-
1
-
-
1542376206
-
Structural analysis of disease-causing mutations in the P-subfamily of forkhead transcription factors
-
S. Banerjee-Basu, and A.D. Baxevanis Structural analysis of disease-causing mutations in the P-subfamily of forkhead transcription factors Proteins 54 2004 639 647
-
(2004)
Proteins
, vol.54
, pp. 639-647
-
-
Banerjee-Basu, S.1
Baxevanis, A.D.2
-
2
-
-
0035167967
-
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
-
C.L. Bennett, J. Christie, F. Ramsdell, M.E. Brunkow, P.J. Ferguson, L. Whitesell, T.E. Kelly, F.T. Saulsbury, P.F. Chance, and H.D. Ochs The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 Nat. Genet. 27 2001 20 21
-
(2001)
Nat. Genet.
, vol.27
, pp. 20-21
-
-
Bennett, C.L.1
Christie, J.2
Ramsdell, F.3
Brunkow, M.E.4
Ferguson, P.J.5
Whitesell, L.6
Kelly, T.E.7
Saulsbury, F.T.8
Chance, P.F.9
Ochs, H.D.10
-
3
-
-
17044393922
-
Foxp3 interacts with nuclear factor of activated T cells and NF-κ B to repress cytokine gene expression and effector functions of T helper cells
-
E. Bettelli, M. Dastrange, and M. Oukka Foxp3 interacts with nuclear factor of activated T cells and NF-κ B to repress cytokine gene expression and effector functions of T helper cells Proc. Natl. Acad. Sci. USA 102 2005 5138 5143
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 5138-5143
-
-
Bettelli, E.1
Dastrange, M.2
Oukka, M.3
-
4
-
-
3543012707
-
Crystallography & NMR system: A new software suite for macromolecular structure determination
-
A.T. Brunger, P.D. Adams, G.M. Clore, W.L. DeLano, P. Gros, R.W. Grosse-Kunstleve, J.S. Jiang, J. Kuszewski, M. Nilges, and N.S. Pannu Crystallography & NMR system: a new software suite for macromolecular structure determination Acta Crystallogr. D Biol. Crystallogr. 54 1998 905 921
-
(1998)
Acta Crystallogr. D Biol. Crystallogr.
, vol.54
, pp. 905-921
-
-
Brunger, A.T.1
Adams, P.D.2
Clore, G.M.3
Delano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
Jiang, J.S.7
Kuszewski, J.8
Nilges, M.9
Pannu, N.S.10
-
5
-
-
0035162560
-
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
-
M.E. Brunkow, E.W. Jeffery, K.A. Hjerrild, B. Paeper, L.B. Clark, S.A. Yasayko, J.E. Wilkinson, D. Galas, S.F. Ziegler, and F. Ramsdell Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse Nat. Genet. 27 2001 68 73
-
(2001)
Nat. Genet.
, vol.27
, pp. 68-73
-
-
Brunkow, M.E.1
Jeffery, E.W.2
Hjerrild, K.A.3
Paeper, B.4
Clark, L.B.5
Yasayko, S.A.6
Wilkinson, J.E.7
Galas, D.8
Ziegler, S.F.9
Ramsdell, F.10
-
6
-
-
0036387193
-
Forkhead transcription factors: Key players in development and metabolism
-
P. Carlsson, and M. Mahlapuu Forkhead transcription factors: key players in development and metabolism Dev. Biol. 250 2002 1 23
-
(2002)
Dev. Biol.
, vol.250
, pp. 1-23
-
-
Carlsson, P.1
Mahlapuu, M.2
-
7
-
-
0034526617
-
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome
-
T.A. Chatila, F. Blaeser, N. Ho, H.M. Lederman, C. Voulgaropoulos, C. Helms, and A.M. Bowcock JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome J. Clin. Invest. 106 2000 R75 R81
-
(2000)
