Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Susan L Naylor"'
Autor:
Amelie G Ramirez, Nancy S Weiss, Alan E C Holden, Lucina Suarez, Sharon P Cooper, Edgar Munoz, Susan L Naylor
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35573 (2012)
Hepatocellular carcinoma (HCC) is increasing in the U.S. despite a decline in cancer overall. Latinos have higher rates of HCC than the general population according to the Surveillance, Epidemiology, and End Results (SEER) Program. Not included in SE
Externí odkaz:
https://doaj.org/article/6430bb0a09e34bc29304f44fb9965a24
Autor:
Sunil Sudarshan, Karthigayan Shanmugasundaram, Susan L Naylor, Shu Lin, Carolina B Livi, Christine F O'Neill, Dipen J Parekh, I-Tien Yeh, Lu-Zhe Sun, Karen Block
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e21037 (2011)
Germline mutations of FH, the gene that encodes for the tricarboxylic acid TCA (TCA) cycle enzyme fumarate hydratase, are associated with an inherited form of cancer referred to as Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC). Individuals
Externí odkaz:
https://doaj.org/article/afe678de0b564340818bc772790d6cab
Autor:
Jun Wu, Jeong Soon Park, Hongzhi Li, Jianxin Lu, Deborah M. Holstein, RuiHua Xiang, Janice Jianhong Deng, Lokendra Kumar Sharma, Yidong Bai, Susan L. Naylor, James D. Lechleiter
Publikováno v:
Human Molecular Genetics. 18:1578-1589
Mitochondrial alteration has been long proposed to play a major role in tumorigenesis. Recently, mitochondrial DNA (mtDNA) mutations have been found in a variety of cancer cells. In this study, we examined the contribution of mtDNA mutation and mitoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aea270fff4a7020b85504ac840606009
https://doi.org/10.1093/hmg/ddp069
https://doi.org/10.1093/hmg/ddp069
Autor:
Jennifer D. Akunowicz, Marc F. Hansen, Elizabeth A. Saria, Bina B. Patel, Robin J. Leach, Richard Gorlick, Amit M. Deshpande, Xavier T. Reveles, Susan L. Naylor
Publikováno v:
Oncogene. 26:1714-1722
PHC3, a component of the hPRC-H complex, associates with E2F6 during G 0 and is lost in osteosarcoma tumors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::505e5aef22f27d95dc281545573a0ceb
https://doi.org/10.1038/sj.onc.1209988
https://doi.org/10.1038/sj.onc.1209988
Publikováno v:
Disease Markers, Vol 20, Iss 2, Pp 117-128 (2004)
Disease markers
Disease markers
Approximately 1 man in 6 will be diagnosed with prostate cancer during his life lifetime, and over 200,000 men in the U.S. are diagnosed with prostate cancer annually. Since the widespread adoption of PSA testing, about 60–70% of men at risk in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3618638d359ab0f6c843968ffc3e0376
https://doaj.org/article/587014fe154e4f4cbbc3f2dcb7c8920b
https://doaj.org/article/587014fe154e4f4cbbc3f2dcb7c8920b
Autor:
Brad H. Pollock, Ian M. Thompson, Robin J. Leach, Susan L. Naylor, Dean A. Troyer, Joseph W. Basler
Publikováno v:
Urologic Clinics of North America. 30:227-237
By 2004-2005, the final results of the Prostate Cancer Prevention Trial should be available. Within several years thereafter, results of the SELECT should be available. The growing list of potential agents for prostate cancer prevention continues to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::885865b816fb00d7b6ebc367d8385d7d
https://doi.org/10.1016/s0094-0143(02)00178-7
https://doi.org/10.1016/s0094-0143(02)00178-7
Autor:
Susan L. Naylor, Angela Johnson, Polly Brinkman-Mills, Nobuyoshi Shimizu, Antonio Baldini, M. Ali Riazi, Heather E. McDermid, Shinsei Minoshima
Publikováno v:
Genomics. 62:90-94
Duplication of a segment of the long arm of human chromosome 3 (3q26.3–q27) results in a syndrome characterized by multiple congenital abnormalities and neurological anomalies in some patients. We have identified a novel gene (KCNMB3) that maps to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fbc21cd2bfec04dcf6ceb454256fd31
https://doi.org/10.1006/geno.1999.5975
https://doi.org/10.1006/geno.1999.5975
Autor:
Mariola Ilnicka, John C. Hunter, Douglas Kenneth Rabert, Susan L. Naylor, Ronald C. Herman, Lakshmi Sangameswaran, Rena Obernolte, Richard M. Eglen, Bruce D. Koch
Publikováno v:
Pain. 78:107-114
Neuropathic pain may be produced, at least in part, by the increased activity of primary afferent neurons. Studies have suggested that an accumulation of voltage-gated sodium channels at the site of peripheral nerve injury is a primary precursory eve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b14f6304c36062cda3d56fe80b8d8d3
https://doi.org/10.1016/s0304-3959(98)00120-1
https://doi.org/10.1016/s0304-3959(98)00120-1
Publikováno v:
Genomics. 50:378-381
We have determined the chromosomal localization of the gene for the regulatory subunit RII alpha of cAMP-dependent protein kinase (locus PRKAR2A) to human chromosome 3 using polymerase chain reaction (PCR) and Southern blot analysis of two different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f64635f8815d5d299e486917eb862390
https://doi.org/10.1006/geno.1998.5326
https://doi.org/10.1006/geno.1998.5326
Autor:
Jan-Olof Winberg, Karen Kerbacher, Nadja Hammami-Hauasli, Mirjam Zimmermann, Susan L. Naylor, Øivind Nilssen, Ingrun Anton-Lamprecht, Peter Krajci, Tobias Gedde-Dahl, Leena Bruckner-Tuderman
Publikováno v:
Human Molecular Genetics. 6:1125-1135
Dystrophic epidermolysis bullosa (EBD) is a clinically heterogeneous skin disorder, characterized by abnormal anchoring fibrils (AF) and loss of dermal-epidermal adherence. EBD has been linked to the COL7A1 gene at chromosome 3p21 which encodes colla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0db7f7055ce292bb5d57c863fdc7f35
https://doi.org/10.1093/hmg/6.7.1125
https://doi.org/10.1093/hmg/6.7.1125