Gerard Gacon

Paris, 75014, France

Last Updated: 09/26/2026

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Found 10 publications

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.

Journal: American journal of human genetics

Published: June 30, 2019

Corrigendum: Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.

Corrigendum: Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.

Journal: Human molecular genetics

Published: December 06, 2018

Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.

Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.

Journal: Human molecular genetics

Published: December 21, 2017

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.

Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.

Journal: American journal of human genetics

Published: March 19, 2016

Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia.

Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia.

Journal: Basic and clinical andrology

Published: August 25, 2015

OCRL-mutated fibroblasts from patients with Dent-2 disease exhibit INPP5B-independent phenotypic variability relatively to Lowe syndrome cells.

OCRL-mutated fibroblasts from patients with Dent-2 disease exhibit INPP5B-independent phenotypic variability relatively to Lowe syndrome cells.

Journal: Human molecular genetics

Published: October 12, 2014

Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse.

Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse.

Journal: Developmental biology

Published: June 23, 2013

Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

Journal: American journal of human genetics

Published: November 17, 2012

The tumor suppressor HACE1 targets Rac1 to ubiquitin-mediated proteasomal degradation

The tumor suppressor HACE1 targets Rac1 to ubiquitin-mediated proteasomal degradation

Journal: Medecine sciences : M/S

Published: February 01, 2012

The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation.

The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation.

Journal: Human molecular genetics

Published: November 29, 2011

Showing 1-10 of 10

Last Updated: 09/26/2026