J. Clin. Invest.
, vol.106
-
-
Chatila, T.A.1
Blaeser, F.2
Ho, N.3
Lederman, H.M.4
Voulgaropoulos, C.5
Helms, C.6
Bowcock, A.M.7
-
8
-
-
0032485391
-
Structure of the DNA-binding domains from NFAT, Fos and Jun bound specifically to DNA
-
L. Chen, J.N. Glover, P.G. Hogan, A. Rao, and S.C. Harrison Structure of the DNA-binding domains from NFAT, Fos and Jun bound specifically to DNA Nature 392 1998 42 48
-
(1998)
Nature
, vol.392
, pp. 42-48
-
-
Chen, L.1
Glover, J.N.2
Hogan, P.G.3
Rao, A.4
Harrison, S.C.5
-
9
-
-
20844452590
-
Specificity of cell-cell adhesion by classical cadherins: Critical role for low-affinity dimerization through β-strand swapping
-
C.P. Chen, S. Posy, A. Ben-Shaul, L. Shapiro, and B.H. Honig Specificity of cell-cell adhesion by classical cadherins: critical role for low-affinity dimerization through β-strand swapping Proc. Natl. Acad. Sci. USA 102 2005 8531 8536
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 8531-8536
-
-
Chen, C.P.1
Posy, S.2
Ben-Shaul, A.3
Shapiro, L.4
Honig, B.H.5
-
10
-
-
0027270989
-
Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5
-
K.L. Clark, E.D. Halay, E. Lai, and S.K. Burley Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5 Nature 364 1993 412 420
-
(1993)
Nature
, vol.364
, pp. 412-420
-
-
Clark, K.L.1
Halay, E.D.2
Lai, E.3
Burley, S.K.4
-
11
-
-
0031820442
-
Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
-
R.J. Clifton-Bligh, J.M. Wentworth, P. Heinz, M.S. Crisp, R. John, J.H. Lazarus, M. Ludgate, and V.K. Chatterjee Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia Nat. Genet. 19 1998 399 401
-
(1998)
Nat. Genet.
, vol.19
, pp. 399-401
-
-
Clifton-Bligh, R.J.1
Wentworth, J.M.2
Heinz, P.3
Crisp, M.S.4
John, R.5
Lazarus, J.H.6
Ludgate, M.7
Chatterjee, V.K.8
-
12
-
-
0024556115
-
Multiple hepatocyte-enriched nuclear factors function in the regulation of transthyretin and α 1-antitrypsin genes
-
R.H. Costa, D.R. Grayson, and J.E. Darnell Jr. Multiple hepatocyte-enriched nuclear factors function in the regulation of transthyretin and α 1-antitrypsin genes Mol. Cell. Biol. 9 1989 1415 1425
-
(1989)
Mol. Cell. Biol.
, vol.9
, pp. 1415-1425
-
-
Costa, R.H.1
Grayson, D.R.2
Darnell Jr., J.E.3
-
13
-
-
0033646615
-
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
-
J. Fang, S.L. Dagenais, R.P. Erickson, M.F. Arlt, M.W. Glynn, J.L. Gorski, L.H. Seaver, and T.W. Glover Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome Am. J. Hum. Genet. 67 2000 1382 1388
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1382-1388
-
-
Fang, J.1
Dagenais, S.L.2
Erickson, R.P.3
Arlt, M.F.4
Glynn, M.W.5
Gorski, J.L.6
Seaver, L.H.7
Glover, T.W.8
-
14
-
-
0035873625
-
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
-
D.N. Finegold, M.A. Kimak, E.C. Lawrence, K.L. Levinson, E.M. Cherniske, B.R. Pober, J.W. Dunlap, and R.E. Ferrell Truncating mutations in FOXC2 cause multiple lymphedema syndromes Hum. Mol. Genet. 10 2001 1185 1189
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1185-1189
-
-
Finegold, D.N.1
Kimak, M.A.2
Lawrence, E.C.3
Levinson, K.L.4
Cherniske, E.M.5
Pober, B.R.6
Dunlap, J.W.7
Ferrell, R.E.8
-
15
-
-
0033535507
-
Exposing the human nude phenotype
-
J. Frank, C. Pignata, A.A. Panteleyev, D.M. Prowse, H. Baden, L. Weiner, L. Gaetaniello, W. Ahmad, N. Pozzi, and P.B. Cserhalmi-Friedman Exposing the human nude phenotype Nature 398 1999 473 474
-
(1999)
Nature
, vol.398
, pp. 473-474
-
-
Frank, J.1
Pignata, C.2
Panteleyev, A.A.3
Prowse, D.M.4
Baden, H.5
Weiner, L.6
Gaetaniello, L.7
Ahmad, W.8
Pozzi, N.9
Cserhalmi-Friedman, P.B.10
-
16
-
-
0033019592
-
Dynamic DNA contacts observed in the NMR structure of winged helix protein-DNA complex
-
C. Jin, I. Marsden, X. Chen, and X. Liao Dynamic DNA contacts observed in the NMR structure of winged helix protein-DNA complex J. Mol. Biol. 289 1999 683 690
-
(1999)
