BACKGROUND: Infertility affects ~10-15% of couples trying to have children, in which the rate of male fertility problems is approximately at 30-50%. Copy number variations (CNVs) are DNA sequences greater than or equal to 1 kb in length sharing a high level of similarity, and present at a variable number of copies in the genome; in our study, we used the canine species as an animal model to detect CNVs responsible for male infertility. We aim to identify CNVs associated with male infertility in the dog genome with a two-pronged approach: we performed a sperm analysis using the CASA system and a cytogenetic-targeted analysis on genes involved in male gonad development and spermatogenesis with fluorescence in situ hybridization (FISH), usi...
Identification of genomic variants within dogs is important for understanding genetic factors contri...
Molecular cytogenetic studies have been instrumental in defining the nature of numerical and structu...
Structural variation is an important and abundant source of genetic and phenotypic variation. Here w...
Mechanisms that regulate sexual chromosome distribution in the canine ejaculate are not quite unders...
BACKGROUND: Copy number variants (CNVs) account for substantial variation between genomes and are a ...
International audienceABSTRACT: BACKGROUND: Copy number variants (CNVs) account for substantial vari...
WOS: 000449849900037PubMed: 30085374Male reproductive parameters are often used for the functional e...
Background: Substantial contribution to phenotypic diversity is accounted for by copy number variant...
Impaired fertility associated with disorders of sex development (DSDs) due to genetic causes in dogs...
Although the disorder of sex development in dogs with female karyotype (XX DSD) is quite common, its...
Abstract. Effective preselection of sex has been accomplished in several species of livestock and al...
Effective preselection of sex has been accomplished in several species of livestock and also in huma...
Male infertility is an emerging problem in both humans and animals, and the knowledge of its causes ...
BACKGROUND: Copy number variants (CNVs) occupy a significant portion of the human genome and may hav...
Cryptorchidism, or retained testicles, is one of the most common congenital developmental defects i...
Identification of genomic variants within dogs is important for understanding genetic factors contri...
Molecular cytogenetic studies have been instrumental in defining the nature of numerical and structu...
Structural variation is an important and abundant source of genetic and phenotypic variation. Here w...
Mechanisms that regulate sexual chromosome distribution in the canine ejaculate are not quite unders...
BACKGROUND: Copy number variants (CNVs) account for substantial variation between genomes and are a ...
International audienceABSTRACT: BACKGROUND: Copy number variants (CNVs) account for substantial vari...
WOS: 000449849900037PubMed: 30085374Male reproductive parameters are often used for the functional e...
Background: Substantial contribution to phenotypic diversity is accounted for by copy number variant...
Impaired fertility associated with disorders of sex development (DSDs) due to genetic causes in dogs...
Although the disorder of sex development in dogs with female karyotype (XX DSD) is quite common, its...
Abstract. Effective preselection of sex has been accomplished in several species of livestock and al...
Effective preselection of sex has been accomplished in several species of livestock and also in huma...
Male infertility is an emerging problem in both humans and animals, and the knowledge of its causes ...
BACKGROUND: Copy number variants (CNVs) occupy a significant portion of the human genome and may hav...
Cryptorchidism, or retained testicles, is one of the most common congenital developmental defects i...
Identification of genomic variants within dogs is important for understanding genetic factors contri...
Molecular cytogenetic studies have been instrumental in defining the nature of numerical and structu...
Structural variation is an important and abundant source of genetic and phenotypic variation. Here w...