-
2
-
-
0030714605
-
A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function
-
Anderson DM, Maraskovsky E, Billingsley WL, Dougall WC, Tometsko ME, Roux ER, Teepe MC, et al (1997) A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function. Nature 390:175-179
-
(1997)
Nature
, vol.390
, pp. 175-179
-
-
Anderson, D.M.1
Maraskovsky, E.2
Billingsley, W.L.3
Dougall, W.C.4
Tometsko, M.E.5
Roux, E.R.6
Teepe, M.C.7
-
3
-
-
0029032394
-
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
-
Bellus GA, McIntosh I, Smith EA, Aylsworth AS, Kaitila I, Horton WA, Greenhaw GA, et al, (1995) A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. Nat Genet 10: 357-359
-
(1995)
Nat Genet
, vol.10
, pp. 357-359
-
-
Bellus, G.A.1
McIntosh, I.2
Smith, E.A.3
Aylsworth, A.S.4
Kaitila, I.5
Horton, W.A.6
Greenhaw, G.A.7
-
4
-
-
0025821019
-
Noonan-like/multiple giant cell lesion syndrome
-
Cohen M, Gorlin RJ (1991) Noonan-like/multiple giant cell lesion syndrome. Am J Med Genet 40:159-166
-
(1991)
Am J Med Genet
, vol.40
, pp. 159-166
-
-
Cohen, M.1
Gorlin, R.J.2
-
5
-
-
0014512221
-
Cherubism - Hereditary fibrous dysplasia of the jaws - Roentgenographic features
-
Cornelius GA, McClendon JL (1969) Cherubism - hereditary fibrous dysplasia of the jaws - roentgenographic features. Am J Roentgenol Radium Ther Nucl Med 106:136-143
-
(1969)
Am J Roentgenol Radium Ther Nucl Med
, vol.106
, pp. 136-143
-
-
Cornelius, G.A.1
McClendon, J.L.2
-
6
-
-
0022452412
-
Cherubism, gingival fibromatosis, epilepsy, and mental deficiency (Ramon syndrome) with juvenile rheumatoid arthritis
-
De Pina-Neto JM, Moreno AFC, Silva LR, Velludo MASL, Ribeiro MVM, Athayde-Junior L, Voltarelli JC (1986) Cherubism, gingival fibromatosis, epilepsy, and mental deficiency (Ramon syndrome) with juvenile rheumatoid arthritis. Am J Med Genet 25:433-441
-
(1986)
Am J Med Genet
, vol.25
, pp. 433-441
-
-
De Pina-Neto, J.M.1
Moreno, A.F.C.2
Silva, L.R.3
Velludo, M.A.S.L.4
Ribeiro, M.V.M.5
Athayde-Junior, L.6
Voltarelli, J.C.7
-
7
-
-
0032574680
-
Retinal changes and tumorogenesis in Ramon syndrome: Follow-up of a Brazilian family
-
De Pina-Neto JM, Vieira de Souza N, Velludo MASL, Perosa GBD, de Freitas MMS, Colafemina JF (1998) Retinal changes and tumorogenesis in Ramon syndrome: follow-up of a Brazilian family. Am J Med Genet 77:43-46
-
(1998)
Am J Med Genet
, vol.77
, pp. 43-46
-
-
De Pina-Neto, J.M.1
Vieira De Souza, N.2
Velludo, M.A.S.L.3
Perosa, G.B.D.4
De Freitas, M.M.S.5
Colafemina, J.F.6
-
8
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
-
10
-
-
0024407271
-
The Noonan syndrome/cherubism association
-
Dunlap C, Neville B, Vickers RA, O'Neil D, Barker B (1989) The Noonan syndrome/cherubism association. Oral Surg Oral Med Oral Pathol 67:698-705
-
(1989)
Oral Surg Oral Med Oral Pathol
, vol.67
, pp. 698-705
-
-
Dunlap, C.1
Neville, B.2
Vickers, R.A.3
O'Neil, D.4
Barker, B.5
-
12
-
-
0028038981
-
Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3
-
Gal A, Xu S, Piczenik Y, Eiberg H, Duvigneau C, Schwinger E, Rosenberg T (1994) Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3. Hum Mol Genet 3:323-325
-
(1994)
Hum Mol Genet
, vol.3
, pp. 323-325
-
-
Gal, A.1
Xu, S.2
Piczenik, Y.3
Eiberg, H.4
Duvigneau, C.5
Schwinger, E.6
Rosenberg, T.7
-
13
-
-
0028077697
-
Mapping a gene for Noonan syndrome to the long arm of chromosome 12
-
Jamieson CR, van der Burgt I, Brady AF, van Ree M, Elsawi MM, Hol F, Jeffery S et al (1994) Mapping a gene for Noonan syndrome to the long arm of chromosome 12. Nat Genet 8:357-360
-