J. Mol. Biol.
, vol.289
, pp. 683-690
-
-
Jin, C.1
Marsden, I.2
Chen, X.3
Liao, X.4
-
17
-
-
84889120137
-
Improved methods for building protein models in electron density maps and the location of errors in these models
-
T.A. Jones, J.Y. Zou, S.W. Cowan, and Kjeldgaard Improved methods for building protein models in electron density maps and the location of errors in these models Acta Crystallogr. A 47 1991 110 119
-
(1991)
Acta Crystallogr. a
, vol.47
, pp. 110-119
-
-
Jones, T.A.1
Zou, J.Y.2
Cowan, S.W.3
Kjeldgaard4
-
18
-
-
0026244229
-
MOLSCRIPT: A program to produce both detailed and schematic plots of protein structures
-
P.J. Kraulis MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures J. Appl. Crystallogr. 24 1991 946 950
-
(1991)
J. Appl. Crystallogr.
, vol.24
, pp. 946-950
-
-
Kraulis, P.J.1
-
19
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
C.S. Lai, S.E. Fisher, J.A. Hurst, F. Vargha-Khadem, and A.P. Monaco A forkhead-domain gene is mutated in a severe speech and language disorder Nature 413 2001 519 523
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
20
-
-
0033753876
-
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma
-
O.J. Lehmann, N.D. Ebenezer, T. Jordan, M. Fox, L. Ocaka, A. Payne, B.P. Leroy, B.J. Clark, R.A. Hitchings, and S. Povey Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma Am. J. Hum. Genet. 67 2000 1129 1135
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1129-1135
-
-
Lehmann, O.J.1
Ebenezer, N.D.2
Jordan, T.3
Fox, M.4
Ocaka, L.5
Payne, A.6
Leroy, B.P.7
Clark, B.J.8
Hitchings, R.A.9
Povey, S.10
-
21
-
-
0037866671
-
Fox's in development and disease
-
O.J. Lehmann, J.C. Sowden, P. Carlsson, T. Jordan, and S.S. Bhattacharya Fox's in development and disease Trends Genet. 19 2003 339 344
-
(2003)
Trends Genet.
, vol.19
, pp. 339-344
-
-
Lehmann, O.J.1
Sowden, J.C.2
Carlsson, P.3
Jordan, T.4
Bhattacharya, S.S.5
-
22
-
-
0035053151
-
Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome
-
E. Levy-Lahad, and R.S. Wildin Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: further evidence for an X-linked lethal syndrome J. Pediatr. 138 2001 577 580
-
(2001)
