-
2
-
-
24644465302
-
Bone structure
-
Martino L, editor. Milan: Elsevier
-
Odgren PR, Gartland A, Mason-Savas A, Marks SC Jr. Bone structure. In: Martino L, editor. Encyclopedia of endocrine diseases. Vol 1. Milan: Elsevier, 2004. p. 392-400.
-
(2004)
Encyclopedia of Endocrine Diseases
, vol.1
, pp. 392-400
-
-
Odgren, P.R.1
Gartland, A.2
Mason-Savas, A.3
Marks Jr., S.C.4
-
3
-
-
4043079307
-
Osteoporosis: A review
-
Lin JT, Lane JM. Osteoporosis: a review. Clin Orthop 2004; 425:126-34.
-
(2004)
Clin Orthop
, vol.425
, pp. 126-134
-
-
Lin, J.T.1
Lane, J.M.2
-
4
-
-
0036797870
-
Molecular genetics of too much bone
-
Janssens K, Van HuI W. Molecular genetics of too much bone. Hum Mol Genet 2002; 11(20):2385-93.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.20
, pp. 2385-2393
-
-
Janssens, K.1
Van Hui, W.2
-
5
-
-
0023025445
-
The osteopetrotic rabbit: General and skeletal features of a new outbred stock
-
Marks SC Jr, Seifert MF, Fox RR. The osteopetrotic rabbit: general and skeletal features of a new outbred stock. Bone 1986; 7(5):359-64.
-
(1986)
Bone
, vol.7
, Issue.5
, pp. 359-364
-
-
Marks Jr., S.C.1
Seifert, M.F.2
Fox, R.R.3
-
6
-
-
0018631124
-
Anemia and osteopetrosis in a dog
-
Lees GE, Sautter JH. Anemia and osteopetrosis in a dog. J Am Vet Med Assoc 1979; 175(8):820-4.
-
(1979)
J Am Vet Med Assoc
, vol.175
, Issue.8
, pp. 820-824
-
-
Lees, G.E.1
Sautter, J.H.2
-
7
-
-
0019333136
-
Hydatidiform moles in Holstein cattle
-
Gopal T, Leipold HW, Dennis SM. Hydatidiform moles in Holstein cattle. Vet Rec 1980; 107(17):395-7.
-
(1980)
Vet Rec
, vol.107
, Issue.17
, pp. 395-397
-
-
Gopal, T.1
Leipold, H.W.2
Dennis, S.M.3
-
8
-
-
0018972928
-
Pathogenesis of virus-induced osteopetrosis in the chicken
-
Smith RE, Ivanyi J. Pathogenesis of virus-induced osteopetrosis in the chicken. J Immunol 1980; 125(2):523-30.
-
(1980)
J Immunol
, vol.125
, Issue.2
, pp. 523-530
-
-
Smith, R.E.1
Ivanyi, J.2
-
9
-
-
0025501874
-
Congenital osteopetrosis in white-tailed deer (Odocoileus virginianus)
-
Smits B, Bubenik GA. Congenital osteopetrosis in white-tailed deer (Odocoileus virginianus). J Wildl Dis 1990; 26(4):567-71.
-
(1990)
J Wildl Dis
, vol.26
, Issue.4
, pp. 567-571
-
-
Smits, B.1
Bubenik, G.A.2
-
10
-
-
0035142015
-
Spontaneous mutation in Mitf gene causes osteopetrosis in silver homozygote quail
-
Kawaguchi N, Ono T, Mochii M, Noda M. Spontaneous mutation in Mitf gene causes osteopetrosis in silver homozygote quail. Dev Dyn 2001; 220(2):133-40.
-
(2001)
Dev Dyn
, vol.220
, Issue.2
, pp. 133-140
-
-
Kawaguchi, N.1
Ono, T.2
Mochii, M.3
Noda, M.4
-
11
-
-
0031907329
-
Role of PU.1 in hematopoiesis
-
Fisher RC, Scott EW. Role of PU.1 in hematopoiesis. Stem Cells 1998; 16(1):25-37.
-
(1998)
Stem Cells
, vol.16
, Issue.1
, pp. 25-37
-
-
Fisher, R.C.1
Scott, E.W.2
-
12
-
-
0028136726
-
Requirement of transcription factor PU.1 in the development of multiple hematopoietic lineages
-
Scott EW, Simon MC, Anastasi J, Singh H. Requirement of transcription factor PU.1 in the development of multiple hematopoietic lineages. Science 1994; 265(5178):1573-7.
-
(1994)
Science
, vol.265
, Issue.5178
, pp. 1573-1577
-
-
Scott, E.W.1
Simon, M.C.2
Anastasi, J.3
Singh, H.4
-
13
-
-
0030933226
-
Osteopetrosis in mice lacking haematopoietic transcription factor PU.1
-
Tondravi MM, McKercher SR, Anderson K, Erdmann JM, Quiroz M, Maki R, et al. Osteopetrosis in mice lacking haematopoietic transcription factor PU.1. Nature 1997; 386(6620):81-4.
-
(1997)
Nature
, vol.386
, Issue.6620
, pp. 81-84
-
-
Tondravi, M.M.1
McKercher, S.R.2
Anderson, K.3
Erdmann, J.M.4
Quiroz, M.5
Maki, R.6
-
14
-
-
0242549003
-
Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities
-
McKercher SR, Torbett BE, Anderson KL, Henkel GW, Vestal DJ, Baribault H, et al. Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities. EMBO J 1996; 15(20):5647-58.
-
(1996)
EMBO J
, vol.15
, Issue.20
, pp. 5647-5658
-
-
McKercher, S.R.1
Torbett, B.E.2
Anderson, K.L.3
Henkel, G.W.4
Vestal, D.J.5
Baribault, H.6
-
15
-
-
0032525250
-
Myeloid development is selectively disrupted in PU.1 null mice
-
Anderson KL, Smith KA, Conners K, McKercher SR, Maki RA, Torbett BE. Myeloid development is selectively disrupted in PU.1 null mice. Blood 1998; 91(10):3702-10.
-
(1998)
Blood
, vol.91
, Issue.10
, pp. 3702-3710
-
-
Anderson, K.L.1
Smith, K.A.2
Conners, K.3
McKercher, S.R.4
Maki, R.A.5
Torbett, B.E.6
-
16
-
-
2642519463
-
Acute myeloid leukemia induced by graded reduction of a lineage-specific transcription factor, PU.1
-
Rosenbauer F, Wagner K, Kutok JL, Iwasaki H, Le Beau MM, Okuno Y, et al. Acute myeloid leukemia induced by graded reduction of a lineage-specific transcription factor, PU.1. Nat Genet 2004; 36(6):624-30.
-
(2004)
Nat Genet
, vol.36
, Issue.6
, pp. 624-630
-
-
Rosenbauer, F.1
Wagner, K.2
Kutok, J.L.3
Iwasaki, H.4
Le Beau, M.M.5
Okuno, Y.6
-
18
-
-
0025332897
-
The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene
-
Yoshida H, Hayashi S, Kunisada T, Ogawa M, Nishikawa S, Okamura H, et al. The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene. Nature 1990; 345(6274):442-4.
-
(1990)
Nature
, vol.345
, Issue.6274
, pp. 442-444
-
-
Yoshida, H.1
Hayashi, S.2
Kunisada, T.3
Ogawa, M.4
Nishikawa, S.5
Okamura, H.6
-
19
-
-
0025622837
-
Molecular biology of macrophage colony-stimulating factor
-
Kawasaki ES, Ladner MB. Molecular biology of macrophage colony-stimulating factor. Immunol Ser 1990; 49:155-76.
-
(1990)
Immunol Ser
, vol.49
, pp. 155-176
-
-
Kawasaki, E.S.1
Ladner, M.B.2
-
20
-
-
0020079296
-
Morphological evidence of reduced bone resorption in osteopetrotic (op) mice
-
Marks SC Jr. Morphological evidence of reduced bone resorption in osteopetrotic (op) mice. Am J Anat 1982; 163(2):157-67.
-
(1982)
Am J Anat
, vol.163
, Issue.2
, pp. 157-167
-
-
Marks Jr., S.C.1
-
21
-
-
0025323482
-
Total absence of colony-stimulating factor 1 in the macrophage-deficient osteopetrotic (op/op) mouse
-
Wiktor-Jedrzejczak W, Bartocci A, Ferrante AW Jr, Ahmed-Ansari A, Sell KW, Pollard JW, et al. Total absence of colony-stimulating factor 1 in the macrophage-deficient osteopetrotic (op/op) mouse. Proc Natl Acad Sci U S A 1990; 87(12):4828-32.
-
(1990)
Proc Natl Acad Sci U S A
, vol.87
, Issue.12
, pp. 4828-4832
-
-
Wiktor-Jedrzejczak, W.1
Bartocci, A.2
Ferrante Jr., A.W.3
Ahmed-Ansari, A.4
Sell, K.W.5
Pollard, J.W.6
-
22
-
-
0029783089
-
Absence of colony-stimulating factor-1 in osteopetrotic (csfmop/csfmop) mice results in male fertility defects
-
Cohen PE, Chisholm O, Arceci RJ, Stanley ER, Pollard JW. Absence of colony-stimulating factor-1 in osteopetrotic (csfmop/csfmop) mice results in male fertility defects. Biol Reprod 1996; 55(2):310-7.
-
(1996)
Biol Reprod
, vol.55
, Issue.2
, pp. 310-317
-
-
Cohen, P.E.1
Chisholm, O.2
Arceci, R.J.3
Stanley, E.R.4
Pollard, J.W.5
-
23
-
-
0000804808
-
Pleiotropic roles for CSF-1 in development defined by the mouse mutation osteopetrotic
-
Pollard JW, Stanley ER. Pleiotropic roles for CSF-1 in development defined by the mouse mutation osteopetrotic. Adv Dev Bioch 1996; 4:153-193.
-
(1996)
Adv Dev Bioch
, vol.4
, pp. 153-193
-
-
Pollard, J.W.1
Stanley, E.R.2
-
24
-
-
10144228401
-
CSF-1 deficiency in mice results in abnormal brain development
-
Michaelson MD, Bieri PL, Mehler MF, Xu H, Arezzo JC, Pollard JW, et al. CSF-1 deficiency in mice results in abnormal brain development. Development 1996; 122(9):2661-72.
-
(1996)
Development
, vol.122
, Issue.9
, pp. 2661-2672
-
-
Michaelson, M.D.1
Bieri, P.L.2
Mehler, M.F.3
Xu, H.4
Arezzo, J.C.5
Pollard, J.W.6
-
25
-
-
0021646131
-
Congenitally osteopetrotic (oplop) mice are not cured by transplants of spleen or bone marrow cells from normal littermates
-
Marks SC Jr, Seifert MF, McGuire JL. Congenitally osteopetrotic (oplop) mice are not cured by transplants of spleen or bone marrow cells from normal littermates. Metab Bone Dis Relat Res 1984; 5(4):183-6.
-
(1984)
Metab Bone Dis Relat Res
, vol.5
, Issue.4
, pp. 183-186
-
-
Marks Jr., S.C.1
Seifert, M.F.2
McGuire, J.L.3
-
26
-
-
0025107432
-
Macrophage colony stimulating factor restores in vivo bone resorption in the op/op osteopetrotic mouse
-
Felix R, Cecchini MG, Fleisch H. Macrophage colony stimulating factor restores in vivo bone resorption in the op/op osteopetrotic mouse. Endocrinology 1990; 127(5):2592-4.
-
(1990)
Endocrinology
, vol.127
, Issue.5
, pp. 2592-2594
-
-
Felix, R.1
Cecchini, M.G.2
Fleisch, H.3
-
27
-
-
0029094162
-
Colony-stimulating factor-1 injections improve but do not cure skeletal sclerosis in osteopetrotic (op) mice
-
Sundquist KT, Cecchini MG, Marks SC Jr. Colony-stimulating factor-1 injections improve but do not cure skeletal sclerosis in osteopetrotic (op) mice. Bone 1995; 16(1):39-46.
-
(1995)
Bone
, vol.16
, Issue.1
, pp. 39-46
-
-
Sundquist, K.T.1
Cecchini, M.G.2
Marks Jr., S.C.3
-
28
-
-
1642541143
-
Incomplete restoration of colony-stimulating factor 1 (CSF-1) function in CSF-1-deficient Csf1op/Csf1op mice by transgenic expression of cell surface CSF-1
-
Dai XM, Zong XH, Sylvestre V, Stanley ER. Incomplete restoration of colony-stimulating factor 1 (CSF-1) function in CSF-1-deficient Csf1op/Csf1op mice by transgenic expression of cell surface CSF-1. Blood 2004; 103(3):1114-23.
-
(2004)
Blood
, vol.103
, Issue.3
, pp. 1114-1123
-
-
Dai, X.M.1
Zong, X.H.2
Sylvestre, V.3
Stanley, E.R.4
-
29
-
-
0027460054
-
Delayed hematopoietic development in osteopetrotic (op/op) mice
-
Begg SK, Radley JM, Pollard JW, Chisholm OT, Stanley ER, Bertoncello I. Delayed hematopoietic development in osteopetrotic (op/op) mice. J Exp Med 1993; 177(1):237-42.
-
(1993)
J Exp Med
, vol.177
, Issue.1
, pp. 237-242
-
-
Begg, S.K.1
Radley, J.M.2
Pollard, J.W.3
Chisholm, O.T.4
Stanley, E.R.5
Bertoncello, I.6
-
30
-
-
2342572812
-
Recruitment of osteoclasts in the mandible of osteopetrotic (op/op) mice
-
Ida-Yonemochi H, Ishibashi O, Sakai H, Saku T. Recruitment of osteoclasts in the mandible of osteopetrotic (op/op) mice. Eur J Oral Sci 2004; 112(2):148-55.
