Literature DB >> 17573525

Role of sperm FISH studies in the genetic reproductive advice of structural reorganization carriers.

E Anton1, F Vidal, J Blanco.   

Abstract

The use of fluorescence in-situ hybridization (FISH) in decondensed spermatozoa from carriers of structural chromosomal abnormalities provides a way to estimate the amount of unbalanced products. This methodology has become a tool of special interest for a better approximation of the reproductive competence of the carriers. Although there is no discussion regarding the cytogenetic value of the information obtained, the usefulness of performing individual sperm FISH studies must be weighed depending on the object of the study. In this paper, we introduce some considerations concerning the convenience of a routine application of sperm FISH analysis in the major populations of structural reorganization carriers. For each group, the significance of the information that can be obtained and its relevance for genetic reproductive advice are discussed.

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Year:  2007        PMID: 17573525     DOI: 10.1093/humrep/dem152

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  14 in total

1.  Sequential FISH allows the determination of the segregation outcome and the presence of numerical anomalies in spermatozoa from a t(1;8;2)(q42;p21;p15) carrier.

Authors:  Anna Godo; Joan Blanco; Francesca Vidal; Mònica Parriego; Montserrat Boada; Ester Anton
Journal:  J Assist Reprod Genet       Date:  2013-08-23       Impact factor: 3.412

2.  Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2).

Authors:  Alina Teresa Midro; Barbara Panasiuk; Beata Stasiewicz-Jarocka; Marta Olszewska; Ewa Wiland; Marta Myśliwiec; Maciej Kurpisz; Lisa G Shaffer; Marzena Gajecka
Journal:  J Hum Genet       Date:  2014-10-16       Impact factor: 3.172

3.  Sperm rates of 7q11.23, 15q11q13 and 22q11.2 deletions and duplications: a FISH approach.

Authors:  Oscar Molina; Ester Anton; Francesca Vidal; Joan Blanco
Journal:  Hum Genet       Date:  2010-10-08       Impact factor: 4.132

4.  Analysis of clinical outcomes and meiotic segregation modes following preimplantation genetic testing for structural rearrangements using aCGH/NGS in couples with balanced chromosome rearrangement.

Authors:  Tatsuya Nakano; Michiko Ammae; Manabu Satoh; Satoshi Mizuno; Yoshiharu Nakaoka; Yoshiharu Morimoto
Journal:  Reprod Med Biol       Date:  2022-06-29

5.  Simultaneous cell by cell study of both DNA fragmentation and chromosomal segregation in spermatozoa from chromosomal rearrangement carriers.

Authors:  Alexandre Rouen; Ketty Pyram; Xavier Pollet-Villard; Capucine Hyon; Maud Dorna; Sandrine Marques; Sandra Chantot-Bastaraud; Nicole Joyé; Nino Guy Cassuto; Jean-Pierre Siffroi
Journal:  J Assist Reprod Genet       Date:  2013-01-04       Impact factor: 3.412

6.  Chromosomal abnormalities in patients with oligozoospermia and non-obstructive azoospermia.

Authors:  Larysa Y Pylyp; Lyudmyla O Spinenko; Natalia V Verhoglyad; Valery D Zukin
Journal:  J Assist Reprod Genet       Date:  2013-04-11       Impact factor: 3.412

7.  High rates of de novo 15q11q13 inversions in human spermatozoa.

Authors:  Oscar Molina; Ester Anton; Francesca Vidal; Joan Blanco
Journal:  Mol Cytogenet       Date:  2012-02-06       Impact factor: 2.009

Review 8.  Cytogenetic determinants of male fertility.

Authors:  R H Martin
Journal:  Hum Reprod Update       Date:  2008-06-04       Impact factor: 15.610

9.  The impact of patient, embryo, and translocation characteristics on the ploidy status of young couples undergoing preimplantation genetic testing for structural rearrangements (PGT-SR) by next generation sequencing (NGS).

Authors:  Fazilet Kubra Boynukalin; Meral Gultomruk; Niyazi Emre Turgut; Carmen Rubio; Lorena Rodrigo; Zalihe Yarkiner; Selen Ecemis; Guvenc Karlikaya; Necati Findikli; Mustafa Bahceci
Journal:  J Assist Reprod Genet       Date:  2021-01-04       Impact factor: 3.412

10.  Inheritance of a Chromosome 3 and 21 Translocation in the Fetuses, with One also Having Trisomy 21, in Three Pregnancies in One Family.

Authors:  A Pazarbasi; O Demirhan; D Alptekin; Ft Ozgunen; L Ozpak; Mb Yilmaz; E Nazlican; N Tanriverdi; U Luleyap; D Gümürdülü
Journal:  Balkan J Med Genet       Date:  2013-12       Impact factor: 0.519

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