-
1
-
-
0029941445
-
A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation
-
Siracusa LD, McGrath R, Ma Q, Moskow JJ, Manne J, Christner PJ, Buchberg AM, Jimenez SA (1996) A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation. Genome Res 6:300-313
-
(1996)
Genome Res
, vol.6
, pp. 300-313
-
-
Siracusa, L.D.1
McGrath, R.2
Ma, Q.3
Moskow, J.J.4
Manne, J.5
Christner, P.J.6
Buchberg, A.M.7
Jimenez, S.A.8
-
2
-
-
0017250167
-
Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton
-
Green MC, Sweet HO, Bunker LE (1976) Tight-skin, a new mutation of the mouse causing excessive growth of connective tissue and skeleton. Am J Pathol 82:493-512
-
(1976)
Am J Pathol
, vol.82
, pp. 493-512
-
-
Green, M.C.1
Sweet, H.O.2
Bunker, L.E.3
-
3
-
-
23644440113
-
Animal models in scleroderma
-
Clark SH (2005) Animal models in scleroderma. Curr Rheumatol Rep 7:150-155
-
(2005)
Curr Rheumatol Rep
, vol.7
, pp. 150-155
-
-
Clark, S.H.1
-
4
-
-
7044247951
-
Animal models of systemic sclerosis: Insights into systemic sclerosis pathogenesis and potential therapeutic approaches
-
Christner PJ, Jimenez SA (2004) Animal models of systemic sclerosis: insights into systemic sclerosis pathogenesis and potential therapeutic approaches. Curr Opin Rheumatol 16:746-752
-
(2004)
Curr Opin Rheumatol
, vol.16
, pp. 746-752
-
-
Christner, P.J.1
Jimenez, S.A.2
-
5
-
-
28444477739
-
Scleroderma: From cell and molecular mechanisms to disease models
-
Abraham DJ, Varga J (2005) Scleroderma: from cell and molecular mechanisms to disease models. Trends Immunol 26:587-595
-
(2005)
Trends Immunol
, vol.26
, pp. 587-595
-
-
Abraham, D.J.1
Varga, J.2
-
6
-
-
0036262665
-
CD19-dependent B lymphocyte signaling thresholds influence skin fibrosis and autoimmunity in the tight-skin mouse
-
Saito E, Fujimoto M, Hasegawa M, Komura K, Hamaguchi Y, Kaburagi Y, Nagaoka T, Takehara K, Tedder TF, Sato S (2002) CD19-dependent B lymphocyte signaling thresholds influence skin fibrosis and autoimmunity in the tight-skin mouse. J Clin Invest 109:1453-1462
-
(2002)
J Clin Invest
, vol.109
, pp. 1453-1462
-
-
Saito, E.1
Fujimoto, M.2
Hasegawa, M.3
Komura, K.4
Hamaguchi, Y.5
Kaburagi, Y.6
Nagaoka, T.7
Takehara, K.8
Tedder, T.F.9
Sato, S.10
-
7
-
-
1542313925
-
Mutant fibrillin 1 from tight skin mice increases extracellular matrix incorporation of microfibril-associated glycoprotein 2 and type I collagen
-
Lemaire R, Farina G, Kissin E, Shipley JM, Bona C, Korn JH, Lafyatis R (2004) Mutant fibrillin 1 from tight skin mice increases extracellular matrix incorporation of microfibril-associated glycoprotein 2 and type I collagen. Arthritis Rheum 50:915-926
-
(2004)
Arthritis Rheum
, vol.50
, pp. 915-926
-
-
Lemaire, R.1
Farina, G.2
Kissin, E.3
Shipley, J.M.4
Bona, C.5
Korn, J.H.6
Lafyatis, R.7
-
8
-
-
25144523631
-
Analysis of the tight skin (Tsk1/+) mouse as a model for testing antifibrotic agents
-
Baxter RM, Crowell TP, McCrann ME, Frew EM, Gardner H (2005) Analysis of the tight skin (Tsk1/+) mouse as a model for testing antifibrotic agents. Lab Invest 85:1199-1209
-
(2005)
Lab Invest
, vol.85
, pp. 1199-1209
-
-
Baxter, R.M.1
Crowell, T.P.2
McCrann, M.E.3
Frew, E.M.4
