Genetic causes of spermatogenic failure. (Q37074590)

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scientific article published on 05 December 2011

Language	Label	Description	Also known as
English	Genetic causes of spermatogenic failure.	scientific article published on 05 December 2011

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scholarly article

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Europe PubMed Central

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17 January 2020

Genetic causes of spermatogenic failure (English)

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Europe PubMed Central

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17 January 2020

2

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17 January 2020

Herman Tournaye

3

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17 January 2020

Katrien Stouffs

4

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17 January 2020

author name string

Annelien Massart

1

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17 January 2020

publication date

5 December 2011

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17 January 2020

Asian Journal of Andrology

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17 January 2020

14

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17 January 2020

1

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17 January 2020

40-48

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17 January 2020

The Y chromosome-linked copy number variations and male fertility

1 reference

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Male infertility: pathogenesis and clinical diagnosis

1 reference

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A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation

1 reference

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DPY19L2 deletion as a major cause of globozoospermia

1 reference

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A comprehensive gene mutation screen in men with asthenozoospermia

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GATA4 regulates Sertoli cell function and fertility in adult male mice

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Mouse models in male fertility research

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Identification of de novo copy number variants associated with human disorders of sexual development

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What about gr/gr deletions and male infertility? Systematic review and meta-analysis

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Genetic variants in Piwi-interacting RNA pathway genes confer susceptibility to spermatogenic failure in a Chinese population

1 reference

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Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1

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A wider context for gene trap mutagenesis

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Gene trap mutagenesis in the mouse.

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Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm

1 reference

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A newly discovered mutation in PICK1 in a human with globozoospermia

1 reference

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The use of transgenic mouse models in the study of male infertility

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Mutations in SOHLH1 gene associate with nonobstructive azoospermia

1 reference

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29 September 2017

Mutation of Eif4g3, encoding a eukaryotic translation initiation factor, causes male infertility and meiotic arrest of mouse spermatocytes

1 reference

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Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent

1 reference

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The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility

1 reference

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29 September 2017

Alterations in the steroid hormone receptor co-chaperone FKBPL are associated with male infertility: a case-control study.

1 reference

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29 September 2017

Clinical Review#: State of the art for genetic testing of infertile men.

1 reference

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29 September 2017

Should non-mosaic Klinefelter syndrome men be labelled as infertile in 2009?

1 reference

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29 September 2017

Differential effect of specific gr/gr deletion subtypes on spermatogenesis in the Chinese Han population

1 reference

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29 September 2017

c.822+126T>G/C: a novel triallelic polymorphism of the TSSK6 gene associated with spermatogenic impairment in a Chinese population

1 reference

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29 September 2017

Y chromosome gr/gr deletions are a risk factor for low semen quality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

29 September 2017

Functional polymorphism in H2BFWT-5'UTR is associated with susceptibility to male infertility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

29 September 2017

Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia

1 reference

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Approaches to improve the diagnosis and management of infertility

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Human male infertility caused by mutations in the CATSPER1 channel protein

1 reference

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A missense mutation in the Capza3 gene and disruption of F-actin organization in spermatids of repro32 infertile male mice

1 reference

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Copy number variation on the human Y chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

29 September 2017

PICK1 deficiency causes male infertility in mice by disrupting acrosome formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

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The will-o'-the-wisp of genetics--hunting for the azoospermia factor gene

1 reference

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Spermatogenesis in a man with complete deletion of USP9Y

1 reference

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The highly conserved NANOS2 protein: testis-specific expression and significance for the human male reproduction

1 reference

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29 September 2017

Single-nucleotide polymorphisms of the PRDM9 (MEISETZ) gene in patients with nonobstructive azoospermia

1 reference

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The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population

1 reference

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Mutations of the SYCP3 gene in women with recurrent pregnancy loss

1 reference

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The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

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Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia

1 reference

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Underlying karyotype abnormalities in IVF/ICSI patients

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Gene polymorphisms/mutations relevant to abnormal spermatogenesis

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The dual bromodomain and WD repeat-containing mouse protein BRWD1 is required for normal spermiogenesis and the oocyte-embryo transition

1 reference

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Sequence alterations in the YBX2 gene are associated with male factor infertility

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Genome-wide expression of azoospermia testes demonstrates a specific profile and implicates ART3 in genetic susceptibility

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Gene polymorphisms and male infertility--a meta-analysis and literature review

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Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia

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A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axoneme

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Male infertility and variation in CAG repeat length in the androgen receptor gene: a meta-analysis

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Male infertility: role of genetic background

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1 reference

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Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure

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Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.

1 reference

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UTP14c is a recently acquired retrogene associated with spermatogenesis and fertility in man.

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SYCP3 mutations are uncommon in patients with azoospermia.

1 reference

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Gene deletions in an infertile man with sperm fibrous sheath dysplasia

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Screening for ZNF230 gene mutation and analysis of its correlation with azoospermia.

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Genetic control of spermiogenesis: insights from the CREM gene and implications for human infertility

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Molecular characterization of heat shock-like factor encoded on the human Y chromosome, and implications for male infertility.

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Azoospermia in patients heterozygous for a mutation in SYCP3

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Genetic dissection of mammalian fertility pathways

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Mouse models of male infertility.

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29 September 2017

Female subfertility

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A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility

1 reference

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29 September 2017

Molecular genetic analysis of two human sperm fibrous sheath proteins, AKAP4 and AKAP3, in men with dysplasia of the fibrous sheath

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

29 September 2017

Prognostic value of Y deletion analysis: what is the clinical prognostic value of Y chromosome microdeletion analysis?

