User profiles for N. Thierry-Mieg

Nicolas Thierry-Mieg

Verified email at imag.fr
Cited by 4934

Interaction networks: from protein functions to drug discovery. A review

E Chautard, N Thierry-Mieg, S Ricard-Blum - Pathologie Biologie, 2009 - Elsevier
Most genes, proteins and other components carry out their functions within a complex network
of interactions and a single molecule can affect a wide range of other cell components. A …

Protein Interaction Mapping in C. elegans Using Proteins Involved in Vulval Development

…, JL Hartley, GF Temple, MA Brasch, N Thierry-Mieg… - Science, 2000 - science.org
… For each hit, we then searched the IST list of Y or Y′ and reiterated the process for several
(n) cycles until the starting bait (X) … Thierry-Mieg, and S. van den Heuvel for support; J. Hitti, L. …

Proto-genes and de novo gene birth

…, GA Brar, JS Weissman, A Regev, N Thierry-Mieg… - Nature, 2012 - nature.com
Novel protein-coding genes can arise either through re-organization of pre-existing genes
or de novo 1 , 2 . Processes involving re-organization of pre-existing genes, notably after …

[PDF][PDF] Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella

…, K Pernet-Gallay, PS Jouk, N Thierry-Mieg… - The American Journal of …, 2014 - cell.com
… None of these variants were detected in our control cohort of 100 individuals of North
African origin. We note that the parents of the subjects could not be analyzed to confirm the …

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

…, S Hennebicq, V Satre, PS Jouk, N Thierry-Mieg… - Nature …, 2018 - nature.com
Spermatogenesis defects concern millions of men worldwide, yet the vast majority remains
undiagnosed. Here we report men with primary infertility due to multiple morphological …

Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP

…, C Triki, S Nef, N Thierry-Mieg… - Human molecular …, 2016 - academic.oup.com
In mammals, sperm–oocyte fusion initiates Ca 2+ oscillations leading to a series of events
called oocyte activation, which is the first stage of embryo development. Ca 2+ signaling is …

[PDF][PDF] Absence of CFAP69 causes male infertility due to multiple morphological abnormalities of the flagella in human and mouse

…, P Lorès, T Karaouzène, N Thierry-Mieg… - The American Journal of …, 2018 - cell.com
The multiple morphological abnormalities of the flagella (MMAF) phenotype is among the
most severe forms of sperm defects responsible for male infertility. The phenotype is …

[PDF][PDF] Bi-allelic mutations in ARMC2 lead to severe astheno-teratozoospermia due to sperm flagellum malformations in humans and mice

…, R Zouari, SH Hosseini, S Nef, N Thierry-Mieg… - The American Journal of …, 2019 - cell.com
… We also compared these variants to an in-house database of 193 control exomes enriched
for North African subjects (n=153) corresponding to the geographical origin of the majority of …

[HTML][HTML] A new pooling strategy for high-throughput screening: the Shifted Transversal Design

N Thierry-Mieg - BMC bioinformatics, 2006 - Springer
… Consider a set of n events which can be true or false, represented by n Boolean variables. …
n, noted Γ(q,n), as the smallest integer γ such that q γ+1 ≥ n. We will simply write Γ for Γ(q,n

[HTML][HTML] A protein–protein interaction map of the Caenorhabditis elegans 26S proteasome

A Davy, P Bello, N ThierryMieg, P Vaglio, J Hitti… - EMBO …, 2001 - embopress.org
… In addition, the 20S structure suggests that α2 is in contact with β5 and that its N‐terminal
tail interacts with the N‐terminal tail of α4 and with an α6 domain (M. Groll, personal …