Gardner, H.5
-
9
-
-
0028335388
-
Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome
-
Kainulainen K, Karttunen L, Puhakka L, Sakai L, Peltonen L (1994) Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome. Nat Genet 6:64-69
-
(1994)
Nat Genet
, vol.6
, pp. 64-69
-
-
Kainulainen, K.1
Karttunen, L.2
Puhakka, L.3
Sakai, L.4
Peltonen, L.5
-
10
-
-
0023002893
-
Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils
-
Sakai LY, Keene DR, Engvall E (1986) Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils. J Cell Biol 103:2499-2509
-
(1986)
J Cell Biol
, vol.103
, pp. 2499-2509
-
-
Sakai, L.Y.1
Keene, D.R.2
Engvall, E.3
-
11
-
-
0028267099
-
Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices
-
Zhang H, Apfelroth SD, Hu W, Davis EC, Sanguineti C, Bonadio J, Mecham RP, Ramirez F (1994) Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices. J Cell Biol 124:855-863
-
(1994)
J Cell Biol
, vol.124
, pp. 855-863
-
-
Zhang, H.1
Apfelroth, S.D.2
Hu, W.3
Davis, E.C.4
Sanguineti, C.5
Bonadio, J.6
Mecham, R.P.7
Ramirez, F.8
-
12
-
-
0025364777
-
TGF-beta 1 binding protein: A component of the large latent complex of TGF-beta 1 with multiple repeat sequences
-
Kanzaki T, Olofsson A, Moren A, Wernstedt C, Hellman U, Miyazono K, Claesson-Welsh L, Heldin CH (1990) TGF-beta 1 binding protein: a component of the large latent complex of TGF-beta 1 with multiple repeat sequences. Cell 61:1051-1061
-
(1990)
Cell
, vol.61
, pp. 1051-1061
-
-
Kanzaki, T.1
Olofsson, A.2
Moren, A.3
Wernstedt, C.4
Hellman, U.5
Miyazono, K.6
Claesson-Welsh, L.7
Heldin, C.H.8
-
13
-
-
0028900639
-
Isolation of a novel latent transforming growth factor-beta binding protein gene (LTBP-3)
-
Yin W, Smiley E, Germiller J, Mecham RP, Florer JB, Wenstrup RJ, Bonadio J (1995) Isolation of a novel latent transforming growth factor-beta binding protein gene (LTBP-3). J Biol Chem 270:10147-10160
-
(1995)
J Biol Chem
, vol.270
, pp. 10147-10160
-
-
Yin, W.1
Smiley, E.2
Germiller, J.3
Mecham, R.P.4
Florer, J.B.5
Wenstrup, R.J.6
Bonadio, J.7
-
14
-
-
0035107364
-
Osteomalacia in hyp mice is associated with abnormal phex expression and with altered bone matrix protein expression and deposition
-
Miao D, Bai X, Panda D, McKee M, Karaplis A, Goltzman D (2001) Osteomalacia in hyp mice is associated with abnormal phex expression and with altered bone matrix protein expression and deposition. Endocrinology 142:926-939
-
(2001)
Endocrinology
, vol.142
, pp. 926-939
-
-
Miao, D.1
Bai, X.2
Panda, D.3
McKee, M.4
Karaplis, A.5
Goltzman, D.6
-
15
-
-
0028626352
-
Marfan's syndrome and other microfibrillar diseases
-
Dietz HC, Ramirez F, Sakai LY (1994) Marfan's syndrome and other microfibrillar diseases. Adv Hum Genet 22:153-186
-
(1994)
Adv Hum Genet
, vol.22
, pp. 153-186
-
-
Dietz, H.C.1
Ramirez, F.2
Sakai, L.Y.3
-
16
-
-
0025900544
-
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes
-
Lee B, Godfrey M, Vitale E, Hori H, Mattei MG, Sarfarazi M, Tsipouras P, Ramirez F, Hollister DW (1991) Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. Nature 352:330-334
-
(1991)
Nature
, vol.352
, pp. 330-334
-
-
Lee, B.1
Godfrey, M.2
Vitale, E.3
Hori, H.4
Mattei, M.G.5
