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K R Bowles

Showing results (1-10 of 12) with videos related to

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Herz|July 25, 2000
The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathyN E Bowles, K R Bowles, J A Towbin
Brain Research Bulletin|August 23, 2011
Gene expression and behaviour in mouse models of HDK R Bowles, S P Brooks, S B Dunnett, et al.
Cellular Signalling|December 19, 2016
SMAD transcription factors are altered in cell models of HD and regulate HTT expressionK R Bowles, T Stone, P Holmans, et al.
Human Genetics|October 30, 1999
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor geneK R Bowles, J Gibson, J Wu, et al.
Human Genetics|January 27, 2000
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathyK R Bowles, C Zintz, S E Abraham, et al.
The Journal of Clinical Investigation|September 15, 1996
Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23K R Bowles, R Gajarski, P Porter, et al.
The Journal of Clinical Investigation|September 7, 2000
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathyS Tsubata, K R Bowles, M Vatta, et al.
Clinical Genetics|February 3, 2015
Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genesE T Rosenthal, K R Bowles, D Pruss, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
Development of MAPT S305 mutation models exhibiting elevated 4R tau expression, resulting in altered neuronal and astrocytic functionK R Bowles, D A Pugh, C Pedicone, et al.
Circulation|March 10, 2001
Novel gene mutations in patients with left ventricular noncompaction or Barth syndromeF Ichida, S Tsubata, K R Bowles, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Herz|July 25, 2000
The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathyN E Bowles, K R Bowles, J A Towbin
Brain Research Bulletin|August 23, 2011
Gene expression and behaviour in mouse models of HDK R Bowles, S P Brooks, S B Dunnett, et al.
Cellular Signalling|December 19, 2016
SMAD transcription factors are altered in cell models of HD and regulate HTT expressionK R Bowles, T Stone, P Holmans, et al.
Human Genetics|October 30, 1999
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor geneK R Bowles, J Gibson, J Wu, et al.
Human Genetics|January 27, 2000
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathyK R Bowles, C Zintz, S E Abraham, et al.
The Journal of Clinical Investigation|September 15, 1996
Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23K R Bowles, R Gajarski, P Porter, et al.
The Journal of Clinical Investigation|September 7, 2000
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathyS Tsubata, K R Bowles, M Vatta, et al.
Clinical Genetics|February 3, 2015
Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genesE T Rosenthal, K R Bowles, D Pruss, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
Development of MAPT S305 mutation models exhibiting elevated 4R tau expression, resulting in altered neuronal and astrocytic functionK R Bowles, D A Pugh, C Pedicone, et al.
Circulation|March 10, 2001
Novel gene mutations in patients with left ventricular noncompaction or Barth syndromeF Ichida, S Tsubata, K R Bowles, et al.
Pageof 2