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1:

Back to basics.

Hardin S.

Genome Biol. 2002 Jul 15;3(8):REPORTS4026. Epub 2002 Jul 15.

PMID: 12186643 [PubMed - indexed for MEDLINE]

2:

Sulfate transport is not impaired in pendred syndrome thyrocytes.

Kraiem Z, Heinrich R, Sadeh O, Shiloni E, Nassir E, Hazani E, Glaser B.

J Clin Endocrinol Metab. 1999 Jul;84(7):2574-6.

PMID: 10404839 [PubMed - indexed for MEDLINE]

3:

Pendred's syndrome and genetic defects in thyroid hormone synthesis.

Kopp P.

Rev Endocr Metab Disord. 2000 Jan;1(1-2):109-21. Review. No abstract available.

PMID: 11704986 [PubMed - indexed for MEDLINE]

4:

[Genetic origin of spermatogenesis impairments: clinical aspects and relationships with mouse models of infertility]

Siffroi JP, Chantot-Bastaraud S, Ravel C.

Gynecol Obstet Fertil. 2003 Jun;31(6):504-15. Review. French.

PMID: 12865188 [PubMed - indexed for MEDLINE]

5:

The locus of sY84 is not associated with spermatogenesis--"is it better to find Adam or study spermatogenesis?--a different opinion".

Tseng SL, Wang YC, Li SY.

Fertil Steril. 1999 Aug;72(2):375-6. No abstract available.

PMID: 10439018 [PubMed - indexed for MEDLINE]

6:

Sex Chromosome Genetics '99. Male infertility and the Y chromosome.

McElreavey K, Krausz C.

Am J Hum Genet. 1999 Apr;64(4):928-33. Review. No abstract available.

PMID: 10090876 [PubMed - indexed for MEDLINE]

7:

The Y chromosome and spermatogenesis.

de Kretser DM, Burger HG.

N Engl J Med. 1997 Feb 20;336(8):576-8. No abstract available.

PMID: 9023097 [PubMed - indexed for MEDLINE]

8:

Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations.

Shaukat S, Fatima Z, Zehra U, Waqar AB.

J Ayub Med Coll Abbottabad. 2003 Jul-Sep;15(3):59-64. Review.

PMID: 14727345 [PubMed - indexed for MEDLINE]

9:

Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2.

Fleming JC, Tartaglini E, Kawatsuji R, Yao D, Fujiwara Y, Bednarski JJ, Fleming MD, Neufeld EJ.

Mol Genet Metab. 2003 Sep-Oct;80(1-2):234-41.

PMID: 14567973 [PubMed - indexed for MEDLINE]

10:

Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assembly.

Brunner S, Colman D, Travis AJ, Luhmann UF, Shi W, Feil S, Imsand C, Nelson J, Grimm C, Rülicke T, Fundele R, Neidhardt J, Berger W.

Biol Reprod. 2008 Oct;79(4):608-17. Epub 2008 Jun 25.

PMID: 18579752 [PubMed - indexed for MEDLINE]

11:

[Phenotypical difference between males of different Y chromosome lineage]

Nakahori Y, Lee JW, Ewis AA, Shinka T.

Tanpakushitsu Kakusan Koso. 2001 Dec;46(16 Suppl):2346-50. Review. Japanese. No abstract available.

PMID: 11802392 [PubMed - indexed for MEDLINE]

12:

Gene polymorphisms/mutations relevant to abnormal spermatogenesis.

Nuti F, Krausz C.

Reprod Biomed Online. 2008 Apr;16(4):504-13. Review.

PMID: 18413059 [PubMed - indexed for MEDLINE]

13:

Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings.

Arellano B, Pera A, Ramírez-Camacho R, Villamar M, Trinidad A, García JR, Moreno F, Hernández-Chico C.

Clin Genet. 2005 May;67(5):438-40. No abstract available.

PMID: 15811013 [PubMed - indexed for MEDLINE]

14:

Y bind RNA for spermatogenesis?

Ruggiu M, Cooke H.

Int J Androl. 1999 Feb;22(1):19-27. Review. No abstract available.

PMID: 10068940 [PubMed - indexed for MEDLINE]

15:

Spermatogenesis and the mouse Y chromosome: specialisation out of decay.

Mitchell MJ.

Results Probl Cell Differ. 2000;28:233-70. Review. No abstract available.

PMID: 10626301 [PubMed - indexed for MEDLINE]

16:

Y chromosome.

Foresta C, Ferlin A, Moro E, Scandellari C.

Lancet. 2000 Jan 15;355(9199):234-5. No abstract available.

PMID: 10675146 [PubMed - indexed for MEDLINE]

17:

[Pendred's syndrome. Current features]

Wémeau JL, Vlaeminck-Guillem V, Dubrulle F, Dumur V, Vincent C.

Presse Med. 2001 Nov 17;30(34):1689-94. Review. French.

PMID: 11760600 [PubMed - indexed for MEDLINE]

18:

Recessive multiple epiphyseal dysplasia (rMED): phenotype delineation in eighteen homozygotes for DTDST mutation R279W.

Ballhausen D, Bonafé L, Terhal P, Unger SL, Bellus G, Classen M, Hamel BC, Spranger J, Zabel B, Cohn DH, Cole WG, Hecht JT, Superti-Furga A.

J Med Genet. 2003 Jan;40(1):65-71. No abstract available.

PMID: 12525546 [PubMed - indexed for MEDLINE]

19:

Impairment of spermatogenesis leading to infertility.

Toshimori K, Ito C, Maekawa M, Toyama Y, Suzuki-Toyota F, Saxena DK.

Anat Sci Int. 2004 Sep;79(3):101-11. Review.

PMID: 15453611 [PubMed - indexed for MEDLINE]

20:

[Animal models: Candidate genes for human male infertility]

Escalier D.

Gynecol Obstet Fertil. 2006 Sep;34(9):827-30. Epub 2006 Aug 23. Review. French.

PMID: 16931095 [PubMed - indexed for MEDLINE]

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