-
(2004)
Eur J Oral Sci
, vol.112
, Issue.2
, pp. 148-155
-
-
Ida-Yonemochi, H.1
Ishibashi, O.2
Sakai, H.3
Saku, T.4
-
31
-
-
0028346644
-
Granulocyte-macrophage colony-stimulating factor corrects macrophage deficiencies, but not osteopetrosis, in the colony-stimulating factor-1-deficient op/ op mouse
-
Wiktor-Jedrzejczak W, Urbanowska E, Szperl M. Granulocyte-macrophage colony-stimulating factor corrects macrophage deficiencies, but not osteopetrosis, in the colony-stimulating factor-1-deficient op/ op mouse. Endocrinology 1994; 134(4):1932-5.
-
(1994)
Endocrinology
, vol.134
, Issue.4
, pp. 1932-1935
-
-
Wiktor-Jedrzejczak, W.1
Urbanowska, E.2
Szperl, M.3
-
32
-
-
0029049021
-
Granulocyte-macrophage colony-stimulating factor is not responsible for the correction of hematopoietic deficiencies in the maturing op/op mouse
-
Nilsson SK, Lieschke GJ, Garcia-Wijnen CC, Williams B, Tzelepis D, Hodgson G, et al. Granulocyte-macrophage colony-stimulating factor is not responsible for the correction of hematopoietic deficiencies in the maturing op/op mouse. Blood 1995; 86(1):66-72.
-
(1995)
Blood
, vol.86
, Issue.1
, pp. 66-72
-
-
Nilsson, S.K.1
Lieschke, G.J.2
Garcia-Wijnen, C.C.3
Williams, B.4
Tzelepis, D.5
Hodgson, G.6
-
33
-
-
0028261070
-
Mice lacking both macrophage- and granulocyte-macrophage colony-stimulating factor have macrophages and coexistent osteopetrosis and severe lung disease
-
Lieschke GJ, Stanley E, Grail D, Hodgson G, Sinickas V, Gall JA, et al. Mice lacking both macrophage- and granulocyte-macrophage colony-stimulating factor have macrophages and coexistent osteopetrosis and severe lung disease. Blood 1994; 84(1):27-35.
-
(1994)
Blood
, vol.84
, Issue.1
, pp. 27-35
-
-
Lieschke, G.J.1
Stanley, E.2
Grail, D.3
Hodgson, G.4
Sinickas, V.5
Gall, J.A.6
-
34
-
-
0028236526
-
Granulocyte/macrophage colony-stimulating factor-deficient mice show no major perturbation of hematopoiesis but develop a characteristic pulmonary pathology
-
Stanley E, Lieschke GJ, Grail D, Metcalf D, Hodgson G, Gall JA, et al. Granulocyte/macrophage colony-stimulating factor-deficient mice show no major perturbation of hematopoiesis but develop a characteristic pulmonary pathology. Proc Natl Acad Sci U S A 1994; 91(12):5592-6.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, Issue.12
, pp. 5592-5596
-
-
Stanley, E.1
Lieschke, G.J.2
Grail, D.3
Metcalf, D.4
Hodgson, G.5
Gall, J.A.6
-
36
-
-
0035525765
-
FLT3 ligand can substitute for macrophage colony-stimulating factor in support of osteoclast differentiation and function
-
Lean JM, Fuller K, Chambers TJ. FLT3 ligand can substitute for macrophage colony-stimulating factor in support of osteoclast differentiation and function. Blood 2001; 98(9):2707-13.
-
(2001)
Blood
, vol.98
, Issue.9
, pp. 2707-2713
-
-
Lean, J.M.1
Fuller, K.2
Chambers, T.J.3
-
37
-
-
0008348421
-
Granulocyte/macrophage colony-stimulating factor and interleukin-3 correct osteopetrosis in mice with osteopetrosis mutation
-
Myint YY, Miyakawa K, Naito M, Shultz LD, Oike Y, Yamamura K, et al. Granulocyte/macrophage colony-stimulating factor and interleukin-3 correct osteopetrosis in mice with osteopetrosis mutation. Am J Pathol 1999; 154(2):553-66.
-
(1999)
Am J Pathol
, vol.154
, Issue.2
, pp. 553-566
-
-
Myint, Y.Y.1
Miyakawa, K.2
Naito, M.3
Shultz, L.D.4
Oike, Y.5
Yamamura, K.6
-
38
-
-
6044270503
-
The origin of hematopoietic cell type diversity
-
Hoang T. The origin of hematopoietic cell type diversity. Oncogene 2004; 23(43):7188-98.
-
(2004)
Oncogene
, vol.23
, Issue.43
, pp. 7188-7198
-
-
Hoang, T.1
-
39
-
-
0346992040
-
Flt3 ligand: Role in control of hematopoietic and immune functions of the bone marrow
-
Wodnar-Filipowicz A. Flt3 ligand: role in control of hematopoietic and immune functions of the bone marrow. News Physiol Sci 2003; 18:247-51.
-
(2003)
News Physiol Sci
, vol.18
, pp. 247-251
-
-
Wodnar-Filipowicz, A.1
-
40
-
-
0033584243
-
Vascular endothelial growth factor can substitute for macrophage colony-stimulating factor in the support of osteoclastic bone resorption
-
Niida S, Kaku M, Amano H, Yoshida H, Kataoka H, Nishikawa S, et al. Vascular endothelial growth factor can substitute for macrophage colony-stimulating factor in the support of osteoclastic bone resorption. J Exp Med 1999; 190(2):293-8.
-
(1999)
J Exp Med
, vol.190
, Issue.2
, pp. 293-298
-
-
Niida, S.1
Kaku, M.2
Amano, H.3
Yoshida, H.4
Kataoka, H.5
Nishikawa, S.6
-
41
-
-
0034640211
-
Vascular endothelial growth factor (VEGF) directly enhances osteoclastic bone resorption and survival of mature osteoclasts
-
Nakagawa M, Kaneda T, Arakawa T, Morita S, Sato T, Yomada T, et al. Vascular endothelial growth factor (VEGF) directly enhances osteoclastic bone resorption and survival of mature osteoclasts. FEBS Lett 2000; 473(2):161-4.
-
(2000)
FEBS Lett
, vol.473
, Issue.2
, pp. 161-164
-
-
Nakagawa, M.1
Kaneda, T.2
Arakawa, T.3
Morita, S.4
Sato, T.5
Yomada, T.6
-
42
-
-
1642485905
-
Estrogen regulates the production of VEGF for osteoclast formation and activity in op/op mice
-
Kodama I, Niida S, Sanada M, Yoshiko Y, Tsuda M, Maeda N, et al. Estrogen regulates the production of VEGF for osteoclast formation and activity in op/op mice. J Bone Miner Res 2004; 19(2):200-6.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.2
, pp. 200-206
-
-
Kodama, I.1
Niida, S.2
Sanada, M.3
Yoshiko, Y.4
Tsuda, M.5
Maeda, N.6
-
43
-
-
0028931593
-
Is the osteopetrotic (op/op mutant) mouse completely deficient in expression of macrophage colony-stimulating factor?
-
Hume DA, Favot P. Is the osteopetrotic (op/op mutant) mouse completely deficient in expression of macrophage colony-stimulating factor? J Interferon Cytokine Res 1995; 15(4):279-84.
-
(1995)
J Interferon Cytokine Res
, vol.15
, Issue.4
, pp. 279-284
-
-
Hume, D.A.1
Favot, P.2
-
44
-
-
0016257950
-
Unerupted dentition secondary to congenital osteopetrosis in the Osborne-Mendel rat
-
Cotton WR, Gaines JF. Unerupted dentition secondary to congenital osteopetrosis in the Osborne-Mendel rat. Proc Soc Exp Biol Med 1974; 146:554-61.
-
(1974)
Proc Soc Exp Biol Med
, vol.146
, pp. 554-561
-
-
Cotton, W.R.1
Gaines, J.F.2
-
45
-
-
0023719161
-
Skeletal biology in the toothless (osteopetrotic) rat
-
Seifert MF, Popoff SN, Marks SC Jr. Skeletal biology in the toothless (osteopetrotic) rat. Am J Anat 1988; 183(2):158-65.
-
(1988)
Am J Anat
, vol.183
, Issue.2
, pp. 158-165
-
-
Seifert, M.F.1
Popoff, S.N.2
Marks Jr., S.C.3
-
46
-
-
0030668359
-
The effects of colony-stimulating factor-1 on the number and ultrastructure of osteoclasts in toothless (tl) rats and osteopetrotic (op) mice
-
Marks SC Jr, Iizuka T, MacKay CA, Mason-Savas A, Cielinski MJ. The effects of colony-stimulating factor-1 on the number and ultrastructure of osteoclasts in toothless (tl) rats and osteopetrotic (op) mice. Tissue Cell 1997; 29(5):589-95.
-
(1997)
Tissue Cell
, vol.29
, Issue.5
, pp. 589-595
-
-
Marks Jr., S.C.1
Iizuka, T.2
MacKay, C.A.3
Mason-Savas, A.4
Cielinski, M.J.5
-
47
-
-
0030273499
-
Abnormalities in bone cell function and endochondral ossification in the osteopetrotic toothless rat
-
Seifert MF. Abnormalities in bone cell function and endochondral ossification in the osteopetrotic toothless rat. Bone 1996; 19(4):329-38.
-
(1996)
Bone
, vol.19
, Issue.4
, pp. 329-338
-
-
Seifert, M.F.1
-
48
-
-
0032980149
-
The toothless osteopetrotic rat has a normal vitamin D-binding protein-macrophage activating factor (DBP-MAF) cascade and chondrodysplasia resistant to treatments with colony stimulating factor-1 (CSF-1) and/or DBP-MAF
-
Odgren PR, Popoff SN, Safadi FF, MacKay CA, Mason-Savas A, Seifert MF, et al. The toothless osteopetrotic rat has a normal vitamin D-binding protein-macrophage activating factor (DBP-MAF) cascade and chondrodysplasia resistant to treatments with colony stimulating factor-1 (CSF-1) and/or DBP-MAF. Bone 1999; 25(2):175-81.
-
(1999)
Bone
, vol.25
, Issue.2
, pp. 175-181
-
-
Odgren, P.R.1
Popoff, S.N.2
Safadi, F.F.3
MacKay, C.A.4
Mason-Savas, A.5
Seifert, M.F.6
-
49
-
-
0342804274
-
Endochondral bone formation in toothless (osteopetrotic) rats: Failures of chondrocyte patterning and type X collagen expression
-
Marks SC Jr, Lundmark C, Christersson C, Wurtz T, Odgren PR, Seifert MF, et al. Endochondral bone formation in toothless (osteopetrotic) rats: failures of chondrocyte patterning and type X collagen expression. Int J Dev Biol 2000; 44(3):309-16.
-
(2000)
Int J Dev Biol
, vol.44
, Issue.3
, pp. 309-316
-
-
Marks Jr., S.C.1
Lundmark, C.2
Christersson, C.3
Wurtz, T.4
Odgren, P.R.5
Seifert, M.F.6
-
50
-
-
0029084809
-
CSF-1 treatment promotes angiogenesis in the metaphysis of osteopetrotic (toothless, tl) rats
-
Aharinejad S, Marks SC Jr, Bock P, Mason-Savas A, MacKay CA, Larson EK, et al. CSF-1 treatment promotes angiogenesis in the metaphysis of osteopetrotic (toothless, tl) rats. Bone 1995; 16(3):315-24.
-
(1995)
Bone
, vol.16
, Issue.3
, pp. 315-324
-
-
Aharinejad, S.1
Marks Jr., S.C.2
Bock, P.3
Mason-Savas, A.4
MacKay, C.A.5
Larson, E.K.6
-
51
-
-
0031043690
-
Ultrastructural evidence of abnormally short and maldistributed actin stress fibers in osteopetrotic (toothless) rat osteoblasts in situ after detergent perfusion
-
Watanabe H, MacKay CA, Kislauskis E, Mason-Savas A, Marks SC Jr. Ultrastructural evidence of abnormally short and maldistributed actin stress fibers in osteopetrotic (toothless) rat osteoblasts in situ after detergent perfusion. Tissue Cell 1997; 29(1):89-98.
-
(1997)
Tissue Cell
, vol.29
, Issue.1
, pp. 89-98
-
-
Watanabe, H.1
MacKay, C.A.2
Kislauskis, E.3
Mason-Savas, A.4
Marks Jr., S.C.5
-
52
-
-
0031781106
-
Actin mRNA isoforms are differentially sorted in normal osteoblasts and sorting is altered in osteoblasts from a skeletal mutation in the rat
-
Watanabe H, Kislauskis EH, Mackay CA, Mason-Savas A, Marks SC Jr. Actin mRNA isoforms are differentially sorted in normal osteoblasts and sorting is altered in osteoblasts from a skeletal mutation in the rat. J Cell Sci 1998; 111 (Pt 9):1287-92.
-
(1998)
J Cell Sci
, vol.111
, Issue.PART 9
, pp. 1287-1292
-
-
Watanabe, H.1
Kislauskis, E.H.2
Mackay, C.A.3
Mason-Savas, A.4
Marks Jr., S.C.5
-
53
-
-
0029946781
-
Decreased growth hormone receptor expression in long bones from toothless (osteopetrotic) rats and restoration by treatment with colony-stimulating factor-1
-
Symons AL, MacKay CA, Leong K, Hume DA, Waters MJ, Marks SC Jr. Decreased growth hormone receptor expression in long bones from toothless (osteopetrotic) rats and restoration by treatment with colony-stimulating factor-1. Growth Factors 1996; 13(1-2):1-10.
-
(1996)
Growth Factors
, vol.13
, Issue.1-2
, pp. 1-10
-
-
Symons, A.L.1
MacKay, C.A.2
Leong, K.3
Hume, D.A.4
Waters, M.J.5
Marks Jr., S.C.6
-
54
-
-
0032767918
-
Insulin-like growth factor-I (IGF-I) and IGF-I receptor (IGF-IR) immunoreactivity in normal and osteopetrotic (toothless, tl/tl) rat tibia
-
Joseph BK, Marks SC Jr, Hume DA, Waters MJ, Symons AL. Insulin-like growth factor-I (IGF-I) and IGF-I receptor (IGF-IR) immunoreactivity in normal and osteopetrotic (toothless, tl/tl) rat tibia. Growth Factors 1999; 16(4):279-91.
