E L Stubbs|J Furth - JoVE Visualize

Showing results (51-60 of 59) with videos related to

Pageof 6

Sort By:

You have reached the last page of results.This site can display upto 59 results.

Journal of Immunology (Baltimore, Md. : 1950)|June 10, 2003

Variations in eosinophil chemokine responses: an investigation of CCR1 and CCR3 function, expression in atopy, and identification of a functional CCR1 promoterRhian M Phillips, Victoria E L Stubbs, Mandy R Henson, et al.

Journal of Cellular Physiology|August 12, 1998

Antioxidants stimulate transcriptional activation of the c-fos gene by multiple pathways in human fetal lung fibroblasts (WI-38)B Keogh, R G Allen, M Tresini, et al.

Mechanisms of Ageing and Development|August 1, 1997

Abundance of alpha 1(I) and alpha 1(III) procollagen and p21 mRNAs in fibroblasts cultured from fetal and postnatal dermisJ J Furth, R G Allen, M Tresini, et al.

Biochemical Genetics|June 1, 1985

Human lactase and the molecular basis of lactase persistenceJ Potter, M W Ho, H Bolton, et al.

Biochimica Et Biophysica Acta|March 20, 1992

Ageing of the human corneal stroma: structural and biochemical changesN S Malik, S J Moss, N Ahmed, et al.

Human Mutation|August 14, 1999

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinismB Glaser, J Furth, C A Stanley, et al.

European Journal of Immunology|March 2, 2005

The carboxyl terminus of the chemokine receptor CCR3 contains distinct domains which regulate chemotactic signaling and receptor down-regulation in a ligand-dependent mannerIan Sabroe, Annelies Jorritsma, Victoria E L Stubbs, et al.

Diabetes, Obesity & Metabolism|August 30, 2012

Glucose metabolism: key endogenous regulator of β-cell replication and survivalD Dadon, S Tornovsky-Babaey, J Furth-Lavi, et al.

Nature Genetics|September 6, 2000

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C geneM Bitner-Glindzicz, K J Lindley, P Rutland, et al.

Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 59 results.

Journal of Immunology (Baltimore, Md. : 1950)|June 10, 2003

Variations in eosinophil chemokine responses: an investigation of CCR1 and CCR3 function, expression in atopy, and identification of a functional CCR1 promoterRhian M Phillips, Victoria E L Stubbs, Mandy R Henson, et al.

Journal of Cellular Physiology|August 12, 1998

Antioxidants stimulate transcriptional activation of the c-fos gene by multiple pathways in human fetal lung fibroblasts (WI-38)B Keogh, R G Allen, M Tresini, et al.

Mechanisms of Ageing and Development|August 1, 1997

Abundance of alpha 1(I) and alpha 1(III) procollagen and p21 mRNAs in fibroblasts cultured from fetal and postnatal dermisJ J Furth, R G Allen, M Tresini, et al.

Biochemical Genetics|June 1, 1985

Human lactase and the molecular basis of lactase persistenceJ Potter, M W Ho, H Bolton, et al.

Biochimica Et Biophysica Acta|March 20, 1992

Ageing of the human corneal stroma: structural and biochemical changesN S Malik, S J Moss, N Ahmed, et al.

Human Mutation|August 14, 1999

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinismB Glaser, J Furth, C A Stanley, et al.

European Journal of Immunology|March 2, 2005

The carboxyl terminus of the chemokine receptor CCR3 contains distinct domains which regulate chemotactic signaling and receptor down-regulation in a ligand-dependent mannerIan Sabroe, Annelies Jorritsma, Victoria E L Stubbs, et al.

Diabetes, Obesity & Metabolism|August 30, 2012

Glucose metabolism: key endogenous regulator of β-cell replication and survivalD Dadon, S Tornovsky-Babaey, J Furth-Lavi, et al.

Nature Genetics|September 6, 2000

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C geneM Bitner-Glindzicz, K J Lindley, P Rutland, et al.

Pageof 6