Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yuval eItan"'
Autor:
Yuval eItan, Jean-Laurent eCasanova
Publikováno v:
Frontiers in Immunology, Vol 6 (2015)
Germline genetic mutations underlie various primary immunodeficiency (PID) diseases. Patients with rare PID diseases (like most non-PID patients and healthy individuals) carry, on average, 20,000 rare and common coding variants detected by high throu
Externí odkaz:
https://doaj.org/article/7a0a4cd88b364301a2ccfdda0ef1bdae
Autor:
Yifat Guthmann, Irit Elmalah, Hila Belhanes-Peled, Yuval Eitan, Natalia Edison, Yelena Yeremenko, Philippe Trougouboff, Mark Raffeld
Publikováno v:
Hum Pathol
Summary We report a case of intestinal indolent T-cell lymphoproliferative disease (TCLPD) occurring after the initiation of tumor necrosis factor– α (TNF- α ) inhibitor therapy for resistant Crohn's disease. A prominent T-cell infiltrate positiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8419af1fd9b7b88a6fa9b4d608cf1932
https://doi.org/10.1016/j.humpath.2016.06.021
https://doi.org/10.1016/j.humpath.2016.06.021
Autor:
Yuval eItan, Jean-Laurent eCasanova
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 6 (2015)
Frontiers in Immunology, Vol 6 (2015)
Germline genetic mutations underlie various primary immunodeficiency (PID) diseases. Patients with rare PID diseases (like most non-PID patients and healthy individuals) carry, on average, 20,000 rare and common coding variants detected by high-throu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36dfd0643e2663e811286efcd9f24313
https://pubmed.ncbi.nlm.nih.gov/25883595
https://pubmed.ncbi.nlm.nih.gov/25883595
Publikováno v:
Tissue engineering. Part C, Methods. 16(4)
We have developed an efficient decellularization process for the isolation of extracellular matrix (ECM) from native cardiac tissue. The isolated ECM exhibited desirable mechanical properties in terms of elasticity, strength and durability-properties
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e4542a0099d6396f87917c2422a894b
https://pubmed.ncbi.nlm.nih.gov/19780649
https://pubmed.ncbi.nlm.nih.gov/19780649
Autor:
Yechezkel Kashi, Yuval Eitan
Publikováno v:
Nucleic Acids Research. 30:62e-62
Analysis of haplotypes is an important tool in population genetics, familial heredity and gene mapping. Determination of haplotypes of multiple single nucleotide polymorphisms (SNPs) or other simple mutations is time consuming and expensive when anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::999c3e8d2396c85f042b14821deb99e0
https://doi.org/10.1093/nar/gnf062
https://doi.org/10.1093/nar/gnf062