-
(1999)
Growth Factors
, vol.16
, Issue.4
, pp. 279-291
-
-
Joseph, B.K.1
Marks Jr., S.C.2
Hume, D.A.3
Waters, M.J.4
Symons, A.L.5
-
55
-
-
0025237103
-
Elevated 1,25-dihydroxyvitamin D3 and intestinal calbindin-D9k in the toothless rat
-
Seifert MF, Gray RW, Bruns ME. Elevated 1,25-dihydroxyvitamin D3 and intestinal calbindin-D9k in the toothless rat. Am J Physiol 1990; 258(2 Pt 1): E377-81.
-
(1990)
Am J Physiol
, vol.258
, Issue.2 PART 1
-
-
Seifert, M.F.1
Gray, R.W.2
Bruns, M.E.3
-
56
-
-
0017368267
-
Osteopetrosis in the toothless (tl) rat: Presence of osteoclasts but failure to respond to parathyroid extract or to be cured by infusion of spleen or bone marrow cells from normal littermates
-
Marks SC Jr. Osteopetrosis in the toothless (tl) rat: presence of osteoclasts but failure to respond to parathyroid extract or to be cured by infusion of spleen or bone marrow cells from normal littermates. Am J Anat 1977; 149(2):289-97.
-
(1977)
Am J Anat
, vol.149
, Issue.2
, pp. 289-297
-
-
Marks Jr., S.C.1
-
57
-
-
0030436988
-
Reduced bone resorption in toothless (osteopetrotic) rats - An abnormality of osteoblasts related to their inability to activate osteoclast activity in vitro
-
Hermey DC, Popoff SN, Marks SC Jr. Reduced bone resorption in toothless (osteopetrotic) rats-an abnormality of osteoblasts related to their inability to activate osteoclast activity in vitro. Connect Tissue Res 1996; 35(1-4):273-8.
-
(1996)
Connect Tissue Res
, vol.35
, Issue.1-4
, pp. 273-278
-
-
Hermey, D.C.1
Popoff, S.N.2
Marks Jr., S.C.3
-
58
-
-
0026608325
-
Administration of colony stimulating factor-1 corrects some macrophage, dental, and skeletal defects in an osteopetrotic mutation (toothless, tl) in the rat
-
Marks SC Jr, Wojtowicz A, Szperl M, Urbanowska E, MacKay CA, Wiktor-Jedrzejczak W, et al. Administration of colony stimulating factor-1 corrects some macrophage, dental, and skeletal defects in an osteopetrotic mutation (toothless, tl) in the rat. Bone 1992; 13(1):89-93.
-
(1992)
Bone
, vol.13
, Issue.1
, pp. 89-93
-
-
Marks Jr., S.C.1
Wojtowicz, A.2
Szperl, M.3
Urbanowska, E.4
MacKay, C.A.5
Wiktor-Jedrzejczak, W.6
-
59
-
-
0034718609
-
Diverse roles of the tumor necrosis factor family member TRANCE in skeletal physiology revealed by TRANCE deficiency and partial rescue by a lymphocyte-expressed TRANCE transgene
-
Kim N, Odgren PR, Kim DK, Marks SC Jr, Choi Y. Diverse roles of the tumor necrosis factor family member TRANCE in skeletal physiology revealed by TRANCE deficiency and partial rescue by a lymphocyte-expressed TRANCE transgene. Proc Natl Acad Sci U S A 2000; 97(20):10905-10.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, Issue.20
, pp. 10905-10910
-
-
Kim, N.1
Odgren, P.R.2
Kim, D.K.3
Marks Jr., S.C.4
Choi, Y.5
-
60
-
-
0035557103
-
Evidence that the rat osteopetrotic mutation toothless (tl) is not in the TNFSF11 (TRANCE, RANKL, ODF, OPGL) gene
-
Odgren PR, Kim N, van Wesenbeeck L, MacKay C, Mason-Savas A, Safadi FF, et al. Evidence that the rat osteopetrotic mutation toothless (tl) is not in the TNFSF11 (TRANCE, RANKL, ODF, OPGL) gene. Int J Dev Biol 2001; 45(8):853-9.
-
(2001)
Int J Dev Biol
, vol.45
, Issue.8
, pp. 853-859
-
-
Odgren, P.R.1
Kim, N.2
Van Wesenbeeck, L.3
MacKay, C.4
Mason-Savas, A.5
Safadi, F.F.6
-
61
-
-
0037195141
-
The osteopetrotic mutation toothless (tl) is a loss-of-function frameshift mutation in the rat Csf1 gene: Evidence of a crucial role for CSF-1 in osteoclastogenesis and endochondral ossification
-
Van Wesenbeeck L, Odgren PR, MacKay CA, D'Angelo M, Safadi FF, Popoff SN, et al. The osteopetrotic mutation toothless (tl) is a loss-of-function frameshift mutation in the rat Csf1 gene: Evidence of a crucial role for CSF-1 in osteoclastogenesis and endochondral ossification. Proc Natl Acad Sci U S A 2002; 99(22):14303-8.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, Issue.22
, pp. 14303-14308
-
-
Van Wesenbeeck, L.1
Odgren, P.R.2
MacKay, C.A.3
D'Angelo, M.4
Safadi, F.F.5
Popoff, S.N.6
-
62
-
-
0036288682
-
Mutation of macrophage colony stimulating factor (Csf1) causes osteopetrosis in the tl rat
-
Dobbins DE, Sood R, Hashiramoto A, Hansen CT, Wilder RL, Remmers EF. Mutation of macrophage colony stimulating factor (Csf1) causes osteopetrosis in the tl rat. Biochem Biophys Res Commun 2002; 294(5):1114-20.
-
(2002)
Biochem Biophys Res Commun
, vol.294
, Issue.5
, pp. 1114-1120
-
-
Dobbins, D.E.1
Sood, R.2
Hashiramoto, A.3
Hansen, C.T.4
Wilder, R.L.5
Remmers, E.F.6
-
63
-
-
0036092801
-
OTargeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects
-
Dai XM, Ryan GR, Hapel AJ, Dominguez MG, Russell RG, Kapp S, et al. oTargeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects. Blood 2002; 99(1):111-20.
-
(2002)
Blood
, vol.99
, Issue.1
, pp. 111-120
-
-
Dai, X.M.1
Ryan, G.R.2
Hapel, A.J.3
Dominguez, M.G.4
Russell, R.G.5
Kapp, S.6
-
64
-
-
15544373018
-
Osteoclast deficiency results in disorganized matrix, reduced mineralization, and abnormal osteoblast behavior in developing bone
-
Dai XM, Zong XH, Akhter MP, Stanley ER. Osteoclast deficiency results in disorganized matrix, reduced mineralization, and abnormal osteoblast behavior in developing bone. J Bone Miner Res 2004; 19(9):1441-51.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.9
, pp. 1441-1451
-
-
Dai, X.M.1
Zong, X.H.2
Akhter, M.P.3
Stanley, E.R.4
-
65
-
-
0036838919
-
Functions of API (Fos/Jun) in bone development
-
Wagner EF. Functions of API (Fos/Jun) in bone development. Ann Rheum Dis 2002; 61 Suppl 2: ii40-2.
-
(2002)
Ann Rheum Dis
, vol.61
, Issue.SUPPL. 2
-
-
Wagner, E.F.1
-
66
-
-
0142249497
-
Signalling in osteoclasts and the role of Fos/AP1 proteins
-
Wagner EF, Matsuo K. Signalling in osteoclasts and the role of Fos/AP1 proteins. Ann Rheum Dis 2003; 62 Suppl 2:ii83-5.
-
(2003)
Ann Rheum Dis
, vol.62
, Issue.SUPPL. 2
-
-
Wagner, E.F.1
Matsuo, K.2
-
67
-
-
3142592253
-
Osteoclasts, mononuclear phagocytes, and c-Fos: New insight into osteoimmunology
-
Matsuo K, Ray N. Osteoclasts, mononuclear phagocytes, and c-Fos: new insight into osteoimmunology. Keio J Med 2004; 53(2):78-84.
-
(2004)
Keio J Med
, vol.53
, Issue.2
, pp. 78-84
-
-
Matsuo, K.1
Ray, N.2
-
68
-
-
0027070472
-
Bone and haematopoietic defects in mice lacking c-fos
-
Wang ZC, Ovitt C, Grigoriadis AE, Mohle-Steinlein U, Ruther U, Wagner EF. Bone and haematopoietic defects in mice lacking c-fos. Nature 1992; 360(6406):741-5.
-
(1992)
Nature
, vol.360
, Issue.6406
, pp. 741-745
-
-
Wang, Z.C.1
Ovitt, C.2
Grigoriadis, A.E.3
Mohle-Steinlein, U.4
Ruther, U.5
Wagner, E.F.6
-
69
-
-
0026486816
-
Pleiotropic effects of a null mutation in the c-fos protooncogene
-
Johnson RS, Spiegelman BM, Papaioannou V. Pleiotropic effects of a null mutation in the c-fos protooncogene. Cell 1992; 71(4):577-86.
-
(1992)
Cell
, vol.71
, Issue.4
, pp. 577-586
-
-
Johnson, R.S.1
Spiegelman, B.M.2
Papaioannou, V.3
-
70
-
-
0028173214
-
C-Fos: A key regulator of osteoclast-macrophage lineage determination and bone remodeling
-
Grigoriadis AE, Wang ZQ, Cecchini MG, Hofstetter W, Felix R, Fleisch HA, et al. c-Fos: a key regulator of osteoclast-macrophage lineage determination and bone remodeling. Science 1994; 266(5184) :443-8.
-
(1994)
Science
, vol.266
, Issue.5184
, pp. 443-448
-
-
Grigoriadis, A.E.1
Wang, Z.Q.2
Cecchini, M.G.3
Hofstetter, W.4
Felix, R.5
Fleisch, H.A.6
-
71
-
-
0033621698
-
Fosl1 is a transcriptional target of c-Fos during osteoclast differentiation
-
Matsuo K, Owens JM, Tonko M, Elliott C, Chambers TJ, Wagner EF. Fosl1 is a transcriptional target of c-Fos during osteoclast differentiation. Nat Genet 2000; 24(2):184-7.
-
(2000)
Nat Genet
, vol.24
, Issue.2
, pp. 184-187
-
-
Matsuo, K.1
Owens, J.M.2
Tonko, M.3
Elliott, C.4
Chambers, T.J.5
Wagner, E.F.6
-
72
-
-
0034312317
-
Fra-1 replaces c-Fos-dependent functions in mice
-
Fleischmann A, Hafezi F, Elliott C, Reme CE, Ruther U, Wagner EF. Fra-1 replaces c-Fos-dependent functions in mice. Genes Dev 2000; 14(21):2695-700.
-
(2000)
Genes Dev
, vol.14
, Issue.21
, pp. 2695-2700
-
-
Fleischmann, A.1
Hafezi, F.2
Elliott, C.3
Reme, C.E.4
Ruther, U.5
Wagner, E.F.6
-
73
-
-
0027219303
-
A null mutation at the c-jun locus causes embryonic lethality and retarded cell growth in culture
-
Johnson RS, van Lingen B, Papaioannou VE, Spiegelman BM. A null mutation at the c-jun locus causes embryonic lethality and retarded cell growth in culture. Genes Dev 1993; 7(7B):1309-17.
-
(1993)
Genes Dev
, vol.7
, Issue.7 B
, pp. 1309-1317
-
-
Johnson, R.S.1
Van Lingen, B.2
Papaioannou, V.E.3
Spiegelman, B.M.4
-
74
-
-
4344697340
-
Critical roles of c-Jun signaling in regulation of NFAT family and RANKL-regulated osteoclast differentiation
-
Ikeda F, Nishimura R, Matsubara T, Tanaka S, Inoue J, Reddy SV, et al. Critical roles of c-Jun signaling in regulation of NFAT family and RANKL-regulated osteoclast differentiation. J Clin Invest 2004; 114(4):475-84.
-
(2004)
J Clin Invest
, vol.114
, Issue.4
, pp. 475-484
-
-
Ikeda, F.1
Nishimura, R.2
Matsubara, T.3
Tanaka, S.4
Inoue, J.5
Reddy, S.V.6
-
75
-
-
0035206443
-
Minireview: The OPG/RANKL/RANK system
-
Khosla S. Minireview: the OPG/RANKL/RANK system. Endocrinology 2001; 142(12):5050-5.
-
(2001)
Endocrinology
, vol.142
, Issue.12
, pp. 5050-5055
-
-
Khosla, S.1
-
76
-
-
0033611467
-
OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis
-
Kong YY, Yoshida H, Sarosi I, Tan HL, Timms E, Capparelli C, et al. OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis. Nature 1999; 397(6717):315-23.
-
(1999)
Nature
, vol.397
, Issue.6717
, pp. 315-323
-
-
Kong, Y.Y.1
Yoshida, H.2
Sarosi, I.3
Tan, H.L.4
Timms, E.5
Capparelli, C.6
-
77
-
-
0037443533
-
RANK ligand and osteoprotegerin in myeloma bone disease
-
Sezer O, Heider U, Zavrski I, Kuhne CA, Hofbauer LC. RANK ligand and osteoprotegerin in myeloma bone disease. Blood 2003; 101(6):2094-8.
-
(2003)
Blood
, vol.101
, Issue.6
, pp. 2094-2098
-
-
Sezer, O.1
Heider, U.2
Zavrski, I.3
Kuhne, C.A.4
Hofbauer, L.C.5
-
78
-
-
4143082697
-
New insight in the mechanism of osteoclast activation and formation in multiple myeloma: Focus on the receptor activator of NF-kappaB ligand (RANKL)
-
Giuliani N, Colla S, Rizzoli V. New insight in the mechanism of osteoclast activation and formation in multiple myeloma: focus on the receptor activator of NF-kappaB ligand (RANKL). Exp Hematol 2004; 32(8):685-91.
