| 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 | 419 | 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 | 309 | 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 | 184 | 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 | 176 | 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 | 167 | 2004 |
| 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 | 135 | 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 | 131 | 1995 |
| 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 | 127 | 2018 |
| 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 | 125 | 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 | 125 | 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 | 117 | 2017 |
| Targeting of Rab GTPases to cellular membranes BR Ali, MC Seabra Biochemical Society Transactions 33 (4), 652-656, 2005 | 110 | 2005 |
| 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 | 107 | 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 | 105 | 2010 |
| 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 | 90 | 1995 |
| 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, 263524, 2017 | 88 | 2017 |
| 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 |
| 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 | 84 | 2010 |
| 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 | 80 | 2013 |
| 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, 274470, 2017 | 72 | 2017 |
lihadh al-gazaliProfessor in Clinical Genetics & Paediatrics在 uaeu.ac.ae 的电子邮件经过验证
