Page last updated: 2024-10-21

4,5,6,7-tetrahydroisoxazolo(4,5-c)pyridin-3-ol and Myelodysplastic Syndromes

4,5,6,7-tetrahydroisoxazolo(4,5-c)pyridin-3-ol has been researched along with Myelodysplastic Syndromes in 1 studies

4,5,6,7-tetrahydroisoxazolo(4,5-c)pyridin-3-ol: inhibitor of GABA uptake systems; RN given refers to parent cpd

Myelodysplastic Syndromes: Clonal hematopoietic stem cell disorders characterized by dysplasia in one or more hematopoietic cell lineages. They predominantly affect patients over 60, are considered preleukemic conditions, and have high probability of transformation into ACUTE MYELOID LEUKEMIA.

Research Excerpts

ExcerptRelevanceReference
"Hereditary thrombocytopenia is a heterogeneous group of congenital disorders with a wide range of symptoms depending on the severity of platelet dysfunction or thrombocytopenia."1.72Novel THPO variant in hereditary thrombocytopenia: A potential candidate variant for predisposition to myeloid neoplasm. ( Jeong, DJ; Kim, MJ; Kwon, S; Kwon, SR; Lee, DS; Lee, YE; Park, JH; Yun, J, 2022)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Kwon, SR1
Kim, MJ1
Lee, YE1
Yun, J1
Jeong, DJ1
Park, JH1
Kwon, S1
Lee, DS1

Other Studies

1 other study available for 4,5,6,7-tetrahydroisoxazolo(4,5-c)pyridin-3-ol and Myelodysplastic Syndromes

ArticleYear
Novel THPO variant in hereditary thrombocytopenia: A potential candidate variant for predisposition to myeloid neoplasm.
    PloS one, 2022, Volume: 17, Issue:12

    Topics: Disease Susceptibility; Humans; Myelodysplastic Syndromes; Myeloproliferative Disorders; Neoplasms;

2022