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Christophe Arnoult
Christophe Arnoult
Directeur de recherche CNRS
Verified email at univ-grenoble-alpes.fr
Title
Cited by
Cited by
Year
Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella
MB Khelifa, C Coutton, R Zouari, T Karaouzène, J Rendu, M Bidart, ...
The American Journal of Human Genetics 94 (1), 95-104, 2014
4052014
Teratozoospermia: spotlight on the main genetic actors in the human
C Coutton, J Escoffier, G Martinez, C Arnoult, PF Ray
Human reproduction update 21 (4), 455-485, 2015
3272015
Ca2+ Entry through Store-operated Channels in Mouse Sperm Is Initiated by Egg ZP3 and Drives the Acrosome Reaction
CMB O'Toole, C Arnoult, A Darszon, RA Steinhardt, HM Florman
Molecular biology of the cell 11 (5), 1571-1584, 2000
3012000
Activation of mouse sperm T-type Ca2+ channels by adhesion to the egg zona pellucida
C Arnoult, RA Cardullo, JR Lemos, HM Florman
Proceedings of the National Academy of Sciences 93 (23), 13004-13009, 1996
2961996
Control of the low voltage-activated calcium channel of mouse sperm by egg ZP3 and by membrane hyperpolarization during capacitation
C Arnoult, IG Kazam, PE Visconti, GS Kopf, M Villaz, HM Florman
Proceedings of the National Academy of Sciences 96 (12), 6757-6762, 1999
2791999
A perspective on the control of mammalian fertilization by egg-activated ion channels in sperm: a tale of two channels
HM Florman, C Arnoult, IG Kazam, C Li, CMB O'Toole
Biology of Reproduction 59 (1), 12-16, 1998
2381998
A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation
R Harbuz, R Zouari, V Pierre, MB Khelifa, M Kharouf, C Coutton, ...
The American Journal of Human Genetics 88 (3), 351-361, 2011
2352011
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human
C Coutton, AS Vargas, A Amiri-Yekta, ZE Kherraf, SF Ben Mustapha, ...
Nature communications 9 (1), 686, 2018
1962018
ZP3-dependent activation of sperm cation channels regulates acrosomal secretion during mammalian fertilization.
C Arnoult, Y Zeng, HM Florman
The Journal of cell biology 134 (3), 637-645, 1996
1931996
Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus
V Pierre, G Martinez, C Coutton, J Delaroche, S Yassine, C Novella, ...
Development 139 (16), 2955-2965, 2012
1892012
Genetic abnormalities leading to qualitative defects of sperm morphology or function
PF Ray, A Toure, C Metzler‐Guillemain, MJ Mitchell, C Arnoult, C Coutton
Clinical Genetics 91 (2), 217-232, 2017
1602017
Pharmacological properties of the T-type Ca2+ current of mouse spermatogenic cells
C Arnoult, M Villaz, HM Florman
Molecular pharmacology 53 (6), 1104-1111, 1998
1561998
The genetic architecture of morphological abnormalities of the sperm tail
A Touré, G Martinez, ZE Kherraf, C Cazin, J Beurois, C Arnoult, PF Ray, ...
Human Genetics 140 (1), 21-42, 2021
1512021
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP
J Escoffier, HC Lee, S Yassine, R Zouari, G Martinez, T Karaouzène, ...
Human molecular genetics 25 (5), 878-891, 2016
1502016
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion
S Treves, C Franzini-Armstrong, L Moccagatta, C Arnoult, C Grasso, ...
The Journal of cell biology 166 (4), 537-548, 2004
1442004
Absence of CFAP69 causes male infertility due to multiple morphological abnormalities of the flagella in human and mouse
FN Dong, A Amiri-Yekta, G Martinez, A Saut, J Tek, L Stouvenel, P Lorès, ...
The American Journal of Human Genetics 102 (4), 636-648, 2018
1352018
Bi-allelic mutations in ARMC2 lead to severe astheno-teratozoospermia due to sperm flagellum malformations in humans and mice
C Coutton, G Martinez, ZE Kherraf, A Amiri-Yekta, M Boguenet, A Saut, ...
The American Journal of Human Genetics 104 (2), 331-340, 2019
1322019
Voltage-dependent modulation of T-type calcium channels by protein tyrosine phosphorylation
C Arnoult, JR Lemos, HM Florman
The EMBO Journal 16 (7), 1593-1599, 1997
1271997
Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations
A Amiri-Yekta, C Coutton, ZE Kherraf, T Karaouzène, P Le Tanno, ...
Human Reproduction, 1-9, 2016
1252016
Bi-allelic DNAH8 variants lead to multiple morphological abnormalities of the sperm flagella and primary male infertility
C Liu, H Miyata, Y Gao, Y Sha, S Tang, Z Xu, M Whitfield, C Patrat, H Wu, ...
The American Journal of Human Genetics 107 (2), 330-341, 2020
1162020
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