-
3
-
-
0026007719
-
Localization of the X inactivation centre on the human X chromosome in Xq13
-
Brown CJ, Lafreniere RG, Powers VE, Sebastio G, Ballabio A, Pettigrew AL, Ledbetter DH, Levy E, Craig IW, Willard HF 1991 Localization of the X inactivation centre on the human X chromosome in Xq13. Nature 349:82-84
-
(1991)
Nature
, vol.349
, pp. 82-84
-
-
Brown, C.J.1
Lafreniere, R.G.2
Powers, V.E.3
Sebastio, G.4
Ballabio, A.5
Pettigrew, A.L.6
Ledbetter, D.H.7
Levy, E.8
Craig, I.W.9
Willard, H.F.10
-
4
-
-
0842287648
-
Controlling X-inactivation in mammals: What does the centre hold?
-
Rougeulle C, Avner P 2003 Controlling X-inactivation in mammals: what does the centre hold? Semin Cell Dev Biol 14:331-340
-
(2003)
Semin Cell Dev Biol
, vol.14
, pp. 331-340
-
-
Rougeulle, C.1
Avner, P.2
-
5
-
-
0027654212
-
Mapping the murine Xce locus with (CA)n repeats
-
Simmler MC, Cattanach BM, Rasberry C, Rougeulle C, Avner P 1993 Mapping the murine Xce locus with (CA)n repeats. Mamm Genome 4:523-530
-
(1993)
Mamm Genome
, vol.4
, pp. 523-530
-
-
Simmler, M.C.1
Cattanach, B.M.2
Rasberry, C.3
Rougeulle, C.4
Avner, P.5
-
6
-
-
16244405272
-
T-cell tolerance and autoimmunity to systemic and tissue-restricted self-antigens
-
Lohr J, Knoechel B, Nagabhushanam V, Abbas AK 2005 T-cell tolerance and autoimmunity to systemic and tissue-restricted self-antigens. Immunol Rev 204:116-127
-
(2005)
Immunol Rev
, vol.204
, pp. 116-127
-
-
Lohr, J.1
Knoechel, B.2
Nagabhushanam, V.3
Abbas, A.K.4
-
7
-
-
17844411238
-
Detection of thyroglobulin mRNA as truncated isoform(s) in mouse thymus
-
Li HS, Carayanniotis G 2005 Detection of thyroglobulin mRNA as truncated isoform(s) in mouse thymus. Immunology 115:85-89
-
(2005)
Immunology
, vol.115
, pp. 85-89
-
-
Li, H.S.1
Carayanniotis, G.2
-
8
-
-
17644395232
-
Getting to the guts of NOD2
-
Kelsall B 2005 Getting to the guts of NOD2. Nat Med 11:383-384
-
(2005)
Nat Med
, vol.11
, pp. 383-384
-
-
Kelsall, B.1
-
9
-
-
0141801751
-
Searching for the autoimmune thyroid disease susceptibility genes: From gene mapping to gene function
-
Tomer Y, Davies TF 2003 Searching for the autoimmune thyroid disease susceptibility genes: From gene mapping to gene function. Endocr Rev 24:694-717
-
(2003)
Endocr Rev
, vol.24
, pp. 694-717
-
-
Tomer, Y.1
Davies, T.F.2
-
10
-
-
0036064287
-
The influence of human leucocyte antigen (HLA) genes on autoimmune thyroid disease (AITD): Results of studies in HLA-DR3 positive AITD families
-
Oxf
-
Ban Y, Davies TF, Greenberg DA, Concepcion ES, Tomer Y 2002 The influence of human leucocyte antigen (HLA) genes on autoimmune thyroid disease (AITD): results of studies in HLA-DR3 positive AITD families. Clin Endocrinol (Oxf) 57:81-88
-
(2002)
Clin Endocrinol
, vol.57
, pp. 81-88
-
-
Ban, Y.1
Davies, T.F.2
Greenberg, D.A.3
Concepcion, E.S.4
Tomer, Y.5
-
11
-
-
8744266374
-
The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease
-
Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, Donaldson PT, Ball SG, James RA, Quinton R, Perros P, Pearce SH 2004 The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease. J Clin Endocrinol Metab 89:5862-5865
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5862-5865
-
-
Velaga, M.R.1
Wilson, V.2
Jennings, C.E.3
Owen, C.J.4
Herington, S.5
Donaldson, P.T.6
Ball, S.G.7
James, R.A.8
Quinton, R.9
Perros, P.10
Pearce, S.H.11
-
12
-
-
0142059659
-
Common and unique susceptibility loci in Graves and Hashimoto diseases: Results of whole-genome screening in a data set of 102 multiplex families