-
(2004)
Exp Hematol
, vol.32
, Issue.8
, pp. 685-691
-
-
Giuliani, N.1
Colla, S.2
Rizzoli, V.3
-
79
-
-
12944262423
-
RANK is the intrinsic hematopoietic cell surface receptor that controls osteoclastogenesis and regulation of bone mass and calcium metabolism
-
Li J, Sarosi I, Yan XQ, Morony S, Capparelli C, Tan HL, et al. RANK is the intrinsic hematopoietic cell surface receptor that controls osteoclastogenesis and regulation of bone mass and calcium metabolism. Proc Natl Acad Sci U S A 2000; 97(4):1566-71.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, Issue.4
, pp. 1566-1571
-
-
Li, J.1
Sarosi, I.2
Yan, X.Q.3
Morony, S.4
Capparelli, C.5
Tan, H.L.6
-
80
-
-
0033568341
-
RANK is essential for osteoclast and lymph node development
-
Dougall WC, Glaccum M, Charrier K, Rohrbach K, Brasel K, De Smedt T, et al. RANK is essential for osteoclast and lymph node development. Genes Dev 1999; 13(18):2412-24.
-
(1999)
Genes Dev
, vol.13
, Issue.18
, pp. 2412-2424
-
-
Dougall, W.C.1
Glaccum, M.2
Charrier, K.3
Rohrbach, K.4
Brasel, K.5
De Smedt, T.6
-
81
-
-
21644469447
-
Malignant autosomal recessive osteopetrosis caused by spontaneous mutation of murine rank
-
Kapur RP, Yao Z, Iida MH, Clarke CM, Doggett B, Xing L, et al. Malignant autosomal recessive osteopetrosis caused by spontaneous mutation of murine rank. J Bone Miner Res 2004; 19(10):1689-1697.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.10
, pp. 1689-1697
-
-
Kapur, R.P.1
Yao, Z.2
Iida, M.H.3
Clarke, C.M.4
Doggett, B.5
Xing, L.6
-
82
-
-
0031005576
-
Osteoprotegerin: A novel secreted protein involved in the regulation of bone density
-
Simonet WS, Lacey DL, Dunstan CR, Kelley M, Chang MS, Luthy R, et al. Osteoprotegerin: a novel secreted protein involved in the regulation of bone density. Cell 1997; 89(2):309-19.
-
(1997)
Cell
, vol.89
, Issue.2
, pp. 309-319
-
-
Simonet, W.S.1
Lacey, D.L.2
Dunstan, C.R.3
Kelley, M.4
Chang, M.S.5
Luthy, R.6
-
83
-
-
0032079445
-
Osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification
-
Bucay N, Sarosi I, Dunstan CR, Morony S, Tarpley J, Capparelli C, et al. osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification. Genes Dev 1998; 12(9):1260-8.
-
(1998)
Genes Dev
, vol.12
, Issue.9
, pp. 1260-1268
-
-
Bucay, N.1
Sarosi, I.2
Dunstan, C.R.3
Morony, S.4
Tarpley, J.5
Capparelli, C.6
-
84
-
-
0032577903
-
Severe osteoporosis in mice lacking osteoclastogenesis inhibitory factor/osteoprotegerin
-
Mizuno A, Amizuka N, Irie K, Murakami A, Fujise N, Kanno T, et al. Severe osteoporosis in mice lacking osteoclastogenesis inhibitory factor/ osteoprotegerin. Biochem Biophys Res Commun 1998; 247(3):610-5.
-
(1998)
Biochem Biophys Res Commun
, vol.247
, Issue.3
, pp. 610-615
-
-
Mizuno, A.1
Amizuka, N.2
Irie, K.3
Murakami, A.4
Fujise, N.5
Kanno, T.6
-
85
-
-
0037314230
-
Osteopetrosis and thalamic hypomyelinosis with synaptic degeneration in DAP12-deficient mice
-
Kaifu T, Nakahara J, Inui M, Mishima K, Momiyama T, Kaji M, et al. Osteopetrosis and thalamic hypomyelinosis with synaptic degeneration in DAP12-deficient mice. J Clin Invest 2003; 111(3):323-32.
-
(2003)
J Clin Invest
, vol.111
, Issue.3
, pp. 323-332
-
-
Kaifu, T.1
Nakahara, J.2
Inui, M.3
Mishima, K.4
Momiyama, T.5
Kaji, M.6
-
86
-
-
1642526619
-
The signaling adapter protein DAP12 regulates multinucleation during osteoclast development
-
Humphrey MB, Ogasawara K, Yao W, Spusta SC, Daws MR, Lane NE, et al. The signaling adapter protein DAP12 regulates multinucleation during osteoclast development. J Bone Miner Res 2004; 19(2):224-34.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.2
, pp. 224-234
-
-
Humphrey, M.B.1
Ogasawara, K.2
Yao, W.3
Spusta, S.C.4
Daws, M.R.5
Lane, N.E.6
-
87
-
-
11144354330
-
Costimulatory signals mediated by the ITAM motif cooperate with RANKL for bone homeostasis
-
Koga T, Inui M, Inoue K, Kim S, Suematsu A, Kobayashi E, et al. Costimulatory signals mediated by the ITAM motif cooperate with RANKL for bone homeostasis. Nature 2004; 428(6984):758-63.
-
(2004)
Nature
, vol.428
, Issue.6984
, pp. 758-763
-
-
Koga, T.1
Inui, M.2
Inoue, K.3
Kim, S.4
Suematsu, A.5
Kobayashi, E.6
-
88
-
-
11144355389
-
The immunomodulatory adapter proteins DAP12 and Fc receptor gamma-chain (FcRgamma) regulate development of functional osteoclasts through the Syk tyrosine kinase
-
Mocsai A, Humphrey MB, Van Ziffle JA, Hu Y, Burghardt A, Spusta SC, et al. The immunomodulatory adapter proteins DAP12 and Fc receptor gamma-chain (FcRgamma) regulate development of functional osteoclasts through the Syk tyrosine kinase. Proc Natl Acad Sci U S A 2004; 101(16):6158-63.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, Issue.16
, pp. 6158-6163
-
-
Mocsai, A.1
Humphrey, M.B.2
Van Ziffle, J.A.3
Hu, Y.4
Burghardt, A.5
Spusta, S.C.6
-
89
-
-
0038706164
-
Signal transduction by receptor activator of nuclear factor kappa B in osteoclasts
-
Lee ZH, Kim HH. Signal transduction by receptor activator of nuclear factor kappa B in osteoclasts. Biochem Biophys Res Commun 2003; 305(2):211-4.
-
(2003)
Biochem Biophys Res Commun
, vol.305
, Issue.2
, pp. 211-214
-
-
Lee, Z.H.1
Kim, H.H.2
-
90
-
-
0037673945
-
Osteoclast differentiation and activation
-
Boyle WJ, Simonet WS, Lacey DL. Osteoclast differentiation and activation. Nature 2003; 423(6937):337-42.
-
(2003)
Nature
, vol.423
, Issue.6937
, pp. 337-42
-
-
Boyle, W.J.1
Simonet, W.S.2
Lacey, D.L.3
-
91
-
-
0027427492
-
Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair
-
Veis DJ, Sorenson CM, Shutter JR, Korsmeyer SJ. Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair. Cell 1993; 75(2):229-40.
-
(1993)
Cell
, vol.75
, Issue.2
, pp. 229-240
-
-
Veis, D.J.1
Sorenson, C.M.2
Shutter, J.R.3
Korsmeyer, S.J.4
-
92
-
-
0034503091
-
The ITAM-bearing transmembrane adaptor DAP12 in lymphoid and myeloid cell function
-
Lanier LL, Bakker AB. The ITAM-bearing transmembrane adaptor DAP12 in lymphoid and myeloid cell function. Immunol Today 2000; 21(12):611-4.
-
(2000)
Immunol Today
, vol.21
, Issue.12
, pp. 611-614
-
-
Lanier, L.L.1
Bakker, A.B.2
-
94
-
-
0037148508
-
A novel member of the leukocyte receptor complex regulates osteoclast differentiation
-
Kim N, Takami M, Rho J, Josien R, Choi Y. A novel member of the leukocyte receptor complex regulates osteoclast differentiation. J Exp Med 2002; 195(2):201-9.
-
(2002)
J Exp Med
, vol.195
, Issue.2
, pp. 201-209
-
-
Kim, N.1
Takami, M.2
Rho, J.3
Josien, R.4
Choi, Y.5
-
95
-
-
3242665399
-
Involvement of FcRgamma in signal transduction of osteoclast-associated receptor (OSCAR)
-
157
-
Ishikawa S, Arase N, Suenaga T, Saita Y, Noda M, Kuriyama T, et al. Involvement of FcRgamma in signal transduction of osteoclast-associated receptor (OSCAR). Int Immunol 2004; 16(7):1019-25.157
-
(2004)
Int Immunol
, vol.16
, Issue.7
, pp. 1019-1025
-
-
Ishikawa, S.1
Arase, N.2
Suenaga, T.3
Saita, Y.4
Noda, M.5
Kuriyama, T.6
-
96
-
-
18744366041
-
Induction and activation of the transcription factor NFATc1 (NFAT2) integrate RANKL signaling in terminal differentiation of osteoclasts
-
Takayanagi H, Kim S, Koga T, Nishina H, Isshiki M, Yoshida H, et al. Induction and activation of the transcription factor NFATc1 (NFAT2) integrate RANKL signaling in terminal differentiation of osteoclasts. Dev Cell 2002; 3(6):889-901.
-
(2002)
Dev Cell
, vol.3
, Issue.6
, pp. 889-901
-
-
Takayanagi, H.1
Kim, S.2
Koga, T.3
Nishina, H.4
Isshiki, M.5
Yoshida, H.6
-
97
-
-
0035475338
-
Tumor necrosis factor receptor-associated factors (TRAFs)
-
Bradley JR, Pober JS. Tumor necrosis factor receptor-associated factors (TRAFs). Oncogene 2001; 20(44):6482-91.
-
(2001)
Oncogene
, vol.20
, Issue.44
, pp. 6482-6491
-
-
Bradley, J.R.1
Pober, J.S.2
-
98
-
-
0034752285
-
TRAF1 is a negative regulator of TNF signaling. Enhanced TNF signaling in TRAF1-deficient mice
-
Tsitsikov EN, Laouini D, Dunn IF, Sannikova TY, Davidson L, Alt FW, et al. TRAF1 is a negative regulator of TNF signaling. Enhanced TNF signaling in TRAF1-deficient mice. Immunity 2001; 15(4):647-57.
-
(2001)
Immunity
, vol.15
, Issue.4
, pp. 647-657
-
-
Tsitsikov, E.N.1
Laouini, D.2
Dunn, I.F.3
Sannikova, T.Y.4
Davidson, L.5
Alt, F.W.6
-
99
-
-
0033889001
-
TRAF4 deficiency leads to tracheal malformation with resulting alterations in air flow to the lungs
-
Shiels H, Li X, Schumacker PT, Maltepe E, Padrid PA, Sperling A, et al. TRAF4 deficiency leads to tracheal malformation with resulting alterations in air flow to the lungs. Am J Pathol 2000; 157(2):679-88.
-
(2000)
Am J Pathol
, vol.157
, Issue.2
, pp. 679-688
-
-
Shiels, H.1
Li, X.2
Schumacker, P.T.3
Maltepe, E.4
Padrid, P.A.5
Sperling, A.6
-
100
-
-
0033578329
-
Targeted disruption of Traf5 gene causes defects in CD40- and CD27-mediated lymphocyte activation
-
Nakano H, Sakon S, Koseki H, Takemori T, Tada K, Matsumoto M, et al. Targeted disruption of Traf5 gene causes defects in CD40- and CD27-mediated lymphocyte activation. Proc Natl Acad Sci U S A 1999; 96(17):9803-8.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, Issue.17
, pp. 9803-9808
-
-
Nakano, H.1
Sakon, S.2
Koseki, H.3
Takemori, T.4
Tada, K.5
Matsumoto, M.6
-
101
-
-
0033561039
-
TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling
-
Lomaga MA, Yeh WC, Sarosi I, Duncan GS, Furlonger C, Ho A, et al. TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling. Genes Dev 1999; 13(8):1015-24.
-
(1999)
Genes Dev
, vol.13
, Issue.8
, pp. 1015-1024
-
-
Lomaga, M.A.1
Yeh, W.C.2
Sarosi, I.3
Duncan, G.S.4
Furlonger, C.5
Ho, A.6
-
102
-
-
6544270833
-
Severe osteopetrosis, defective interleukin-1 signalling and lymph node organogenesis in TRAF6-deficient mice
-
Naito A, Azuma S, Tanaka S, Miyazaki T, Takaki S, Takatsu K, et al. Severe osteopetrosis, defective interleukin-1 signalling and lymph node organogenesis in TRAF6-deficient mice. Genes Cells 1999; 4(6):353-62.
-
(1999)
Genes Cells
, vol.4
, Issue.6
, pp. 353-362
-
-
Naito, A.1
Azuma, S.2
Tanaka, S.3
Miyazaki, T.4
Takaki, S.5
Takatsu, K.6
-
103
-
-
0037113931
-
A RANK/TRAF6-dependent signal transduction pathway is essential for osteoclast cytoskeletal organization and resorptive function
-
Armstrong AP, Tometsko ME, Glaccum M, Sutherland CL, Cosman D, Dougall WC. A RANK/TRAF6-dependent signal transduction pathway is essential for osteoclast cytoskeletal organization and resorptive function. J Biol Chem 2002; 277(46):44347-56.
-
(2002)
J Biol Chem
, vol.277
, Issue.46
, pp. 44347-44356
-
-
Armstrong, A.P.1
Tometsko, M.E.2
Glaccum, M.3
Sutherland, C.L.4
Cosman, D.5
Dougall, W.C.6
-
104
-
-
0029874138
-
The NF-kappa B and I kappa B proteins: New discoveries and insights
-
Baldwin AS Jr. The NF-kappa B and I kappa B proteins: new discoveries and insights. Annu Rev Immunol 1996; 14:649-83.
-
(1996)
Annu Rev Immunol
, vol.14
, pp. 649-683
-
-
Baldwin Jr., A.S.1
-
105
-
-
0028804551
-
Targeted disruption of the p50 subunit of NF-kappa B leads to multifocal defects in immune responses
-
Sha WC, Liou HC, Tuomanen EI, Baltimore D. Targeted disruption of the p50 subunit of NF-kappa B leads to multifocal defects in immune responses. Cell 1995; 80(2):321-30.
