Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Gabriel Lidzbarsky"'
Cloning of the wheat Yr15 resistance gene sheds light on the plant tandem kinase-pseudokinase family
Autor:
Valentina Klymiuk, Elitsur Yaniv, Lin Huang, Dina Raats, Andrii Fatiukha, Shisheng Chen, Lihua Feng, Zeev Frenkel, Tamar Krugman, Gabriel Lidzbarsky, Wei Chang, Marko J. Jääskeläinen, Christian Schudoma, Lars Paulin, Pia Laine, Harbans Bariana, Hanan Sela, Kamran Saleem, Chris Khadgi Sørensen, Mogens S. Hovmøller, Assaf Distelfeld, Boulos Chalhoub, Jorge Dubcovsky, Abraham B. Korol, Alan H. Schulman, Tzion Fahima
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
Yellow rust fungus severely limits global wheat production and breeding of durable resistance is challenging. Here Klymiuk et al. isolate the broad-spectrum Yr15 resistance gene from wild emmer wheat and show that it is a member of a distinct tandem
Externí odkaz:
https://doaj.org/article/2c039f0c17bd49bda9be577c91659dba
Publikováno v:
Frontiers in Medicine, Vol 5 (2018)
As average life span and elderly people prevalence in the western world population is gradually increasing, the incidence of age-related diseases such as cancer, heart diseases, diabetes, and dementia is increasing, bearing social and economic conseq
Externí odkaz:
https://doaj.org/article/51e181d297274a698bf425b09af7fb46
Autor:
Merav Birk-Bachar, Hadar Cohen, Efrat Sofrin-Drucker, Nesia Kropach-Gilad, Naama Orenstein, Gabriel Lidzbarsky, Liora Kornreich, Rotem Tal, Gil Amarilyo, Yoel Levinsky, Meirav Sokolov, Eyal Raveh, Motti Gerlic, Liora Harel
Cryopyrin-associated periodic syndromes (CAPS) also known as NLRP3-associated auto-inflammatory diseases, are a spectrum of rare auto-inflammatory diseases caused by gain-of-function mutations in the NLRP3 gene, resulting in inflammasome hyper-activa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::002ff43c275b94bffaed968a3afa8a1b
https://doi.org/10.1101/2023.05.05.23289337
https://doi.org/10.1101/2023.05.05.23289337
Autor:
Orli Michaeli, Hagay Ladany, Ayelet Erez, Shay Ben Shachar, Shai Izraeli, Gabriel Lidzbarsky, Lina Basel‐Salmon, Saskia Biskup, Yosef E. Maruvka, Helen Toledano, Yael Goldberg
Publikováno v:
Clinical Genetics. 101:442-447
Polymerase proofreading-associated polyposis (PPAP) and Lynch syndrome, caused by mutated POLE and mismatch repair (MMR) genes, respectively, are associated with adult-onset cancer. PPAP and MMR-deficient tumors are both hypermutated, and each has a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76dcbc66cbbbf0dd22e80012b248d1be
https://doi.org/10.1111/cge.14106
https://doi.org/10.1111/cge.14106
Autor:
Nimrod Sachs, Oded Wechsberg, Yuval E. Landau, Irit Krause, Ifat Israel Elgali, Malak Darawshe, Noam Shomron, Gabriel Lidzbarsky, Naama Orenstein
Publikováno v:
Gene. 874:147483
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb6531b78422316b7318a9bd0405bf56
https://doi.org/10.1016/j.gene.2023.147483
https://doi.org/10.1016/j.gene.2023.147483
Autor:
Gabriel Lidzbarsky, Hadassa Goldberg-Stern, Lina Basel-Salmon, Noa Lev-El Halabi, Naama Orenstein, Alan R. Shuldiner, Claudia Gonzaga-Jauregui, Avi Fellner, Tomer Stern
Publikováno v:
American Journal of Medical Genetics Part A. 185:901-908
A male patient with a de novo mutation in the YWHAG gene and mild phenotype is presented. He had normal delivery and normal development, with normal speech and social milestones. At the age of 9 months, myoclonic seizures started, with generalized ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e87b5641503d712e5695ee4263442c05
https://doi.org/10.1002/ajmg.a.62026
https://doi.org/10.1002/ajmg.a.62026
Autor:
Marina Michelson, Gabriel Lidzbarsky, Daniella Nishri, Ifat Israel‐Elgali, Rachel Berger, Michal Gafner, Noam Shomron, Dorit Lev, Yael Goldberg
Publikováno v:
American journal of medical genetics. Part A. 188(7)
Interstitial deletions of 16q24.1-q24.2 are associated with alveolar capillary dysplasia, congenital renal malformations, neurodevelopmental disorders, and congenital abnormalities. Lymphedema-Distichiasis syndrome (LDS; OMIM # 153400) is a dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abea2f2eb05ed76e1be3a4cf30673d55
https://pubmed.ncbi.nlm.nih.gov/35312147
https://pubmed.ncbi.nlm.nih.gov/35312147
Autor:
Joris Deelen, Claudia Gonzaga-Jauregui, Patrick Sin-Chan, Tina Gao, Nir Barzilai, Gil Atzmon, A. R. Shuldiner, Danielle Gutman, Gabriel Lidzbarsky, Sofiya Milman
Publikováno v:
Aging Cell
Centenarians (exceptionally long‐lived individuals—ELLI) are a unique segment of the population, exhibiting long human lifespan and healthspan, despite generally practicing similar lifestyle habits as their peers. We tested disease‐associated m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f57c04ba6647f6174f7c13f9f88b2d
https://hdl.handle.net/21.11116/0000-000B-2D86-C
https://hdl.handle.net/21.11116/0000-000B-2D86-C
Autor:
Avi, Fellner, Noa, Ruhrman-Shahar, Naama, Orenstein, Gabriel, Lidzbarsky, Alan R, Shuldiner, Claudia, Gonzaga-Jauregui, Hadar, Brown-Shalev, Ofir, Hagari-Bechar, Lily, Bazak, Lina, Basel-Salmon
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 23(6)
To investigate the effectiveness of phenotype-based search approaches using publicly available online databases.We included consecutively solved cases from our exome database. For each case, the combination of Human Phenotype Ontology terms reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c725ffb6e475c74968fadde1727b4f9
https://pubmed.ncbi.nlm.nih.gov/33473205
https://pubmed.ncbi.nlm.nih.gov/33473205
Autor:
Andrii Fatiukha, Abraham B. Korol, Curtis J. Pozniak, Tzion Fahima, Naveh Filler, Tamar Krugman, Itamar Lupo, Gabriel Lidzbarsky, Valentyna Klymiuk
Publikováno v:
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik. 133(1)
Genetic dissection of GPC and TKW in tetraploid durum × WEW RIL population, based on high-density SNP genetic map, revealed 12 GPC QTLs and 11 TKW QTLs, with favorable alleles for 11 and 5 QTLs, respectively, derived from WEW. Wild emmer wheat (Trit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7ba68bd079e9ef641403fccce78957b
https://pubmed.ncbi.nlm.nih.gov/31562566
https://pubmed.ncbi.nlm.nih.gov/31562566