1 reference

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29 September 2017

Preserved male fertility despite decreased androgen sensitivity caused by a mutation in the ligand-binding domain of the androgen receptor gene

1 reference

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29 September 2017

The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility

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29 September 2017

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y

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Mouse mutagenesis-systematic studies of mammalian gene function

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Large scale ENU screens in the mouse: genetics meets genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

29 September 2017

CAG-repeat variant in the polymerase γ gene and male infertility in the Chinese population: a meta-analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

27 June 2018

TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

27 June 2018

Cytogenetics of infertile men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

27 June 2018

Towards the molecular localisation of the AZF locus: mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

27 June 2018

Abnormal methylation of the promoter of CREM is broadly associated with male factor infertility and poor sperm quality but is improved in sperm selected by density gradient centrifugation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Molecular analysis of guanidinoacetate-n-methyltransferase (GAMT) and creatine transporter (SLC6A8) gene by using denaturing high pressure liquid chromatography (DHPLC) as a possible source of human male infertility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Polymorphisms in MTHFR and MTRR genes associated with blood plasma homocysteine concentration and sperm counts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Complete deletion of the AZFb interval from the Y chromosome in an oligozoospermic man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) and idiopathic male infertility: novel perspectives versus facts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Role of glutathione S-transferase Mu-1 (GSTM1) polymorphism in oligospermic infertile males

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Single nucleotide polymorphism (SNP) of the endothelial nitric oxide synthase (eNOS) gene (Glu298Asp variant) in infertile men with asthenozoospermia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Association of CYP1A1*2A polymorphism with male infertility in Indian population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Glutathione S-transferase M1 and T1 polymorphism in men with idiopathic infertility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Expansion of CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene in idiopathic oligozoospermia patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Focal spermatogenesis originates in euploid germ cells in classical Klinefelter patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

FAS and FASLG polymorphisms and susceptibility to idiopathic azoospermia or severe oligozoospermia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Association of CYP1A1 and glutathione S-transferase polymorphisms with male factor infertility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Associations of MTHFR DNMT3b 4977 bp deletion in mtDNA and GSTM1 deletion, and aberrant CpG island hypermethylation of GSTM1 in non-obstructive infertility in Indian men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Natural transmission of USP9Y gene mutations: a new perspective on the role of AZFa genes in male fertility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

The role of the testis-specific gene hTAF7L in the aetiology of male infertility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

MTHFR C677T polymorphism, GSTM1 deletion and male infertility: a possible suggestion of a gene-gene interaction?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Gene functional research using polyethylenimine-mediated in vivo gene transfection into mouse spermatogenic cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Fluorescence in situ hybridization and molecular studies in infertile men with dysplasia of the fibrous sheath.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Single nucleotide polymorphisms of the heat shock protein 90 gene in varicocele-associated infertility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Molecular genetics of male infertility: stem cell factor/c-kit system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Homozygous methylenetetrahydrofolate reductase C677T mutation and male infertility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Increased frequencies of cytochrome P4501A1 polymorphisms in infertile men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

Wild-type endoderm abrogates the ventral developmental defects associated with GATA-4 deficiency in the mouse.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 September 2018

The choice and outcome of the fertility treatment of 38 couples in whom the male partner has a Yq microdeletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 December 2018

Genetic Abnormalities among Severely Oligospermic Men Who Are Candidates for Intracytoplasmic Sperm Injection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 December 2018

EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 December 2018

CATSPER2, a human autosomal nonsyndromic male infertility gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3735159

4 December 2018

The role of endothelial nitric oxide synthase (eNOS) T-786C, G894T, and 4a/b gene polymorphisms in the risk of idiopathic male infertility

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase C677T polymorphism and the risk of male infertility: a meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NANOS3 gene mutations in men with isolated sterility phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is a genetic defect in Fkbp6 a common cause of azoospermia in humans?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multilocus analyses of estrogen-related genes reveal involvement of the ESR1 gene in male infertility and the polygenic nature of the pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the hemochromatosis mutations C282Y and H63D in infertile men

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion of a novel heat shock gene on the Y chromosome associated with azoospermia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rare Y chromosome missense mutation in exon 25 of human USP9Y revealed by pyrosequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sperm chromosome analysis and outcome of IVF in patients with non-mosaic Klinefelter's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between male infertility and genetic variability at the PON1/2 and GSTM1/T1 gene loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AZFa deletions in Sertoli cell-only syndrome: a retrospective study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New mouse genetic models for human contraceptive development

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MTHFR 677C>T and 1298A>C polymorphisms and male infertility risk: a meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of genetic markers within the KIT and KITLG genes with human male infertility

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-based screening for Y chromosome deletions in Taiwanese men presenting with spermatogenic failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensorineural deafness and male infertility: a contiguous gene deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in cell death pathway genes are associated with altered sperm apoptosis and poor semen quality

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in CYP1A1 gene are associated with male infertility in a Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of USP9Y and DBY in infertile patients with severely impaired spermatogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association of 4a4b polymorphism of endothelial nitric oxide synthase (eNOS) gene with the sperm morphology in Korean infertile men

1 reference

https://pubmed.ncbi.nlm.nih.gov/22138898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/AJA.2011.67

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22138898%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22138898%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22138898%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

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