Linda M. Scott

researcher

Linda M. Scott is …
instance of (P31):
humanQ5

External links are
P496ORCID iD0000-0003-0334-1479
P3829Publons author ID2733758
P1053ResearcherIDD-9777-2012
P1153Scopus author ID55555303800

P734family nameScottQ12800811
ScottQ12800811
ScottQ12800811
P735given nameLindaQ1136594
LindaQ1136594
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q38139915Acquired mutations that affect pre-mRNA splicing in hematologic malignancies and solid tumors
Q53563972Alpha4 and beta2 integrins have nonredundant roles for asthma development, but for optimal allergen sensitization only alpha4 is critical.
Q34988228Deletion of alpha4 integrins from adult hematopoietic cells reveals roles in homeostasis, regeneration, and homing.
Q38540370Deregulated JAK/STAT signalling in lymphomagenesis, and its implications for the development of new targeted therapies
Q39901451Inhibition of the Bcl-xL deamidation pathway in myeloproliferative disorders
Q42006793JAK2 V617F impairs hematopoietic stem cell function in a conditional knock-in mouse model of JAK2 V617F-positive essential thrombocythemia
Q42742283Lack of alpha4 integrin expression in stem cells restricts competitive function and self-renewal activity
Q38075971Lymphoid malignancies: Another face to the Janus kinases.
Q34775393MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort.
Q43757332Molecular pathways in bone marrow homing: dominant role of alpha(4)beta(1) over beta(2)-integrins and selectins
Q50721189Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations, and role in leukemic transformation.
Q54531488Mutations in exon 12 of JAK2 are mainly found in JAK2 V617F-negative polycythaemia vera patients.
Q46355702Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome
Q50662979Prevalance of JAK2 V617F and exon 12 mutations in polycythaemia vera.
Q38717569Progenitor genotyping reveals a complex clonal architecture in a subset of CALR-mutated myeloproliferative neoplasms.
Q50624557Rapid identification of JAK2 exon 12 mutations using high resolution melting analysis.
Q26859843Revisiting the case for genetically engineered mouse models in human myelodysplastic syndrome research
Q37146068SOCS3 tyrosine phosphorylation as a potential bio-marker for myeloproliferative neoplasms associated with mutant JAK2 kinases
Q53959801Synergistic mobilization of hemopoietic progenitor cells using concurrent beta1 and beta2 integrin blockade or beta2-deficient mice.
Q35132280The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms
Q46735262The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders
Q46868807The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels
Q44881600Transgenic Cre expression mice for generation of erythroid-specific gene alterations
Q35847871VCAM-1 expression in adult hematopoietic and nonhematopoietic cells is controlled by tissue-inductive signals and reflects their developmental origin.

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