Results 221 to 230 of about 10,781,581 (397)
Human adult T-cell leukemia virus: complete nucleotide sequence of the provirus genome integrated in leukemia cell DNA. [PDF]
Motoharu Seiki+3 more
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Germline variants in CDKN2A wild‐type melanoma prone families
Among melanoma‐prone families, wild‐type for CDKN2A and CDK4, some have pathogenic variants in genes not usually linked to melanoma. Furthermore, rare XP‐related variants and variants in MC1R are enriched in such families. Germline pathogenic variants in CDKN2A are well established as an underlying cause of familial malignant melanoma. While pathogenic
Gjertrud T. Iversen+5 more
wiley +1 more source
The Genome of Human Coronavirus Strain 229E
M. R. Macnaughton, M. H. Madge
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Chronic TGF‐β exposure drives epithelial HCC cells from a senescent state to a TGF‐β resistant mesenchymal phenotype. This transition is characterized by the loss of Smad3‐mediated signaling, escape from senescence, enhanced invasiveness and metastatic potential, and upregulation of key resistance modulators such as MARK1 and GRM8, ultimately promoting
Minenur Kalyoncu+11 more
wiley +1 more source
Publisher Summary This chapter discusses genomic imprinting in humans, which is a recently recognized phenomenon. It has already been implicated in a number of developmental and pathological processes. However, it is still unclear in terms of its functions in normal development, although there is evidence that some imprinted genes are important in ...
openaire +3 more sources
We identified adaptor protein ShcD as upregulated in triple‐negative breast cancer and found its expression to be correlated with reduced patient survival and increased invasion in cell models. Using a proteomic screen, we identified novel ShcD binding partners involved in EGFR signaling pathways.
Hayley R. Lau+11 more
wiley +1 more source
The distribution of interspersed repeats is nonuniform and conserved in the mouse and human genomes. [PDF]
Philippe Soriano+2 more
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