-
Tomer Y, Ban Y, Concepcion E, Barbesino G, Villanueva R, Greenberg DA, Davies TF 2003 Common and unique susceptibility loci in Graves and Hashimoto diseases: Results of whole-genome screening in a data set of 102 multiplex families. Am J Hum Genet 73:736-747
-
(2003)
Am J Hum Genet
, vol.73
, pp. 736-747
-
-
Tomer, Y.1
Ban, Y.2
Concepcion, E.3
Barbesino, G.4
Villanueva, R.5
Greenberg, D.A.6
Davies, T.F.7
-
13
-
-
0036149916
-
Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases
-
Tomer Y, Greenberg DA, Concepcion E, Ban Y, Davies TF 2002 Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases. J Clin Endocrinol Metab 87:404-407
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 404-407
-
-
Tomer, Y.1
Greenberg, D.A.2
Concepcion, E.3
Ban, Y.4
Davies, T.F.5
-
14
-
-
0344303638
-
Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease
-
USA
-
Ban Y, Greenberg DA, Concepcion E, Skrabanek L, Villanueva R, Tomer Y 2003 Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease. Proc Natl Acad Sci USA 100:15119-15124
-
(2003)
Proc Natl Acad Sci
, vol.100
, pp. 15119-15124
-
-
Ban, Y.1
Greenberg, D.A.2
Concepcion, E.3
Skrabanek, L.4
Villanueva, R.5
Tomer, Y.6
-
15
-
-
0030042952
-
X-inactivation patterns in monozygotic and dizygotic female twins
-
Goodship J, Carter J, Burn J 1996 X-inactivation patterns in monozygotic and dizygotic female twins. Am J Med Genet 61:205-208
-
(1996)
Am J Med Genet
, vol.61
, pp. 205-208
-
-
Goodship, J.1
Carter, J.2
Burn, J.3
-
16
-
-
0034825344
-
Autoimmune thyroid syndrome in women with Turner's syndrome - The association with karyotype
-
Oxf
-
Elsheikh M, Wass JA, Conway GS 2001 Autoimmune thyroid syndrome in women with Turner's syndrome-the association with karyotype. Clin Endocrinol (Oxf) 55:223-226
-
(2001)
Clin Endocrinol
, vol.55
, pp. 223-226
-
-
Elsheikh, M.1
Wass, J.A.2
Conway, G.S.3
-
17
-
-
18544413131
-
Skewed X chromosome inactivation in blood cells of women with scleroderma
-
Ozbalkan Z, Bagislar S, Kiraz S, Akyerli CB, Ozer HT, Yavuz S, Birlik AM, Calguneri M, Ozcelik T 2005 Skewed X chromosome inactivation in blood cells of women with scleroderma. Arthritis Rheum 52:1564-1570
-
(2005)
Arthritis Rheum
, vol.52
, pp. 1564-1570
-
-
Ozbalkan, Z.1
Bagislar, S.2
Kiraz, S.3
Akyerli, C.B.4
Ozer, H.T.5
Yavuz, S.6
Birlik, A.M.7
Calguneri, M.8
Ozcelik, T.9
-
18
-
-
27744454481
-
High frequency of skewed X-chromosome inactivation in females with autoimmune thyroid disease: A possible explanation for the female predisposition to thyroid autoimmunity
-
Brix TH, Knudsen GPS, Kristiansen M, Kyvik KO, Ørstavik KH, Hegedüs L 2005 High frequency of skewed X-chromosome inactivation in females with autoimmune thyroid disease: a possible explanation for the female predisposition to thyroid autoimmunity. J Clin Endocrinol Metab 90:5949-5953
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 5949-5953
-
-
Brix, T.H.1
Knudsen, G.P.S.2
Kristiansen, M.3
Kyvik, K.O.4
Ørstavik, K.H.5
Hegedüs, L.6
-
19
-
-
0031834892
-
A population-based study of Graves' disease in Danish twins
-
Oxf
-
Brix TH, Christensen K, Holm NV, Harvald B, Hegedüs L 1998 A population-based study of Graves' disease in Danish twins. Clin Endocrinol (Oxf) 48:397-400
-
(1998)
Clin Endocrinol
, vol.48
, pp. 397-400
-
-
Brix, T.H.1
Christensen, K.2
Holm, N.V.3
Harvald, B.4
Hegedüs, L.5
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