-
(1995)
Cell
, vol.80
, Issue.2
, pp. 321-330
-
-
Sha, W.C.1
Liou, H.C.2
Tuomanen, E.I.3
Baltimore, D.4
-
106
-
-
0031964855
-
Mice deficient in nuclear factor (NF)-kappa B/p52 present with defects in humoral responses, germinal center reactions, and splenic microarchitecrure
-
Franzoso G, Carlson L, Poljak L, Shores EW, Epstein S, Leonardi A, et al. Mice deficient in nuclear factor (NF)-kappa B/p52 present with defects in humoral responses, germinal center reactions, and splenic microarchitecrure. J Exp Med 1998; 187(2):147-59.
-
(1998)
J Exp Med
, vol.187
, Issue.2
, pp. 147-159
-
-
Franzoso, G.1
Carlson, L.2
Poljak, L.3
Shores, E.W.4
Epstein, S.5
Leonardi, A.6
-
107
-
-
0030715563
-
Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2
-
Iotsova V, Caamano J, Loy J, Yang Y, Lewin A, Bravo R. Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2. Nat Med 1997; 3(11):1285-9.
-
(1997)
Nat Med
, vol.3
, Issue.11
, pp. 1285-1289
-
-
Iotsova, V.1
Caamano, J.2
Loy, J.3
Yang, Y.4
Lewin, A.5
Bravo, R.6
-
108
-
-
15444357762
-
Requirement for NF-kappaB in osteoclast and B-cell development
-
Franzoso G, Carlson L, Xing L, Poljak L, Shores EW, Brown KD, et al. Requirement for NF-kappaB in osteoclast and B-cell development. Genes Dev 1997; 11(24):3482-96.
-
(1997)
Genes Dev
, vol.11
, Issue.24
, pp. 3482-3496
-
-
Franzoso, G.1
Carlson, L.2
Xing, L.3
Poljak, L.4
Shores, E.W.5
Brown, K.D.6
-
109
-
-
0036085510
-
NF-kappaB p50 and p52 expression is not required for RANK-expressing osteoclast progenitor formation but is essential for RANK- and cytokine-mediated osteoclastogenesis
-
Xing L, Bushnell TP, Carlson L, Tai Z, Tondravi M, Siebenlist U, et al. NF-kappaB p50 and p52 expression is not required for RANK-expressing osteoclast progenitor formation but is essential for RANK- and cytokine-mediated osteoclastogenesis. J Bone Miner Res 2002; 17(7):1200-10.
-
(2002)
J Bone Miner Res
, vol.17
, Issue.7
, pp. 1200-1210
-
-
Xing, L.1
Bushnell, T.P.2
Carlson, L.3
Tai, Z.4
Tondravi, M.5
Siebenlist, U.6
-
110
-
-
0028789866
-
Insight into the microphthalmia gene
-
Moore KJ. Insight into the microphthalmia gene. Trends Genet 1995; 11(11):442-8.
-
(1995)
Trends Genet
, vol.11
, Issue.11
, pp. 442-448
-
-
Moore, K.J.1
-
111
-
-
0027204149
-
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
-
Hodgkinson CA, Moore KJ, Nakayama A, Steingrimsson E, Copeland NG, Jenkins NA, et al. Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 1993; 74(2):395-404.
-
(1993)
Cell
, vol.74
, Issue.2
, pp. 395-404
-
-
Hodgkinson, C.A.1
Moore, K.J.2
Nakayama, A.3
Steingrimsson, E.4
Copeland, N.G.5
Jenkins, N.A.6
-
112
-
-
0015813915
-
The osteopetrotic syndrome in the microphthalmic mutant mouse
-
Murphy HM. The osteopetrotic syndrome in the microphthalmic mutant mouse. Calcif Tissue Res 1973; 13(1):19-26.
-
(1973)
Calcif Tissue Res
, vol.13
, Issue.1
, pp. 19-26
-
-
Murphy, H.M.1
-
113
-
-
0028879371
-
Mild osteopetrosis in the microphthalmia-oak ridge mouse. A model for intermediate autosomal recessive osteopetrosis in humans
-
Nii A, Steingrimsson E, Copeland NG, Jenkins NA, Ward JM. Mild osteopetrosis in the microphthalmia-oak ridge mouse. A model for intermediate autosomal recessive osteopetrosis in humans. Am J Pathol 1995; 147(6):1871-82.
-
(1995)
Am J Pathol
, vol.147
, Issue.6
, pp. 1871-1882
-
-
Nii, A.1
Steingrimsson, E.2
Copeland, N.G.3
Jenkins, N.A.4
Ward, J.M.5
-
114
-
-
0028091741
-
Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences
-
Steingrimsson E, Moore KJ, Lamoreux ML, Ferre-D'Amare AR, Burley SK, Zimring DC, et al. Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences. Nat Genet 1994; 8(3):256-63.
-
(1994)
Nat Genet
, vol.8
, Issue.3
, pp. 256-263
-
-
Steingrimsson, E.1
Moore, K.J.2
Lamoreux, M.L.3
Ferre-D'Amare, A.R.4
Burley, S.K.5
Zimring, D.C.6
-
115
-
-
0028062014
-
Microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family
-
Hemesath TJ, Steingrimsson E, McGill G, Hansen MJ, Vaught J, Hodgkinson CA, et al. microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family. Genes Dev 1994; 8(22):2770-80.
-
(1994)
Genes Dev
, vol.8
, Issue.22
, pp. 2770-2780
-
-
Hemesath, T.J.1
Steingrimsson, E.2
McGill, G.3
Hansen, M.J.4
Vaught, J.5
Hodgkinson, C.A.6
-
116
-
-
0016811449
-
Bone resorption restored in osteopetrotic mice by transplants of normal bone marrow and spleen cells
-
Walker DG. Bone resorption restored in osteopetrotic mice by transplants of normal bone marrow and spleen cells. Science 1975; 190(4216):784-5.
-
(1975)
Science
, vol.190
, Issue.4216
, pp. 784-785
-
-
Walker, D.G.1
-
117
-
-
0016700933
-
Spleen cells transmit osteopetrosis in mice
-
Walker DG. Spleen cells transmit osteopetrosis in mice. Science 1975; 190(4216):785-7.
-
(1975)
Science
, vol.190
, Issue.4216
, pp. 785-787
-
-
Walker, D.G.1
-
118
-
-
0019348074
-
The ultrastructure of osteoclasts in microphthalmic mice
-
Holtrop ME, Cox KA, Eilon G, Simmons HA, Raisz LG. The ultrastructure of osteoclasts in microphthalmic mice. Metab Bone Dis Relat Res 1981; 3(2):123-9.
-
(1981)
Metab Bone Dis Relat Res
, vol.3
, Issue.2
, pp. 123-129
-
-
Holtrop, M.E.1
Cox, K.A.2
Eilon, G.3
Simmons, H.A.4
Raisz, L.G.5
-
119
-
-
0022007383
-
Fusion disability of embryonic osteoclast precursor cells and macrophages in the microphthalmic osteopetrotic mouse
-
Thesingh CW, Scherft JP. Fusion disability of embryonic osteoclast precursor cells and macrophages in the microphthalmic osteopetrotic mouse. Bone 1985; 6(1):43-52.
-
(1985)
Bone
, vol.6
, Issue.1
, pp. 43-52
-
-
Thesingh, C.W.1
Scherft, J.P.2
-
120
-
-
0037007031
-
Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development
-
Steingrimsson E, Tessarollo L, Pathak B, Hou L, Arnheiter H, Copeland NG, et al. Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development. Proc Natl Acad Sci U S A 2002; 99(7):4477-82.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, Issue.7
, pp. 4477-4482
-
-
Steingrimsson, E.1
Tessarollo, L.2
Pathak, B.3
Hou, L.4
Arnheiter, H.5
Copeland, N.G.6
-
121
-
-
0034052945
-
The microphthalmia transcription factor regulates expression of the tartrate-resistant acid phosphatase gene during terminal differentiation of osteoclasts
-
Luchin A, Purdom G, Murphy K, Clark MY, Angel N, Cassady AI, et al. The microphthalmia transcription factor regulates expression of the tartrate-resistant acid phosphatase gene during terminal differentiation of osteoclasts. J Bone Miner Res 2000; 15(3):451-60.
-
(2000)
J Bone Miner Res
, vol.15
, Issue.3
, pp. 451-460
-
-
Luchin, A.1
Purdom, G.2
Murphy, K.3
Clark, M.Y.4
Angel, N.5
Cassady, A.I.6
-
122
-
-
0035826866
-
Linking osteopetrosis and pycnodysostosis: Regulation of cathepsin K expression by the microphthalmia transcription factor family
-
Motyckova G, Weilbaecher KN, Horstmann M, Rieman DJ, Fisher DZ, Fisher DE. Linking osteopetrosis and pycnodysostosis: regulation of cathepsin K expression by the microphthalmia transcription factor family. Proc Natl Acad Sci U S A 2001; 98(10):5798-803.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, Issue.10
, pp. 5798-5803
-
-
Motyckova, G.1
Weilbaecher, K.N.2
Horstmann, M.3
Rieman, D.J.4
Fisher, D.Z.5
Fisher, D.E.6
-
123
-
-
18444418797
-
Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability
-
McGill GG, Horstmann M, Widlund HR, Du J, Motyckova G, Nishimura EK, et al. Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability. Cell 2002; 109(6):707-18.
-
(2002)
Cell
, vol.109
, Issue.6
, pp. 707-718
-
-
McGill, G.G.1
Horstmann, M.2
Widlund, H.R.3
Du, J.4
Motyckova, G.5
Nishimura, E.K.6
-
124
-
-
0025507537
-
Early and transient osteopetrosis in microphthalmic MIB-rats
-
Wojtowicz A, Moutier R, Grzesik W, Dziedzic-Goclawska A, Lamendin H, Ostrowski K. Early and transient osteopetrosis in microphthalmic MIB-rats. Arch Ital Anat Embriol 1990; 95(3-4):209-21.
-
(1990)
Arch Ital Anat Embriol
, vol.95
, Issue.3-4
, pp. 209-221
-
-
Wojtowicz, A.1
Moutier, R.2
Grzesik, W.3
Dziedzic-Goclawska, A.4
Lamendin, H.5
Ostrowski, K.6
-
125
-
-
0029149487
-
Bone metabolism in the osteopetrotic rat mutation microphthalmia blanc
-
Cielinski MJ, Marks SC Jr. Bone metabolism in the osteopetrotic rat mutation microphthalmia blanc. Bone 1995; 16(5):567-74.
-
(1995)
Bone
, vol.16
, Issue.5
, pp. 567-574
-
-
Cielinski, M.J.1
Marks Jr., S.C.2
-
126
-
-
0032473407
-
Age-resolving osteopetrosis: A rat model implicating microphthalmia and the related transcription factor TFE3
-
Weilbaecher KN, Hershey CL, Takemoto CM, Horstmann MA, Hemesath TJ, Tashjian AH, et al. Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3. J Exp Med 1998; 187(5):775-85.
-
(1998)
J Exp Med
, vol.187
, Issue.5
, pp. 775-785
-
-
Weilbaecher, K.N.1
Hershey, C.L.2
Takemoto, C.M.3
Horstmann, M.A.4
Hemesath, T.J.5
Tashjian, A.H.6
-
127
-
-
0031928169
-
The rat microphthalmia-associated transcription factor gene (Mitf) maps at 4q34-q41 and is mutated in the mib rats
-
Opdecamp K, Vanvooren P, Riviere M, Arnheiter H, Motta R, Szpirer J, et al. The rat microphthalmia-associated transcription factor gene (Mitf) maps at 4q34-q41 and is mutated in the mib rats. Mamm Genome 1998; 9(8):617-21.
-
(1998)
Mamm Genome
, vol.9
, Issue.8
, pp. 617-621
-
-
Opdecamp, K.1
Vanvooren, P.2
Riviere, M.3
Arnheiter, H.4
Motta, R.5
Szpirer, J.6
-
128
-
-
0032523187
-
Spontaneous transdifferentiation of quail pigmented epithelial cell is accompanied by a mutation in the Mitf gene
-
Mochii M, Ono T, Matsubara Y, Eguchi G. Spontaneous transdifferentiation of quail pigmented epithelial cell is accompanied by a mutation in the Mitf gene. Dev Biol 1998; 196(2):145-59.
-
(1998)
Dev Biol
, vol.196
, Issue.2
, pp. 145-159
-
-
Mochii, M.1
Ono, T.2
Matsubara, Y.3
Eguchi, G.4
-
129
-
-
0036423664
-
Formation and function of the ruffled border in osteoclasts
-
Stenbeck G. Formation and function of the ruffled border in osteoclasts. Semin Cell Dev Biol 2002; 13(4):285-92.
-
(2002)
Semin Cell Dev Biol
, vol.13
, Issue.4
, pp. 285-292
-
-
Stenbeck, G.1
-
130
-
-
0031439247
-
Cellular functions regulated by Src family kinases
-
Thomas SM, Brugge JS. Cellular functions regulated by Src family kinases. Annu Rev Cell Dev Biol 1997; 13:513-609.
-
(1997)
Annu Rev Cell Dev Biol
, vol.13
, pp. 513-609
-
-
Thomas, S.M.1
Brugge, J.S.2
-
131
-
-
0026023289
-
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
-
Soriano P, Montgomery C, Geske R, Bradley A. Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice. Cell 1991; 64(4):693-702.
-
(1991)
Cell
, vol.64
, Issue.4
, pp. 693-702
-
-
Soriano, P.1
Montgomery, C.2
Geske, R.3
Bradley, A.4
-
132
-
-
0027318189
-
Osteopetrosis in Src-deficient mice is due to an autonomous defect of osteoclasts
-
Lowe C, Yoneda T, Boyce BF, Chen H, Mundy GR, Soriano P. Osteopetrosis in Src-deficient mice is due to an autonomous defect of osteoclasts. Proc Natl Acad Sci U S A 1993; 90(10):4485-9.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, Issue.10
, pp. 4485-4489
-
-
Lowe, C.1
Yoneda, T.2
Boyce, B.F.3
Chen, H.4
Mundy, G.R.5
Soriano, P.6
-
133
-
-
0026612467
-
Requirement of pp60c-src expression for osteoclasts to form ruffled borders and resorb bone in mice
-
Boyce BF, Yoneda T, Lowe C, Soriano P, Mundy GR. Requirement of pp60c-src expression for osteoclasts to form ruffled borders and resorb bone in mice. J Clin Invest 1992; 90(4):1622-7.
