Works by Amiri-Yekta, Amir

Results: 26

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.
Published in:
Human Genetics, 2021, v. 140, n. 9, p. 1367, doi. 10.1007/s00439-021-02313-z
By:
- Shen, Qunshan;
- Martinez, Guillaume;
- Liu, Hongbin;
- Beurois, Julie;
- Wu, Huan;
- Amiri-Yekta, Amir;
- Liang, Dan;
- Kherraf, Zine-Eddine;
- Bidart, Marie;
- Cazin, Caroline;
- Celse, Tristan;
- Satre, Véronique;
- Thierry-Mieg, Nicolas;
- Whitfield, Marjorie;
- Touré, Aminata;
- Song, Bing;
- Lv, Mingrong;
- Li, Kuokuo;
- Liu, Chunyu;
- Tao, Fangbiao
Publication type:
Article
Correction to: 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.
Published in:
2021
By:
- Lorès, Patrick;
- Kherraf, Zine-Eddine;
- Amiri-Yekta, Amir;
- Whitfield, Marjorie;
- Daneshipour, Abbas;
- Stouvenel, Laurence;
- Cazin, Caroline;
- Cavarocchi, Emma;
- Coutton, Charles;
- Llabador, Marie-Astrid;
- Arnoult, Christophe;
- Thierry-Mieg, Nicolas;
- Ferreux, Lucile;
- Patrat, Catherine;
- Hosseini, Seyedeh-Hanieh;
- Mustapha, Selima Fourati Ben;
- Zouari, Raoudha;
- Dulioust, Emmanuel;
- Ray, Pierre F.;
- Touré, Aminata
Publication type:
Correction Notice
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.
Published in:
Human Genetics, 2021, v. 140, n. 7, p. 1031, doi. 10.1007/s00439-021-02270-7
By:
- Lorès, Patrick;
- Kherraf, Zine-Eddine;
- Amiri-Yekta, Amir;
- Whitfield, Marjorie;
- Daneshipour, Abbas;
- Stouvenel, Laurence;
- Cazin, Caroline;
- Cavarocchi, Emma;
- Coutton, Charles;
- Llabador, Marie-Astrid;
- Arnoult, Christophe;
- Thierry-Mieg, Nicolas;
- Ferreux, Lucile;
- Patrat, Catherine;
- Hosseini, Seyedeh-Hanieh;
- Mustapha, Selima Fourati Ben;
- Zouari, Raoudha;
- Dulioust, Emmanuel;
- Ray, Pierre F.;
- Touré, Aminata
Publication type:
Article
CYP19A1 Promoters Activity in Human Granulosa Cells: A Comparison between PCOS and Normal Subjects.
Published in:
Cell Journal (Yakhteh), 2022, v. 24, n. 4, p. 170, doi. 10.22074/cellj.2022.7787
By:
- Hashemain, Zohreh;
- Amiri-Yekta, Amir;
- Khosravifar, Mona;
- Alvandian, Faezeh;
- Shahhosseini, Maryam;
- Hosseinkhani, Saman;
- Afsharian, Parvaneh
Publication type:
Article
Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients.
Published in:
Cell Journal (Yakhteh), 2021, v. 22, p. 148, doi. 10.22074/cellj.2020.7524
By:
- Salehi, Najmeh;
- Amiri-Yekta, Amir;
- Totonchi, Mehdi
Publication type:
Article
Designing A Transgenic Chicken: Applying New Approaches toward A Promising Bioreactor.
Published in:
Cell Journal (Yakhteh), 2020, v. 22, n. 2, p. 133, doi. 10.22074/cellj.2020.6738
By:
- Bahrami, Salahadin;
- Amiri-Yekta, Amir;
- Daneshipour, Abbas;
- Jazayeri, Seyedeh Hoda;
- Mozdziak, Paul Edward;
- Sanati, Mohammad Hossein;
- Gourabi, Hamid
Publication type:
Article
Regulated Acyl-CoA Synthetase Short-Chain Family Member 2 Accumulation during Spermatogenesis.
Published in:
Cell Journal (Yakhteh), 2020, v. 22, n. 1, p. 66, doi. 10.22074/cellj.2020.6306
By:
- Goudarzi, Afsaneh;
- Amiri-Yekta, Amir
Publication type:
Article
Optimization of The Electroporation Conditions for Transfection of Human Factor IX into The Goat Fetal Fibroblasts.
