Search Results - "Fellous, M"

Fluctuating synaptic conductances recreate in vivo-like activity in neocortical neurons by Destexhe, A, Rudolph, M, Fellous, J.-M, Sejnowski, T.J

“…To investigate the basis of the fluctuating activity present in neocortical neurons in vivo, we have combined computational models with whole-cell recordings…”
Get full text

Synaptic background noise controls the input/output characteristics of single cells in an in vitro model of in vivo activity by Fellous, J.-M, Rudolph, M, Destexhe, A, Sejnowski, T.J

“…In vivo, in vitro and computational studies were used to investigate the impact of the synaptic background activity observed in neocortical neurons in vivo. We…”
Get full text

A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency by Fauchereau, F., Shalev, S., Chervinsky, E., Beck-Fruchter, R., Legois, B., Fellous, M., Caburet, S., Veitia, R.A.

“…Primary ovarian insufficiency (POI) results in an early loss of ovarian function, and remains idiopathic in about 80% of cases. Here, we have performed a…”
Get full text

Face recognition by elastic bunch graph matching by Wiskott, L., Fellous, J.-M., Kuiger, N., von der Malsburg, C.

“…We present a system for recognizing human faces from single images out of a large database containing one image per person. Faces are represented by labeled…”
Get full text

Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2 by Laissue, P, Lakhal, B, Benayoun, B A, Dipietromaria, A, Braham, R, Elghezal, H, Philibert, P, Saâd, A, Sultan, C, Fellous, M, Veitia, R A

“…FOXL2 encodes a forkhead transcription factor whose mutations are responsible for the blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), involving…”
Get more information

FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD) by Hersmus, R, Kalfa, N, de Leeuw, B, Stoop, H, Oosterhuis, JW, de Krijger, R, Wolffenbuttel, KP, Drop, SLS, Veitia, RA, Fellous, M, Jaubert, F, Looijenga, LHJ

“…The transcription factors SOX9 and FOXL2 are required for male and female mammalian gonadal development. We have used specific antibodies to investigate the…”
Get full text

Evolution and expression of FOXL2 by Cocquet, J, Pailhoux, E, Jaubert, F, Servel, N, Xia, X, Pannetier, M, De Baere, E, Messiaen, L, Cotinot, C, Fellous, M, Veitia, R A

Get full text

Linkage and association of the glutamate receptor 6 gene with autism by Jamain, S, Betancur, C, Quach, H, Philippe, A, Fellous, M, Giros, B, Gillberg, C, Leboyer, M, Bourgeron, T

Get full text

Frequency Dependence of Spike Timing Reliability in Cortical Pyramidal Cells and Interneurons by Fellous, J.-M, Houweling, A. R, Modi, R. H, Rao, R.P.N, Tiesinga, P.H.E, Sejnowski, T. J

“…  1 Computational Neurobiology Laboratory, Howard Hughes Medical Institute, Sloan Center for Theoretical Neurobiology, The Salk Institute for Biological…”
Get full text

Linkage and association of the glutamate receptor 6 gene with autism by JAMAIN, S, BETANCUR, C, QUACH, H, PHILIPPE, A, FELLOUS, M, GIROS, B, GILLBERG, C, LEBOYER, M, BOURGERON, T

“…A genome scan was previously performed and pointed to chromosome 6q21 as a candidate region for autism. This region contains the glutamate receptor 6 (GluR6 or…”
Get full text

The mutations and potential targets of the forkhead transcription factor FOXL2 by Moumné, L., Batista, F., Benayoun, B.A., Nallathambi, J., Fellous, M., Sundaresan, P., Veitia, R.A.

“…Mutations of FOXL2, a gene encoding a forkhead transcription factor, have been shown to cause the blepharophimosis–ptosis–epicanthus inversus syndrome (BPES)…”
Get full text

P-015: Association of FOXD1 variants with pregnancy failures in mice and humans by Laissue, P, Lakhal, B, Vatin, M, Batista, F, Burgio, G, Dos Santos, E, Buffat, C, Sierra-Diaz, A.C, Renault, G, Montagutelli, X, Salmon, J, Monget, P, Veitia, R.A, Méhats, C, Fellous, M, Cocquet, J, Vaiman, D, Gris, J.-C

Get full text

A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation by Caburet, S, Demarez, A, Moumné, L, Fellous, M, De Baere, E, Veitia, R A

“…Blepharophimosis syndrome is an autosomal dominant disease characterised by eyelid malformations, associated or not with premature ovarian failure. It is…”
Get full text

Structure, evolution and expression of the FOXL2 transcription unit by Cocquet, J, De Baere, E, Gareil, M, Pannetier, M, Xia, X, Fellous, M, Veitia, R A

“…FOXL2 is a putative transcription factor involved in ovarian development and function. Its mutations in humans are responsible for the blepharophimosis…”
Get more information

Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency by BOUHALI, Kamal, DIPIETROMARIA, Aurélie, FONTAINE, Anastasia, CABURET, Sandrine, BARBIERI, Ottavia, BELLESSORT, Brice, FELLOUS, Marc, VEITIA, Reiner A, LEVI, Giovanni

“…Primary ovarian insufficiency (POI) is characterized by the loss of ovarian function before the age of 40 in humans. Although most cases of POI are idiopathic,…”
Get full text

A new correlation-based measure of spike timing reliability by Schreiber, S., Fellous, J.M., Whitmer, D., Tiesinga, P., Sejnowski, T.J.

“…We introduce a new correlation-based measure of spike timing reliability. Unlike other measures, it does not require the definition of a posteriori “events”…”
Get full text

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome by Beysen, D., Raes, J., Leroy, B.P., Lucassen, A., Yates, J.R.W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J.P., Kim, J.R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L.M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R.A., De Paepe, A., De Baere, E.

“…The expression of a gene requires not only a normal coding sequence but also intact regulatory regions, which can be located at large distances from the target…”
Get full text

The Processing of Color, Motion, and Stimulus Timing Are Anatomically Segregated in the Bumblebee Brain by Paulk, Angelique C, Phillips-Portillo, James, Dacks, Andrew M, Fellous, Jean-Marc, Gronenberg, Wulfila

“…Animals use vision to perform such diverse behaviors as finding food, interacting socially with other animals, choosing a mate, and avoiding predators. These…”
Get full text

Genetic Counseling for the Orthodox Jewish Couple Undergoing Preimplantation Genetic Diagnosis by David, B. E., Weitzman, G. A., Hervé, C., Fellous, M.

“…Orthodox Jewish patients who seek genetic counseling are often placed in a difficult position of having to choose between their desire to follow Jewish…”
Get full text

Regulation of Persistent Activity by Background Inhibition in an In Vitro Model of a Cortical Microcircuit by Fellous, Jean-Marc, Sejnowski, Terrence J.

“…We combined in vitro intracellular recording from prefrontal cortical neurons with simulated synaptic activity of a layer 5 prefrontal microcircuit using a…”
Get full text