Abdullah Mahmood Ali
Abdullah Mahmood Ali
Columbia University Medical Center
Verified email at columbia.edu - Homepage
Cited by
Cited by
MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM
TR Singh, D Saro, AM Ali, XF Zheng, C Du, MW Killen, A Sachpatzidis, ...
Molecular cell 37 (6), 879-886, 2010
Physiologic Expression of Sf3b1K700E Causes Impaired Erythropoiesis, Aberrant Splicing, and Sensitivity to Therapeutic Spliceosome Modulation
EA Obeng, RJ Chappell, M Seiler, MC Chen, DR Campagna, PJ Schmidt, ...
Cancer Cell 30 (3), 404-417, 2016
BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase–double Holliday junction dissolvasome
TR Singh, AM Ali, V Busygina, S Raynard, Q Fan, C Du, PR Andreassen, ...
Genes & development 22 (20), 2856-2868, 2008
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway
C Ling, M Ishiai, AM Ali, AL Medhurst, K Neveling, R Kalb, Z Yan, Y Xue, ...
The EMBO journal 26 (8), 2104-2114, 2007
Disease-associated mutation in SRSF2 misregulates splicing by altering RNA-binding affinities
J Zhang, YK Lieu, AM Ali, A Penson, KS Reggio, R Rabadan, A Raza, ...
Proceedings of the National Academy of Sciences 112 (34), E4726-E4734, 2015
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M
TR Singh, ST Bakker, S Agarwal, M Jansen, E Grassman, BC Godthelp, ...
Blood 114 (1), 174-180, 2009
Role of CYP1B1, MYOC, OPTN and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients
A Kumar, MG Basavaraj, SK Gupta, I Qamar, AM Ali, V Bajaj, TK Ramesh, ...
Molecular vision 13, 667, 2007
FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway
AM Ali, A Pradhan, TR Singh, C Du, J Li, K Wahengbam, E Grassman, ...
Blood 119 (14), 3285-3294, 2012
U2AF35(S34F) Promotes Transformation by Directing Aberrant ATG7 Pre-mRNA 3′ End Formation
SM Park, J Ou, L Chamberlain, TM Simone, H Yang, CM Virbasius, AM Ali, ...
Molecular cell 62 (4), 479-490, 2016
ATR-Dependent Phosphorylation of FANCM at Serine 1045 is Essential for FANCM Functions
TR Singh, AM Ali, M Paramasivam, A Pradhan, K Wahengbam, ...
Cancer research 73 (14), 4300-4310, 2013
Identification and characterization of mutations in FANCL gene: A second case of Fanconi anemia belonging to FA‐L complementation group
AM Ali, M Kirby, M Jansen, FP Lach, J Schulte, TR Singh, SD Batish, ...
Human mutation 30 (7), E761-E770, 2009
Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway
M Huang, R Kennedy, AM Ali, LA Moreau, AR Meetei, AD D’Andrea, ...
DNA repair 10 (12), 1203-1212, 2011
FANCM–FAAP24 and FANCJ: FA proteins that metabolize DNA
AM Ali, TR Singh, AR Meetei
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 668 (1 …, 2009
Ectopic HOXB4 overcomes the inhibitory effect of tumor necrosis factor-α on Fanconi anemia hematopoietic stem and progenitor cells
MD Milsom, B Schiedlmeier, J Bailey, MO Kim, D Li, M Jansen, AM Ali, ...
Blood 113 (21), 5111-5120, 2009
Gene-edited stem cells enable CD33-directed immune therapy for myeloid malignancies
F Borot, H Wang, Y Ma, T Jafarov, A Raza, AM Ali, S Mukherjee
Proceedings of the National Academy of Sciences 116 (24), 11978-11987, 2019
Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex
M Ali, SC Girimaji, M Markandaya, AK Shukla, S Sacchidanand, A Kumar
Acta Neurologica Scandinavica 111 (1), 54-63, 2005
Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations
M Ali, C Venkatesh, A Ragunath, A Kumar
Ophthalmic Genetics 25 (4), 247-255, 2004
Disease-causing mutations in SF3B1 alter splicing by disrupting interaction with SUGP1
J Zhang, AM Ali, YK Lieu, Z Liu, J Gao, R Rabadan, A Raza, S Mukherjee, ...
Molecular cell 76 (1), 82-95. e7, 2019
DEK is required for homologous recombination repair of DNA breaks
EA Smith, B Gole, NA Willis, R Soria, LM Starnes, EF Krumpelbeck, ...
Scientific reports 7, 44662, 2017
Identification of a core promoter and a novel isoform of the human TSC1 gene transcript and structural comparison with mouse homolog
M Ali, SC Girimaji, A Kumar
Gene 320, 145-154, 2003
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