Published in:
Cell Journal (Yakhteh), 2012, v. 14, n. 4, p. 270
By:
- Amiri Yekta, Amir;
- Dalman, Azam;
- Hossein Sanati, Mohammad;
- Fatemi, Nayeralsadat;
- Vazirinasab, Hamed;
- Zomorodipour, Alireza;
- Chehrazi, Mohammad;
- Gourabi, Hamid
Publication type:
Article
Vector and Cell Line Engineering Technologies Toward Recombinant Protein Expression in Mammalian Cell Lines.
Published in:
Applied Biochemistry & Biotechnology, 2018, v. 185, n. 4, p. 986, doi. 10.1007/s12010-017-2689-8
By:
- Jazayeri, Seyedeh Hoda;
- Amiri-Yekta, Amir;
- Bahrami, Salahadin;
- Gourabi, Hamid;
- Sanati, Mohammad Hossein;
- Khorramizadeh, Mohammad Reza
Publication type:
Article
Pathophysiologic Mechanisms of Insulin Secretion and Signaling-Related Genes in Etiology of Polycystic Ovary Syndrome.
Published in:
Genetics Research, 2021, p. 1, doi. 10.1155/2021/7781823
By:
- Shaaban, Zahra;
- Khoradmehr, Arezoo;
- Amiri-Yekta, Amir;
- Nowzari, Fariborz;
- Jafarzadeh Shirazi, Mohammad Reza;
- Tamadon, Amin
Publication type:
Article
Comparative Assessment on the Expression Level of Recombinant Human Follicle-Stimulating Hormone (FSH) in Serum-Containing Versus Protein-Free Culture Media.
Published in:
Molecular Biotechnology, 2017, v. 59, n. 11/12, p. 490, doi. 10.1007/s12033-017-0037-4
By:
- Jazayeri, Seyedeh;
- Amiri-Yekta, Amir;
- Gourabi, Hamid;
- Abd Emami, Baharak;
- Halfinezhad, Zahra;
- Abolghasemi, Somayeh;
- Fatemi, Nayeralsadat;
- Daneshipour, Abbas;
- Ghahremani, Mohammad;
- Sanati, Mohammad;
- Khorramizadeh, Mohammad
Publication type:
Article
Integration and gene co-expression network analysis of scRNA-seq transcriptomes reveal heterogeneity and key functional genes in human spermatogenesis.
Published in:
Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98267-3
By:
- Salehi, Najmeh;
- Karimi-Jafari, Mohammad Hossein;
- Totonchi, Mehdi;
- Amiri-Yekta, Amir
Publication type:
Article
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human.
Published in:
Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02792-7
By:
- Coutton, Charles;
- Vargas, Alexandra S.;
- Amiri-Yekta, Amir;
- Kherraf, Zine-Eddine;
- Ben Mustapha, Selima Fourati;
- Le Tanno, Pauline;
- Wambergue-Legrand, Clémentine;
- Karaouzène, Thomas;
- Martinez, Guillaume;
- Crouzy, Serge;
- Daneshipour, Abbas;
- Hosseini, Seyedeh Hanieh;
- Mitchell, Valérie;
- Halouani, Lazhar;
- Marrakchi, Ouafi;
- Makni, Mounir;
- Latrous, Habib;
- Kharouf, Mahmoud;
- Deleuze, Jean-François;
- Boland, Anne
Publication type:
Article
Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non‐obstructive azoospermia in an Iranian family.
Published in:
Clinical Genetics, 2024, v. 106, n. 5, p. 625, doi. 10.1111/cge.14584
By:
- Amiri‐Yekta, Amir;
- Sen, Sharanya;
- Hazane‐Puch, Florence;
- Tebbakh, Célia;
- Roux‐Buisson, Nathalie;
- Cazin, Caroline;
- Thierry‐Mieg, Nicolas;
- Bouras, Ahmed;
- Mohammad Ali, Sadighi‐Gilani;
- Hosseini, Seyedeh‐Hanieh;
- Goodarzian, Maedeh;
- Gourabi, Hamid;
- Ray, Pierre F.;
- Kherraf, Zine‐Eddine
Publication type:
Article
CCDC65, encoding a component of the axonemal Nexin‐Dynein regulatory complex, is required for sperm flagellum structure in humans.
