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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 21, 2011
Carbon monoxide protects against oxidant-induced apoptosis via inhibition of Kv2.1
Mark L Dallas, John P Boyle, Carol J Milligan, et al.
Diabetes Care
|
April 24, 2019
Response to Comment on Johnson et al. Cost-effectiveness Analysis of Routine Screening Using Massively Parallel Sequencing for Maturity-Onset Diabetes of the Young in a Pediatric Diabetes Cohort: Reduced Health System Costs and Improved Patient Quality of Life. Diabetes Care 2019;42:69-76
Stephanie R Johnson, Hannah E Carter, Paul Leo, et al.
Journal of Paediatrics and Child Health
|
June 21, 2013
Response to growth hormone treatment in Prader-Willi syndrome: auxological criteria versus genetic diagnosis
Elly Scheermeyer, Ian Hughes, Mark Harris, et al.
The Journal of General Virology
|
March 31, 2021
Corrigendum: A novel substitution in NS5A enhances resistance of hepatitis C virus genotype 3 to daclatasvir
Guilherme Rodrigues Fernandes Campos, Joseph Ward, Shucheng Chen, et al.
Journal of Paediatrics and Child Health
|
June 24, 2014
Comparison of Centers for Disease Control and Prevention and World Health Organization references/standards for height in contemporary Australian children: analyses of the Raine Study and Australian National Children's Nutrition and Physical Activity cohorts
Ian Hughes, Mark Harris, Andrew Cotterill, et al.
BMJ Open
|
February 3, 2024
Community health navigator-assisted transition of care from hospital to community: protocol for a randomised controlled trial
Sharon M Parker, Parisa Aslani, Ben Harris-Roxas, et al.
Transfusion
|
June 6, 2014
The p.R168Q mutation is associated with the Bw phenotype and a predicted decrease in the stability of the resulting ABO glycosyltransferase
Seung Yeob Lee, Chunhwa Ihm, Dong-Jun Shin, et al.
Journal of Korean Medical Science
|
June 29, 2007
A dispermic chimera with mixed field blood group B and mosaic 46,XY/47,XYY karyotype
Duck Cho, Sang Ku Lee, Mark Harris Yazer, et al.
The Journal of Pathology
|
June 25, 2013
Selective modulation through the glucocorticoid receptor ameliorates muscle pathology in mdx mice
Tony Huynh, Kitipong Uaesoontrachoon, James L Quinn, et al.
The Korean Journal of Laboratory Medicine
|
March 4, 2010
The M142T mutation causes B3 phenotype: three cases and an in vitro expression study
Duck Cho, Dong-Jun Shin, Mark Harris Yazer, et al.
Page
of 43
Search research articles
Search
Showing results (371-380 of 430) with videos related to
Sort By:
Page
of 43
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 21, 2011
Carbon monoxide protects against oxidant-induced apoptosis via inhibition of Kv2.1
Mark L Dallas, John P Boyle, Carol J Milligan, et al.
Diabetes Care
|
April 24, 2019
Response to Comment on Johnson et al. Cost-effectiveness Analysis of Routine Screening Using Massively Parallel Sequencing for Maturity-Onset Diabetes of the Young in a Pediatric Diabetes Cohort: Reduced Health System Costs and Improved Patient Quality of Life. Diabetes Care 2019;42:69-76
Stephanie R Johnson, Hannah E Carter, Paul Leo, et al.
Journal of Paediatrics and Child Health
|
June 21, 2013
Response to growth hormone treatment in Prader-Willi syndrome: auxological criteria versus genetic diagnosis
Elly Scheermeyer, Ian Hughes, Mark Harris, et al.
The Journal of General Virology
|
March 31, 2021
Corrigendum: A novel substitution in NS5A enhances resistance of hepatitis C virus genotype 3 to daclatasvir
Guilherme Rodrigues Fernandes Campos, Joseph Ward, Shucheng Chen, et al.
Journal of Paediatrics and Child Health
|
June 24, 2014
Comparison of Centers for Disease Control and Prevention and World Health Organization references/standards for height in contemporary Australian children: analyses of the Raine Study and Australian National Children's Nutrition and Physical Activity cohorts
Ian Hughes, Mark Harris, Andrew Cotterill, et al.
BMJ Open
|
February 3, 2024
Community health navigator-assisted transition of care from hospital to community: protocol for a randomised controlled trial
Sharon M Parker, Parisa Aslani, Ben Harris-Roxas, et al.
Transfusion
|
June 6, 2014
The p.R168Q mutation is associated with the Bw phenotype and a predicted decrease in the stability of the resulting ABO glycosyltransferase
Seung Yeob Lee, Chunhwa Ihm, Dong-Jun Shin, et al.
Journal of Korean Medical Science
|
June 29, 2007
A dispermic chimera with mixed field blood group B and mosaic 46,XY/47,XYY karyotype
Duck Cho, Sang Ku Lee, Mark Harris Yazer, et al.
The Journal of Pathology
|
June 25, 2013
Selective modulation through the glucocorticoid receptor ameliorates muscle pathology in mdx mice
Tony Huynh, Kitipong Uaesoontrachoon, James L Quinn, et al.
The Korean Journal of Laboratory Medicine
|
March 4, 2010
The M142T mutation causes B3 phenotype: three cases and an in vitro expression study
Duck Cho, Dong-Jun Shin, Mark Harris Yazer, et al.
Page
of 43