(1994)
Nat Genet
, vol.8
, pp. 357-360
-
-
Jamieson, C.R.1
Van Der Burgt, I.2
Brady, A.F.3
Van Ree, M.4
Elsawi, M.M.5
Hol, F.6
Jeffery, S.7
-
14
-
-
84882914596
-
Familial multilocular cystic disease of the jaws
-
Jones WA (1933) Familial multilocular cystic disease of the jaws. Am J Cancer 17:946-950
-
(1933)
Am J Cancer
, vol.17
, pp. 946-950
-
-
Jones, W.A.1
-
15
-
-
50549218724
-
Cherubism: A thumbnail sketch of its diagnosis and a conservative method of treatment
-
-(1965) Cherubism: a thumbnail sketch of its diagnosis and a conservative method of treatment. Oral Surg Oral Med Oral Pathol 20:648-653
-
(1965)
Oral Surg Oral Med Oral Pathol
, vol.20
, pp. 648-653
-
-
-
16
-
-
0026561913
-
Cherubism: Report of a case showing regression without treatment
-
Katz JO, Dunlap CL, Annis RL (1992) Cherubism: report of a case showing regression without treatment. J Oral Maxillofac Surg 50:301-303
-
(1992)
J Oral Maxillofac Surg
, vol.50
, pp. 301-303
-
-
Katz, J.O.1
Dunlap, C.L.2
Annis, R.L.3
-
17
-
-
0026509974
-
Cherubism; Diagnosis, treatment, and comparison with central giant cell granulomas and giant cell tumors
-
Kaugars GE, Niamtu J III, Svirsky JA (1992) Cherubism; diagnosis, treatment, and comparison with central giant cell granulomas and giant cell tumors. Oral Surg Oral Med Oral Pathol 73:369-374
-
(1992)
Oral Surg Oral Med Oral Pathol
, vol.73
, pp. 369-374
-
-
Kaugars, G.E.1
Niamtu J. III2
Svirsky, J.A.3
-
18
-
-
0021850103
-
Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
-
Lathrop GM, Lalouel JM, Julier C, Ott J (1985) Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 37:482-498
-
(1985)
Am J Hum Genet
, vol.37
, pp. 482-498
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
21
-
-
0027270053
-
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa
-
McLaughlin ME, Sandberg MA, Berson EL, Dryja TP (1993) Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa. Nat Genet 4:130-134
-
(1993)
Nat Genet
, vol.4
, pp. 130-134
-
-
McLaughlin, M.E.1
Sandberg, M.A.2
Berson, E.L.3
Dryja, T.P.4
-
22
-
-
0028793472
-
Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
-
Meyers GA, Orlow SJ, Munro IR, Przylepa KA, Jabs EW (1995) Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. Nat Genet 11:462-464
-
(1995)
Nat Genet
, vol.11
, pp. 462-464
-
-
Meyers, G.A.1
Orlow, S.J.2
Munro, I.R.3
Przylepa, K.A.4
Jabs, E.W.5
-
23
-
-
0043048571
-
Sequential tests for the detection of linkage
-
Morton NE (1955) Sequential tests for the detection of linkage. Am J Hum Genet 7:277-318
-
(1955)
Am J Hum Genet
, vol.7
, pp. 277-318
-
-
Morton, N.E.1
-
24
-
-
15444351110
-
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
-
Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, et al (1997) Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. Cell 89:773-779
-
(1997)
Cell
, vol.89
, pp. 773-779
-
-
Mundlos, S.1
Otto, F.2
Mundlos, C.3
Mulliken, J.B.4
Aylsworth, A.S.5
Albright, S.6
Lindhout, D.7
-
25
-
-
0029153893
-
Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism
-
Quan F, Grompe M, Jakobs P, Popovich BW (1995) Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism. Hum Mol Genet 4:1681-1684
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1681-1684
-
-
Quan, F.1
Grompe, M.2
Jakobs, P.3
Popovich, B.W.4
-
26
-
-
0014141822
-
Gingival fibromatosis combined with cherubism
-
Ramon Y, Berman W, Bubis JJ (1967) Gingival fibromatosis combined with cherubism. Oral Surg 24:436-448
-
(1967)
Oral Surg
, vol.24
, pp. 436-448
-
-
Ramon, Y.1
Berman, W.2
Bubis, J.J.3
-
27
-
-
0028093135
