עקוב אחר
Prof. Rajech Sharkia
Prof. Rajech Sharkia
Beit-Berl College and Triangle R&D Center
כתובת אימייל מאומתת בדומיין beitberl.ac.il
כותרת
צוטט על ידי
צוטט על ידי
שנה
The effect of nucleotides and mitochondrial chaperonin 10 on the structure and chaperone activity of mitochondrial chaperonin 60
G Levy‐Rimler, P Viitanen, C Weiss, R Sharkia, A Greenberg, A Niv, ...
European journal of biochemistry 268 (12), 3465-3472, 2001
1302001
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
M Mallaret, M Synofzik, J Lee, CA Sagum, M Mahajnah, R Sharkia, ...
Brain 137 (2), 411-419, 2014
1192014
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia
M Minnerop, D Kurzwelly, H Wagner, AS Soehn, J Reichbauer, F Tao, ...
Brain 140 (6), 1561-1578, 2017
1032017
Bicarbonate uptake in the marine macroalga Ulva sp. is inhibited by classical probes of anion exchange by red blood cells
Z Drechsler, R Sharkia, ZI Cabantchik, S Beer
Planta 191, 34-40, 1993
1031993
The changing pattern of consanguinity in a selected region of the Israeli Arab community
R Sharkia, M Zaid, A Athamna, D Cohen, A Azem, A Zalan
American Journal of Human Biology 20 (1), 72-77, 2008
462008
The relationship of arginine groups to photosynthetic HCO 3 - uptake inUlva sp. mediated by a putative anion exchanger
Z Drechsler, R Sharkia, ZI Cabantchik, S Beer
Planta 194, 250-255, 1994
371994
On the oligomeric state of chloroplast chaperonin 10 and chaperonin 20
R Sharkia, AL Bonshtien, I Mizrahi, C Weiss, A Niv, A Lustig, PV Viitanen, ...
Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics 1651 (1-2), 76-84, 2003
312003
Clinical characteristics of autism spectrum disorder in Israel: impact of ethnic and social diversities
M Mahajnah, R Sharkia, H Shalabe, R Terkel-Dawer, A Akawi, N Zelnik
BioMed Research International 2015, 2015
302015
A membrane-located polypeptide of Ulva sp. which may be involved in HCO 3 - uptake is recognized by antibodies raised against the …
R Sharkia, S Beer, ZI Cabantchik
Planta 194, 247-249, 1994
301994
CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis
H Hengel, A Magee, M Mahanjah, JM Vallat, R Ouvrier, M Abu-Rashid, ...
Neurology: Genetics 3 (2), e144, 2017
282017
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery
H Hengel, R Buchert, M Sturm, TB Haack, Y Schelling, M Mahajnah, ...
European Journal of Human Genetics 28 (8), 1034-1043, 2020
272020
Changes in marriage patterns among the Arab community in Israel over a 60-year period
R Sharkia, M Mahajnah, E Athamny, M Khatib, A Sheikh-Muhammad, ...
Journal of biosocial science 48 (2), 283-287, 2016
272016
A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome
R Sharkia, A Zalan, A Jabareen-Masri, H Zahalka, M Mahajnah
European journal of medical genetics 62 (11), 103549, 2019
262019
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus
AK Mayer, M Mahajnah, MG Thomas, Y Cohen, A Habib, M Schulze, ...
Brain 142 (6), 1528-1534, 2019
262019
Clinical, radiological, and genetic characteristics of 16 patients with ACO2 gene defects: Delineation of an emerging neurometabolic syndrome
R Sharkia, KJ Wierenga, A Kessel, A Azem, E Bertini, R Carrozzo, ...
Journal of inherited metabolic disease 42 (2), 264-275, 2019
232019
Differential effects of co-chaperonin homologs on cpn60 oligomers
AL Bonshtien, A Parnas, R Sharkia, A Niv, I Mizrahi, A Azem, C Weiss
Cell Stress and Chaperones 14 (5), 509-519, 2009
222009
Comparative screening of FMF mutations in various communities of the Israeli society
R Sharkia, M Mahajnah, A Zalan, M Athamna, A Azem, K Badarneh, ...
European Journal of Medical Genetics 56 (7), 351-355, 2013
202013
The relationship between parental stress and mastery, forgiveness, and social support among parents of children with autism
M Weinberg, N Gueta, J Weinberg, MA Much, A Akawi, R Sharkia, ...
Research in Autism Spectrum Disorders 81, 101712, 2021
192021
Novel missense variants in ADAT3 as a cause of syndromic intellectual disability
E Thomas, AM Lewis, Y Yang, S Chanprasert, L Potocki, DA Scott
Journal of Pediatric Genetics 8 (04), 244-251, 2019
182019
Mental retardation and consanguinity in a selected region of the Israeli Arab community
R Sharkia, A Azem, Q Kaiyal, N Zelnik, M Mahajnah
Central European journal of medicine 5, 91-96, 2010
182010
המערכת אינה יכולה לבצע את הפעולה כעת. נסה שוב מאוחר יותר.
מאמרים 1–20