-
(1992)
J Clin Invest
, vol.90
, Issue.4
, pp. 1622-1627
-
-
Boyce, B.F.1
Yoneda, T.2
Lowe, C.3
Soriano, P.4
Mundy, G.R.5
-
134
-
-
0033766934
-
Progressive increase in bone mass and development of odontomas in aging osteopetrotic c-src-deficient mice
-
Amling M, Neff L, Priemel M, Schilling AF, Rueger JM, Baron R. Progressive increase in bone mass and development of odontomas in aging osteopetrotic c-src-deficient mice. Bone 2000; 27(5):603-10.
-
(2000)
Bone
, vol.27
, Issue.5
, pp. 603-610
-
-
Amling, M.1
Neff, L.2
Priemel, M.3
Schilling, A.F.4
Rueger, J.M.5
Baron, R.6
-
136
-
-
0035862994
-
Genetic evidence for a role for Src family kinases in TNF family receptor signaling and cell survival
-
Xing L, Venegas AM, Chen A, Garrett-Beal L, Boyce BF, Varmus HE, et al. Genetic evidence for a role for Src family kinases in TNF family receptor signaling and cell survival. Genes Dev 2001; 15(2):241-53.
-
(2001)
Genes Dev
, vol.15
, Issue.2
, pp. 241-253
-
-
Xing, L.1
Venegas, A.M.2
Chen, A.3
Garrett-Beal, L.4
Boyce, B.F.5
Varmus, H.E.6
-
137
-
-
2342442847
-
Src kinase activity is essential for osteoclast function
-
Miyazaki T, Sanjay A, Neff L, Tanaka S, Home WC, Baron R. Src kinase activity is essential for osteoclast function. J Biol Chem 2004; 279(17):17660-6.
-
(2004)
J Biol Chem
, vol.279
, Issue.17
, pp. 17660-17666
-
-
Miyazaki, T.1
Sanjay, A.2
Neff, L.3
Tanaka, S.4
Home, W.C.5
Baron, R.6
-
138
-
-
0026770377
-
Integrins: Versatility, modulation, and signaling in cell adhesion
-
Hynes RO. Integrins: versatility, modulation, and signaling in cell adhesion. Cell 1992; 69(1):11-25.
-
(1992)
Cell
, vol.69
, Issue.1
, pp. 11-25
-
-
Hynes, R.O.1
-
139
-
-
0029087897
-
Function and regulation of the beta 3 integrins in hemostasis and vascular biology
-
Shattil SJ. Function and regulation of the beta 3 integrins in hemostasis and vascular biology. Thromb Haemost 1995; 74(1):149-55.
-
(1995)
Thromb Haemost
, vol.74
, Issue.1
, pp. 149-155
-
-
Shattil, S.J.1
-
140
-
-
0034194652
-
Integrins and signaling in osteoclast function
-
Duong LT, Lakkakorpi P, Nakamura I, Rodan GA. Integrins and signaling in osteoclast function. Matrix Biol 2000; 19(2):97-105.
-
(2000)
Matrix Biol
, vol.19
, Issue.2
, pp. 97-105
-
-
Duong, L.T.1
Lakkakorpi, P.2
Nakamura, I.3
Rodan, G.A.4
-
141
-
-
0032590042
-
Beta3-integrin-deficient mice are a model for Glanzmann thrombasthenia showing placental defects and reduced survival
-
Hodivala-Dilke KM, McHugh KP, Tsakiris DA, Rayburn H, Crowley D, Ullman-Cullere M, et al. Beta3-integrin-deficient mice are a model for Glanzmann thrombasthenia showing placental defects and reduced survival. J Clin Invest 1999; 103(2):229-38.
-
(1999)
J Clin Invest
, vol.103
, Issue.2
, pp. 229-238
-
-
Hodivala-Dilke, K.M.1
McHugh, K.P.2
Tsakiris, D.A.3
Rayburn, H.4
Crowley, D.5
Ullman-Cullere, M.6
-
142
-
-
0033621890
-
Mice lacking beta3 integrins are osteosclerotic because of dysfunctional osteoclasts
-
McHugh KP, Hodivala-Dilke K, Zheng MH, Namba N, Lam J, Novack D, et al. Mice lacking beta3 integrins are osteosclerotic because of dysfunctional osteoclasts. J Clin Invest 2000; 105(4):433-40.
-
(2000)
J Clin Invest
, vol.105
, Issue.4
, pp. 433-440
-
-
McHugh, K.P.1
Hodivala-Dilke, K.2
Zheng, M.H.3
Namba, N.4
Lam, J.5
Novack, D.6
-
143
-
-
0035015396
-
A Glanzmann's mutation in beta 3 integrin specifically impairs osteoclast function
-
Feng X, Novack DV, Faccio R, Ory DS, Aya K, Boyer MI, et al. A Glanzmann's mutation in beta 3 integrin specifically impairs osteoclast function. J Clin Invest 2001; 107(9):1137-44.
-
(2001)
J Clin Invest
, vol.107
, Issue.9
, pp. 1137-1144
-
-
Feng, X.1
Novack, D.V.2
Faccio, R.3
Ory, D.S.4
Aya, K.5
Boyer, M.I.6
-
144
-
-
0033994430
-
The cell biology of osteoclast function
-
Vaananen HK, Zhao H, Mulari M, Halleen JM. The cell biology of osteoclast function. J Cell Sci 2000; 113(Pt 3):377-81.
-
(2000)
J Cell Sci
, vol.113
, Issue.PART 3
, pp. 377-381
-
-
Vaananen, H.K.1
Zhao, H.2
Mulari, M.3
Halleen, J.M.4
-
145
-
-
0032748995
-
Atp6i-deficient mice exhibit severe osteopetrosis due to loss of osteoclast-mediated extracellular acidification
-
Li YP, Chen W, Liang Y, Li E, Stashenko P. Atp6i-deficient mice exhibit severe osteopetrosis due to loss of osteoclast-mediated extracellular acidification. Nat Genet 1999; 23(4):447-51.
-
(1999)
Nat Genet
, vol.23
, Issue.4
, pp. 447-451
-
-
Li, Y.P.1
Chen, W.2
Liang, Y.3
Li, E.4
Stashenko, P.5
-
146
-
-
0021949202
-
Morphological evidence of reduced bone resorption in the osteosclerotic (oc) mouse
-
Seifert MF, Marks SC Jr. Morphological evidence of reduced bone resorption in the osteosclerotic (oc) mouse. Am J Anat 1985; 172(2):141-53.
-
(1985)
Am J Anat
, vol.172
, Issue.2
, pp. 141-153
-
-
Seifert, M.F.1
Marks Jr., S.C.2
-
147
-
-
0023100637
-
Congenitally osteosclerotic (oc/oc) mice are resistant to cure by transplantation of bone marrow or spleen cells from normal littermates
-
Seifert MF, Marks SC Jr. Congenitally osteosclerotic (oc/oc) mice are resistant to cure by transplantation of bone marrow or spleen cells from normal littermates. Tissue Cell 1987; 19(1):29-37.
-
(1987)
Tissue Cell
, vol.19
, Issue.1
, pp. 29-37
-
-
Seifert, M.F.1
Marks Jr., S.C.2
-
148
-
-
0023113981
-
Failure of normal osteoclasts to resorb calcified cartilage from osteosclerotic (oc/oc) mice in vitro
-
Van Slyke MA, Marks SC Jr. Failure of normal osteoclasts to resorb calcified cartilage from osteosclerotic (oc/oc) mice in vitro. Bone 1987; 8(1):39-44.
-
(1987)
Bone
, vol.8
, Issue.1
, pp. 39-44
-
-
Van Slyke, M.A.1
Marks Jr., S.C.2
-
149
-
-
0023023080
-
Congenital murine osteopetrosis inherited with osteosclerotic (oc) gene: Hematological characterization
-
Wiktor-Jedrzejczak W, Szczylik C, Ratajczak MZ, Ahmed A. Congenital murine osteopetrosis inherited with osteosclerotic (oc) gene: hematological characterization. Exp Hematol 1986; 14(9):819-26.
-
(1986)
Exp Hematol
, vol.14
, Issue.9
, pp. 819-826
-
-
Wiktor-Jedrzejczak, W.1
Szczylik, C.2
Ratajczak, M.Z.3
Ahmed, A.4
-
150
-
-
0026740979
-
Lack of bone resorption in osteosclerotic (oc/oc) mice is due to a defect in osteoclast progenitors rather than the local microenvironment provided by osteoblastic cells
-
Udagawa N, Sasald T, Akatsu T, Takahashi N, Tanaka S, Tamura T, et al. Lack of bone resorption in osteosclerotic (oc/oc) mice is due to a defect in osteoclast progenitors rather than the local microenvironment provided by osteoblastic cells. Biochem Biophys Res Commun 1992; 184(1):67-72.
-
(1992)
Biochem Biophys Res Commun
, vol.184
, Issue.1
, pp. 67-72
-
-
Udagawa, N.1
Sasald, T.2
Akatsu, T.3
Takahashi, N.4
Tanaka, S.5
Tamura, T.6
-
151
-
-
18344407785
-
The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants
-
Scimeca JC, Franchi A, Trojani C, Parrinello H, Grosgeorge J, Robert C, et al. The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants. Bone 2000; 26(3):207-13.
-
(2000)
Bone
, vol.26
, Issue.3
, pp. 207-213
-
-
Scimeca, J.C.1
Franchi, A.2
Trojani, C.3
Parrinello, H.4
Grosgeorge, J.5
Robert, C.6
-
152
-
-
0031015595
-
Lack of vacuolar proton ATPase association with the cytoskeleton in osteoclasts of osteosclerotic (oc/oc) mice
-
Nakamura I, Takahashi N, Udagawa N, Moriyama Y, Kurokawa T, Jimi E, et al. Lack of vacuolar proton ATPase association with the cytoskeleton in osteoclasts of osteosclerotic (oc/oc) mice. FEBS Lett 1997; 401(2-3):207-12.
-
(1997)
FEBS Lett
, vol.401
, Issue.2-3
, pp. 207-212
-
-
Nakamura, I.1
Takahashi, N.2
Udagawa, N.3
Moriyama, Y.4
Kurokawa, T.5
Jimi, E.6
-
153
-
-
0035951282
-
Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man
-
Kornak U, Kasper D, Bosl MR, Kaiser E, Schweizer M, Schulz A, et al. Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man. Cell 2001; 104(2):205-15.
-
(2001)
Cell
, vol.104
, Issue.2
, pp. 205-215
-
-
Kornak, U.1
Kasper, D.2
Bosl, M.R.3
Kaiser, E.4
Schweizer, M.5
Schulz, A.6
-
155
-
-
0032506007
-
Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice
-
Saftig P, Hunziker E, Wehmeyer O, Jones S, Boyde A, Rommerskirch W, et al. Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice. Proc Natl Acad Sci U S A 1998; 95(23):13453-8.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, Issue.23
, pp. 13453-13458
-
-
Saftig, P.1
Hunziker, E.2
Wehmeyer, O.3
Jones, S.4
Boyde, A.5
Rommerskirch, W.6
-
156
-
-
0032859323
-
Cathepsin K knockout mice develop osteopetrosis due to a deficit in matrix degradation but not demineralization
-
Gowen M, Lazner F, Dodds R, Kapadia R, Feild J, Tavaria M, et al. Cathepsin K knockout mice develop osteopetrosis due to a deficit in matrix degradation but not demineralization. J Bone Miner Res 1999; 14(10):1654-63.
-
(1999)
J Bone Miner Res
, vol.14
, Issue.10
, pp. 1654-1663
-
-
Gowen, M.1
Lazner, F.2
Dodds, R.3
Kapadia, R.4
Feild, J.5
Tavaria, M.6
-
157
-
-
0142178312
-
Potential function for the ROS-generating activity of TRACP
-
Halleen JM, Raisanen SR, Alatalo SL, Vaananen HK. Potential function for the ROS-generating activity of TRACP. J Bone Miner Res 2003; 18(10):1908-11.
-
(2003)
J Bone Miner Res
, vol.18
, Issue.10
, pp. 1908-1911
-
-
Halleen, J.M.1
Raisanen, S.R.2
Alatalo, S.L.3
Vaananen, H.K.4
-
158
-
-
0142178314
-
TRACP as an osteopontin phosphatase
-
Andersson G, Ek-Rylander B, Hollberg K, Ljusberg-Sjolander J, Lang P, Norgard M, et al. TRACP as an osteopontin phosphatase. J Bone Miner Res 2003; 18(10):1912-5.
-
(2003)
J Bone Miner Res
, vol.18
, Issue.10
, pp. 1912-1915
-
-
Andersson, G.1
Ek-Rylander, B.2
Hollberg, K.3
Ljusberg-Sjolander, J.4
Lang, P.5
Norgard, M.6
-
159
-
-
0029851956
-
Mice lacking tartrate-resistant acid phosphatase (Acp 5) have disrupted endochondral ossification and mild osteopetrosis
-
Hayman AR, Jones SJ, Boyde A, Foster D, Colledge WH, Carlton MB, et al. Mice lacking tartrate-resistant acid phosphatase (Acp 5) have disrupted endochondral ossification and mild osteopetrosis. Development 1996; 122(10):3151-62.
-
(1996)
Development
, vol.122
, Issue.10
, pp. 3151-3162
-
-
Hayman, A.R.1
Jones, S.J.2
Boyde, A.3
Foster, D.4
Colledge, W.H.5
Carlton, M.B.6
-
160
-
-
0036405426
-
Osteoclasts from mice deficient in tartrate-resistant acid phosphatase have altered ruffled borders and disturbed intracellular vesicular transport
-
Hollberg K, Hultenby K, Hayman A, Cox T, Andersson G. Osteoclasts from mice deficient in tartrate-resistant acid phosphatase have altered ruffled borders and disturbed intracellular vesicular transport. Exp Cell Res 2002; 279(2):227-38.
