Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Patricia Bocangel"'
Publikováno v:
Molecular and Cellular Biochemistry. 275:75-84
The molecular mechanisms by which Mesenchyme Homeobox 2 (Meox2) regulates the proliferation, differentiation and migration of vascular smooth muscle cells and cardiomyocytes are not known. The discovery of MEOX2 binding proteins will aid in understan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1539fbf4a669c4ec6ac8aa6e017abfba
https://doi.org/10.1007/s11010-005-0823-3
https://doi.org/10.1007/s11010-005-0823-3
Publikováno v:
Journal of genetic counseling. 23(5)
Paper-based surveys are an effective means of evaluating the quality of a clinical service. As part of ongoing quality improvement initiatives within our Genetics Program, new patients were invited to participate in a paper-based survey. Issues relat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6c370705bc169dba46b27df5fdea6d6
https://pubmed.ncbi.nlm.nih.gov/24647747
https://pubmed.ncbi.nlm.nih.gov/24647747
Autor:
David Cheung, Hae K. Kim, Shunzhen Zhang, Josette M. Douville, Shannon A. Baxter, David D. Eisenstat, Patricia Bocangel, Krista L. Herbert, Jaganmohan Reddy Jangamreddy, Jeffrey T. Wigle
Publikováno v:
Biochimica et biophysica acta. 1813(1)
The homeobox transcription factor PROX1 is essential for the development and maintenance of lymphatic vasculature. How PROX1 regulates lymphatic endothelial cell fate remains undefined. PROX1 has been shown to upregulate the expression of Cyclin E, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07f66e532fb89439fd0dee04d280832a
https://pubmed.ncbi.nlm.nih.gov/21040746
https://pubmed.ncbi.nlm.nih.gov/21040746
Autor:
Elizabeth Spriggs, Terri Berk, Angela Mitri, Cheryl R. Greenberg, B. N. Chodirker, Lily Ramyar, Hong Cheng, Jack H. Jung, George S. Charames, Bharati Bapat, Patricia Bocangel
Publikováno v:
Human genetics. 124(5)
Familial adenomatous polyposis (FAP) is an autosomal dominant syndrome caused by the inheritance of germline mutations in the APC tumour suppressor gene. The vast majority of these are nonsense and frameshift mutations resulting in a truncated protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f799272c5974dce211804091a85b889
https://pubmed.ncbi.nlm.nih.gov/18982352
https://pubmed.ncbi.nlm.nih.gov/18982352
Publikováno v:
Molecular & Cellular Biochemistry; Jul2005, Vol. 275 Issue 1/2, p75-84, 10p