Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of XPD (Lys751Gln) and XRCC1 (Arg280His) gene polymorphisms in myelodysplastic syndrome.

Annals of hematology - 1 Jan 2016

Joshi Dolly, Korgaonkar Seema, Shanmukhaiah Chandrakala, Vundinti Babu Rao

Abstract excerpt

Myelodysplastic syndromes (MDSs) are heterogeneous hematopoietic disease characterized by ineffective haematopoiesis that frequently transforms into acute leukaemia. Alterations in many individual biologic pathways have been reported in MDS pathophysiology. Disease progression along the MDS, acute myeloid leukemia (AML) continuum is believed to be a consequence of stepwise accumulation of DNA mutations which...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Arginine
Share to Genetic Association Studies
Share to Glutamine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Histidine

Share to Lysine

Share to Myelodysplastic Syndromes

Share to X-ray Repair Cross Complementing Protein 1

Share to Xeroderma Pigmentosum Group D Protein

Source

Identifiers

PMID: 26482462
DOI: 10.1007/s00277-015-2528-3

Genes

XRCC1
OGG1
RAD51
XRCC3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of XPD (Lys751Gln) and XRCC1 (Arg280His) gene polymorphisms in myelodysplastic syndrome.PMID 26482462Read ↗

Investigation of DNA repair gene variants on myelodysplastic syndromes in a Turkish population.Semantic proximity Read ↗

Polymorphisms of DNA repair genes are related to the pathogenesis of myelodysplastic syndrome.Semantic proximity Read ↗

Polymorphisms of detoxification and DNA repair enzymes in myelodyplastic syndromes.Semantic proximity Read ↗

DNA repair gene variants are associated with an increased risk of myelodysplastic syndromes in a Czech population.Semantic proximity Read ↗

Detoxification and DNA repair genes polymorphisms and susceptibility of primary myelodysplastic syndromes in Chinese population.Semantic proximity Read ↗

Association of A(313)G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome.Semantic proximity Read ↗

New polymorphisms of Xeroderma Pigmentosum DNA repair genes in myelodysplastic syndrome.Semantic proximity Read ↗

Genetic variants involved in oxidative stress, base excision repair, DNA methylation, and folate metabolism pathways influence myeloid neoplasias susceptibility and prognosis.Semantic proximity Read ↗

Polymorphism of XRCC1, XRCC3, and XPD genes and risk of chronic myeloid leukemia.Semantic proximity Read ↗

XRCC1 Arg194Trp and Arg399Gln polymorphisms are significantly associated with shorter survival in acute myeloid leukemia.Semantic proximity Read ↗

Base excision repair dysfunction in a subgroup of patients with myelodysplastic syndrome.Semantic proximity Read ↗

Influence of XPC, XPD, XPF, and XPG gene polymorphisms on the risk and the outcome of acute myeloid leukemia in a Romanian population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.