Lista de obras - Abdullah M. Ali - Dominio Público Uruguay

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

artículo científico publicado en 2013

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

artículo científico publicado en 2008

DEK is required for homologous recombination repair of DNA breaks

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 2009

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

artículo científico publicado en 2007

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

artículo científico publicado en 2012

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

artículo científico publicado en 2019

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

artículo científico publicado en 2011

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

artículo científico publicado en 2009

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

artículo científico publicado en 2003

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

artículo científico publicado en 2010

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

artículo científico publicado en 2013

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

artículo científico publicado en 2004

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

artículo científico publicado en 2005

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

artículo científico publicado en 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.