Các bài viết có thể truy cập công khai - abdussalam azemTìm hiểu thêm
Không có ở bất kỳ nơi nào: 2
Cooperation of TOM and TIM23 complexes during translocation of proteins into mitochondria
K Waegemann, D Popov-Čeleketić, W Neupert, A Azem, D Mokranjac
Journal of Molecular Biology 427 (5), 1075-1084, 2015
Các cơ quan ủy nhiệm: German Research Foundation
The TIM23 mitochondrial protein import complex: function and dysfunction
K Demishtein-Zohary, A Azem
Cell and Tissue Research 367, 33-41, 2017
Các cơ quan ủy nhiệm: German Research Foundation
Có tại một số nơi: 23
Role of Tim50 in the transfer of precursor proteins from the outer to the inner membrane of mitochondria
D Mokranjac, M Sichting, D Popov-Čeleketić, K Mapa, ...
Molecular biology of the cell 20 (5), 1400-1407, 2009
Các cơ quan ủy nhiệm: German Research Foundation
GroEL and CCT are catalytic unfoldases mediating out-of-cage polypeptide refolding without ATP
S Priya, SK Sharma, V Sood, RUH Mattoo, A Finka, A Azem, ...
Proceedings of the National Academy of Sciences 110 (18), 7199-7204, 2013
Các cơ quan ủy nhiệm: Swiss National Science Foundation
Structural basis for active single and double ring complexes in human mitochondrial Hsp60-Hsp10 chaperonin
Y Gomez-Llorente, F Jebara, M Patra, R Malik, S Nisemblat, ...
Nature Communications 11 (1), 1916, 2020
Các cơ quan ủy nhiệm: US National Science Foundation, US National Institutes of Health
Methylation-controlled J-protein MCJ acts in the import of proteins into human mitochondria
C Schusdziarra, M Blamowska, A Azem, K Hell
Human molecular genetics 22 (7), 1348-1357, 2013
Các cơ quan ủy nhiệm: German Research Foundation
Effects of a Mutation in the HSPE1 Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental …
AS Bie, P Fernandez-Guerra, RID Birkler, S Nisemblat, D Pelnena, X Lu, ...
Frontiers in molecular biosciences 3, 65, 2016
Các cơ quan ủy nhiệm: German Research Foundation
Mitochondrial epileptic encephalopathy, 3‐methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutations
MA Shahrour, O Staretz‐Chacham, D Dayan, J Stephen, A Weech, ...
Clinical genetics 91 (5), 690-696, 2017
Các cơ quan ủy nhiệm: US National Institutes of Health
Role of Tim17 in coupling the import motor to the translocation channel of the mitochondrial presequence translocase
K Demishtein-Zohary, U Günsel, M Marom, R Banerjee, W Neupert, ...
Elife 6, e22696, 2017
Các cơ quan ủy nhiệm: German Research Foundation, Federal Ministry of Education and Research, Germany
GxxxG motifs hold the TIM23 complex together
K Demishtein‐Zohary, M Marom, W Neupert, D Mokranjac, A Azem
The FEBS journal 282 (11), 2178-2186, 2015
Các cơ quan ủy nhiệm: German Research Foundation
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
Các cơ quan ủy nhiệm: German Research Foundation
Dynamic complexes in the chaperonin-mediated protein folding cycle
C Weiss, F Jebara, S Nisemblat, A Azem
Frontiers in molecular biosciences 3, 80, 2016
Các cơ quan ủy nhiệm: US National Science Foundation
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
Các cơ quan ủy nhiệm: German Research Foundation, Fondazione Telethon, Italy
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
Các cơ quan ủy nhiệm: Research Foundation (Flanders), German Research Foundation, National …
Haploinsufficiency due to a novel ACO2 deletion causes mitochondrial dysfunction in fibroblasts from a patient with dominant optic nerve atrophy
MAC Neumann, D Grossmann, S Schimpf-Linzenbold, D Dayan, K Stingl, ...
Scientific reports 10 (1), 16736, 2020
Các cơ quan ủy nhiệm: German Research Foundation, Luxembourg National Research Fund, Federal …
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
Các cơ quan ủy nhiệm: German Research Foundation
A mutagenesis analysis of Tim50, the major receptor of the TIM23 complex, identifies regions that affect its interaction with Tim23
D Dayan, M Bandel, U Günsel, I Nussbaum, G Prag, D Mokranjac, ...
Scientific Reports 9 (1), 2012, 2019
Các cơ quan ủy nhiệm: German Research Foundation
In vivo dissection of the intrinsically disordered receptor domain of Tim23
U Günsel, E Paz, R Gupta, I Mathes, A Azem, D Mokranjac
Journal of Molecular Biology 432 (10), 3326-3337, 2020
Các cơ quan ủy nhiệm: German Research Foundation
A novel biallelic loss‐of‐function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro‐facio‐thoracic dysplasia
R Sharkia, A Zalan, A Jabareen‐Masri, H Hengel, L Schöls, A Kessel, ...
American Journal of Medical Genetics Part A 179 (7), 1338-1345, 2019
Các cơ quan ủy nhiệm: German Research Foundation, State of Califonia
A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay and polyneuropathy
M Patra, C Weiss, B Abu-Libdeh, M Ashhab, S Abuzer, O Elpeleg, ...
European Journal of Human Genetics 27 (7), 1072-1080, 2019
Các cơ quan ủy nhiệm: German Research Foundation
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