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Helvise Morse

Researcher at University of Colorado Denver

Publications -  12
Citations -  370

Helvise Morse is an academic researcher from University of Colorado Denver. The author has contributed to research in topics: Leukemia & Chromosomal translocation. The author has an hindex of 9, co-authored 12 publications receiving 369 citations. Previous affiliations of Helvise Morse include Jewish Hospital & Boston Children's Hospital.

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Remission of relapsed leukæmia during a graft-versus-host reaction a "graft-versus-leukæmia reaction" in man?

TL;DR: The prolonged bone-marrow remission in the face of active and even massive extramedullary leukaemia suggests a graft-versus-leukaemia reaction in these two patients.
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Acute nonlymphoblastic leukemia in childhood. High incidence of clonal abnormalities and nonrandom changes

TL;DR: Cytogenetic studies have been done on a group of childhood patients over a period of 3 1/2 years in which Giemsa trypsin banding was applied to all specimens and no correlation could be found between the disease subgroup and the karyotypic aberration in patients with anomalies involving a common chromosome.
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4;11 translocation in acute lymphoblastic leukemia: a specific syndrome.

TL;DR: Three patients with acute lymphoblastic leukemia having t(4;11) (q21;q23) are described and their clinical characteristics are compared with ten other published cases all involving similar histories and poor prognoses.
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Chromosome mapping of biological pathways by fluorescence-activated cell sorting and cell fusion: human interferon gamma receptor as a model system

TL;DR: The segregation of cells on the basis of a biological effect by fluorescence-activated cell sorting and reconstitution by hybrid fusion provides a strategy by which some biological pathways can be mapped at a chromosomal level.
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Karyotyping of bone-marrow cells in hematologic diseases.

TL;DR: Cultures of bone-marrow cells incubated for 5 h at 4° had cells in metaphase with elongated chromosomes which were easily Giemsa banded, making possible routine karyotyping of patients with leukemia and other hematological diseases in which the detection of aberrations was otherwise difficult.