-
(2002)
Exp Cell Res
, vol.279
, Issue.2
, pp. 227-238
-
-
Hollberg, K.1
Hultenby, K.2
Hayman, A.3
Cox, T.4
Andersson, G.5
-
161
-
-
0142178313
-
Tartrate-resistant acid phosphatase knockout mice
-
Hayman AR, Cox TM. Tartrate-resistant acid phosphatase knockout mice. J Bone Miner Res 2003; 18(10):1905-7.
-
(2003)
J Bone Miner Res
, vol.18
, Issue.10
, pp. 1905-1907
-
-
Hayman, A.R.1
Cox, T.M.2
-
162
-
-
14844313875
-
Intracellular machinery for matrix degradation in bone-resorbing osteoclasts
-
Vaaraniemi J, Halleen JM, Kaarlonen K, Ylipahkala H, Alatalo SL, Andersson G, et al. Intracellular machinery for matrix degradation in bone-resorbing osteoclasts. J Bone Miner Res 2004; 19(9):1432-40.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.9
, pp. 1432-1440
-
-
Vaaraniemi, J.1
Halleen, J.M.2
Kaarlonen, K.3
Ylipahkala, H.4
Alatalo, S.L.5
Andersson, G.6
-
163
-
-
0142240453
-
Regulation of the murine TRACP gene promoter
-
Cassady AI, Luchin A, Ostrowski MC, Hume DA. Regulation of the murine TRACP gene promoter. J Bone Miner Res 2003; 18(10):1901-4.
-
(2003)
J Bone Miner Res
, vol.18
, Issue.10
, pp. 1901-1904
-
-
Cassady, A.I.1
Luchin, A.2
Ostrowski, M.C.3
Hume, D.A.4
-
164
-
-
0030792031
-
Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system
-
Saftig P, Hartmann D, Lullmann-Rauch R, Wolff J, Evers M, Koster A, et al. Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system. J Biol Chem 1997; 272(30):18628-35.
-
(1997)
J Biol Chem
, vol.272
, Issue.30
, pp. 18628-18635
-
-
Saftig, P.1
Hartmann, D.2
Lullmann-Rauch, R.3
Wolff, J.4
Evers, M.5
Koster, A.6
-
165
-
-
0035208079
-
Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient mice
-
Suter A, Everts V, Boyde A, Jones SJ, Lullmann-Rauch R, Hartmann D, et al. Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient mice. Development 2001; 128(23):4899-910.
-
(2001)
Development
, vol.128
, Issue.23
, pp. 4899-4910
-
-
Suter, A.1
Everts, V.2
Boyde, A.3
Jones, S.J.4
Lullmann-Rauch, R.5
Hartmann, D.6
-
166
-
-
0035047413
-
The mouse osteopetrotic grey-lethal mutation induces a defect in osteoclast maturation/function
-
Rajapurohitam V, Chalhoub N, Benachenhou N, Neff L, Baron R, Vacher J. The mouse osteopetrotic grey-lethal mutation induces a defect in osteoclast maturation/function. Bone 2001; 28(5):513-23.
-
(2001)
Bone
, vol.28
, Issue.5
, pp. 513-523
-
-
Rajapurohitam, V.1
Chalhoub, N.2
Benachenhou, N.3
Neff, L.4
Baron, R.5
Vacher, J.6
-
167
-
-
0037393446
-
Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human
-
Chalhoub N, Benachenhou N, Rajapurohitam V, Pata M, Ferron M, Frattini A, et al. Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human. Nat Med 2003; 9(4):399-406.
-
(2003)
Nat Med
, vol.9
, Issue.4
, pp. 399-406
-
-
Chalhoub, N.1
Benachenhou, N.2
Rajapurohitam, V.3
Pata, M.4
Ferron, M.5
Frattini, A.6
-
168
-
-
0037478669
-
Promotion of G alpha i3 subunit down-regulation by GIPN, a putative E3 ubiquitin ligase that interacts with RGS-GAIP
-
Fischer T, De Vries L, Meerloo T, Farquhar MG. Promotion of G alpha i3 subunit down-regulation by GIPN, a putative E3 ubiquitin ligase that interacts with RGS-GAIP. Proc Natl Acad Sci U S A 2003; 100(14):8270-5.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, Issue.14
, pp. 8270-8275
-
-
Fischer, T.1
De Vries, L.2
Meerloo, T.3
Farquhar, M.G.4
-
169
-
-
0031710927
-
RGS-GAIP, a GTPase-activating protein for Galphai heterotrimeric G proteins, is located on clathrin-coated vesicles
-
De Vries L, Elenko E, McCaffery JM, Fischer T, Hubler L, McQuistan T, et al. RGS-GAIP, a GTPase-activating protein for Galphai heterotrimeric G proteins, is located on clathrin-coated vesicles. Mol Biol Cell 1998; 9(5):1123-34.
-
(1998)
Mol Biol Cell
, vol.9
, Issue.5
, pp. 1123-1134
-
-
De Vries, L.1
Elenko, E.2
McCaffery, J.M.3
Fischer, T.4
Hubler, L.5
McQuistan, T.6
-
171
-
-
0024427435
-
Osteoclast biology in the osteopetrotic (op) rat
-
Marks SC Jr, Popoff SN. Osteoclast biology in the osteopetrotic (op) rat. Am J Anat 1989; 186(4):325-34.
-
(1989)
Am J Anat
, vol.186
, Issue.4
, pp. 325-334
-
-
Marks Jr., S.C.1
Popoff, S.N.2
-
173
-
-
0030449258
-
Localization of the gene responsible for the op (osteopetrotic) defect in rats on chromosome 10
-
Remmers EF, Du Y, Ding YP, Kotake S, Ge L, Zha H, et al. Localization of the gene responsible for the op (osteopetrotic) defect in rats on chromosome 10. J Bone Miner Res 1996; 11(12):1856-61.
-
(1996)
J Bone Miner Res
, vol.11
, Issue.12
, pp. 1856-1861
-
-
Remmers, E.F.1
Du, Y.2
Ding, Y.P.3
Kotake, S.4
Ge, L.5
Zha, H.6
-
174
-
-
0036785367
-
Localization of the mutation responsible for osteopetrosis in the op rat to a 1.5-cM genetic interval on rat chromosome 10: Identification of positional candidate genes by radiation hybrid mapping
-
Dobbins DE, Joe B, Hashiramoto A, Salstrom JL, Dracheva S, Ge L, et al. Localization of the mutation responsible for osteopetrosis in the op rat to a 1.5-cM genetic interval on rat chromosome 10: identification of positional candidate genes by radiation hybrid mapping. J Bone Miner Res 2002; 17(10):1761-7.
-
(2002)
J Bone Miner Res
, vol.17
, Issue.10
, pp. 1761-1767
-
-
Dobbins, D.E.1
Joe, B.2
Hashiramoto, A.3
Salstrom, J.L.4
Dracheva, S.5
Ge, L.6
-
175
-
-
0015889762
-
Pathogenesis of osteopetrosis in the ia rat: Reduced bone resorption due to reduced osteoclast function
-
Marks SC Jr. Pathogenesis of osteopetrosis in the ia rat: reduced bone resorption due to reduced osteoclast function. Am J Anat 1973; 138(2):165-89.
-
(1973)
Am J Anat
, vol.138
, Issue.2
, pp. 165-189
-
-
Marks Jr., S.C.1
-
176
-
-
0017113477
-
Osteopetrosis in the IA rat cured by spleen cells from a normal littermate
-
Marks SC Jr. Osteopetrosis in the IA rat cured by spleen cells from a normal littermate. Am J Anat 1976; 146(3):331-8.
-
(1976)
Am J Anat
, vol.146
, Issue.3
, pp. 331-338
-
-
Marks Jr., S.C.1
-
177
-
-
0033568206
-
Extensive clear zone and defective ruffled border formation in osteoclasts of osteopetrotic (ia/ia) rats: Implications for secretory function
-
Reinholt FP, Hultenby K, Heinegard D, Marks SC Jr, Norgard M, Anderson G. Extensive clear zone and defective ruffled border formation in osteoclasts of osteopetrotic (ia/ia) rats: implications for secretory function. Exp Cell Res 1999; 251(2):477-91.
-
(1999)
Exp Cell Res
, vol.251
, Issue.2
, pp. 477-491
-
-
Reinholt, F.P.1
Hultenby, K.2
Heinegard, D.3
Marks Jr., S.C.4
Norgard, M.5
Anderson, G.6
-
178
-
-
1642526675
-
Localization of the gene causing the osteopetrotic phenotype in the incisors absent (ia) rat on chromosome 10q32.1
-
Van Wesenbeeck L, Odgren PR, Mackay CA, Van Hul W. Localization of the gene causing the osteopetrotic phenotype in the incisors absent (ia) rat on chromosome 10q32.1. J Bone Miner Res 2004; 19(2):183-9.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.2
, pp. 183-189
-
-
Van Wesenbeeck, L.1
Odgren, P.R.2
Mackay, C.A.3
Van Hul, W.4
-
179
-
-
0023114684
-
The osteopetrotic rabbit: Skeletal cytology and ultrastructure
-
Marks SC Jr, MacKay CA, Seifert MF. The osteopetrotic rabbit: skeletal cytology and ultrastructure. Am J Anat 1987; 178(3):300-7.
-
(1987)
Am J Anat
, vol.178
, Issue.3
, pp. 300-307
-
-
Marks Jr., S.C.1
MacKay, C.A.2
Seifert, M.F.3
-
180
-
-
0025316220
-
Defective osteoclast differentiation and function in the osteopetrotic (os) rabbit
-
Lenhard S, Popoff SN, Marks SC Jr. Defective osteoclast differentiation and function in the osteopetrotic (os) rabbit. Am J Anat 1990; 188(4):438-44.
-
(1990)
Am J Anat
, vol.188
, Issue.4
, pp. 438-444
-
-
Lenhard, S.1
Popoff, S.N.2
Marks Jr., S.C.3
-
181
-
-
0025992035
-
Congenitally osteosderotic (os/os) rabbits are not cured by bone marrow transplantation from normal littermates
-
Popoff SN, Marks SC Jr. Congenitally osteosderotic (os/os) rabbits are not cured by bone marrow transplantation from normal littermates. Am J Anat 1991; 192(3):274-80.
-
(1991)
Am J Anat
, vol.192
, Issue.3
, pp. 274-280
-
-
Popoff, S.N.1
Marks Jr., S.C.2
-
182
-
-
0017401403
-
Animal model: Osteopetrosis in Angus and Hereford calves
-
Leipold HW, Cook JE. Animal model: osteopetrosis in Angus and Hereford calves. Am J Pathol 1977; 86(3):745-8.
-
(1977)
Am J Pathol
, vol.86
, Issue.3
, pp. 745-748
-
-
Leipold, H.W.1
Cook, J.E.2
-
184
-
-
0001690310
-
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification
-
Sly WS, Hewett-Emmett D, Whyte MP, Yu YS, Tashian RE. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. Proc Natl Acad Sci U S A 1983; 80(9):2752-6.
-
(1983)
Proc Natl Acad Sci U S A
, vol.80
, Issue.9
, pp. 2752-2756
-
-
Sly, W.S.1
Hewett-Emmett, D.2
Whyte, M.P.3
Yu, Y.S.4
Tashian, R.E.5
-
185
-
-
0024121523
-
N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: An animal model for human carbonic anhydrase II deficiency syndrome
-
Lewis SE, Erickson RP, Barnett LB, Venta PJ, Tashian RE. N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome. Proc Natl Acad Sci U S A 1988; 85(6):1962-6.
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, Issue.6
, pp. 1962-1966
-
-
Lewis, S.E.1
Erickson, R.P.2
Barnett, L.B.3
Venta, P.J.4
Tashian, R.E.5
-
186
-
-
0021284365
-
The value of inherited deficiencies of human carbonic anhydrase isozymes in understanding their cellular roles
-
Tashian RE, Hewett-Emmett D, Dodgson SJ, Forster RE 2nd, Sly WS. The value of inherited deficiencies of human carbonic anhydrase isozymes in understanding their cellular roles. Ann N Y Acad Sci 1984; 429:262-75.
-
(1984)
Ann N Y Acad Sci
, vol.429
, pp. 262-275
-
-
Tashian, R.E.1
Hewett-Emmett, D.2
Dodgson, S.J.3
Forster II, R.E.4
Sly, W.S.5
-
187
-
-
0034641590
-
Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosis
-
Kornak U, Schulz A, Friedrich W, Uhlhaas S, Kremens B, Voit T, et al. Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosis. Hum Mol Genet 2000; 9(13):2059-63.
-
(2000)
Hum Mol Genet
, vol.9
, Issue.13
, pp. 2059-2063
-
-
Kornak, U.1
Schulz, A.2
Friedrich, W.3
Uhlhaas, S.4
Kremens, B.5
Voit, T.6
-
188
-
-
0033946477
-
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis
-
Frattini A, Orchard PJ, Sobacchi C, Giliani S, Abinun M, Mattsson JP, et al. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. Nat Genet 2000; 25(3):343-6.
-
(2000)
Nat Genet
, vol.25
, Issue.3
, pp. 343-346
-
-
Frattini, A.1
Orchard, P.J.2
Sobacchi, C.3
Giliani, S.4
Abinun, M.5
Mattsson, J.P.6
-
189
-
-
0022461459
-
Lethal osteopetrosis with multiple fractures in utero
-
el Khazen N, Faverly D, Vamos E, Van Regemorter N, Flament-Durand J, Carton B, et al. Lethal osteopetrosis with multiple fractures in utero. Am J Med Genet 1986; 23(3):811-9.