Sarfarazi, M.6
Tsipouras, P.7
Ramirez, F.8
Hollister, D.W.9
-
17
-
-
0025886783
-
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
-
Dietz HC, Cutting GR, Pyeritz RE, Maslen CL, Sakai LY, Corson GM, Puffenberger EG, Hamosh A, Nanthakumar EJ, Curristin SM, et al. (1991) Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature 352:337-339
-
(1991)
Nature
, vol.352
, pp. 337-339
-
-
Dietz, H.C.1
Cutting, G.R.2
Pyeritz, R.E.3
Maslen, C.L.4
Sakai, L.Y.5
Corson, G.M.6
Puffenberger, E.G.7
Hamosh, A.8
Nanthakumar, E.J.9
Curristin, S.M.10
-
18
-
-
3543013177
-
Heterozygous TGFBR2 mutations in Marfan syndrome
-
Mizuguchi T, Collod-Beroud G, Akiyama T, Abifadel M, Harada N, Morisaki T, Allard D, Varret M, Claustres M, Morisaki H, Ihara M, Kinoshita A, Yoshiura K, Junien C, Kajii T, Jondeau G, Ohta T, Kishino T, Furukawa Y, Nakamura Y, Niikawa N, Boileau C, Matsumoto N (2004) Heterozygous TGFBR2 mutations in Marfan syndrome. Nat Genet 36:855-860
-
(2004)
Nat Genet
, vol.36
, pp. 855-860
-
-
Mizuguchi, T.1
Collod-Beroud, G.2
Akiyama, T.3
Abifadel, M.4
Harada, N.5
Morisaki, T.6
Allard, D.7
Varret, M.8
Claustres, M.9
Morisaki, H.10
Ihara, M.11
Kinoshita, A.12
Yoshiura, K.13
Junien, C.14
Kajii, T.15
Jondeau, G.16
Ohta, T.17
Kishino, T.18
Furukawa, Y.19
Nakamura, Y.20
Niikawa, N.21
Boileau, C.22
Matsumoto, N.23
more..
-
20
-
-
4043070821
-
Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome
-
Judge DP, Biery NJ, Keene DR, Geubtner J, Myers L, Huso DL, Sakai LY, Dietz HC (2004) Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome. J Clin Invest 114:172-181
-
(2004)
J Clin Invest
, vol.114
, pp. 172-181
-
-
Judge, D.P.1
Biery, N.J.2
Keene, D.R.3
Geubtner, J.4
Myers, L.5
Huso, D.L.6
Sakai, L.Y.7
Dietz, H.C.8
-
21
-
-
33750208100
-
Fibrillin in Marfan syndrome and tight skin mice provides new insights into transforming growth factor-beta regulation and systemic sclerosis
-
Lemaire R, Bayle J, Lafyatis R (2006) Fibrillin in Marfan syndrome and tight skin mice provides new insights into transforming growth factor-beta regulation and systemic sclerosis. Curr Opin Rheumatol 18:582-587
-
(2006)
Curr Opin Rheumatol
, vol.18
, pp. 582-587
-
-
Lemaire, R.1
Bayle, J.2
Lafyatis, R.3
-
22
-
-
0035503934
-
Reduction in dermal fibrosis in the tight-skin (Tsk) mouse after local application of halofuginone
-
Pines M, Domb A, Ohana M, Inbar J, Genina O, Alexiev R, Nagler A (2001) Reduction in dermal fibrosis in the tight-skin (Tsk) mouse after local application of halofuginone. Biochem Pharmacol 62:1221-1227
-
(2001)
Biochem Pharmacol
, vol.62
, pp. 1221-1227
-
-
Pines, M.1
Domb, A.2
Ohana, M.3
Inbar, J.4
Genina, O.5
Alexiev, R.6
Nagler, A.7
-
23
-
-
0035995041
-
Effect of halofuginone on the development of tight skin (TSK) syndrome
-
McGaha T, Kodera T, Phelps R, Spiera H, Pines M, Bona C (2002) Effect of halofuginone on the development of tight skin (TSK) syndrome. Autoimmunity 35:277-282
-
(2002)
Autoimmunity
, vol.35
, pp. 277-282
-
-
McGaha, T.1
Kodera, T.2
Phelps, R.3
Spiera, H.4
Pines, M.5
Bona, C.6
-
24
-
-
0035138260
-
Lack of skin fibrosis in tight skin (TSK) mice with targeted mutation in the interleukin-4R alpha and transforming growth factor-beta genes
