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Bassam R Ali
Bassam R Ali
Professor of Molecular Genetics, College of Medicine, United Arab Emirates University
Bestätigte E-Mail-Adresse bei uaeu.ac.ae - Startseite
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Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
V Cantagrel, JL Silhavy, SL Bielas, D Swistun, SE Marsh, JY Bertrand, ...
The American Journal of Human Genetics 83 (2), 170-179, 2008
4352008
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder
V Cantagrel, DJ Lefeber, BG Ng, Z Guan, JL Silhavy, SL Bielas, L Lehle, ...
Cell 142 (2), 203-217, 2010
3272010
Membrane targeting of Rab GTPases is influenced by the prenylation motif
AQ Gomes, BR Ali, JS Ramalho, RF Godfrey, DC Barral, AN Hume, ...
Molecular biology of the cell 14 (5), 1882-1899, 2003
1892003
Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia
JHM Schuurs-Hoeijmakers, MT Geraghty, EJ Kamsteeg, S Ben-Salem, ...
The American Journal of Human Genetics 91 (6), 1073-1081, 2012
1822012
Multiple regions contribute to membrane targeting of Rab GTPases
BR Ali, C Wasmeier, L Lamoreux, M Strom, MC Seabra
Journal of cell science 117 (26), 6401-6412, 2004
1742004
DNA methylation and repressive H3K9 and H3K27 trimethylation in the promoter regions of PD-1, CTLA-4, TIM-3, LAG-3, TIGIT, and PD-L1 genes in human primary breast cancer
V Sasidharan Nair, H El Salhat, RZ Taha, A John, BR Ali, E Elkord
Clinical epigenetics 10, 1-12, 2018
1462018
Faulty initiation of proteoglycan synthesis causes cardiac and joint defects
S Baasanjav, L Al-Gazali, T Hashiguchi, S Mizumoto, B Fischer, D Horn, ...
The American Journal of Human Genetics 89 (1), 15-27, 2011
1452011
The non-catalytic cellulose-binding domain of a novel cellulase from Pseudomonas fluorescens subsp. cellulosa is important for the efficient hydrolysis of Avicel
J Hall, GW Black, LMA Ferreira, SJ Millward-Sadler, BRS Ali, ...
Biochemical Journal 309 (3), 749-756, 1995
1321995
Preferential accumulation of regulatory T cells with highly immunosuppressive characteristics in breast tumor microenvironment
ASS Khaja, SM Toor, H El Salhat, I Faour, NU Haq, BR Ali, E Elkord
Oncotarget 8 (20), 33159, 2017
1302017
Rab GTPases containing a CAAX motif are processed post-geranylgeranylation by proteolysis and methylation
KF Leung, R Baron, BR Ali, AI Magee, MC Seabra
Journal of Biological Chemistry 282 (2), 1487-1497, 2007
1282007
Cellulases and hemicellulases of the anaerobic fungus Piromyces constitute a multiprotein cellulose-binding complex and are encoded by multigene families
BRS Ali, L Zhou, FM Graves, RB Freedman, GW Black, HJ Gilbert, ...
FEMS microbiology letters 125 (1), 15-21, 1995
1281995
Dual inhibition of STAT1 and STAT3 activation downregulates expression of PD-L1 in human breast cancer cells
V Sasidharan Nair, SM Toor, BR Ali, E Elkord
Expert opinion on therapeutic targets 22 (6), 547-557, 2018
1202018
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts
GH Mochida, VS Ganesh, JM Felie, D Gleason, RS Hill, KR Clapham, ...
The American Journal of Human Genetics 87 (6), 882-889, 2010
1142010
Targeting of Rab GTPases to cellular membranes
BR Ali, MC Seabra
Biochemical Society Transactions 33 (4), 652-656, 2005
1132005
Intratumoral FoxP3+Helios+ Regulatory T Cells Upregulating Immunosuppressive Molecules Are Expanded in Human Colorectal Cancer
AS Syed Khaja, SM Toor, H El Salhat, BR Ali, E Elkord
Frontiers in Immunology 8, 619, 2017
942017
A non-modular endo-β-1,4-mannanase from Pseudomonas fluorescens subspecies cellulosa
KL Braithwaite, GW Black, GP Hazlewood, BRS Ali, HJ Gilbert
Biochemical Journal 305 (3), 1005-1010, 1995
931995
Prevalence and novel mutations of lysosomal storage disorders in United Arab Emirates: LSD in UAE
FA Al-Jasmi, N Tawfig, A Berniah, BR Ali, M Taleb, JL Hertecant, F Bastaki, ...
JIMD Reports-Volume 10, 1-9, 2013
872013
Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patients
BR Ali, H Xu, NA Akawi, A John, NS Karuvantevida, R Langer, L Al-Gazali, ...
Human molecular genetics 19 (11), 2239-2250, 2010
872010
Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE)
L Al‐Gazali, BR Ali
Human mutation 31 (5), 505-520, 2010
852010
Pharmaceutical chaperones and proteostasis regulators in the therapy of lysosomal storage disorders: current perspective and future promises
FE Mohamed, L Al-Gazali, F Al-Jasmi, BR Ali
Frontiers in pharmacology 8, 448, 2017
742017
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