Published in:
Clinical Genetics, 2024, v. 105, n. 3, p. 317, doi. 10.1111/cge.14459
By:
- Jreijiri, Fadwa;
- Cavarocchi, Emma;
- Amiri‐Yekta, Amir;
- Cazin, Caroline;
- Hosseini, Seyedeh‐Hanieh;
- El Khouri, Elma;
- Patrat, Catherine;
- Thierry‐Mieg, Nicolas;
- Ray, Pierre F.;
- Dulioust, Emmanuel;
- Whitfield, Marjorie;
- Touré, Aminata
Publication type:
Article
Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations.
Published in:
Clinical Genetics, 2019, v. 96, n. 5, p. 394, doi. 10.1111/cge.13604
By:
- Kherraf, Zine‐Eddine;
- Cazin, Caroline;
- Coutton, Charles;
- Amiri‐Yekta, Amir;
- Martinez, Guillaume;
- Boguenet, Magalie;
- Fourati Ben Mustapha, Selima;
- Kharouf, Mahmoud;
- Gourabi, Hamid;
- Hosseini, Seyedeh Hanieh;
- Daneshipour, Abbas;
- Touré, Aminata;
- Thierry‐Mieg, Nicolas;
- Zouari, Raoudha;
- Arnoult, Christophe;
- Ray, Pierre F.
Publication type:
Article
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse.
Published in:
eLife, 2024, p. 1, doi. 10.7554/eLife.86845
By:
- Muroňová, Jana;
- Kherraf, Zine Eddine;
- Giordani, Elsa;
- Lambert, Emeline;
- Eckert, Simon;
- Cazin, Caroline;
- Amiri-Yekta, Amir;
- Court, Magali;
- Chevalier, Geneviève;
- Martinez, Guillaume;
- Neirijnck, Yasmine;
- Kühne, Francoise;
- Wehrli, Lydia;
- Klena, Nikolai;
- Hamel, Virginie;
- De Macedo, Lisa;
- Escoffier, Jessica;
- Guichard, Paul;
- Coutton, Charles;
- Ben Mustapha, Selima Fourati
Publication type:
Article
Pathophysiologic mechanisms of obesity- and chronic inflammation-related genes in etiology of polycystic ovary syndrome.
Published in:
Iranian Journal of Basic Medical Sciences, 2019, v. 22, n. 12, p. 1378, doi. 10.22038/IJBMS.2019.14029
By:
- Shaaban, Zahra;
- Khoradmehr, Arezoo;
- Amiri-Yekta, Amir;
- Jafarzadeh Shirazi, Mohammad Reza;
- Tamadon, Amin
Publication type:
Article
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.
Published in:
International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2559, doi. 10.3390/ijms24032559
By:
- Martinez, Guillaume;
- Barbotin, Anne-Laure;
- Cazin, Caroline;
- Wehbe, Zeina;
- Boursier, Angèle;
- Amiri-Yekta, Amir;
- Daneshipour, Abbas;
- Hosseini, Seyedeh-Hanieh;
- Rives, Nathalie;
- Feraille, Aurélie;
- Thierry-Mieg, Nicolas;
- Bidart, Marie;
- Satre, Véronique;
- Arnoult, Christophe;
- Ray, Pierre F.;
- Kherraf, Zine-Eddine;
- Coutton, Charles
Publication type:
Article
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice.
Published in:
EMBO Molecular Medicine, 2018, v. 10, n. 5, p. 1, doi. 10.15252/emmm.201708515
By:
- Christou‐Kent, Marie;
- Kherraf, Zine‐Eddine;
- Amiri‐Yekta, Amir;
- Le Blévec, Emilie;
- Karaouzène, Thomas;
- Conne, Béatrice;
- Escoffier, Jessica;
- Assou, Said;
- Guttin, Audrey;
- Lambert, Emeline;
- Martinez, Guillaume;
- Boguenet, Magalie;
- Fourati Ben Mustapha, Selima;
- Cedrin Durnerin, Isabelle;
- Halouani, Lazhar;
- Marrakchi, Ouafi;
- Makni, Mounir;
- Latrous, Habib;
- Kharouf, Mahmoud;
- Coutton, Charles
Publication type:
Article
SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes.
