about
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathwayMHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCMFAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathwayATR-dependent phosphorylation of FANCM at serine 1045 is essential for FANCM functions.Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations.Disease-associated mutation in SRSF2 misregulates splicing by altering RNA-binding affinities.DEK is required for homologous recombination repair of DNA breaks.Ectopic HOXB4 overcomes the inhibitory effect of tumor necrosis factor-{alpha} on Fanconi anemia hematopoietic stem and progenitor cells.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) activatioIdentification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.U2AF35(S34F) Promotes Transformation by Directing Aberrant ATG7 Pre-mRNA 3' End Formation.Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway.Characterization of the human SLC22A18 gene promoter and its regulation by the transcription factor Sp1.Identification of a core promoter and a novel isoform of the human TSC1 gene transcript and structural comparison with mouse homolog.Physiologic Expression of Sf3b1(K700E) Causes Impaired Erythropoiesis, Aberrant Splicing, and Sensitivity to Therapeutic Spliceosome Modulation.Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex.Gene-edited stem cells enable CD33-directed immune therapy for myeloid malignancies
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Q24301340-72659CB9-6C3D-4082-9B7B-7432E76D5FB2Q24305020-CBA8E422-1F08-4E89-AFCB-11228541A329Q24305406-5A104744-A502-4A10-A88D-E2A2B4F1B028Q30411898-0B8CE349-1385-4353-9040-193CCE0D007EQ34380159-8691894E-5EA4-4146-A158-2AB8DECA1534Q36008365-C247A18C-D712-4030-801A-7643FD58A6E9Q36314320-2E25E632-35B4-48BD-B87F-B0DE01489849Q37201960-C837847B-F37A-4AA1-B809-BF26DEE017C3Q37333676-095D71A7-7307-4652-AAC6-77165E263D14Q37384036-C0FEE5D3-B516-48A9-ADC7-E154C3C8C23BQ38770604-852550DD-C45B-4676-A70D-54F2BE533156Q39462876-A43A91C9-9BA2-4670-A942-547022BD117DQ39919624-6CAD3C67-B932-4CFD-A4B7-C4DA19EB161BQ40620346-4102E91C-B055-4B01-B842-D19D60F01F4FQ41091296-F724C1B4-4C2A-4503-A0E1-B83CAFA49CD1Q45185112-2A073A66-8A00-47E8-B448-A5D22EAB0E08Q92355483-64CC1135-08FE-43D1-A99A-97FD091A9B45
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Abdullah M. Ali
@ast
Abdullah M. Ali
@en
Abdullah M. Ali
@es
Abdullah M. Ali
@nl
Abdullah M. Ali
@sl
type
label
Abdullah M. Ali
@ast
Abdullah M. Ali
@en
Abdullah M. Ali
@es
Abdullah M. Ali
@nl
Abdullah M. Ali
@sl
prefLabel
Abdullah M. Ali
@ast
Abdullah M. Ali
@en
Abdullah M. Ali
@es
Abdullah M. Ali
@nl
Abdullah M. Ali
@sl
P106
P1153
16232374800
P21
P31
P496
0000-0002-4007-6769