A. Amiri-Yekta

发表

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.

Creation of knock out and knock in mice by CRISPR/Cas9 to validate candidate genes for human male infertility, interest, difficulties and feasibility

B. Conne, P. Ray, S. Nef, 2018, Molecular and Cellular Endocrinology.

Comparative Assessment on the Expression Level of Recombinant Human Follicle-Stimulating Hormone (FSH) in Serum-Containing Versus Protein-Free Culture Media

M. Ghahremani, M. Khorramizadeh, M. Sanati, 2017, Molecular Biotechnology.

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.

Pathophysiologic mechanisms of obesity- and chronic inflammation-related genes in etiology of polycystic ovary syndrome

A. Khoradmehr, Amin Tamadon, M. R. Jafarzadeh Shirazi, 2019, Iranian journal of basic medical sciences.

CYP19A1 Promoters Activity in Human Granulosa Cells: A Comparison between PCOS and Normal Subjects

S. Hosseinkhani, P. Afsharian, M. Shahhosseini, 2022, Cell journal.

Integration and gene co-expression network analysis of scRNA-seq transcriptomes reveal heterogeneity and key functional genes in human spermatogenesis

N. Salehi, M. H. Karimi-Jafari, M. Totonchi, 2021, Scientific Reports.

Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice

P. Ray, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations

N. Thierry-Mieg, P. Ray, H. Gourabi, 2019, Clinical genetics.

Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH 2 mutations

N. Thierry-Mieg, P. Ray, H. Gourabi, 2019 .

Designing A Transgenic Chicken: Applying New Approaches toward A Promising Bioreactor

P. Mozdziak, M. Sanati, H. Gourabi, 2019, Cell journal.

SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes

Thomas Karaouzene, Nicolas Thierry-Mieg, Serge Nef, 2017, EMBO molecular medicine.

Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice.

N. Thierry-Mieg, B. Conne, P. Ray, 2019, American journal of human genetics.

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.

PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice

N. Thierry-Mieg, B. Conne, P. Ray, 2018, EMBO Molecular Medicine.

A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.

M. Blum, N. Thierry-Mieg, P. Ray, 2018, American journal of human genetics.

KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole.

P. Ray, M. Totonchi, Navid Almadani, 2021, European journal of obstetrics, gynecology, and reproductive biology.

CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report.

N. Thierry-Mieg, S. Brouillet, P. Ray, 2019, Human reproduction.

Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility

Yong Zhu, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

Cloning and Expression of Iranian Turkmen-thoroughbred Horse Follicle Stimulating Hormone in Pichia pastoris.

M. Sanati, H. Gourabi, F. Vakhshiteh, 2015, Iranian journal of biotechnology.

A Heterozygous Missense Variant in DLX3 Leads to Uterine Leiomyomas and Pregnancy Losses in a Consanguineous Iranian Family.

M. Mazaheri, M. Totonchi, Navid Almadani, 2023, Gene.

Regulated Acyl-CoA Synthetase Short-Chain Family Member 2 Accumulation during Spermatogenesis

A. Goudarzi, A. Amiri-Yekta, Amir Amiri-Yekta, 2019, Cell journal.

Vector and Cell Line Engineering Technologies Toward Recombinant Protein Expression in Mammalian Cell Lines

M. Khorramizadeh, M. Sanati, H. Gourabi, 2018, Applied Biochemistry and Biotechnology.

Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.

M. Sabbaghian, P. Ray, M. Sanati, 2016, Human reproduction.

“Conservation cloning” of vulnerable Esfahan mouflon (Ovis orientalis isphahanica): in vitro and in vivo studies

M. Nasr-Esfahani, M. Hajian, H. Gourabi, 2011, European Journal of Wildlife Research.

Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2018, Human reproduction.

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

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

Lack of CCDC 146 , a ubiquitous centriole and microtubule-associated protein , 2 leads to non-syndromic male infertility in human and mouse 3 4 5

N. Thierry-Mieg, S. Geimer, P. Ray, 2023 .

New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella

N. Thierry-Mieg, P. Ray, Zine-Eddine Kherraf, 2023, International journal of molecular sciences.

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.

Pathophysiologic Mechanisms of Insulin Secretion and Signaling-Related Genes in Etiology of Polycystic Ovary Syndrome

A. Khoradmehr, M. R. Jafarzadeh Shirazi, A. Amiri-Yekta, 2021, Genetics research.

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.

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.

Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients

N. Salehi, M. Totonchi, A. Amiri-Yekta, 2020, Cell journal.