J. Pediatr.
, vol.138
, pp. 577-580
-
-
Levy-Lahad, E.1
Wildin, R.S.2
-
23
-
-
0027133451
-
DNA-binding properties and secondary structural model of the hepatocyte nuclear factor 3/fork head domain
-
C. Li, and P.W. Tucker DNA-binding properties and secondary structural model of the hepatocyte nuclear factor 3/fork head domain Proc. Natl. Acad. Sci. USA 90 1993 11583 11587
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 11583-11587
-
-
Li, C.1
Tucker, P.W.2
-
24
-
-
0347986673
-
Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions
-
S. Li, J. Weidenfeld, and E.E. Morrisey Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions Mol. Cell. Biol. 24 2004 809 822
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 809-822
-
-
Li, S.1
Weidenfeld, J.2
Morrisey, E.E.3
-
25
-
-
0036893049
-
Solution structure of the DNA-binding domain of interleukin enhancer binding factor 1 (FOXK1a)
-
P.P. Liu, Y.C. Chen, C. Li, Y.H. Hsieh, S.W. Chen, S.H. Chen, W.Y. Jeng, and W.J. Chuang Solution structure of the DNA-binding domain of interleukin enhancer binding factor 1 (FOXK1a) Proteins 49 2002 543 553
-
(2002)
Proteins
, vol.49
, pp. 543-553
-
-
Liu, P.P.1
Chen, Y.C.2
Li, C.3
Hsieh, Y.H.4
Chen, S.W.5
Chen, S.H.6
Jeng, W.Y.7
Chuang, W.J.8
-
26
-
-
0141888247
-
Phylogenetic relationships of the Fox (Forkhead) gene family in the Bilateria
-
F. Mazet, J.K. Yu, D.A. Liberles, L.Z. Holland, and S.M. Shimeld Phylogenetic relationships of the Fox (Forkhead) gene family in the Bilateria Gene 316 2003 79 89
-
(2003)
Gene
, vol.316
, pp. 79-89
-
-
Mazet, F.1
Yu, J.K.2
Liberles, D.A.3
Holland, L.Z.4
Shimeld, S.M.5
-
27
-
-
0032231330
-
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly
-
A.J. Mears, T. Jordan, F. Mirzayans, S. Dubois, T. Kume, M. Parlee, R. Ritch, B. Koop, W.L. Kuo, and C. Collins Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly Am. J. Hum. Genet. 63 1998 1316 1328
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1316-1328
-
-
Mears, A.J.1
Jordan, T.2
Mirzayans, F.3
Dubois, S.4
Kume, T.5
Parlee, M.6
Ritch, R.7
Koop, B.8
Kuo, W.L.9
Collins, C.10
-
28
-
-
0033993639
-
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25
-
F. Mirzayans, D.B. Gould, E. Heon, G.D. Billingsley, J.C. Cheung, A.J. Mears, and M.A. Walter Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25 Eur. J. Hum. Genet. 8 2000 71 74
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 71-74
-
-
Mirzayans, F.1
Gould, D.B.2
Heon, E.3
Billingsley, G.D.4
Cheung, J.C.5
Mears, A.J.6
Walter, M.A.7
-
29
-
-
0030956416
-
Constitutive binding of the transcription factor interleukin-2 (IL-2) enhancer binding factor to the IL-2 promoter
-
A. Nirula, D.J. Moore, and R.B. Gaynor Constitutive binding of the transcription factor interleukin-2 (IL-2) enhancer binding factor to the IL-2 promoter J. Biol. Chem. 272 1997 7736 7745
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 7736-7745
-
-
Nirula, A.1
Moore, D.J.2
Gaynor, R.B.3
-
30
-
-
17344368672
-
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
-
D.Y. Nishimura, R.E. Swiderski, W.L. Alward, C.C. Searby, S.R. Patil, S.R. Bennet, A.B. Kanis, J.M. Gastier, E.M. Stone, and V.C. Sheffield The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 Nat. Genet. 19 1998 140 147
-
(1998)
Nat. Genet.
, vol.19
, pp. 140-147
-
-
Nishimura, D.Y.1
Swiderski, R.E.2
Alward, W.L.3
Searby, C.C.4
Patil, S.R.5
Bennet, S.R.6
Kanis, A.B.7
Gastier, J.M.8
Stone, E.M.9
Sheffield, V.C.10
-
31
-
-
0035125059
-
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye
-
D.Y. Nishimura, C.C. Searby, W.L. Alward, D. Walton, J.E. Craig, D.A. Mackey, K. Kawase, A.B. Kanis, S.R. Patil, E.M. Stone, and V.C. Sheffield A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye Am. J. Hum. Genet. 68 2001 364 372
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 364-372
-
-
Nishimura, D.Y.1
Searby, C.C.2
Alward, W.L.3
Walton, D.4
Craig, J.E.5
MacKey, D.A.6
Kawase, K.7
Kanis, A.B.8
Patil, S.R.9
Stone, E.M.10
Sheffield, V.C.11
-
32
-
-
0031059866
-
Processing of X-ray diffraction data collected in oscillation mode
-
C.W.J. Carter R.M. Sweet Academic Press New York
-
Z. Otwinowski, and W. Minor Processing of X-ray diffraction data collected in oscillation mode C.W.J. Carter R.M. Sweet Methods in Enzymology 1997 Academic Press New York 307 326
-
(1997)
Methods in Enzymology
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
33
-
-
0031808074
-
A helix propensity scale based on experimental studies of peptides and proteins
-
C.N. Pace, and J.M. Scholtz A helix propensity scale based on experimental studies of peptides and proteins Biophys. J. 75 1998 422 427
-
(1998)
Biophys. J.
