1 |
Nesterova TB, Johnston CM, Appanah R, Newall AE, Godwin J, Alexiou M, et al. Skewing X chromosome choice by modulating sense transcription across the Xist locus. Genes Dev 2003;17: 2177-90.
DOI
|
2 |
Hendrich BD, Plenge RM, Willard HF. Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation. Nucleic Acids Res 1997;25:2661-71.
DOI
|
3 |
Sato K, Uehara S, Hashiyada M, Nabeshima H, Sugawara J, Terada Y, et al. Genetic significance of skewed X-chromosome inactivation in premature ovarian failure. Am J Med Genet A 2004; 130:240-4.
|
4 |
Anasti JN. Premature ovarian failure: an update. Fertil Steril 1998;70:1-15.
|
5 |
Nelson LM. Clinical practice: primary ovarian insufficiency. N Engl J Med 2009;360:606-14.
DOI
|
6 |
Coulam CB, Adamson SC, Annegers JF. Incidence of premature ovarian failure. Obstet Gynecol 1986;67:604-6.
|
7 |
Goswami D, Conway GS. Premature ovarian failure. Hum Reprod Update 2005;11:391-410.
DOI
|
8 |
Herzing LB, Romer JT, Horn JM, Ashworth A. Xist has properties of the X-chromosome inactivation centre. Nature 1997;386:272-5.
DOI
|
9 |
Lyon MF. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature 1961;190:372-3.
DOI
|
10 |
Brown CJ, Ballabio A, Rupert JL, Lafreniere RG, Grompe M, Tonlorenzi R, et al. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome. Nature 1991;349:38-44.
DOI
|
11 |
Wengler G, Gorlin JB, Williamson JM, Rosen FS, Bing DH. Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome. Blood 1995; 85:2471-7.
|
12 |
Orstavik KH, Orstavik RE, Eiklid K, Tranebjaerg L. Inheritance of skewed X chromosome inactivation in a large family with an Xlinked recessive deafness syndrome. Am J Med Genet 1996;64: 31-4.
DOI
|
13 |
Devriendt K, Matthijs G, Legius E, Schollen E, Blockmans D, van Geet C, et al. Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita. Am J Hum Genet 1997;60:581-7.
|
14 |
Plenge RM, Hendrich BD, Schwartz C, Arena JF, Naumova A, Sapienza C, et al. A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation. Nat Genet 1997;17:353-6.
DOI
|
15 |
Marahrens Y, Loring J, Jaenisch R. Role of the Xist gene in X chromosome choosing. Cell 1998;92:657-64.
DOI
|
16 |
Newall AE, Duthie S, Formstone E, Nesterova T, Alexiou M, Johnston C, et al. Primary non-random X inactivation associated with disruption of Xist promoter regulation. Hum Mol Genet 2001;10: 581-9.
DOI
|
17 |
Therman E, Laxova R, Susman B. The critical region on the human Xq. Hum Genet 1990;85:455-61.
|
18 |
Pugacheva EM, Tiwari VK, Abdullaev Z, Vostrov AA, Flanagan PT, Quitschke WW, et al. Familial cases of point mutations in the XIST promoter reveal a correlation between CTCF binding and pre-emptive choices of X chromosome inactivation. Hum Mol Genet 2005;14:953-65.
DOI
|
19 |
Yoon SH, Choi YM, Hong MA, Kang BM, Kim JJ, Min EG, et al. X chromosome inactivation patterns in patients with idiopathic premature ovarian failure. Hum Reprod 2008;23:688-92.
DOI
|
20 |
Pereira LV, Zatz M. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed Xchromosome inactivation. Am J Med Genet 1999;87:86-7.
DOI
|
21 |
Davis CJ, Davison RM, Payne NN, Rodeck CH, Conway GS. Female sex preponderance for idiopathic familial premature ovarian failure suggests an X chromosome defect: opinion. Hum Reprod 2000;15:2418-22.
DOI
|