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Journal of Medical Genetics
|
July 28, 2018
Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children
Lamia Mestek-Boukhibar, Emma Clement, Wendy D Jones, et al.
Nature
|
June 26, 1997
Congenital leptin deficiency is associated with severe early-onset obesity in humans
C T Montague, I S Farooqi, J P Whitehead, et al.
Journal of Medical Genetics
|
March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
B B de Vries, S M White, S J Knight, et al.
European Journal of Human Genetics : EJHG
|
June 30, 2005
Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation
David A Koolen, William Reardon, Elisabeth M Rosser, et al.
American Journal of Medical Genetics
|
December 11, 1996
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families
R M Hughes-Benzie, G Pilia, J Y Xuan, et al.
Cancer Research
|
May 19, 2026
Ketogenic Diet Prevents Obesity-Associated Pancreatic Cancer Independent of Weight Loss and Induces Pancreatic Metabolic Reprogramming
Ericka Vélez-Bonet, Kristyn Gumpper-Fedus, Kaylin M Chasser, et al.
Circulation
|
July 12, 2013
Mitochondrial DNA damage can promote atherosclerosis independently of reactive oxygen species through effects on smooth muscle cells and monocytes and correlates with higher-risk plaques in humans
Emma Yu, Patrick A Calvert, John R Mercer, et al.
Journal of Medical Genetics
|
July 4, 2009
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome
H Vega, A H Trainer, M Gordillo, et al.
Molecular and Cellular Biology
|
May 18, 2016
Novel MicroRNA Regulators of Atrial Natriuretic Peptide Production
Connie Wu, Pankaj Arora, Obiajulu Agha, et al.
Circulation
|
March 26, 2014
Response to letter regarding article, "Mitochondrial DNA damage can promote atherosclerosis independently of reactive oxygen species through effects on smooth muscle cells and monocytes and correlates with higher-risk plaques in humans"
Emma Yu, Patrick A Calvert, John R Mercer, et al.
Page
of 48
Search research articles
Search
Showing results (431-440 of 476) with videos related to
Sort By:
Page
of 48
Journal of Medical Genetics
|
July 28, 2018
Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children
Lamia Mestek-Boukhibar, Emma Clement, Wendy D Jones, et al.
Nature
|
June 26, 1997
Congenital leptin deficiency is associated with severe early-onset obesity in humans
C T Montague, I S Farooqi, J P Whitehead, et al.
Journal of Medical Genetics
|
March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
B B de Vries, S M White, S J Knight, et al.
European Journal of Human Genetics : EJHG
|
June 30, 2005
Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation
David A Koolen, William Reardon, Elisabeth M Rosser, et al.
American Journal of Medical Genetics
|
December 11, 1996
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families
R M Hughes-Benzie, G Pilia, J Y Xuan, et al.
Cancer Research
|
May 19, 2026
Ketogenic Diet Prevents Obesity-Associated Pancreatic Cancer Independent of Weight Loss and Induces Pancreatic Metabolic Reprogramming
Ericka Vélez-Bonet, Kristyn Gumpper-Fedus, Kaylin M Chasser, et al.
Circulation
|
July 12, 2013
Mitochondrial DNA damage can promote atherosclerosis independently of reactive oxygen species through effects on smooth muscle cells and monocytes and correlates with higher-risk plaques in humans
Emma Yu, Patrick A Calvert, John R Mercer, et al.
Journal of Medical Genetics
|
July 4, 2009
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome
H Vega, A H Trainer, M Gordillo, et al.
Molecular and Cellular Biology
|
May 18, 2016
Novel MicroRNA Regulators of Atrial Natriuretic Peptide Production
Connie Wu, Pankaj Arora, Obiajulu Agha, et al.
Circulation
|
March 26, 2014
Response to letter regarding article, "Mitochondrial DNA damage can promote atherosclerosis independently of reactive oxygen species through effects on smooth muscle cells and monocytes and correlates with higher-risk plaques in humans"
Emma Yu, Patrick A Calvert, John R Mercer, et al.
Page
of 48