, vol.75
, pp. 422-427
-
-
Pace, C.N.1
Scholtz, J.M.2
-
34
-
-
0035813231
-
Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation
-
L.A. Schubert, E. Jeffery, Y. Zhang, F. Ramsdell, and S.F. Ziegler Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation J. Biol. Chem. 276 2001 37672 37679
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 37672-37679
-
-
Schubert, L.A.1
Jeffery, E.2
Zhang, Y.3
Ramsdell, F.4
Ziegler, S.F.5
-
35
-
-
0028986780
-
Structural basis of cell-cell adhesion by cadherins
-
L. Shapiro, A.M. Fannon, P.D. Kwong, A. Thompson, M.S. Lehmann, G. Grubel, J.F. Legrand, J. Als-Nielsen, D.R. Colman, and W.A. Hendrickson Structural basis of cell-cell adhesion by cadherins Nature 374 1995 327 337
-
(1995)
Nature
, vol.374
, pp. 327-337
-
-
Shapiro, L.1
Fannon, A.M.2
Kwong, P.D.3
Thompson, A.4
Lehmann, M.S.5
Grubel, G.6
Legrand, J.F.7
Als-Nielsen, J.8
Colman, D.R.9
Hendrickson, W.A.10
-
36
-
-
0035920153
-
Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors
-
W. Shu, H. Yang, L. Zhang, M.M. Lu, and E.E. Morrisey Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors J. Biol. Chem. 276 2001 27488 27497
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 27488-27497
-
-
Shu, W.1
Yang, H.2
Zhang, L.3
Lu, M.M.4
Morrisey, E.E.5
-
37
-
-
0034681284
-
Solution structure and dynamics of the DNA-binding domain of the adipocyte-transcription factor FREAC-11
-
M.J. van Dongen, A. Cederberg, P. Carlsson, S. Enerback, and M. Wikstrom Solution structure and dynamics of the DNA-binding domain of the adipocyte-transcription factor FREAC-11 J. Mol. Biol. 296 2000 351 359
-
(2000)
J. Mol. Biol.
, vol.296
, pp. 351-359
-
-
Van Dongen, M.J.1
Cederberg, A.2
Carlsson, P.3
Enerback, S.4
Wikstrom, M.5
-
38
-
-
0042591396
-
Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional repressors
-
B. Wang, D. Lin, C. Li, and P. Tucker Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional repressors J. Biol. Chem. 278 2003 24259 24268
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 24259-24268
-
-
Wang, B.1
Lin, D.2
Li, C.3
Tucker, P.4
-
39
-
-
0035918516
-
Solution structure of the DNA binding domain of the human forkhead transcription factor AFX (FOXO4)
-
J. Weigelt, I. Climent, K. Dahlman-Wright, and M. Wikstrom Solution structure of the DNA binding domain of the human forkhead transcription factor AFX (FOXO4) Biochemistry 40 2001 5861 5869
-
(2001)
Biochemistry
, vol.40
, pp. 5861-5869
-
-
Weigelt, J.1
Climent, I.2
Dahlman-Wright, K.3
Wikstrom, M.4
-
40
-
-
0035163909
-
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
-
R.S. Wildin, F. Ramsdell, J. Peake, F. Faravelli, J.L. Casanova, N. Buist, E. Levy-Lahad, M. Mazzella, O. Goulet, and L. Perroni X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy Nat. Genet. 27 2001 18 20
-
(2001)
Nat. Genet.
, vol.27
, pp. 18-20
-
-
Wildin, R.S.1
Ramsdell, F.2
Peake, J.3
Faravelli, F.4
Casanova, J.L.5
Buist, N.6
Levy-Lahad, E.7
Mazzella, M.8
Goulet, O.9
Perroni, L.10
|