-
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
-
Rousseau F, Bonaventure J, Legeai-Mallet L, Pelet A, Rozet J-M, Maroteaux P, Le Merrer M, et al (1994) Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature 371:252-254
-
(1994)
Nature
, vol.371
, pp. 252-254
-
-
Rousseau, F.1
Bonaventure, J.2
Legeai-Mallet, L.3
Pelet, A.4
Rozet, J.-M.5
Maroteaux, P.6
Le Merrer, M.7
-
29
-
-
0027964261
-
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
-
Shiang R, Thompson LM, Zhu YZ, Church DM, Fielder TJ, Bocian M, Winokur ST et al. (1994) Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 78:335-342
-
(1994)
Cell
, vol.78
, pp. 335-342
-
-
Shiang, R.1
Thompson, L.M.2
Zhu, Y.Z.3
Church, D.M.4
Fielder, T.J.5
Bocian, M.6
Winokur, S.T.7
-
30
-
-
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, Nguyen HQ, et al (1997) Osteoprotegerin: a novel secreted protein involved in the regulation of bone density. Cell 89:309-319
-
(1997)
Cell
, vol.89
, 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
Nguyen, H.Q.7
-
31
-
-
0028924820
-
A common FGFR3 gene mutation is present in achondroplasia but not in hypochondroplasia
-
Stoilov I, Kilpatrick MW, Tsipouras PA (1995) A common FGFR3 gene mutation is present in achondroplasia but not in hypochondroplasia. Am J Med Genet 55:127-133
-
(1995)
Am J Med Genet
, vol.55
, pp. 127-133
-
-
Stoilov, I.1
Kilpatrick, M.W.2
Tsipouras, P.A.3
-
32
-
-
0001099859
-
Multiple giant cell tumors - Report of a case
-
Thompson ER (1962) Multiple giant cell tumors - report of a case. Oral Surg Oral Med Oral Pathol 15: 69-73
-
(1962)
Oral Surg Oral Med Oral Pathol
, vol.15
, pp. 69-73
-
-
Thompson, E.R.1
-
33
-
-
0029705334
-
Cherubism: Regression of the lesions and spontaneous bone regeneration
-
Timosca GC (1996) Cherubism: regression of the lesions and spontaneous bone regeneration. Rev Stomatol Chir Maxillofac 97:172-177
-
(1996)
Rev Stomatol Chir Maxillofac
, vol.97
, pp. 172-177
-
-
Timosca, G.C.1
-
34
-
-
0018223665
-
Cherubism: A report on three cases
-
Wayman JB (1978) Cherubism: a report on three cases. Br J Oral Surg 16:47-56
-
(1978)
Br J Oral Surg
, vol.16
, pp. 47-56
-
-
Wayman, J.B.1
-
35
-
-
0031439265
-
TRANCE (tumor necrosis factor [TNF]-related activation-induced cytokine), a new TNF family member predominantly expressed in T cells, is a dendritic cell-specific survival factor
-
Wong BR, Josien R, Lee SY, Sauter B, Li HL, Steinman RM, Choi Y (1997) TRANCE (tumor necrosis factor [TNF]-related activation-induced cytokine), a new TNF family member predominantly expressed in T cells, is a dendritic cell-specific survival factor. J Exp Med 186:2075-2080
-
(1997)
J Exp Med
, vol.186
, pp. 2075-2080
-
-
Wong, B.R.1
Josien, R.2
Lee, S.Y.3
Sauter, B.4
Li, H.L.5
Steinman, R.M.6
Choi, Y.7
-
36
-
-
0032584208
-
Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/ RANKL
-
Yasuda H, Shima N, Nakagawa N, Yamaguchi K, Kinosaki M, Mochizuki SI, Tomoyasu A, et al (1998) Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/ RANKL. Proc Natl Acad Sci USA 95:3597-3602
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3597-3602
-
-
Yasuda, H.1
Shima, N.2
Nakagawa, N.3
Yamaguchi, K.4
Kinosaki, M.5
Mochizuki, S.I.6
Tomoyasu, A.7
-
37
-
-
0027272951
-
Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4
-
Zuo J, Robbins C, Baharloo S, Cox DR, Myers RM (1993) Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4. Hum Mol Genet 2:889-899
-
(1993)
Hum Mol Genet
, vol.2
, pp. 889-899
-
-
Zuo, J.1
Robbins, C.2
Baharloo, S.3
Cox, D.R.4
Myers, R.M.5
|