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Barbara H. Jung

Researcher at University of California, San Diego

Publications -  42
Citations -  1621

Barbara H. Jung is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Colorectal cancer & Signal transduction. The author has an hindex of 22, co-authored 39 publications receiving 1507 citations. Previous affiliations of Barbara H. Jung include University of California & Northwestern University.

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A Gαi–GIV Molecular Complex Binds Epidermal Growth Factor Receptor and Determines Whether Cells Migrate or Proliferate

TL;DR: How this cellular decision is made is revealed by showing that a Gαi–GIV molecular complex interacts with EGF receptor and programs growth factor signaling, triggering migration when assembled and favoring mitosis when assembly is prevented.
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Loss of activin receptor type 2 protein expression in microsatellite unstable colon cancers.

TL;DR: ACVR2 mutations are highly frequent in MSI-H colon cancers and in most cases cause loss of ACVR2 expression, indicating biallelic inactivation of the gene.
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Bone morphogenetic protein signaling and growth suppression in colon cancer

TL;DR: BMP signaling is intact and growth suppressive in human colon cancer cells, and in addition to SMADs, BMP may utilize SMAD4-independent pathways for growth suppression in colon cancers.
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Epigenetic and genetic alterations in Netrin-1 receptors UNC5C and DCC in human colon cancer.

TL;DR: The majority of CRCs harbor defects in Netrin-1 receptors, emphasizing the importance of this growth regulatory pathway in cancer, and the timing of the molecular alterations in the Netrin -1 receptors is not random.
Journal Article

Overexpression of Lerk-5/Eplg5 messenger RNA: a novel marker for increased tumorigenicity and metastatic potential in human malignant melanomas.

TL;DR: Increased Lerk-5 expression possibly reflects or induces an increased potential of growth, tumorigenicity, and metastatic abilities in human melanomas, which makes the yet to be elucidated eph-related receptor tyrosine kinase/Lerk signaling system a potential new source for molecular markers as well as a target for new therapies.