Bilaketaren emaitzak - Hugh Watkins
- Erakusten 1 - 20 emaitzak -- 182
- Go to Next Page
-
1
Time to Think Differently About Sarcomere-Negative Hypertrophic Cardiomyopathy nork Hugh Watkins
Argitaratua 2021Revisão -
2
-
3
-
4
-
5
Inherited Cardiomyopathies nork Hugh Watkins, Houman Ashrafian, Charles Redwood
Argitaratua 2011Revisão -
6
-
7
Personalized medicine: hope or hype? nork Keyan Salari, Hugh Watkins, Euan A. Ashley
Argitaratua 2012Revisão -
8
Genetic Cardiomyopathies Causing Heart Failure nork Thomas J. Cahill, Houman Ashrafian, Hugh Watkins
Argitaratua 2013Revisão -
9
Disease Pathways and Novel Therapeutic Targets in Hypertrophic Cardiomyopathy nork Houman Ashrafian, William J. McKenna, Hugh Watkins
Argitaratua 2011Revisão -
10
-
11
-
12
-
13
Truncated Estrogen Receptor α 46-kDa Isoform in Human Endothelial Cells nork Gemma A. Figtree, Denise McDonald, Hugh Watkins, Keith M. Channon
Argitaratua 2003Artigo -
14
-
15
Mavacamten rescues increased myofilament calcium sensitivity and dysregulation of Ca<sup>2+</sup> flux caused by thin filament hypertrophic cardiomyopathy mutations nork Alexander J. Sparrow, Hugh Watkins, Matthew J. Daniels, Charles Redwood, Paul Robinson
Argitaratua 2020Artigo -
16
-
17
-
18
-
19
-
20
Alterations in Thin Filament Regulation Induced by a Human Cardiac Troponin T Mutant That Causes Dilated Cardiomyopathy Are Distinct from Those Induced by Troponin T Mutants That C... nork Paul Robinson, M Mirza, Adam Knott, Hassan Abdulrazzak, Ruth Willott, Steven B. Marston, Hugh Watkins, Charles Redwood
Argitaratua 2002Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Medicine
Internal medicine
Biology
Gene
Genetics
Cardiology
Hypertrophic cardiomyopathy
Heart failure
Cardiomyopathy
Genotype
Endocrinology
Mutation
Biochemistry
Disease
Single-nucleotide polymorphism
Computational biology
Bioinformatics
Cell biology
Coronary artery disease
Genome-wide association study
Chemistry
Myocardial infarction
Allele
Blood pressure
Pathology
Phenotype
Exome sequencing
Genetic association
Myocyte
Missense mutation