Bassam R Ali

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lihadh al-gazaliProfessor in Clinical Genetics & PaediatricsDirección de correo verificada de uaeu.ac.ae
Salma Ben-SalemEarly is Good, IncDirección de correo verificada de earlyisgood.com
Joseph G. GleesonUniversity of California, San DiegoDirección de correo verificada de ucsd.edu
Theodora KatsilaResearch Associate Professor-Head of Lab at National Hellenic Research FoundationDirección de correo verificada de eie.gr
Eyad ElkordProfessor; Dept of Biosciences&Bioinformatics-School of Science-XJTLU; Uni of Salford; Abu Dhabi UniDirección de correo verificada de xjtlu.edu.cn
harry gilbertInstitute for Cell and Molecular Biosciences, Newcastle UniversityDirección de correo verificada de ncl.ac.uk
Reham M. MilhemMedComms | ResearchDirección de correo verificada de uaeu.ac.ae
Prof. Gary BlackNorthumbria UniversityDirección de correo verificada de northumbria.ac.uk
Ron WeversProfessor in Clinical Chemistry in NijmegenDirección de correo verificada de radboudumc.nl
Hudson FreezeHuman Genetics ProgramDirección de correo verificada de sanfordburnham.org
Christopher A WalshBoston Children's HospitalDirección de correo verificada de childrens.harvard.edu
Noushad KaruvantevidaMohammed Bin Rashid University of Medicine and Health Sciences, DubaiDirección de correo verificada de dubaihealth.ae
Edgar Otto, PhDAssociate Research Scientist, Internal Medicine-Nephrology, University of MichiganDirección de correo verificada de umich.edu
Duarte BarralCEDOC, NOVA Medical School | Faculdade de Ciências Médicas, Universidade Nova de LisboaDirección de correo verificada de fcm.unl.pt
Jose RamalhoCEDOC - NOVA Medical School - NOVA University of LisbonDirección de correo verificada de sicgen.pt
Angela BrandMaastricht UniversityDirección de correo verificada de maastrichtuniversity.nl
Adrián LLerena MD PhD Professor Cli...INUBE Biosanitary University Research Institute. University of Extremadura. CICAB Clinical ResearchDirección de correo verificada de unex.es
Diego Forero, MD, PhDResearcher, School of Health and Sport Sciences, Fundación Universitaria del Área AndinaDirección de correo verificada de areandina.edu.co
Paul LaissueLATAM Medical Director. Orphan Diseases Unit. Biopas Laboratoires. BIOPAS Group. Inserm U1016, CNRSDirección de correo verificada de biopasgroup.com
Prof Ambroise Wonkam, MD, DMedSc,...Division of Human Genetics - Faculty of Health Sciences - University of Cape Town - South AfricaDirección de correo verificada de uct.ac.za

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Bassam R Ali

Professor of Molecular Genetics, College of Medicine, United Arab Emirates University

Dirección de correo verificada de uaeu.ac.ae - Página principal

Genetics Genetic Disorders Pharmacogenomics Membrane Trafficking Protein Misfolding


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
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	435	2008
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	326	2010
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	189	2003
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	182	2012
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	174	2004
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	146	2018
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	145	2011
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	132	1995
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	131	2017
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	128	2007
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	128	1995
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	120	2018
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	114	2010
Targeting of Rab GTPases to cellular membranes BR Ali, MC Seabra Biochemical Society Transactions 33 (4), 652-656, 2005	113	2005
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	94	2017
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	93	1995
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	87	2013
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	87	2010
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	85	2010
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	74	2017

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