Literature DB >> 7661932

PCR analysis of the Y chromosome long arm in azoospermic patients: evidence for a second locus required for spermatogenesis.

K Kobayashi1, K Mizuno, A Hida, R Komaki, K Tomita, I Matsushita, M Namiki, T Iwamoto, S Tamura, S Minowada.   

Abstract

We analyzed DNA from 63 Japanese men with either azoospermia or severe oligospermia whose Y chromosomes were cytogenetically normal. A total of 16 loci were examined: 15 loci on the long arm between DYS7E and DYZ1, and the YRRM1 locus, a candidate gene for the azoospermic factor, AZF. One patient with a pericentric inversion of the Y chromosome was also included. We detected micro-deletions in ten individuals. The YRRM1 gene was involved in only three of them. The remaining seven patients showed deletion between DYS7C and DYS239 in common, indicating the presence of at least one additional gene, deletion of which causes azoospermia.

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Year:  1994        PMID: 7661932     DOI: 10.1093/hmg/3.11.1965

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  20 in total

1.  Multiplex PCR for screening of microdeletions on the Y chromosome.

Authors:  P Bor; J Hindkjaer; H J Ingerslev; S Kølvraa
Journal:  J Assist Reprod Genet       Date:  2001-05       Impact factor: 3.412

Review 2.  Genetically determined male infertility and assisted reproduction techniques.

Authors:  T Hargreave
Journal:  J Endocrinol Invest       Date:  2000-11       Impact factor: 4.256

3.  Does junk DNA regulate gene expression in humans?

Authors:  M A Hultén; M Stacey; S J Armstrong
Journal:  Clin Mol Pathol       Date:  1995-06

4.  Study of microdeletions in the Y chromosome of infertile men with idiopathic oligo- or azoospermia.

Authors:  G Yao; G Chen; T Pan
Journal:  J Assist Reprod Genet       Date:  2001-11       Impact factor: 3.412

5.  Expression of DAZ, an azoospermia factor candidate, in human spermatogonia.

Authors:  D B Menke; G L Mutter; D C Page
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

6.  Widening of a Y-chromosome interval-6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to the RBM1 and DAZ genes.

Authors:  L Stuppia; G Calabrese; P G Franchi; R Mingarelli; V Gatta; G Palka; B Dallapiccola
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

7.  Semen characteristics: Advancement in andrological assessment.

Authors:  R S Sharma; K K Gaur; P C Pal; Monika Manocha; Deepak Tomar; Arif Azam Khan; Vinita Tripathi; Vineeta Chattree; A Kriplani
Journal:  Indian J Clin Biochem       Date:  2005-01

8.  SRY and AZF gene variation in male infertility: a cytogenetic and molecular approach.

Authors:  Ozturk Ozdemir; Eylem Gul; Hakan Kilicarslan; Gökhan Gokce; Fatma Y Beyaztas; Semih Ayan; Ihan Sezgin
Journal:  Int Urol Nephrol       Date:  2007-08-31       Impact factor: 2.370

9.  Idiopathic cases of male infertility from a region in India show low incidence of Y-chromosome microdeletion.

Authors:  R Ambasudhan; K Singh; J K Agarwal; S K Singh; A Khanna; R K Sah; I Singh; R Raman
Journal:  J Biosci       Date:  2003-09       Impact factor: 1.826

10.  Members of the CDY family have different expression patterns: CDY1 transcripts have the best correlation with complete spermatogenesis.

Authors:  Sandra E Kleiman; Leah Yogev; Ron Hauser; Amnon Botchan; Batia Bar-Shira Maymon; Letizia Schreiber; Gedalia Paz; Haim Yavetz
Journal:  Hum Genet       Date:  2003-09-03       Impact factor: 4.132

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