Literature DB >> 24458834

Relevance of genetic investigation in male infertility.

P Asero1, A E Calogero, R A Condorelli, L Mongioi', E Vicari, F Lanzafame, R Crisci, S La Vignera.   

Abstract

Genetic causes can be directly responsible for various clinical conditions of male infertility and spermatogenic impairment. With the increased use of assisted reproduction technologies our understanding of genetic basis of male infertility has large implications not only for understanding the causes of infertility but also in determining the prognosis and management of such couples. For these reasons, the genetic investigations represent today an essential and useful tool in the treatment of male infertility. Several evidences are available for the clinical practice regarding the diagnosis; however, there are less information relative to the treatment of the genetic causes of male infertility. Focus of this review is to discuss the main and more common genetic causes of male infertility to better direct the genetics investigation in the treatment of spermatogenic impairment.

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Year:  2014        PMID: 24458834     DOI: 10.1007/s40618-014-0053-1

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  114 in total

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5.  Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure.

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Review 10.  CAG repeat testing of androgen receptor polymorphism: is this necessary for the best clinical management of hypogonadism?

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  11 in total

1.  MicroRNAs association with azoospermia, oligospermia, asthenozoospermia, and teratozoospermia: a systematic review.

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Authors:  Filipe Tenorio Lira Neto; Phil Vu Bach; Bobby Baback Najari; Philip Shihua Li; Marc Goldstein
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3.  Association of polymorphisms in tektin-t gene with idiopathic asthenozoospermia in Sichuan, China.

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Journal:  J Assist Reprod Genet       Date:  2015-11-19       Impact factor: 3.412

Review 4.  The evolving role of genetic tests in reproductive medicine.

Authors:  Federica Cariati; Valeria D'Argenio; Rossella Tomaiuolo
Journal:  J Transl Med       Date:  2019-08-14       Impact factor: 5.531

5.  Leukocytospermia in late adolescents: possible clinical interpretations.

Authors:  S La Vignera; R Cannarella; A Aversa; R Rago; R A Condorelli; A E Calogero
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6.  Expression Analysis of the CRISP2, CATSPER1, PATE1 and SEMG1 in the Sperm of Men with Idiopathic Asthenozoospermia.

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Journal:  J Reprod Infertil       Date:  2019 Apr-Jun

Review 7.  Genetic Landscape of Nonobstructive Azoospermia and New Perspectives for the Clinic.

Authors:  Miriam Cerván-Martín; José A Castilla; Rogelio J Palomino-Morales; F David Carmona
Journal:  J Clin Med       Date:  2020-01-21       Impact factor: 4.241

8.  Genetics in human reproduction.

Authors:  Vivian de Oliveira Rodrigues; Fernanda Polisseni; Gabriel Duque Pannain; Miralva Aurora Galvão Carvalho
Journal:  JBRA Assist Reprod       Date:  2020-10-06

9.  Integration and gene co-expression network analysis of scRNA-seq transcriptomes reveal heterogeneity and key functional genes in human spermatogenesis.

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Journal:  Sci Rep       Date:  2021-09-27       Impact factor: 4.379

10.  Update on genetic screening and treatment for infertile men with genetic disorders in the era of assisted reproductive technology.

Authors:  Seung Ryeol Lee; Tae Ho Lee; Seung-Hun Song; Dong Suk Kim; Kyung Hwa Choi; Jae Ho Lee; Dae Keun Kim
Journal:  Clin Exp Reprod Med       Date:  2021-11-23
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