Hamid Dolatshad

Oxford, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 22 publications

Identification of new candidate drugs in myelodysplastic syndromes with splicing factor mutations by transcriptional profiling and connectivity map analysis.

Identification of new candidate drugs in myelodysplastic syndromes with splicing factor mutations by transcriptional profiling and connectivity map analysis.

Journal: British journal of haematology

Published: November 26, 2024

Effects of prolactin on movement disorders and APOE, GFAP, and PRL receptor gene expression following intracerebral hemorrhage in rats.

Effects of prolactin on movement disorders and APOE, GFAP, and PRL receptor gene expression following intracerebral hemorrhage in rats.

Journal: Iranian journal of basic medical sciences

Published: July 05, 2021

ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine.

ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine.

Journal: Blood cancer journal

Published: February 08, 2021

The protective effects of prolactin on brain injury.

The protective effects of prolactin on brain injury.

Journal: Life sciences

Published: June 30, 2020

SF3B1 mutations induce R-loop accumulation and DNA damage in MDS and leukemia cells with therapeutic implications.

SF3B1 mutations induce R-loop accumulation and DNA damage in MDS and leukemia cells with therapeutic implications.

Journal: Leukemia

Published: November 20, 2019

Application of induced pluripotent stem cell technology for the investigation of hematological disorders.

Application of induced pluripotent stem cell technology for the investigation of hematological disorders.

Journal: Advances in biological regulation

Published: September 20, 2018

Generation of Knock-out Primary and Expanded Human NK Cells Using Cas9 Ribonucleoproteins.

Generation of Knock-out Primary and Expanded Human NK Cells Using Cas9 Ribonucleoproteins.

Journal: Journal of visualized experiments : JoVE

Published: July 10, 2018

Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations.

Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations.

Journal: Blood

Published: April 06, 2018

Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 Gene Editing Technique in Xenotransplantation.

Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 Gene Editing Technique in Xenotransplantation.

Journal: Frontiers in immunology

Published: December 21, 2017

The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.

The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.

Journal: The Journal of clinical investigation

Published: September 02, 2017

The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.

The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.

Journal: The Journal of clinical investigation

Published: October 21, 2016

Cryptic splicing events in the iron transporter ABCB7 and other key target genes in SF3B1-mutant myelodysplastic syndromes.

Cryptic splicing events in the iron transporter ABCB7 and other key target genes in SF3B1-mutant myelodysplastic syndromes.

Journal: Leukemia

Published: March 11, 2016

Showing 1-12 of 22

Last Updated: 09/26/2026