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R Williamson

Showing results (831-840 of 1,955) with videos related to

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Journal of Medical Genetics|May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosisC P Bennett, J Burn, G E Moore, et al.
Antimicrobial Agents and Chemotherapy|December 1, 1986
Involvement of penicillin-binding protein 2 with other penicillin-binding proteins in lysis of Escherichia coli by some beta-lactam antibiotics alone and in synergistic lytic effect of amdinocillin (mecillinam)L Gutmann, S Vincent, D Billot-Klein, et al.
Human Genetics|October 30, 1999
G130V, a common FRDA point mutation, appears to have arisen from a common founderM B Delatycki, M Knight, M Koenig, et al.
Molecular and Cellular Endocrinology|January 28, 1999
Genetics of polycystic ovary syndromeS Franks, N Gharani, D Waterworth, et al.
Gene Therapy|October 1, 1995
Gene delivery and expression mediated by an integrin-binding peptideS L Hart, R P Harbottle, R Cooper, et al.
Human Genetics|April 1, 1990
The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndromeA Ivens, N Flavin, R Williamson, et al.
Trials|February 9, 2010
Feasibility study to inform the design of a randomised controlled trial to eradicate Pseudomonas aeruginosa infection in individuals with cystic fibrosisHelen R Hickey, Ashley P Jones, Warren Lenney, et al.
Biomaterials|September 14, 2007
The role of endothelial cell attachment to elastic fibre molecules in the enhancement of monolayer formation and retention, and the inhibition of smooth muscle cell recruitmentMatthew R Williamson, Adrian Shuttleworth, Ann E Canfield, et al.
Epilepsia|May 25, 2002
Carbamazepine versus valproate monotherapy for epilepsy: a meta-analysisAnthony G Marson, Paula R Williamson, Helen Clough, et al.
Development (Cambridge, England)|January 1, 1988
The application of molecular genetics to detection of craniofacial abnormalityG Moore, A Ivens, J Chambers, et al.
Pageof 196

Showing results (831-840 of 1,955) with videos related to

Sort By:
Pageof 196
Journal of Medical Genetics|May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosisC P Bennett, J Burn, G E Moore, et al.
Antimicrobial Agents and Chemotherapy|December 1, 1986
Involvement of penicillin-binding protein 2 with other penicillin-binding proteins in lysis of Escherichia coli by some beta-lactam antibiotics alone and in synergistic lytic effect of amdinocillin (mecillinam)L Gutmann, S Vincent, D Billot-Klein, et al.
Human Genetics|October 30, 1999
G130V, a common FRDA point mutation, appears to have arisen from a common founderM B Delatycki, M Knight, M Koenig, et al.
Molecular and Cellular Endocrinology|January 28, 1999
Genetics of polycystic ovary syndromeS Franks, N Gharani, D Waterworth, et al.
Gene Therapy|October 1, 1995
Gene delivery and expression mediated by an integrin-binding peptideS L Hart, R P Harbottle, R Cooper, et al.
Human Genetics|April 1, 1990
The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndromeA Ivens, N Flavin, R Williamson, et al.
Trials|February 9, 2010
Feasibility study to inform the design of a randomised controlled trial to eradicate Pseudomonas aeruginosa infection in individuals with cystic fibrosisHelen R Hickey, Ashley P Jones, Warren Lenney, et al.
Biomaterials|September 14, 2007
The role of endothelial cell attachment to elastic fibre molecules in the enhancement of monolayer formation and retention, and the inhibition of smooth muscle cell recruitmentMatthew R Williamson, Adrian Shuttleworth, Ann E Canfield, et al.
Epilepsia|May 25, 2002
Carbamazepine versus valproate monotherapy for epilepsy: a meta-analysisAnthony G Marson, Paula R Williamson, Helen Clough, et al.
Development (Cambridge, England)|January 1, 1988
The application of molecular genetics to detection of craniofacial abnormalityG Moore, A Ivens, J Chambers, et al.
Pageof 196