Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yehuda Kling"'
Autor:
David A. Zeevi, Sophie Kirshberg, Dina Kort, Sharon Zeligson, Aharon Peretz, Ephrat Levy-Lahad, Tal Dror, Gheona Altarescu, Yehuda Kling, Fouad Zahdeh, Tzvia Rosen, Reeval Segel, Daniel Backenroth, Efrat Burak, David Zangen, Shai Carmi
Publikováno v:
Genetics in Medicine. 21:1390-1399
To develop an economical, user-friendly, and accurate all-in-one next-generation sequencing (NGS)-based workflow for single-cell gene variant detection combined with comprehensive chromosome screening in a 24-hour workflow protocol. We subjected sing
Autor:
Zohar Argov, Yehuda Kling, Sharona Elgavish, Ilan Sela, L. Yakovlev, Stella Mitrani-Rosenbaum, A. Harazi, Yuval Nevo, Michal Becker Cohen, Hadar Benyamini
Publikováno v:
Journal of Neuromuscular Diseases
Background Mutations in GNE cause a recessive, adult onset myopathy characterized by slowly progressive distal and proximal muscle weakness. Knock-in mice carrying the most frequent mutation in GNE myopathy patients, GneM743T/M743T, usually die few d
PURPOSE: Pre-implantation genetic diagnosis (PGD) for molecular disorders requires the construction of parental haplotypes. Classically, haplotype resolution (“phasing”) is obtained by genotyping multiple polymorphic markers in both parents and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11d4642757ec77139640c2470d02a709
https://europepmc.org/articles/PMC6504987/
https://europepmc.org/articles/PMC6504987/
Autor:
Gheona Altarescu, David A. Zeevi, Hananel E.G. Holzer, Paul Renbaum, Tzvia Rosen, Raphael Ron-El, Talia Eldar-Geva, Ephrat Levy-Lahad, Yehuda Kling, Fouad Zahdeh
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
Scientific Reports
Scientific Reports
Prenatal genetic testing is not generally applicable to the very early stages of pregnancy (prior to week 8 gestation), a time period that is crucial to pregnant couples with high risk for transmission of genetic disease to their fetus. Therefore, we
Autor:
David A. Zeevi, Yehuda Kling, Fouad Zahdeh, Daniel Backenroth, Aaron Perez, Gheona Altarescu, Ephrat Levy-Lahad, Shai Carmi, Tzvia Rosen
Publikováno v:
Reproductive BioMedicine Online. 38:e13
Introduction Recent technological advances have enabled combined gene mutation detection and comprehensive chromosome screening (CCS) from a single embryo biopsy by means of microarray or high coverage next generation sequencing (NGS) technologies. H
Autor:
Gheona Altarescu, Ephrat Levy-Lahad, Paul Renbaum, Shai Carmi, Yehuda Kling, Fouad Zahdeh, David A. Zeevi
Publikováno v:
Reproductive BioMedicine Online. 36:e34