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Molecular Carcinogenesis
|
May 23, 2000
Development of a prostate cDNA microarray and statistical gene expression analysis package
A J Carlisle, V V Prabhu, A Elkahloun, et al.
JAMA
|
May 14, 1997
Endolymphatic sac tumors. A source of morbid hearing loss in von Hippel-Lindau disease
T J Manski, D K Heffner, G M Glenn, et al.
Emerging Infectious Diseases
|
November 6, 2013
Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein
Jonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 2006
Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice
Emmanuel A Asante, Jacqueline M Linehan, Ian Gowland, et al.
Neurology
|
August 22, 2007
Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129
S Mead, T E F Webb, T A Campbell, et al.
Electrophoresis
|
July 13, 2000
Proteomic analysis of laser capture microdissected human prostate cancer and in vitro prostate cell lines
D K Ornstein, J W Gillespie, C P Paweletz, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 14, 1998
Phase II study of suramin plus aminoglutethimide in two cohorts of patients with androgen-independent prostate cancer: simultaneous antiandrogen withdrawal and prior antiandrogen withdrawal
N Dawson, W D Figg, O W Brawley, et al.
Journal of Neuropathology and Experimental Neurology
|
August 22, 2008
First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutation
Thomas E F Webb, Suvankar Pal, Durrenajaf Siddique, et al.
Nature Communications
|
July 10, 2014
Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked
Malin K Sandberg, Huda Al-Doujaily, Bernadette Sharps, et al.
Journal of the American College of Surgeons
|
January 21, 2014
Assessment of tumor growth in pancreatic neuroendocrine tumors in von Hippel Lindau syndrome
Allison B Weisbrod, Mio Kitano, Francine Thomas, et al.
Page
of 45
Search research articles
Search
Showing results (401-410 of 443) with videos related to
Sort By:
Page
of 45
Molecular Carcinogenesis
|
May 23, 2000
Development of a prostate cDNA microarray and statistical gene expression analysis package
A J Carlisle, V V Prabhu, A Elkahloun, et al.
JAMA
|
May 14, 1997
Endolymphatic sac tumors. A source of morbid hearing loss in von Hippel-Lindau disease
T J Manski, D K Heffner, G M Glenn, et al.
Emerging Infectious Diseases
|
November 6, 2013
Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein
Jonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 2006
Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice
Emmanuel A Asante, Jacqueline M Linehan, Ian Gowland, et al.
Neurology
|
August 22, 2007
Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129
S Mead, T E F Webb, T A Campbell, et al.
Electrophoresis
|
July 13, 2000
Proteomic analysis of laser capture microdissected human prostate cancer and in vitro prostate cell lines
D K Ornstein, J W Gillespie, C P Paweletz, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 14, 1998
Phase II study of suramin plus aminoglutethimide in two cohorts of patients with androgen-independent prostate cancer: simultaneous antiandrogen withdrawal and prior antiandrogen withdrawal
N Dawson, W D Figg, O W Brawley, et al.
Journal of Neuropathology and Experimental Neurology
|
August 22, 2008
First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutation
Thomas E F Webb, Suvankar Pal, Durrenajaf Siddique, et al.
Nature Communications
|
July 10, 2014
Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked
Malin K Sandberg, Huda Al-Doujaily, Bernadette Sharps, et al.
Journal of the American College of Surgeons
|
January 21, 2014
Assessment of tumor growth in pancreatic neuroendocrine tumors in von Hippel Lindau syndrome
Allison B Weisbrod, Mio Kitano, Francine Thomas, et al.
Page
of 45