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New insights into protein-protein interaction data lead to increased estimates of the S. cerevisiae interactome size.
Laure Sambourg
,
Nicolas Thierry-Mieg
Journal articles
hal-00807360v1
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MatrixDB: integration of new data with a focus on glycosaminoglycan interactions
Olivier Clerc
,
Madeline Deniaud
,
Sylvain Vallet
,
Alexandra Naba
,
Alain Rivet
et al.
Journal articles
hal-02109904v1
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Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations
Zine‐eddine Kherraf
,
Caroline Cazin
,
Charles Coutton
,
Amir Amiri‐yekta
,
Guillaume Martinez
et al.
Journal articles
hal-02347512v1
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The [PSI+] prion and HSP104 modulate cytochrome c oxidase deficiency caused by deletion of COX12
Pawan Kumar Saini
,
Hannah Dawitz
,
Andreas Aufschnaiter
,
Jinsu Thomas
,
Amélie Amblard
et al.
2021
Preprints, Working Papers, ...
hal-03402829v1
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A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.
Zine-Eddine Kherraf
,
Amir Amiri-Yekta
,
Denis Dacheux
,
Thomas Karaouzène
,
Charles Coutton
et al.
Journal articles
hal-01863586v1
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New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella
Guillaume Martinez
,
Anne-Laure Barbotin
,
Caroline Cazin
,
Zeina Wehbe
,
Angèle Boursier
et al.
Journal articles
hal-04011973v1
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From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the ZMYND15 gene
Zine-Eddine Kherraf
,
Caroline Cazin
,
Florence Lestrade
,
Jana Muronova
,
Charles Coutton
et al.
Journal articles
hal-03720221v1
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A new pooling strategy for high-throughput screening: the Shifted Transversal Design.
Nicolas Thierry-Mieg
Journal articles
hal-00198315v1
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CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia.
Julie Beurois
,
Guillaume Martinez
,
Caroline Cazin
,
Zine-Eddine Kherraf
,
Amir Amiri-Yekta
et al.
Journal articles
hal-02322935v1
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Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player
Tristan Celse
,
Caroline Cazin
,
Flore Mietton
,
Guillaume Martinez
,
Delphine Martinez
et al.
Journal articles
hal-03025179v1
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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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PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Marie Christou‐kent
,
Zine‐eddine Kherraf
,
Amir Amiri‐yekta
,
Emilie Le Blévec
,
Thomas Karaouzène
et al.
Journal articles
hal-01877992v1
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Mapping interactomes with high coverage and efficiency using the shifted transversal design.
Xiaofeng Xin
,
Charles Boone
,
Nicolas Thierry-Mieg
Journal articles
hal-00807350v1
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Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.
Mariem Ben Khelifa
,
Charles Coutton
,
Raoudha Zouari
,
Thomas Karaouzène
,
John Rendu
et al.
Journal articles
pasteur-01061012v1
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Pooling in systems biology becomes smart.
Nicolas Thierry-Mieg
Journal articles
hal-00198318v1
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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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Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP
Jessica Escoffier
,
Hoi Chang Lee
,
Sandra Yassine
,
Raoudha Zouari
,
Guillaume Martinez
et al.
Journal articles
hal-01877966v1
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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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Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa
Caroline Cazin
,
Yasmine Boumerdassi
,
Guillaume Martinez
,
Selima Fourati Ben Mustapha
,
Marjorie Whitfield
et al.
Journal articles
hal-03365058v1
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MatrixDB, the extracellular matrix interaction database.
Emilie Chautard
,
Marie Fatoux-Ardore
,
Lionel Ballut
,
Nicolas Thierry-Mieg
,
Sylvie Ricard-Blum
et al.
Journal articles
hal-00807349v1
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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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The [PSI + ] prion modulates cytochrome c oxidase deficiency caused by deletion of COX12
Pawan Kumar Saini
,
Hannah Dawitz
,
Andreas Aufschnaiter
,
Stanislav Bondarev
,
Jinsu Thom
et al.
Journal articles
hal-03836554v1
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Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia
Zine-Eddine Kherraf
,
Caroline Cazin
,
Amine Bouker
,
Selima Fourati Ben Mustapha
,
Sylviane Hennebicq
et al.
Journal articles
hal-03718022v1
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Interpool: interpreting smart-pooling results
Nicolas Thierry-Mieg
,
Gilles Bailly
Journal articles
hal-01894176v1
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Systems biology: from yesterday's concepts to tomorrow's discoveries
Anne-Ruxandra Carvunis
,
Elisa Gomez
,
Nicolas Thierry-Mieg
,
Laurent Trilling
,
Marc Vidal
et al.
Journal articles
hal-03266023v1
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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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Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse
Qunshan Shen
,
Guillaume Martinez
,
Hongbin Liu
,
Julie Beurois
,
Huan Wu
et al.
Journal articles
hal-03365264v1
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Defect in the nuclear pore membrane glycoprotein 210-like gene is associated with extreme uncondensed sperm nuclear chromatin and male infertility: a case report
Karim Arafah
,
Fabrice Lopez
,
Caroline Cazin
,
Zine‐eddine Kherraf
,
Virginie Tassistro
et al.
Journal articles
hal-02985525v1
|
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Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella
Guillaume Martinez
,
Zine-Eddine Kherraf
,
Raoudha Zouari
,
Selima Fourati Ben Mustapha
,
Antoine Saut
et al.
Journal articles
hal-01877993v1
|
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Selective termination of lncRNA transcription promotes heterochromatin silencing and cell differentiation
Leila Touat‐todeschini
,
Yuichi Shichino
,
Mathieu Dangin
,
Nicolas Thierry-Mieg
,
Benoit Gilquin
et al.
Journal articles
hal-01877979v1
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