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Journal of Medical Genetics
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May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosis
C 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 founder
M B Delatycki, M Knight, M Koenig, et al.
Molecular and Cellular Endocrinology
|
January 28, 1999
Genetics of polycystic ovary syndrome
S Franks, N Gharani, D Waterworth, et al.
Gene Therapy
|
October 1, 1995
Gene delivery and expression mediated by an integrin-binding peptide
S 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 syndrome
A 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 fibrosis
Helen 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 recruitment
Matthew R Williamson, Adrian Shuttleworth, Ann E Canfield, et al.
Epilepsia
|
May 25, 2002
Carbamazepine versus valproate monotherapy for epilepsy: a meta-analysis
Anthony G Marson, Paula R Williamson, Helen Clough, et al.
Development (Cambridge, England)
|
January 1, 1988
The application of molecular genetics to detection of craniofacial abnormality
G Moore, A Ivens, J Chambers, et al.
Page
of 196
Search research articles
Search
Showing results (831-840 of 1,955) with videos related to
Sort By:
Page
of 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 stenosis
C 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 founder
M B Delatycki, M Knight, M Koenig, et al.
Molecular and Cellular Endocrinology
|
January 28, 1999
Genetics of polycystic ovary syndrome
S Franks, N Gharani, D Waterworth, et al.
Gene Therapy
|
October 1, 1995
Gene delivery and expression mediated by an integrin-binding peptide
S 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 syndrome
A 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 fibrosis
Helen 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 recruitment
Matthew R Williamson, Adrian Shuttleworth, Ann E Canfield, et al.
Epilepsia
|
May 25, 2002
Carbamazepine versus valproate monotherapy for epilepsy: a meta-analysis
Anthony G Marson, Paula R Williamson, Helen Clough, et al.
Development (Cambridge, England)
|
January 1, 1988
The application of molecular genetics to detection of craniofacial abnormality
G Moore, A Ivens, J Chambers, et al.
Page
of 196