Similar articles for PMID: 12161610

Year	Number of Results
1988	1
1991	2
1992	1
1993	1
1994	1
1995	2
1998	3
1999	5
2000	6
2001	4
2002	8
2003	2
2004	7
2005	1
2006	4
2007	4
2008	4
2009	2
2010	5
2011	5
2012	4
2013	1
2014	1
2015	3
2016	2
2017	3
2018	2
2019	1
2024	0

1

FOXL2 mutation screening in a large panel of POF patients and XX males.

De Baere E, Lemercier B, Christin-Maitre S, Durval D, Messiaen L, Fellous M, Veitia R. De Baere E, et al. J Med Genet. 2002 Aug;39(8):e43. doi: 10.1136/jmg.39.8.e43. J Med Genet. 2002. PMID: 12161610 Free PMC article. No abstract available.

2

Identification of novel mutations in FOXL2 associated with premature ovarian failure.

Harris SE, Chand AL, Winship IM, Gersak K, Aittomäki K, Shelling AN. Harris SE, et al. Mol Hum Reprod. 2002 Aug;8(8):729-33. doi: 10.1093/molehr/8.8.729. Mol Hum Reprod. 2002. PMID: 12149404

3

Screening for FOXL2 gene mutations in women with premature ovarian failure: an Indian experience.

Chatterjee S, Modi D, Maitra A, Kadam S, Patel Z, Gokrall J, Meherji P. Chatterjee S, et al. Reprod Biomed Online. 2007 Nov;15(5):554-60. doi: 10.1016/s1472-6483(10)60388-4. Reprod Biomed Online. 2007. PMID: 18028747

4

Genes and translocations involved in POF.

Schlessinger D, Herrera L, Crisponi L, Mumm S, Percesepe A, Pellegrini M, Pilia G, Forabosco A. Schlessinger D, et al. Am J Med Genet. 2002 Aug 15;111(3):328-33. doi: 10.1002/ajmg.10565. Am J Med Genet. 2002. PMID: 12210333 Review.

5

Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure.

Watkins WJ, Umbers AJ, Woad KJ, Harris SE, Winship IM, Gersak K, Shelling AN. Watkins WJ, et al. Fertil Steril. 2006 Nov;86(5):1518-21. doi: 10.1016/j.fertnstert.2006.03.054. Epub 2006 Sep 18. Fertil Steril. 2006. PMID: 16979636 Free article. Clinical Trial.

6

[Advance in mutation analysis of the candidate genes in premature ovarian failure].

Tan YQ, Cheng DH, Lu GX. Tan YQ, et al. Yi Chuan. 2006 Nov;28(11):1467-71. doi: 10.1360/yc-006-1467. Yi Chuan. 2006. PMID: 17098720 Review. Chinese.

7

Evolution and expression of FOXL2.

Cocquet J, Pailhoux E, Jaubert F, Servel N, Xia X, Pannetier M, De Baere E, Messiaen L, Cotinot C, Fellous M, Veitia RA. Cocquet J, et al. J Med Genet. 2002 Dec;39(12):916-21. doi: 10.1136/jmg.39.12.916. J Med Genet. 2002. PMID: 12471206 Free PMC article. No abstract available.

8

[Sex genetics].

Vilain E, Elreavey KM, Richaud F, Fellous M. Vilain E, et al. Presse Med. 1992 May 16;21(18):852-6. Presse Med. 1992. PMID: 1535151 Review. French.

9

An autosomal or X linked mutation results in true hermaphrodites and 46,XX males in the same family.

Slaney SF, Chalmers IJ, Affara NA, Chitty LS. Slaney SF, et al. J Med Genet. 1998 Jan;35(1):17-22. doi: 10.1136/jmg.35.1.17. J Med Genet. 1998. PMID: 9475089 Free PMC article. Review.

10

A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development.

McElreavey K, Vilain E, Abbas N, Herskowitz I, Fellous M. McElreavey K, et al. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3368-72. doi: 10.1073/pnas.90.8.3368. Proc Natl Acad Sci U S A. 1993. PMID: 8475082 Free PMC article.

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