Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nurit Edri"'
Autor:
Jeffrey Bruffaerts, Inbar Kesten, Keren Buhnik-Rosenblau, Anthony Cohen, Nurit Edri, Morgan Cormier, Yuanfei Zhang, Guo-Ming Ho, Itai Massad, Hila Halfon-Verner, Yechezkel Kashi, Ilan Marek
Publikováno v:
Angewandte Chemie International Edition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c59246a3b0c2fd93adcc9058b9ef5ac
https://doi.org/10.1002/anie.202306343
https://doi.org/10.1002/anie.202306343
Autor:
Tzipora C. Falik-Zaccai, Nurit Edri, Nehama Cohen-Kfir, Irith Weissman, Lena Sagi-Dain, Hadas Shasha Lavski, Limor Kalfon, Amir Peleg
Publikováno v:
Birth Defects Research. 112:316-320
BACKGROUND Isolated populations with high rates of consanguinity and genetic disorders can be found in most parts of the world. The aim of our paper was to highlight the unique challenges faced in genetic counseling for such patients and to discuss t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ef7b70139a62aaa6e80b6f226baaf45
https://doi.org/10.1002/bdr2.1633
https://doi.org/10.1002/bdr2.1633
Autor:
Itai Massad, Yuanfei Zhang, Morgan Cormier, Yechezkel Kashi, Keren Buhnik-Rosenblau, Inbar Kesten, Anthony Cohen, Fabian Glaser, Ilan Marek, Nurit Edri, Guy Horev, Guo-Ming Ho, Jeffrey Bruffaerts, Hila Halfon-Verner
Selective undirected functionalization of strong primary C-H bonds of linear alkanes, that do not possess directing groups, historically stands as one of the most challenging transformation in chemistry. In this Article, we report a two-step sequenti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcbe00681573c12d1ce81f56ec92f30b
https://doi.org/10.21203/rs.3.rs-133031/v1
https://doi.org/10.21203/rs.3.rs-133031/v1
Autor:
Limor, Kalfon, Irit, Weissman, Miriam, Hershkovits, Nadra, Nasser Samra, Nurit, Edri, Morad, Khayat, Mary, Tanus, Shihab, Shihab, Hanna, Mandel, Tzipora, Falik-Zaccai
Publikováno v:
Harefuah. 156(3)
Primary Hyperoxaluria type I (PH1) is a rare autosomal recessive disease caused by lack or dysfunction of the liver peroxisomal enzyme alanine: glyoxylate aminotransferase, AGT.To conduct clinical and genetic characterization of Druze and Muslim Arab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9bd3664f4530c66fa1566309d59a43e4
https://pubmed.ncbi.nlm.nih.gov/28551940
https://pubmed.ncbi.nlm.nih.gov/28551940
Autor:
Michele Zaccai, Nurit Edri
Publikováno v:
Scientia Horticulturae. 95:333-340
Floral transition was studied in lisianthus [Eustoma grandiflorum (Raf.) Shinn.] plants grown in a greenhouse at two planting times (winter and summer) under two photoperiod regimes: long day (LD) and short day (SD), 16 h/8 h and 8 h/16 h (light/dark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bd51774214aa785a053d43450449d1f
https://doi.org/10.1016/s0304-4238(02)00057-2
https://doi.org/10.1016/s0304-4238(02)00057-2