J Burn|J Goodship - JoVE Visualize

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Clinical Science (London, England : 1979)|March 1, 2002

Skeletal muscle mRNA levels for cathepsin B, but not components of the ubiquitin-proteasome pathway, are increased in patients with lung cancer referred for thoracotomyR Thomas Jagoe, Christopher P F Redfern, Russell G Roberts, et al.

Pediatric Cardiology|January 1, 1984

Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary taleJ Burn, M Baraitser, D T Hughes, et al.

Human Mutation|November 25, 2003

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPAC F Taylor, R S Charlton, J Burn, et al.

Parkinsonism & Related Disorders|February 7, 2006

Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's diseaseDavid J Burn, Watcharee Tiangyou, Liesl M Allcock, et al.

Annals of Human Genetics|July 1, 1993

Germline rearrangement of MCC and APC detected by pulsed field gel electrophoresis and fluorescent in situ hybridizationS Gayther, D Wells, K Gulati, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2009

Levodopa use and sleep in patients with dementia with Lewy bodiesSophie Molloy, Thais Minett, John T O'Brien, et al.

Journal of Medical Genetics|October 1, 1986

A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndromeR D Jefferson, J Burn, K L Gaunt, et al.

The British Journal of Radiology|May 19, 2000

Distribution of cranial MRI abnormalities in patients with symptomatic and subclinical CADASILA Coulthard, S C Blank, K Bushby, et al.

Oncogene|March 21, 1996

The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromasP J Biggs, P Chapman, S R Lakhani, et al.

Neuropsychologia|October 19, 2013

The basal ganglia in perceptual timing: timing performance in Multiple System Atrophy and Huntington's diseaseThomas E Cope, Manon Grube, Baldev Singh, et al.

Pageof 58

Showing results (201-210 of 571) with videos related to

Sort By:

Pageof 58

Clinical Science (London, England : 1979)|March 1, 2002

Skeletal muscle mRNA levels for cathepsin B, but not components of the ubiquitin-proteasome pathway, are increased in patients with lung cancer referred for thoracotomyR Thomas Jagoe, Christopher P F Redfern, Russell G Roberts, et al.

Pediatric Cardiology|January 1, 1984

Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary taleJ Burn, M Baraitser, D T Hughes, et al.

Human Mutation|November 25, 2003

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPAC F Taylor, R S Charlton, J Burn, et al.

Parkinsonism & Related Disorders|February 7, 2006

Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's diseaseDavid J Burn, Watcharee Tiangyou, Liesl M Allcock, et al.

Annals of Human Genetics|July 1, 1993

Germline rearrangement of MCC and APC detected by pulsed field gel electrophoresis and fluorescent in situ hybridizationS Gayther, D Wells, K Gulati, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2009

Levodopa use and sleep in patients with dementia with Lewy bodiesSophie Molloy, Thais Minett, John T O'Brien, et al.

Journal of Medical Genetics|October 1, 1986

A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndromeR D Jefferson, J Burn, K L Gaunt, et al.

The British Journal of Radiology|May 19, 2000

Distribution of cranial MRI abnormalities in patients with symptomatic and subclinical CADASILA Coulthard, S C Blank, K Bushby, et al.

Oncogene|March 21, 1996

The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromasP J Biggs, P Chapman, S R Lakhani, et al.

Neuropsychologia|October 19, 2013

The basal ganglia in perceptual timing: timing performance in Multiple System Atrophy and Huntington's diseaseThomas E Cope, Manon Grube, Baldev Singh, et al.

Pageof 58