Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Amye M. Harrigan"'
Publikováno v:
Current Oncology, Vol 29, Iss 9, Pp 6419-6432 (2022)
Cancer-associated venous thromboembolism is a devastating complication of cancer and is associated with significant morbidity and mortality. The cornerstone of cancer-associated venous thromboembolism treatment is anticoagulation, and in recent years
Externí odkaz:
https://doaj.org/article/773eca9aa66a4a0ba6370ee75ef33fd5
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Rationale: Alemtuzumab is a monoclonal antibody approved for the treatment of relapsing-remitting multiple sclerosis (RRMS). Many autoimmune-mediated adverse events have been associated with alemtuzumab, including renal-limited anti-glomerular baseme
Externí odkaz:
https://doaj.org/article/c8976202fe4e49999d85e051a78fb074
Autor:
Amye M. Harrigan, Amy M. Trottier
Acute myeloid leukemia with germline CEBPA mutation is a subtype of acute myeloid leukemia that is associated with a favorable prognosis. Most of the reported cases of acute myeloid leukemia with CEBPA germline variants involve a germline variant in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c57b20fd8d1ba35b2e4f860803ef314b
https://doi.org/10.21203/rs.3.rs-2167397/v1
https://doi.org/10.21203/rs.3.rs-2167397/v1
Publikováno v:
Journal of Hematology
TERC variant telomere biology disorders (TBDs) are a rare, heterogenous group of disorders that arise from germline variants in TERC , a gene that encodes for the RNA component of telomerase. Variants in TERC lead to accelerated telomere attrition an
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Canadian Journal of Kidney Health and Disease
Canadian Journal of Kidney Health and Disease
Rationale: Alemtuzumab is a monoclonal antibody approved for the treatment of relapsing-remitting multiple sclerosis (RRMS). Many autoimmune-mediated adverse events have been associated with alemtuzumab, including renal-limited anti-glomerular baseme
Publikováno v:
Genome Biology and Evolution
Approximately 35% of the human genome can be identified as sequence devoid of a selected-effect function, and not derived from transposable elements or repeated sequences. We provide evidence supporting a known origin for a fraction of this sequence.
Publikováno v:
Blood. 136:11-11
TERC variant telomere biology disorders are a rare and heterogenous group of disorders that arise from germline variants in TERC, a gene that encodes for the RNA component of telomerase. Variants in TERC lead to accelerated telomere attrition and can