Homozygosis for (12) CA repeats in the first intron of the human IFN-gamma gene is significantly associated with the risk of aplastic anaemia in Caucasian population
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Current concepts in the pathophysiology and treatment of aplastic anemiaHematopoietic Stem Cell Regulation by Type I and II Interferons in the Pathogenesis of Acquired Aplastic AnemiaInfluence of TNF and IL6 gene polymorphisms on the severity of cytopenias in Argentine patients with myelodysplastic syndromes.Expression of Shelterin component POT1 is associated with decreased telomere length and immunity condition in humans with severe aplastic anemiaAplastica anemia and viral hepatitisIFN-γ causes aplastic anemia by altering hematopoietic stem/progenitor cell composition and disrupting lineage differentiation.The antihypertension drug doxazosin suppresses JAK/STATs phosphorylation and enhances the effects of IFN-α/γ-induced apoptosis.Association of IFN-g+874(T/A) polymorphism with female patients of age-related cataracts.Response of paroxysmal nocturnal hemoglobinuria clone with aplastic anemia to rituximab.Genetic associations in acquired immune-mediated bone marrow failure syndromes: insights in aplastic anemia and chronic idiopathic neutropenia.Identification of novel microRNA signatures linked to acquired aplastic anemia.The role of telomere biology in bone marrow failure and other disordersThe genetics and clinical manifestations of telomere biology disorders.Common polymorphic deletion of glutathione S-transferase theta predisposes to acquired aplastic anemia: Independent cohort and meta-analysis of 609 patients.The diagnosis and treatment of aplastic anemia: a review.Exploring the relationship between polymorphic (TG/CA)n repeats in intron 1 regions and gene expression.miR-146a-Traf6 regulatory axis controls autoimmunity and myelopoiesis, but is dispensable for hematopoietic stem cell homeostasis and tumor suppression.Why is the incidence of aplastic anemia higher in Asia?Acquired severe aplastic anemia after H1N1 influenza virus vaccination successfully treated with allogeneic bone marrow transplantation.Androgen receptor in cancer-associated fibroblasts influences stemness in cancer cells.Association of interferon-gamma +874(T/A) single nucleotide polymorphism with the rate of tryptophan catabolism in healthy individuals.Inflammatory Signaling Pathways in Preleukemic and Leukemic Stem Cells.iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors.Association between the lengths of GT dinucleotide repeat in the PIK3CA gene with breast cancer risk.
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Homozygosis for (12) CA repeats in the first intron of the human IFN-gamma gene is significantly associated with the risk of aplastic anaemia in Caucasian population
description
article
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im September 2004 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
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наукова стаття, опублікована у вересні 2004
@uk
ലേഖനം
@ml
name
Homozygosis for (12) CA repeat ...... naemia in Caucasian population
@en
Homozygosis for
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type
label
Homozygosis for (12) CA repeat ...... naemia in Caucasian population
@en
Homozygosis for
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prefLabel
Homozygosis for (12) CA repeat ...... naemia in Caucasian population
@en
Homozygosis for
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P1476
Homozygosis for (12) CA repeat ...... naemia in Caucasian population
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Achille Iolascon
Agnese Marrone
Andrea Bacigalupo
Anna Paola Iori
Associazione Italiana di Emato-Oncologia Pediatrica (AIEOP)
Carlo Dufour
Carola Pongiglione
Daniela Longoni
Department of Hematology, Ospedale S. Martino, Genoa, Italy
Lucia Giordani
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P356
10.1111/J.1365-2141.2004.05102.X
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P577
2004-09-01T00:00:00Z