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Donor Clonal Hematopoiesis and Recipient Outcomes After Transplantation [PDF]
PURPOSE Clonal hematopoiesis (CH) can be transmitted from a donor to a recipient during allogeneic hematopoietic cell transplantation. Exclusion of candidate donors with CH is controversial since its impact on recipient outcomes and graft alloimmune ...
Christopher J. Gibson +28 more
openalex +2 more sources
Clonal hematopoiesis (CH), the clonal expansion of a blood stem cell and its progeny driven by somatic driver mutations, affects over a third of people, yet remains poorly understood.
Siddhartha P Kar +2 more
exaly +2 more sources
Cancer therapy shapes the fitness landscape of clonal hematopoiesis
Acquired mutations are pervasive across normal tissues. However, understanding of the processes that drive transformation of certain clones to cancer is limited.
Kelly L Bolton +2 more
exaly +2 more sources
Clonal hematopoiesis in human aging and disease
Cryptic signs of aging in our blood Time is not a friend to our DNA. Aging is associated with an accumulation of somatic mutations in normal dividing cells, including the hematopoietic stem cells (HSCs) that give rise to all blood cells.
Siddhartha Jaiswal, Benjamin L Ebert
exaly +2 more sources
Cardiovascular Disease, Aging, and Clonal Hematopoiesis
Traditional risk factors are incompletely predictive of cardiovascular disease development, a leading cause of death in the elderly. Recent epidemiological studies have shown that human aging is associated with an increased frequency of somatic mutations
Soichi Sano, Kenneth Walsh
exaly +2 more sources
Distinction of lymphoid and myeloid clonal hematopoiesis
Abhishek Niroula +2 more
exaly +2 more sources
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
Siddhartha Jaiswal +2 more
exaly +2 more sources
Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes
Rafael Bejar +2 more
exaly +2 more sources
Spectrum of clonal hematopoiesis in VEXAS syndrome.
VEXAS is caused by somatic mutations in UBA1 (UBA1mut) and characterized by heterogenous systemic auto-inflammation and progressive hematologic manifestations, meeting criteria for myelodysplastic syndrome (MDS) and plasma cell dyscrasias.
Fernanda Gutierrez-Rodrigues +35 more
semanticscholar +1 more source
CD14+ monocytes repress gamma globin expression at early stages of erythropoiesis
In β-hemoglobinopathies, reactivation of gamma- at the expense of beta-globin is a prominent therapeutic option. Expression of the globin genes is not strictly intrinsically regulated during erythropoiesis, supported by the observation that fetal ...
Steven Heshusius +3 more
doaj +1 more source

