Large Granular Lymphocyte Leukemia
What's New
Last Posted: Jun 25, 2023
- Genomic landscape of T-large granular lymphocyte leukemia and chronic lymphoproliferative disorder of NK cells: a single institution experience.
Fei Fei, et al. Leukemia & lymphoma 2023 0 1-9 - Inclusion-body myositis and primary Sjögren syndrome: mechanisms for shared etiologies.
Limaye Vidya S, et al. Muscle & nerve 2020 0 (5) 570-574 - Clonal hematopoiesis in adult pure red cell aplasia.
Fujishima Naohito, et al. Scientific reports 2021 0 (1) 2253 - T?? LGLL identifies a subset with more symptomatic disease: analysis of an international cohort of 137 patients.
Barilà Gregorio, et al. Blood 2022 0 - Identification of novel STAT5B mutations and characterization of TCR? signatures in CD4+ T-cell large granular lymphocyte leukemia.
Bhattacharya Dipabarna, et al. Blood cancer journal 2022 0 (2) 31 - Genomic landscape of TCR?? and TCR?? T-large granular lymphocyte leukemia.
Cheon HeeJin, et al. Blood 2022 0 (20) 3058-3072 - Somatic STAT3 mutations in Felty syndrome: an implication for a common pathogenesis with large granular lymphocyte leukemia.
Savola Paula, et al. Haematologica 2017 12 - Cell size variations of large granular lymphocyte leukemia: Implication of a small cell subtype of granular lymphocyte leukemia with STAT3 mutations.
Tanahashi Takahiro, et al. Leukemia research 2016 4 8-13 - STAT3 gene mutations and their association with pure red cell aplasia in large granular lymphocyte leukemia.
Ishida Fumihiro, et al. Cancer science 2014 3 (3) 342-6 - STAT3 mutations indicate the presence of subclinical T-cell clones in a subset of aplastic anemia and myelodysplastic syndrome patients.
Jerez Andres, et al. Blood 2013 10 (14) 2453-9
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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