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List of works by Abdullah M. Ali

ATR-dependent phosphorylation of FANCM at serine 1045 is essential for FANCM functions.

scientific article

Characterization of the human SLC22A18 gene promoter and its regulation by the transcription factor Sp1.

scientific article

DEK is required for homologous recombination repair of DNA breaks

scientific article

Disease-associated mutation in SRSF2 misregulates splicing by altering RNA-binding affinities

scientific article

Ectopic HOXB4 overcomes the inhibitory effect of tumor necrosis factor-{alpha} on Fanconi anemia hematopoietic stem and progenitor cells

scientific article published on 06 March 2009

FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

scientific article

FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway

scientific article

Gene-edited stem cells enable CD33-directed immune therapy for myeloid malignancies

scientific article published on 28 May 2019

Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway

scientific article published on 4 October 2011

Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.

scientific article published on July 2009

Identification of a core promoter and a novel isoform of the human TSC1 gene transcript and structural comparison with mouse homolog.

scientific article published on November 2003

MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM

scientific article

Monopolar spindle 1 (MPS1) protein-dependent phosphorylation of RecQ-mediated genome instability protein 2 (RMI2) at serine 112 is essential for BLM-Topo III α-RMI1-RMI2 (BTR) protein complex function upon spindle assembly checkpoint (SAC) activatio

scientific article published on 09 October 2013

Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations.

scientific article

Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex.

scientific article published in January 2005

Physiologic Expression of Sf3b1(K700E) Causes Impaired Erythropoiesis, Aberrant Splicing, and Sensitivity to Therapeutic Spliceosome Modulation.

scientific article published on September 2016

Taurine deficiency as a driver of aging

scientific article published on 08 June 2023

U2AF35(S34F) Promotes Transformation by Directing Aberrant ATG7 Pre-mRNA 3' End Formation.

scientific article published on 11 May 2016

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