-
McGaha T, Saito S, Phelps RG, Gordon R, Noben-Trauth N, Paul WE, Bona C (2001) Lack of skin fibrosis in tight skin (TSK) mice with targeted mutation in the interleukin-4R alpha and transforming growth factor-beta genes. J Invest Dermatol 116:136-143
-
(2001)
J Invest Dermatol
, vol.116
, pp. 136-143
-
-
McGaha, T.1
Saito, S.2
Phelps, R.G.3
Gordon, R.4
Noben-Trauth, N.5
Paul, W.E.6
Bona, C.7
-
25
-
-
0036133690
-
Use of type I collagen green fluorescent protein transgenes to identify subpopulations of cells at different stages of the osteoblast lineage
-
Kalajzic I, Kalajzic Z, Kaliterna M, Gronowicz G, Clark SH, Lichtler AC, Rowe D (2002) Use of type I collagen green fluorescent protein transgenes to identify subpopulations of cells at different stages of the osteoblast lineage. J Bone Miner Res 17:15-25
-
(2002)
J Bone Miner Res
, vol.17
, pp. 15-25
-
-
Kalajzic, I.1
Kalajzic, Z.2
Kaliterna, M.3
Gronowicz, G.4
Clark, S.H.5
Lichtler, A.C.6
Rowe, D.7
-
26
-
-
21644486143
-
Expression profile of osteoblast lineage at defined stages of differentiation
-
Kalajzic I, Staal A, Yang WP, Wu Y, Johnson SE, Feyen JH, Krueger W, Maye P, Yu F, Zhao Y, Kuo L, Gupta RR, Achenie LE, Wang HW, Shin DG, Rowe DW (2005) Expression profile of osteoblast lineage at defined stages of differentiation. J Biol Chem 280:24618-24626
-
(2005)
J Biol Chem
, vol.280
, pp. 24618-24626
-
-
Kalajzic, I.1
Staal, A.2
Yang, W.P.3
Wu, Y.4
Johnson, S.E.5
Feyen, J.H.6
Krueger, W.7
Maye, P.8
Yu, F.9
Zhao, Y.10
Kuo, L.11
Gupta, R.R.12
Achenie, L.E.13
Wang, H.W.14
Shin, D.G.15
Rowe, D.W.16
-
27
-
-
21644482444
-
Comparison of the action of transient and continuous PTH on primary osteoblast cultures expressing differentiation stage-specific GFP
-
Wang YH, Liu Y, Buhl K, Rowe DW (2005) Comparison of the action of transient and continuous PTH on primary osteoblast cultures expressing differentiation stage-specific GFP. J Bone Miner Res 20:5-14
-
(2005)
J Bone Miner Res
, vol.20
, pp. 5-14
-
-
Wang, Y.H.1
Liu, Y.2
Buhl, K.3
Rowe, D.W.4
-
28
-
-
0029610915
-
The tight skin 2 mouse. An animal model of scleroderma displaying cutaneous fibrosis and mononuclear cell infiltration
-
Christner PJ, Peters J, Hawkins D, Siracusa LD, Jimenez SA (1995) The tight skin 2 mouse. An animal model of scleroderma displaying cutaneous fibrosis and mononuclear cell infiltration. Arthritis Rheum 38:1791-1798
-
(1995)
Arthritis Rheum
, vol.38
, pp. 1791-1798
-
-
Christner, P.J.1
Peters, J.2
Hawkins, D.3
Siracusa, L.D.4
Jimenez, S.A.5
-
30
-
-
0019126423
-
Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S
-
McLeod MJ (1980) Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S. Teratology 22:299-301
-
(1980)
Teratology
, vol.22
, pp. 299-301
-
-
McLeod, M.J.1
-
31
-
-
17844402483
-
Histological analysis of GFP expression in murine bone
-
Jiang X, Kalajzic Z, Maye P, Braut A, Bellizzi J, Mina M, Rowe DW (2005) Histological analysis of GFP expression in murine bone. J Histochem Cytochem 53:593-602
-
(2005)
J Histochem Cytochem
, vol.53
, pp. 593-602
-
-
Jiang, X.1
Kalajzic, Z.2
Maye, P.3
Braut, A.4
Bellizzi, J.5
Mina, M.6
Rowe, D.W.7
-
32
-
-
