P. Lorès

发表

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

S. Amselem, B. Crestani, B. Copin, 2016, American journal of human genetics.

Escherichia coli Producing CNF1 Toxin Hijacks Tollip to Trigger Rac1‐Dependent Cell Invasion

P. Cossart, E. Lemichez, A. Doye, 2011, Traffic.

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.

N. Thierry-Mieg, S. Brouillet, P. Ray, 2018, American journal of human genetics.

The SWI/SNF protein BAF60b is ubiquitinated through a signalling process involving Rac GTPase and the RING finger protein Unkempt

R. Luna, E. Lemichez, P. Lorès, 2010, The FEBS journal.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

Constitutive (pro)insulin release from pancreas of transgenic mice expressing monomeric insulin.

J. Jami, G. Grodsky, P. Lorès, 1995, Endocrinology.

Transgenic Expression of CD95 Ligand on Thyroid Follicular Cells Confers Immune Privilege upon Thyroid Allografts

B. Malassagne, F. Batteux, P. Lorès, 2001, The Journal of Immunology.

Transgenic Expression of Fas Ligand On

P. Lorès, C. Batteux, D. Bucchini, 2013 .

Transgenic Expression of Fas Ligand on Thyroid Follicular Cells Prevents Autoimmune Thyroiditis1

F. Batteux, P. Lorès, G. Chiocchia, 2000, The Journal of Immunology.

Phenotype on Transgenic B Cells Receptor Confers a Tolerance-Like Expression of a V Region-Less B Cell

A. Vazquez, D. Bucchini, A. Grandien, 2001 .

Expression of a V Region-Less B Cell Receptor Confers a Tolerance-Like Phenotype on Transgenic B Cells1

A. Vazquez, A. Grandien, P. Lorès, 2001, The Journal of Immunology.

Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction

P. Jouk, H. Sartelet, P. Ray, 2018, Clinical genetics.

Soluble Fcγ Receptors: Interaction with Ligands and Biological Consequences

J. Galon, W. Fridman, J. Jami, 1997 .

An insulinoma nuclear factor binding to GGGCCC motifs in human insulin gene.

J. Jami, P. Lorès, G. Gacon, 1993, Nucleic acids research.

Enhanced apoptosis in the thymus of transgenic mice expressing constitutively activated forms of human Rac2GTPase

R. Luna, P. Lorès, G. Gacon, 1997, Oncogene.

A mouse minialbumin gene is specifically expressed in differentiated hepatoma cells but not in transgenic mice.

J. Jami, P. Lorès, C. Besnard, 1988, Differentiation; research in biological diversity.

Pancreatic expression of human insulin gene in transgenic mice.

R. Pictet, D. Bucchini, J. Jami, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Slc26a3 deficiency is associated with epididymis dysplasia and impaired sperm fertilization potential in the mouse

F. Saez, A. Touré, E. El Khouri, 2018, Molecular reproduction and development.

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

T. Dirami, T. Bienvenu, A. Edelman, 2012, Human molecular genetics.

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

D. Huylebroeck, T. Kurosaki, M. Hikida, 2014, Developmental biology.

Conditional ablation of dendritic cells in transgenic mice.

P. Rácz, D. Klatzmann, J. Jami, 1994, Journal of immunology.

In-vitro effects of Thymus munbyanus essential oil and thymol on human sperm motility and function.

J. Auger, A. Schmitt, Daniel Vaiman, 2015, Reproductive biomedicine online.

Absence of annulus in human asthenozoospermia: case report.

T. Dirami, T. Bienvenu, D. Escalier, 2009, Human reproduction.

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

P. Ray, S. Savinov, F. Guillonneau, 2019, American journal of human genetics.

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

S. Amselem, P. Ray, S. Savinov, 2018, Human molecular genetics.

BAF60A mediates interactions between the microphthalmia‐associated transcription factor and the BRG1‐containing SWI/SNF complex during melanocyte differentiation

P. Lorès, I. L. de la Serna, S. Saladi, 2018, Journal of cellular physiology.

Expression of human CD4 in transgenic mice does not confer sensitivity to human immunodeficiency virus infection.

F. Barré-Sinoussi, J. Weill, J. Jami, 1992, AIDS research and human retroviruses.

Activated Rac1, but not the tumorigenic variant Rac1b, is ubiquitinated on Lys 147 through a JNK‐regulated process

E. Lemichez, P. Lorès, G. Gacon, 2008, The FEBS journal.

Characterization of an intronless CD4 minigene expressed in mature CD4 and CD8 T cells, but not expressed in immature thymocytes.

D. Klatzmann, J. Jami, P. Lorès, 1996, Journal of immunology.

The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility

N. Thierry-Mieg, P. Santulli, P. Ray, 2021, Clinical genetics.

Novel axonemal protein ZMYND12 is required for flagellum function and male fertility

N. Thierry-Mieg, P. Ray, J. Dupuy, 2023 .

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

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2021, Human Genetics.

Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.

P. Santulli, A. Schmitt, A. Touré, 2021, Human reproduction.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

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.

S. Amselem, P. Ray, S. Savinov, 2018, Human molecular genetics.

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human

N. Thierry-Mieg, B. Conne, P. Jouk, 2018, Nature Communications.

Pre-B-cell development in the absence of λ5 in transgenic mice expressing a heavy-chain disease protein

J. Cesbron, D. Bucchini, J. Jami, 1995, Current Biology.

Pre-B-cell development in the absence of lambda 5 in transgenic mice expressing a heavy-chain disease protein.

J. Cesbron, D. Bucchini, J. Jami, 1995, Current biology : CB.

Conditional ablation of dendritic cells in mice: comparison of two animal models.

P. Rácz, D. Klatzmann, J. Jami, 1995, Advances in experimental medicine and biology.

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function

N. Thierry-Mieg, P. Ray, J. Dupuy, 2023, bioRxiv.

Absence of CFAP 69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

N. Thierry-Mieg, S. Brouillet, P. Ray, 2018 .

Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans

N. Thierry-Mieg, P. Ray, Caroline Cazin, 2023, iScience.

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

S. Amselem, B. Crestani, B. Copin, 2016, American journal of human genetics.

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

T. Bienvenu, A. Edelman, A. Touré, 2012, Human molecular genetics.