Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Rebecca S. Henkhaus"'
Autor:
Rebecca S. Henkhaus, Upal Kunal Basu Roy, Dora Cavallo-Medved, Bonnie F. Sloane, Eugene W. Gerner, Natalia A. Ignatenko
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 10, Iss 2, Pp 140-148 (2008)
Kallikreins are secreted proteases that may play a functional role and/or serve as a serum biomarker for the presence or progression of certain types of cancers. Kallikrein 6 (KLK6) has been shown to be upregulated in several types of cancers, includ
Externí odkaz:
https://doaj.org/article/22e57fd41b4a4c16b15f6ee3d6043d4f
Autor:
Natalia A. Ignatenko, Chiara Cremolini, Rebecca S. Henkhaus, Fotios Loupakis, Upal K. Basu Roy, Eugene W. Gerner
Publikováno v:
International Journal of Cancer. 133:43-57
Caveolin-1 is an essential component of membrane caveolae. It is an important regulator of cellular processes such as signal transduction and endocytosis. We report here, for the first time, that caveolin-1 is a target of the K-RAS oncogene in colon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a60b5868171c04adf438dd57b0f25a7
https://doi.org/10.1002/ijc.28001
https://doi.org/10.1002/ijc.28001
Publikováno v:
Gene. 498:5-12
To determine if ethanol consumption and alcoholism cause global DNA methylation disturbances, we examined alcoholics and controls using methylation specific microarrays to detect all annotated gene and non-coding micro-RNA promoters and their CpG isl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b511bf0d445489d96e34ad308f1dc875
https://doi.org/10.1016/j.gene.2012.01.096
https://doi.org/10.1016/j.gene.2012.01.096
Publikováno v:
European Journal of Medical Genetics. 55:32-36
Intellectual disability affects approximately 2% of the population with males outnumbering females due to involvement of over 300 genes on the X chromosome. The most common form of X-linked intellectual disability (XLID) is fragile X syndrome. We rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7c849d440b1b5c873b11eed537e6daa
https://doi.org/10.1016/j.ejmg.2011.08.004
https://doi.org/10.1016/j.ejmg.2011.08.004
Publikováno v:
Journal of neurodevelopmental disorders
Prader-Willi syndrome (PWS) is a genetic imprinting disease that causes developmental and behavioral disturbances resulting from loss of expression of genes from the paternal chromosome 15q11-q13 region. In about 70% of subjects, this portion of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf17bcb76ef8474f877a49f6ecc3308e
https://doi.org/10.1007/s11689-010-9051-6
https://doi.org/10.1007/s11689-010-9051-6
Autor:
Natalia A. Ignatenko, Upal K. Basu Roy, Jessica Mora, Kimberly Elizabeth Fultz, Rebecca S. Henkhaus, Eugene W. Gerner
Publikováno v:
Molecular Carcinogenesis. 47:947-955
Genetic evidence suggests that caveolin-1, an essential component of membrane caveolae, acts as a tumor promoter in some, and a tumor suppressor in other cancers. The role of caveolin-1 in colon carcinogenesis is controversial. We report here, for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8ee429954452399d0c797e7f6acfce
https://doi.org/10.1002/mc.20451
https://doi.org/10.1002/mc.20451
Autor:
Natalia A. Ignatenko, Dora Cavallo-Medved, Eugene W. Gerner, Bonnie F. Sloane, Rebecca S. Henkhaus, Upal K. Basu Roy
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 10, Iss 2, Pp 140-148 (2008)
Biological Sciences Publications
Biological Sciences Publications
Kallikreins are secreted proteases that may play a functional role and/or serve as a serum biomarker for the presence or progression of certain types of cancers. Kallikrein 6 (KLK6) has been shown to be upregulated in several types of cancers, includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46bebb353bd258152b138cba27d86c59
http://www.sciencedirect.com/science/article/pii/S1476558608800607
http://www.sciencedirect.com/science/article/pii/S1476558608800607
Publikováno v:
Chemical communications (Cambridge, England). 51(78)
Mammalian cells acquire cholesterol, a critical membrane constituent, through multiple mechanisms. We synthesized mimics of cholesterol, fluorescent N-alkyl-3β-cholesterylamine-glutamic acids, that are rapidly incorporated into cellular plasma membr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae4b51f3a934525314f9b6b489838e25
https://pubmed.ncbi.nlm.nih.gov/26287483
https://pubmed.ncbi.nlm.nih.gov/26287483
Background The pathogenesis of autistic disorder (AD) is not clearly understood but genetic factors and the immune system have been implicated. Disturbed immunoglobulin levels and autoantibodies to neuronal elements have been reported in AD including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83090a3cfd45dd0a3e953a12f472a68e
https://europepmc.org/articles/PMC6675569/
https://europepmc.org/articles/PMC6675569/
Autor:
Merlin G. Butler, Rebecca S. Henkhaus, Daniel J. Driscoll, Virginia Kimonis, June-Anne Gold, Soo Jeong Kim, Elisabeth M. Dykens
Publikováno v:
Genetic testing and molecular biomarkers. 16(3)
Purpose: Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are complex neurodevelopmental disorders caused by loss of expression of imprinted genes from the 15q11-q13 region depending on the parent of origin. Methylation-specific multiplex ligat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c757987c8a93c063c192a07335a89a0
https://pubmed.ncbi.nlm.nih.gov/21977908
https://pubmed.ncbi.nlm.nih.gov/21977908