0021731952
-
Construction of DNA sequences complementary to rat alpha 1 and alpha 2 collagen mRNA and their use in studying the regulation of type I collagen synthesis by 1,25-dihydroxyvitamin D
-
Genovese C, Rowe D, Kream B (1984) Construction of DNA sequences complementary to rat alpha 1 and alpha 2 collagen mRNA and their use in studying the regulation of type I collagen synthesis by 1,25-dihydroxyvitamin D. Biochemistry 23:6210-6216
-
(1984)
Biochemistry
, vol.23
, pp. 6210-6216
-
-
Genovese, C.1
Rowe, D.2
Kream, B.3
-
33
-
-
0022760002
-
Isolation of the human gene for bone gla protein utilizing mouse and rat cDNA clones
-
Celeste AJ, Rosen V, Buecker JL, Kriz R, Wang EA, Wozney JM (1986) Isolation of the human gene for bone gla protein utilizing mouse and rat cDNA clones. EMBO J 5:1885-1890
-
(1986)
EMBO J
, vol.5
, pp. 1885-1890
-
-
Celeste, A.J.1
Rosen, V.2
Buecker, J.L.3
Kriz, R.4
Wang, E.A.5
Wozney, J.M.6
-
34
-
-
0028370599
-
Murine bone sialoprotein (BSP): CDNA cloning, mRNA expression, and genetic mapping
-
Young MF, Ibaraki K, Kerr JM, Lyu MS, Kozak CA (1994) Murine bone sialoprotein (BSP): cDNA cloning, mRNA expression, and genetic mapping. Mamm Genome 5:108-111
-
(1994)
Mamm Genome
, vol.5
, pp. 108-111
-
-
Young, M.F.1
Ibaraki, K.2
Kerr, J.M.3
Lyu, M.S.4
Kozak, C.A.5
-
35
-
-
33749320619
-
Increased levels of transforming growth factor beta receptor type I and up-regulation of matrix gene program: A model of scleroderma
-
Pannu J, Gardner H, Shearstone JR, Smith E, Trojanowska M (2006) Increased levels of transforming growth factor beta receptor type I and up-regulation of matrix gene program: a model of scleroderma. Arthritis Rheum 54:3011-3021
-
(2006)
Arthritis Rheum
, vol.54
, pp. 3011-3021
-
-
Pannu, J.1
Gardner, H.2
Shearstone, J.R.3
Smith, E.4
Trojanowska, M.5
-
36
-
-
11144328149
-
Fibrillin microfibrils: Multipurpose extracellular networks in organismal physiology
-
Ramirez F, Sakai LY, Dietz HC, Rifkin DB (2004) Fibrillin microfibrils: multipurpose extracellular networks in organismal physiology. Physiol Genomics 19:151-154
-
(2004)
Physiol Genomics
, vol.19
, pp. 151-154
-
-
Ramirez, F.1
Sakai, L.Y.2
Dietz, H.C.3
Rifkin, D.B.4
-
37
-
-
13044266360
-
Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1
-
Pereira L, Lee SY, Gayraud B, Andrikopoulos K, Shapiro SD, Bunton T, Biery NJ, Dietz HC, Sakai LY, Ramirez F (1999) Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1. Proc Natl Acad Sci USA 96:3819-3823
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 3819-3823
-
-
Pereira, L.1
Lee, S.Y.2
Gayraud, B.3
Andrikopoulos, K.4
Shapiro, S.D.5
Bunton, T.6
Biery, N.J.7
Dietz, H.C.8
Sakai, L.Y.9
Ramirez, F.10
-
38
-
-
33845503048
-
Bone mineral density in Marfan syndrome. a large case-control study
-
Moura B, Tubach F, Sulpice M, Boileau C, Jondeau G, Muti C, Chevallier B, Ounnoughene Y, Le Parc JM (2006) Bone mineral density in Marfan syndrome. A large case-control study. Joint Bone Spine 73:733-735
-
(2006)
Joint Bone Spine
, vol.73
, pp. 733-735
-
-
Moura, B.1
Tubach, F.2
Sulpice, M.3
Boileau, C.4
Jondeau, G.5
Muti, C.6
Chevallier, B.7
Ounnoughene, Y.8
Le Parc, J.M.9
-
39
-
-
33947375691
