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Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
Frederick Dong
,
Amir Amiri-Yekta
,
Guillaume Martinez
,
Antoine Saut
,
Julie Tek
et al.
Journal articles
hal-01877985v1
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Mutations in DNAJB13 , Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility
Elma El Khouri
,
Lucie Thomas
,
Ludovic Jeanson
,
Emilie Bequignon
,
Benoit Vallette
et al.
Journal articles
inserm-03875562v1
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Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility
Chunyu Liu
,
Haruhiko Miyata
,
Yang Gao
,
Yanwei Sha
,
Shuyan Tang
et al.
Journal articles
hal-03004971v1
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Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility
Guillaume Martinez
,
Julie Beurois
,
Denis Dacheux
,
Caroline Cazin
,
Marie Bidart
et al.
Journal articles
hal-03004959v1
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Zika virus and reproduction: facts, questions and current management
Sylvie Epelboin
,
Emmanuel Dulioust
,
Loïc Epelboin
,
Alexandra Benachi
,
Françoise Merlet
et al.
Journal articles
hal-01844532v1
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Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in $Trypanosoma$ and human.
Charles Coutton
,
Alexandra S. Vargas
,
Amir Amiri-Yekta
,
Zine-Eddine Kherraf
,
Selima Fourati Ben Mustapha
et al.
Journal articles
hal-01724640v1
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A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl Syndrome
Patrick Lorès
,
Zine-Eddine Kherraf
,
Amir Amiri-Yekta
,
Marjorie Whitfield
,
Abbas Daneshipour
et al.
Journal articles
hal-03369854v1
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Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility
Patrick Lorès
,
Denis Dacheux
,
Zine-Eddine Kherraf
,
Jean-Fabrice Nsota Mbango
,
Charles Coutton
et al.
Journal articles
hal-02370384v1
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Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.
Thassadite Dirami
,
Baptiste Rode
,
Mathilde Jollivet
,
Nathalie da Silva
,
Denise Escalier
et al.
Journal articles
hal-00990664v1
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The sodium/proton exchanger SLC9C1 ( sNHE ) is essential for human sperm motility and fertility
Emma Cavarocchi
,
Marjorie Whitfield
,
Ahmed Chargui
,
Laurence Stouvenel
,
Patrick Lorès
et al.
Journal articles
hal-03369825v1
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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
Patrick Lorès
,
Charles Coutton
,
Elma El Khouri
,
Laurence Stouvenel
,
Maelle Givelet
et al.
Journal articles
hal-02346745v1
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Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia
Thassadite Dirami
,
Baptiste Rode
,
Jean-Philippe Wolf
,
Gérard Gacon
,
Emmanuel Dulioust
et al.
Journal articles
inserm-01244340v1
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Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum
Lucile Ferreux
,
Mathilde Bourdon
,
Ahmed Chargui
,
Alain Schmitt
,
Laurence Stouvenel
et al.
Journal articles
hal-03873460v1
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