Published in:
EMBO Molecular Medicine, 2017, v. 9, n. 8, p. 1132, doi. 10.15252/emmm.201607461
By:
- Kherraf, Zine ‐ Eddine;
- Christou ‐ Kent, Marie;
- Karaouzene, Thomas;
- Amiri ‐ Yekta, Amir;
- Martinez, Guillaume;
- Vargas, Alexandra S;
- Lambert, Emeline;
- Borel, Christelle;
- Dorphin, Béatrice;
- Aknin ‐ Seifer, Isabelle;
- Mitchell, Michael J;
- Metzler ‐ Guillemain, Catherine;
- Escoffier, Jessica;
- Nef, Serge;
- Grepillat, Mariane;
- Thierry ‐ Mieg, Nicolas;
- Satre, Véronique;
- Bailly, Marc;
- Boitrelle, Florence;
- Pernet ‐ Gallay, Karin
Publication type:
Article
Production of transgenic goats expressing human coagulation factor IX in the mammary glands after nuclear transfer using transfected fetal fibroblast cells.
Published in:
Transgenic Research, 2013, v. 22, n. 1, p. 131, doi. 10.1007/s11248-012-9634-y
By:
- Amiri Yekta, Amir;
- Dalman, Azam;
- Eftekhari-Yazdi, Poopak;
- Sanati, Mohammad;
- Shahverdi, Abdol;
- Fakheri, Rahman;
- Vazirinasab, Hamed;
- Daneshzadeh, Mohammad;
- Vojgani, Mahdi;
- Zomorodipour, Alireza;
- Fatemi, Nayeralsadat;
- Vahabi, Zeinab;
- Mirshahvaladi, Shahab;
- Ataei, Fariba;
- Bahraminejad, Elmira;
- Masoudi, Najmehsadat;
- Rezazadeh Valojerdi, Mojtaba;
- Gourabi, Hamid
Publication type:
Article
CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report.
Published in:
2019
By:
- Beurois, Julie;
- Martinez, Guillaume;
- Cazin, Caroline;
- Kherraf, Zine-Eddine;
- Amiri-Yekta, Amir;
- Thierry-Mieg, Nicolas;
- Bidart, Marie;
- Petre, Graciane;
- Satre, Véronique;
- Brouillet, Sophie;
- Touré, Aminata;
- Arnoult, Christophe;
- Ray, Pierre F;
- Coutton, Charles
Publication type:
journal article
Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.
Published in:
2018
By:
- Martinez, Guillaume;
- Kherraf, Zine-Eddine;
- Zouari, Raoudha;
- Mustapha, Selima Fourati Ben;
- Saut, Antoine;
- Pernet-Gallay, Karin;
- Bertrand, Anne;
- Bidart, Marie;
- Hograindleur, Jean Pascal;
- Amiri-Yekta, Amir;
- Fourati Ben Mustapha, Selima;
- Kharouf, Mahmoud;
- Karaouzène, Thomas;
- Thierry-Mieg, Nicolas;
- Dacheux-Deschamps, Denis;
- Satre, Véronique;
- Bonhivers, Mélanie;
- Touré, Aminata;
- Arnoult, Christophe;
- Ray, Pierre F
Publication type:
journal article
Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
Published in:
2016
By:
- Amiri-Yekta, Amir;
- Coutton, Charles;
- Kherraf, Zine-Eddine;
- Karaouzène, Thomas;
- Le Tanno, Pauline;
- Sanati, Mohammad Hossein;
- Sabbaghian, Marjan;
- Almadani, Navid;
- Gilani, Mohammad Ali Sadighi;
- Hosseini, Seyedeh Hanieh;
- Bahrami, Salahadin;
- Daneshipour, Abbas;
- Bini, Maurizio;
- Arnoult, Christophe;
- Colombo, Roberto;
- Gourabi, Hamid;
- Ray, Pierre F.;
- Sadighi Gilani, Mohammad Ali
Publication type:
journal article
Direct visualization of pre-protamine 2 detects protamine assembly failures and predicts ICSI success.
Published in:
Molecular Human Reproduction, 2022, v. 28, n. 2, p. 1, doi. 10.1093/molehr/gaac004
By:
- Rezaei-Gazik, Maryam;
- Vargas, Alexandra;
- Amiri-Yekta, Amir;
- Vitte, Anne-Laure;
- Akbari, Arvand;
- Barral, Sophie;
- Esmaeili, Vahid;
- Chuffart, Florent;
- Sadighi-Gilani, Mohammad Ali;
- Couté, Yohann;
- Eftekhari-Yazdi, Poopak;
- Khochbin, Saadi;
- Rousseaux, Sophie;
- Totonchi, Mehdi
Publication type:
Article