-
Symposium on the musculoskeletal aspects of Marfan syndrome: Meeting report and state of the science
-
Jones KB, Sponseller PD, Erkula G, Sakai L, Ramirez F, Dietz HC 3rd, Kost-Byerly S, Bridwell KH, Sandell L (2007) Symposium on the musculoskeletal aspects of Marfan syndrome: meeting report and state of the science. J Orthop Res 25:413-422
-
(2007)
J Orthop Res
, vol.25
, pp. 413-422
-
-
Jones, K.B.1
Sponseller, P.D.2
Erkula, G.3
Sakai, L.4
Ramirez, F.5
Dietz III, H.C.6
Kost-Byerly, S.7
Bridwell, K.H.8
Sandell, L.9
-
40
-
-
0030920251
-
Apoptosis and proliferation of fibroblasts during postnatal skin development and scleroderma in the tight-skin mouse
-
Pablos JL, Carreira PE, Serrano L, Del Castillo P, Gomez-Reino JJ (1997) Apoptosis and proliferation of fibroblasts during postnatal skin development and scleroderma in the tight-skin mouse. J Histochem Cytochem 45:711-719
-
(1997)
J Histochem Cytochem
, vol.45
, pp. 711-719
-
-
Pablos, J.L.1
Carreira, P.E.2
Serrano, L.3
Del Castillo, P.4
Gomez-Reino, J.J.5
-
41
-
-
0019267041
-
The tight-skin mouse: An animal model of inherited emphysema
-
suppl
-
Rossi GA, Hunninghake GW, Szapiel SV, Gadek JE, Fulmer JD, Kawanami O, Ferrans VJ, Crystal RG (1980) The tight-skin mouse: an animal model of inherited emphysema. Bull Eur Physiopathol Respir 16(suppl):157-166
-
(1980)
Bull Eur Physiopathol Respir
, vol.16
, pp. 157-166
-
-
Rossi, G.A.1
Hunninghake, G.W.2
Szapiel, S.V.3
Gadek, J.E.4
Fulmer, J.D.5
Kawanami, O.6
Ferrans, V.J.7
Crystal, R.G.8
-
42
-
-
0019522086
-
Hereditary emphysema in the tight-skin (Tsk/+) mouse
-
Szapiel SV, Fulmer JD, Hunninghake GW, Elson NA, Kawanami O, Ferrans VJ, Crystal RG (1981) Hereditary emphysema in the tight-skin (Tsk/+) mouse. Am Rev Respir Dis 123:680-685
-
(1981)
Am Rev Respir Dis
, vol.123
, pp. 680-685
-
-
Szapiel, S.V.1
Fulmer, J.D.2
Hunninghake, G.W.3
Elson, N.A.4
Kawanami, O.5
Ferrans, V.J.6
Crystal, R.G.7
-
43
-
-
0021260399
-
Hereditary emphysema in the tight-skin mouse. Evaluation of pathogenesis
-
Rossi GA, Hunninghake GW, Gadek JE, Szapiel SV, Kawanami O, Ferrans VJ, Crystal RG (1984) Hereditary emphysema in the tight-skin mouse. Evaluation of pathogenesis. Am Rev Respir Dis 129:850-855
-
(1984)
Am Rev Respir Dis
, vol.129
, pp. 850-855
-
-
Rossi, G.A.1
Hunninghake, G.W.2
Gadek, J.E.3
Szapiel, S.V.4
Kawanami, O.5
Ferrans, V.J.6
Crystal, R.G.7
-
46
-
-
0032752728
-
The vascular perspective of systemic sclerosis: Of chickens, mice and men
-
Sgonc R (1999) The vascular perspective of systemic sclerosis: of chickens, mice and men. Int Arch Allergy Immunol 120:169-176
-
(1999)
Int Arch Allergy Immunol
, vol.120
, pp. 169-176
-
-
Sgonc, R.1
-
47
-
-
0031252407
-
Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome
-
Pereira L, Andrikopoulos K, Tian J, Lee SY, Keene DR, Ono R, Reinhardt DP, Sakai LY, Biery NJ, Bunton T, Dietz HC, Ramirez F (1997) Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome. Nat Genet 17:218-222
-
(1997)
Nat Genet
, vol.17
, pp. 218-222
-
-
Pereira, L.1
Andrikopoulos, K.2
Tian, J.3
Lee, S.Y.4
Keene, D.R.5
Ono, R.6
Reinhardt, D.P.7
Sakai, L.Y.8
Biery, N.J.9
Bunton, T.10
Dietz, H.C.11
Ramirez, F.12
|