Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Barbara LeMaire"'
Autor:
A. Vijaya Rao, Barbara LeMaire, Anthony R. Kalica, Janet Wittes, James H. Ware, Frank D. Goebel, Yu Lou, John F. French, Bonita T. Mangura, W. Kenneth Poole, Lee B. Reichman, Kim Clayton, Bert J. Shapiro, Joanne Huitsing, Virjilio Clemente, Jeanne M. Wallace, Judith Katzin, Norman Markowitz, Philip C. Hopewell, Lori Meiselman, Janet Au, Louis O. Saravolatz, Kim K. Manghisi, Jeffrey Glassroth, Gerard N. Turino, John G. Bartlett, Saundra Barnes, Albert Miller, Dixie E. Snider, Ronald P. Daniele, Nellie I. Hansen, Paul A. Kvale, Thomas H. Kalb, David Myers, Barbara Richer, Christopher Cardozo, Anne H. Coulson, Dennis Osmond, James Thompson, Matthew C. Jordan, Annmarie Krystoforski, Mark J. Rosen, Reuben Cherniak, Timothy C. Wilcosky, Christine Cole Johnson, John E. Connett, Melinda Mossar, Robert E. Hirschtick, John Stansell, Joan Turner, Roslyn F. Schneider, Steve Game, William Fulkerson, Dean Follmann, Robert A. Wise, Lisa Lavange
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 152:738-745
To determine the prevalence, incidence, and types of lung diseases that occur in association with HIV infection, 1,353 subjects, including HIV-seropositive homosexual men, injection drug users, female sexual partners of HIV-positive men, and HIV-sero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7e541e0b1e3ecee15a7bc19f221745
https://doi.org/10.1164/ajrccm.152.2.7633736
https://doi.org/10.1164/ajrccm.152.2.7633736
Autor:
Annette Hammes, Pierre Lacombe, Marie Monet-Leprêtre, Anne Joutel, Valérie Domenga, Andreas Schedl, Claudia Gosele, Sabine Schmidt, Barbara Lemaire-Carrette, Norbert Hubner, Céline Baron-Menguy
Cerebral ischemic small vessel disease (SVD) is the leading cause of vascular dementia and a major contributor to stroke in humans. Dominant mutations in NOTCH3 cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencepha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d6408d09653850a6dbad8317672606
https://europepmc.org/articles/PMC2810078/
https://europepmc.org/articles/PMC2810078/
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain
Autor:
Valérie Domenga, Barbara Lemaire, Ophélia Godin, Marie Monet-Leprêtre, Hugues Chabriat, Anne Joutel, Michel Cohen-Tannoudji, Elisabeth Tournier-Lasserve, Boris Bardot, Martin Dichgans
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
Brain-A Journal of Neurology, 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
International audience; Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant small-vessel disease of the brain caused by mutations in the NOTCH3 receptor. The highly stereotyped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dacaef39e41c7561d7752f2965cea348
https://hal-pasteur.archives-ouvertes.fr/pasteur-02075498
https://hal-pasteur.archives-ouvertes.fr/pasteur-02075498
Autor:
Barbara Lemaire, E.-J. Belin de Chantemele, Kevin Retailleau, Arnaud Bocquet, Christophe Baufreton, Frédéric Pinaud, Valérie Domenga, Daniel Henrion, Anne-Laure Guihot, Laurent Loufrani, Emilie Vessières, Anne Joutel
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2008, 28 (12), pp.2216-24. ⟨10.1161/ATVBAHA.108.171751⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2008, 28 (12), pp.2216-24. ⟨10.1161/ATVBAHA.108.171751⟩
Objective— Notch3, a member of the evolutionary conserved Notch receptor family, is primarily expressed in vascular smooth muscle cells. Genetic studies in human and mice revealed a critical role for Notch3 in the structural integrity of distal res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55e744d611751c8d65f79ebe0146dfab
https://pubmed.ncbi.nlm.nih.gov/18818417
https://pubmed.ncbi.nlm.nih.gov/18818417
Autor:
Elisabeth Tournier-Lasserve, Charles Babinet, Anne Joutel, Valérie Domenga, Thomas Gridley, Francina Langa, Celine Souilhol, Barbara Lemaire, Michel Cohen-Tannoudji, Marie Monet
Publikováno v:
Human molecular genetics. 16(8)
Cerebral Autosomal Dominant Arteriopathy with Subcortical infarcts and Leukoencephalopathy (CADASIL) is the most prominent known cause of inherited stroke and vascular dementia in human adult. The disease gene, NOTCH3, encodes a transmembrane recepto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::787882e32048ea3b9ed17615abb10a00
https://pubmed.ncbi.nlm.nih.gov/17331978
https://pubmed.ncbi.nlm.nih.gov/17331978