Greaves, M. F. (Melvyn F.), 1941-
Greaves, Melvyn F. 1941-
Melvyn Greaves biologist
Greaves, Melvyn Francis, 1941-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Greaves, M. F.
Greaves, Mel
Greaves, Melvyn F. (Melvyn Francis), 1941-
Greaves, Melvyn
Greaves, Melvyn Francis
Greaves, M. F. (Melvyn F.)
VIAF ID: 79085829 (Personal)
Permalink: http://viaf.org/viaf/79085829
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Greaves
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, Mel
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Greaves
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Melvyn
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200 _ 1 ‡a Greaves ‡b Melvyn F. ‡f 1941-
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100 1 _ ‡a Greaves, M. F.
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Greaves, M. F.
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(Melvyn F.)
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100 1 _ ‡a Greaves, M. F. ‡q (Melvyn F.), ‡d 1941-
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100 1 _ ‡a Greaves, M. F. ‡q (Melvyn F.), ‡d 1941-
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100 1 _ ‡a Greaves, M. F. ‡q (Melvyn F.), ‡d 1941-
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100 1 _
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Greaves, M. F.
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(Melvyn F.),
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1941-
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100 1 _ ‡a Greaves, M. F. ‡q (Melvyn F.), ‡d 1941-
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100 1 _ ‡a Greaves, Mel
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Greaves, Melvyn F,
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1941-
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100 1 _ ‡a Greaves, Melvyn F. ‡d (1941- ).
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100 1 _
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Greaves, Melvyn F.
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1941-
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100 1 _ ‡a Greaves, Melvyn F. ‡q (Melvyn Francis), ‡d 1941-
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100 1 _ ‡a Greaves, Melvyn Francis
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100 1 _
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Greaves, Melvyn Francis,
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1941-....
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100 0 _
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Melvyn Greaves
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biologist
4xx's: Alternate Name Forms (31)
Works
| Title | Sources |
|---|---|
| The association of a distinctive allele of NAD(P)H:quinone oxidoreductase with pediatric acute lymphoblastic leukemias with MLL fusion genes in Japan. |
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| Atlas of blood cells : function and pathology |
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| Blut. |
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| Cancer : the evolutionary legacy |
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| Chromosome translocations and covert leukemic clones are generated during normal fetal development |
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| Darwin and evolutionary tales in leukemia. The Ham-Wasserman Lecture |
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| Darwinian medicine: a case for cancer |
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| Developmental impact of leukemic fusion genes on stem cell fate |
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| Developmental timing of mutations revealed by whole-genome sequencing of twins with acute lymphoblastic leukemia |
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| Directing oncogenic fusion genes into stem cells via an SCL enhancer |
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| Epidemiology of leukemia and lymphoma : report of the Leukemia Research Fund International Workshop, Oxford, UK, September 1984 |
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| Erratum: Corrigendum: Signatures of mutational processes in human cancer |
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| Evolutionary Adaptations to Risk of Cancer: Evidence From Cancer Resistance in Elephants |
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| Fetal origins of the TEL-AML1 fusion gene in identical twins with leukemia |
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| Fusion genes in cord blood. |
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| Gan : Shinka no isan |
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| Genes and cancer : proceedings of a CETUS/UCLA Symposium held in Steamboat Springs, Colorado, March 11-17, 1984 |
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| Genetic variegation of clonal architecture and propagating cells in leukaemia |
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| Godwits and blast crises: in memory of David Galton. |
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| The histone deacetylase 9 gene encodes multiple protein isoforms |
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| Immunologically silent cancer clone transmission from mother to offspring |
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| In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia |
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| Infection and the Perils of B-cell Activation |
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| Initiating and cancer-propagating cells in TEL-AML1-associated childhood leukemia |
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| Krebs - der blinde Passagier der Evolution |
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| Leukaemia 'firsts' in cancer research and treatment |
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| Leukemia : progress and controversies : Keystone Symposium on Molecular and Cellular Biology, 6-12 April, 1991, Big Sky, Montana, USA |
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| Leukemogenesis and ageing: 'fit for transformation'? |
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| MLL chimeric protein activation renders cells vulnerable to chromosomal damage: an explanation for the very short latency of infant leukemia |
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| Modeling first-hit functions of the t(12;21) TEL-AML1 translocation in mice |
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| Modern trends in human leukemia : the Xth Wilsede Meeting on Leukemia Research |
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| Molecular diagnostics of human cancer, 1989: |
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| Molecular pathogenesis of MLL-associated leukemias |
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| Monoclonal antibodies to receptors : probes for receptor structure and function |
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| n82257895 |
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| NOTCH1 mutation can be an early, prenatal genetic event in T-ALL. |
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| Nothing in cancer makes sense except…. |
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| Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer |
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| P-24: a human leukemia-associated and lymphohemopoietic progenitor cell surface structure identified with monoclonal antibody |
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| Processed pseudogenes acquired somatically during cancer development |
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| Protracted dormancy of pre-leukemic stem cells |
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| Protracted postnatal natural histories in childhood leukemia |
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| RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia |
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| Recept. recogn. Ser. A |
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| Receptors and Recognition. |
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| Retrospective. Janet Rowley (1925-2013). |
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| The role of the MLL gene in infant leukemia |
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| La sfida più difficile : l'eredità evolutiva del cancro / Mel Greaves ; traduzione di Adria Tissoni |
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| Single-cell mutational profiling and clonal phylogeny in cancer |
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| The small oligomerization domain of gephyrin converts MLL to an oncogene |
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| Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia. |
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| The subclonal complexity of STIL-TAL1+ T-cell acute lymphoblastic leukaemia. |
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| T and B lymphocytes : origins, properties and roles in immune responses |
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| The TEL-AML1 leukemia fusion gene dysregulates the TGF-beta pathway in early B lineage progenitor cells |
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| Tyrosine kinase inhibitor insensitivity of non-cycling CD34+ human acute myeloid leukaemia cells with FMS-like tyrosine kinase 3 mutations. |
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| Ubiquitous cell-surface glycoprotein on tumor cells is proliferation-associated receptor for transferrin |
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| Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk |
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| Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood. |
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| Was skin cancer a selective force for black pigmentation in early hominin evolution? |
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| When one mutation is all it takes |
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| White blood personal journeys with childhood leukaemia |
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| がん : 進化の遺産 |
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