-
(1986)
Am J Med Genet
, vol.23
, Issue.3
, pp. 811-819
-
-
Khazen, N.1
Faverly, D.2
Vamos, E.3
Van Regemorter, N.4
Flament-Durand, J.5
Carton, B.6
-
190
-
-
0036137583
-
Macrophage colony-stimulating factor and receptor activator NF-kappaB ligand fail to rescue osteoclast-poor human malignant infantile osteopetrosis in vitro
-
Flanagan AM, Massey HM, Wilson C, Vellodi A, Horton MA, Steward CG. Macrophage colony-stimulating factor and receptor activator NF-kappaB ligand fail to rescue osteoclast-poor human malignant infantile osteopetrosis in vitro. Bone 2002; 30(1):85-90.
-
(2002)
Bone
, vol.30
, Issue.1
, pp. 85-90
-
-
Flanagan, A.M.1
Massey, H.M.2
Wilson, C.3
Vellodi, A.4
Horton, M.A.5
Steward, C.G.6
-
191
-
-
0019195835
-
Osteopetrosis: Further heterogeneity
-
Horton WA, Schimke RN, Iyama T. Osteopetrosis: further heterogeneity. J Pediatr 1980; 97(4):580-5.
-
(1980)
J Pediatr
, vol.97
, Issue.4
, pp. 580-585
-
-
Horton, W.A.1
Schimke, R.N.2
Iyama, T.3
-
192
-
-
0033987358
-
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis
-
Hughes AE, Ralston SH, Marken J, Bell C, MacPherson H, Wallace RG, et al. Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis. Nat Genet 2000; 24(1):45-8.
-
(2000)
Nat Genet
, vol.24
, Issue.1
, pp. 45-48
-
-
Hughes, A.E.1
Ralston, S.H.2
Marken, J.3
Bell, C.4
MacPherson, H.5
Wallace, R.G.6
-
193
-
-
0036133351
-
Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis
-
Whyte MP, Hughes AE. Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis. J Bone Miner Res 2002; 17(1):26-9.
-
(2002)
J Bone Miner Res
, vol.17
, Issue.1
, pp. 26-29
-
-
Whyte, M.P.1
Hughes, A.E.2
-
194
-
-
0037130183
-
Osteoprotegerin deficiency and juvenile Paget's disease
-
Whyte MP, Obrecht SE, Finnegan PM, Jones JL, Podgornik MN, McAlister WH, et al. Osteoprotegerin deficiency and juvenile Paget's disease. N Engl J Med 2002; 347(3):175-84.
-
(2002)
N Engl J Med
, vol.347
, Issue.3
, pp. 175-184
-
-
Whyte, M.P.1
Obrecht, S.E.2
Finnegan, P.M.3
Jones, J.L.4
Podgornik, M.N.5
McAlister, W.H.6
-
195
-
-
18544371504
-
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
-
Cundy T, Hegde M, Naot D, Chong B, King A, Wallace R, et al. A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype. Hum Mol Genet 2002; 11(18):2119-27.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.18
, pp. 2119-2127
-
-
Cundy, T.1
Hegde, M.2
Naot, D.3
Chong, B.4
King, A.5
Wallace, R.6
-
196
-
-
0033945864
-
Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts
-
Paloneva J, Kestila M, Wu J, Salminen A, Bohling T, Ruotsalainen V, et al. Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts. Nat Genet 2000; 25(3):357-61.
-
(2000)
Nat Genet
, vol.25
, Issue.3
, pp. 357-361
-
-
Paloneva, J.1
Kestila, M.2
Wu, J.3
Salminen, A.4
Bohling, T.5
Ruotsalainen, V.6
-
197
-
-
10744222733
-
Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy-PLOSL): A dementia associated with bone cystic lesions. From clinical to genetic and molecular aspects
-
Bianchin MM, Capella HM, Chaves DL, Steindel M, Grisard EC, Ganev GG, et al. Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy-PLOSL): a dementia associated with bone cystic lesions. From clinical to genetic and molecular aspects. Cell Mol Neurobiol 2004; 24(1):1-24.
-
(2004)
Cell Mol Neurobiol
, vol.24
, Issue.1
, pp. 1-24
-
-
Bianchin, M.M.1
Capella, H.M.2
Chaves, D.L.3
Steindel, M.4
Grisard, E.C.5
Ganev, G.G.6
-
198
-
-
0034045615
-
Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF
-
Smith SD, Kelley PM, Kenyon JB, Hoover D. Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF. J Med Genet 2000; 37(6):446-8.
-
(2000)
J Med Genet
, vol.37
, Issue.6
, pp. 446-448
-
-
Smith, S.D.1
Kelley, P.M.2
Kenyon, J.B.3
Hoover, D.4
-
199
-
-
0030012628
-
Analyses of loss-of-function mutations of the MITF gene suggest that haploinsufficiency is a cause of Waardenburg syndrome type 2A
-
Nobukuni Y, Watanabe A, Takeda K, Skarka H, Tachibana M. Analyses of loss-of-function mutations of the MITF gene suggest that haploinsufficiency is a cause of Waardenburg syndrome type 2A. Am J Hum Genet 1996; 59(1):76-83.
-
(1996)
Am J Hum Genet
, vol.59
, Issue.1
, pp. 76-83
-
-
Nobukuni, Y.1
Watanabe, A.2
Takeda, K.3
Skarka, H.4
Tachibana, M.5
-
200
-
-
0343245112
-
A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance
-
Tietz W. A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance. Am J Hum Genet 1963; 15:259-64.
-
(1963)
Am J Hum Genet
, vol.15
, pp. 259-264
-
-
Tietz, W.1
-
201
-
-
0030739603
-
Waardenburg syndrome
-
Read AP, Newton VE. Waardenburg syndrome. J Med Genet 1997; 34(8):656-65.
-
(1997)
J Med Genet
, vol.34
, Issue.8
, pp. 656-665
-
-
Read, A.P.1
Newton, V.E.2
-
202
-
-
0242391859
-
Apoptotic gene expression in Paget's disease: A possible role for Bcl-2
-
Brandwood CP, Hoyland JA, Hillarby MC, Berry JL, Davies M, Selby PL, et al. Apoptotic gene expression in Paget's disease: a possible role for Bcl-2. J Pathol 2003; 201(3):504-12.
-
(2003)
J Pathol
, vol.201
, Issue.3
, pp. 504-512
-
-
Brandwood, C.P.1
Hoyland, J.A.2
Hillarby, M.C.3
Berry, J.L.4
Davies, M.5
Selby, P.L.6
-
203
-
-
0036849578
-
Glanzmann's thrombasthenia: Updated
-
Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D. Glanzmann's thrombasthenia: updated. Platelets 2002; 13(7):387-93.
-
(2002)
Platelets
, vol.13
, Issue.7
, pp. 387-393
-
-
Nair, S.1
Ghosh, K.2
Kulkarni, B.3
Shetty, S.4
Mohanty, D.5
-
204
-
-
0141651720
-
Upregulation of osteoclast alpha2beta1 integrin compensates for lack of alphavbeta3 vitronectin receptor in Iraqi-Jewish-type Glanzmann thrombasthenia
-
Horton MA, Massey HM, Rosenberg N, Nicholls B, Seligsohn U, Flanagan AM. Upregulation of osteoclast alpha2beta1 integrin compensates for lack of alphavbeta3 vitronectin receptor in Iraqi-Jewish-type Glanzmann thrombasthenia. Br J Haematol 2003; 122(6):950-7.
-
(2003)
Br J Haematol
, vol.122
, Issue.6
, pp. 950-957
-
-
Horton, M.A.1
Massey, H.M.2
Rosenberg, N.3
Nicholls, B.4
Seligsohn, U.5
Flanagan, A.M.6
-
205
-
-
0037938844
-
Osteopetrosis and Glanzmann's thrombasthenia in a child
-
Yarali N, Fisgin T, Duru F, Kara A. Osteopetrosis and Glanzmann's thrombasthenia in a child. Ann Hematol 2003; 82(4):254-6.
-
(2003)
Ann Hematol
, vol.82
, Issue.4
, pp. 254-256
-
-
Yarali, N.1
Fisgin, T.2
Duru, F.3
Kara, A.4
-
207
-
-
18244389008
-
Albers-Schonberg disease (autosomal dominant Osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene
-
Cleiren E, Benichou O, Van Hul E, Gram J, Bollerslev J, Singer FR, et al. Albers-Schonberg disease (autosomal dominant Osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene. Hum Mol Genet 2001; 10(25):2861-7.
-
(2001)
Hum Mol Genet
, vol.10
, Issue.25
, pp. 2861-2867
-
-
Cleiren, E.1
Benichou, O.2
Van Hul, E.3
Gram, J.4
Bollerslev, J.5
Singer, F.R.6
-
208
-
-
0037315475
-
Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive Osteopetrosis
-
Campos-Xavier AB, Saraiva JM, Ribeiro LM, Munnich A, Cormier-Daire V. Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive Osteopetrosis. Hum Genet 2003; 112(2):186-9.
-
(2003)
Hum Genet
, vol.112
, Issue.2
, pp. 186-189
-
-
Campos-Xavier, A.B.1
Saraiva, J.M.2
Ribeiro, L.M.3
Munnich, A.4
Cormier-Daire, V.5
-
209
-
-
0029809357
-
Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency
-
Gelb BD, Shi GP, Chapman HA, Desnick RJ. Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science 1996; 273(5279):1236-8.
-
(1996)
Science
, vol.273
, Issue.5279
, pp. 1236-1238
-
-
Gelb, B.D.1
Shi, G.P.2
Chapman, H.A.3
Desnick, R.J.4
-
210
-
-
2342632645
-
Identification of a novel mutation in the coding region of the grey-lethal gene OSTM1 in human malignant infantile osteopetrosis
-
Ramirez A, Faupel J, Goebel I, Stiller A, Beyer S, Stockle C, et al. Identification of a novel mutation in the coding region of the grey-lethal gene OSTM1 in human malignant infantile osteopetrosis. Hum Mutat 2004; 23(5):471-6.
-
(2004)
Hum Mutat
, vol.23
, Issue.5
, pp. 471-476
-
-
Ramirez, A.1
Faupel, J.2
Goebel, I.3
Stiller, A.4
Beyer, S.5
Stockle, C.6
-
211
-
-
16544384350
-
Severe malignant osteopetrosis caused by a GL gene mutation
-
Quarello P, Forni M, Barberis L, Defilippi C, Campagnoli MF, Silvestro L, et al. Severe malignant osteopetrosis caused by a GL gene mutation. J Bone Miner Res 2004; 19(7):1194-9.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.7
, pp. 1194-1199
-
-
Quarello, P.1
Forni, M.2
Barberis, L.3
Defilippi, C.4
Campagnoli, M.F.5
Silvestro, L.6
-
212
-
-
0037373341
-
Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density
-
Van Wesenbeeck L, Cleiren E, Gram J, Beals RK, Benichou O, Scopelliti D, et al. Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density. Am J Hum Genet 2003; 72(3):763-71.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.3
, pp. 763-771
-
-
Van Wesenbeeck, L.1
Cleiren, E.2
Gram, J.3
Beals, R.K.4
Benichou, O.5
Scopelliti, D.6
-
213
-
-
0024389809
-
Autosomal dominant osteopetrosis: Bone metabolism and epidemiological, clinical, and hormonal aspects
-
Bollerslev J. Autosomal dominant osteopetrosis: bone metabolism and epidemiological, clinical, and hormonal aspects. Endocr Rev 1989; 10(1):45-67.
-
(1989)
Endocr Rev
, vol.10
, Issue.1
, pp. 45-67
-
-
Bollerslev, J.1
-
214
-
-
0027752423
-
Ultrastructural investigations of bone resorptive cells in two types of autosomal dominant osteopetrosis
-
Bollerslev J, Marks SC Jr, Pockwinse S, Kassem M, Brixen K, Steiniche T, et al. Ultrastructural investigations of bone resorptive cells in two types of autosomal dominant osteopetrosis. Bone 1993; 14(6):865-9.
-
(1993)
Bone
, vol.14
, Issue.6
, pp. 865-869
-
-
Bollerslev, J.1
Marks Jr., S.C.2
Pockwinse, S.3
Kassem, M.4
Brixen, K.5
Steiniche, T.6
-
215
-
-
10744224854
-
High bone mass in mice expressing a mutant LRP5 gene
-
Babij P, Zhao W, Small C, Kharode Y, Yaworsky PJ, Bouxsein ML, et al. High bone mass in mice expressing a mutant LRP5 gene. J Bone Miner Res 2003; 18(6):960-74.
-
(2003)
J Bone Miner Res
, vol.18
, Issue.6
, pp. 960-974
-
-
Babij, P.1
Zhao, W.2
Small, C.3
Kharode, Y.4
Yaworsky, P.J.5
Bouxsein, M.L.6
-
216
-
-
0036138175
-
A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait
-
Little RD, Carulli JP, Del Mastro RG, Dupuis J, Osborne M, Folz C, et al. A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait. Am J Hum Genet 2002; 70(1):11-9.
-
(2002)
Am J Hum Genet
, vol.70
, Issue.1
, pp. 11-19
-
-
Little, R.D.1
Carulli, J.P.2
Del Mastro, R.G.3
Dupuis, J.4
Osborne, M.5
Folz, C.6
-
217
-
-
0037118285
-
High bone density due to a mutation in LDL-receptor-related protein 5
-
Boyden LM, Mao J, Belsky J, Mitzner L, Farhi A, Mitnick MA, et al. High bone density due to a mutation in LDL-receptor-related protein 5. N Engl J Med 2002; 346(20):1513-21.
-
(2002)
N Engl J Med
, vol.346
, Issue.20
, pp. 1513-1521
-
-
Boyden, L.M.1
Mao, J.2
Belsky, J.3
Mitzner, L.4
Farhi, A.5
Mitnick, M.A.6
-
218
-
-
13844269808
-
LRP5 and Wnt signaling: A union made for bone
-
Johnson ML, Harnish K, Nusse R, Van Hul W. LRP5 and Wnt signaling: a union made for bone. J Bone Miner Res 2004; 19(11):1749-57.
-
(2004)
J Bone Miner Res
, vol.19
, Issue.11
, pp. 1749-1757
-
-
Johnson, M.L.1
Harnish, K.2
Nusse, R.3
Van Hul, W.4
|