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The Journal of Physiology
|
October 7, 2009
PKC-permitted elevation of sarcolemmal KATP concentration may explain female-specific resistance to myocardial infarction
Andrew G Edwards, Meredith L Rees, Rachel A Gioscia, et al.
Experimental Dermatology
|
June 6, 2000
Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma
F J Smith, M P Fisher, E Healy, et al.
Antimicrobial Agents and Chemotherapy
|
January 20, 2021
Tetracycline Resistance Mediated by <i>tet</i>(M) Has Variable Integrative Conjugative Element Composition in Mycoplasma hominis Strains Isolated in the United Kingdom from 2005 to 2015
Victoria J Chalker, Martin G Sharratt, Christopher L Rees, et al.
Advances in Experimental Medicine and Biology
|
May 23, 1998
Efficacy of allopurinol in ameliorating the progressive renal disease in familial juvenile hyperuricaemic nephropathy (FJHN). A six-year update
M B McBride, H A Simmonds, C S Ogg, et al.
Genomics
|
November 15, 1994
Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129
S A Carter, S D Bryce, C S Munro, et al.
The British Journal of Dermatology
|
February 12, 1998
Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
M A Birch-Machin, E Healy, R Turner, et al.
BMJ Open
|
December 9, 2020
Use of implantable meshes for augmented rotator cuff repair: a systematic review and meta-analysis
Mathew Baldwin, N S Nagra, Gemma Greenall, et al.
The Journal of Investigative Dermatology
|
April 5, 2001
Expression, candidate gene, and population studies of the melanocortin 5 receptor
N Hatta, C Dixon, A J Ray, et al.
Kidney International
|
August 1, 1997
Physiology and biochemistry of endothelial function in children with chronic renal failure
J A Kari, A E Donald, D T Vallance, et al.
The Biochemical Journal
|
January 15, 1993
Site-directed mutation studies of human liver cytochrome P-450 isoenzymes in the CYP2C subfamily
M E Veronese, C J Doecke, P I Mackenzie, et al.
Page
of 50
Search research articles
Search
Showing results (431-440 of 495) with videos related to
Sort By:
Page
of 50
The Journal of Physiology
|
October 7, 2009
PKC-permitted elevation of sarcolemmal KATP concentration may explain female-specific resistance to myocardial infarction
Andrew G Edwards, Meredith L Rees, Rachel A Gioscia, et al.
Experimental Dermatology
|
June 6, 2000
Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma
F J Smith, M P Fisher, E Healy, et al.
Antimicrobial Agents and Chemotherapy
|
January 20, 2021
Tetracycline Resistance Mediated by <i>tet</i>(M) Has Variable Integrative Conjugative Element Composition in Mycoplasma hominis Strains Isolated in the United Kingdom from 2005 to 2015
Victoria J Chalker, Martin G Sharratt, Christopher L Rees, et al.
Advances in Experimental Medicine and Biology
|
May 23, 1998
Efficacy of allopurinol in ameliorating the progressive renal disease in familial juvenile hyperuricaemic nephropathy (FJHN). A six-year update
M B McBride, H A Simmonds, C S Ogg, et al.
Genomics
|
November 15, 1994
Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129
S A Carter, S D Bryce, C S Munro, et al.
The British Journal of Dermatology
|
February 12, 1998
Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
M A Birch-Machin, E Healy, R Turner, et al.
BMJ Open
|
December 9, 2020
Use of implantable meshes for augmented rotator cuff repair: a systematic review and meta-analysis
Mathew Baldwin, N S Nagra, Gemma Greenall, et al.
The Journal of Investigative Dermatology
|
April 5, 2001
Expression, candidate gene, and population studies of the melanocortin 5 receptor
N Hatta, C Dixon, A J Ray, et al.
Kidney International
|
August 1, 1997
Physiology and biochemistry of endothelial function in children with chronic renal failure
J A Kari, A E Donald, D T Vallance, et al.
The Biochemical Journal
|
January 15, 1993
Site-directed mutation studies of human liver cytochrome P-450 isoenzymes in the CYP2C subfamily
M E Veronese, C J Doecke, P I Mackenzie, et al.
Page
of 50