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Cancer Research
|
May 1, 1991
Somatic allelic deletion of nm23 in human cancer
A Leone, O W McBride, A Weston, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 18, 1999
VHL gene deletion and enhanced VEGF gene expression detected in the stromal cells of retinal angioma
C C Chan, A O Vortmeyer, E Y Chew, et al.
Human Molecular Genetics
|
September 1, 1996
The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene
S K Sidhar, J Clark, S Gill, et al.
Journal of the Neurological Sciences
|
February 7, 2018
Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein
Susan Joiner, Emmanuel A Asante, Jacqueline M Linehan, et al.
Acta Neuropathologica Communications
|
November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases
Lilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.
Annals of Surgery
|
November 1, 1990
Surgical management of pheochromocytoma with the use of metyrosine
R R Perry, H R Keiser, J A Norton, et al.
Cancer Research
|
March 1, 1997
Generation and genetic characterization of immortal human prostate epithelial cell lines derived from primary cancer specimens
R K Bright, C D Vocke, M R Emmert-Buck, et al.
Human Molecular Genetics
|
July 1, 1993
Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis
F M Richards, M E Phipps, F Latif, et al.
JAMA Psychiatry
|
March 26, 2015
Dialectical behavior therapy for high suicide risk in individuals with borderline personality disorder: a randomized clinical trial and component analysis
Marsha M Linehan, Kathryn E Korslund, Melanie S Harned, et al.
Lancet (London, England)
|
December 13, 2006
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report
Stephen J Wroe, Suvankar Pal, Durrenajaf Siddique, et al.
Page
of 45
Search research articles
Search
Showing results (331-340 of 443) with videos related to
Sort By:
Page
of 45
Cancer Research
|
May 1, 1991
Somatic allelic deletion of nm23 in human cancer
A Leone, O W McBride, A Weston, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 18, 1999
VHL gene deletion and enhanced VEGF gene expression detected in the stromal cells of retinal angioma
C C Chan, A O Vortmeyer, E Y Chew, et al.
Human Molecular Genetics
|
September 1, 1996
The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene
S K Sidhar, J Clark, S Gill, et al.
Journal of the Neurological Sciences
|
February 7, 2018
Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein
Susan Joiner, Emmanuel A Asante, Jacqueline M Linehan, et al.
Acta Neuropathologica Communications
|
November 21, 2013
Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases
Lilla Reiniger, Ilaria Mirabile, Ana Lukic, et al.
Annals of Surgery
|
November 1, 1990
Surgical management of pheochromocytoma with the use of metyrosine
R R Perry, H R Keiser, J A Norton, et al.
Cancer Research
|
March 1, 1997
Generation and genetic characterization of immortal human prostate epithelial cell lines derived from primary cancer specimens
R K Bright, C D Vocke, M R Emmert-Buck, et al.
Human Molecular Genetics
|
July 1, 1993
Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis
F M Richards, M E Phipps, F Latif, et al.
JAMA Psychiatry
|
March 26, 2015
Dialectical behavior therapy for high suicide risk in individuals with borderline personality disorder: a randomized clinical trial and component analysis
Marsha M Linehan, Kathryn E Korslund, Melanie S Harned, et al.
Lancet (London, England)
|
December 13, 2006
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report
Stephen J Wroe, Suvankar Pal, Durrenajaf Siddique, et al.
Page
of 45