Search research articles
Contact Us
Filters
Showing results (271-280 of 439) with videos related to
Page
of 44
Sort By:
Vaccines
|
September 20, 2017
Targeting Host Cell Surface Nucleolin for RSV Therapy: Challenges and Opportunities
Peter Mastrangelo, Michael J Norris, Wenming Duan, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
May 8, 2015
Upregulation of UGT2B4 Expression by 3'-Phosphoadenosine-5'-Phosphosulfate Synthase Knockdown: Implications for Coordinated Control of Bile Acid Conjugation
Kathleen G Barrett, Hailin Fang, Daniela Cukovic, et al.
Andrology
|
April 29, 2025
Gonadal function in males with WFS1 spectrum disorder (Wolfram syndrome)-A European cohort perspective
Julia Rohayem, Olivia Cunningham, Denise Williams, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
September 24, 2004
Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature
S Iyer, M Korada, L Rainbow, et al.
American Journal of Veterinary Research
|
June 28, 2013
Evaluation of neutrophil apoptosis in horses with acute abdominal disease
Kathryn M Krista, Nathaniel A White, Jennifer G Barrett, et al.
Journal of Evolutionary Biology
|
August 22, 2012
Variation in infectivity and aggressiveness in space and time in wild host-pathogen systems: causes and consequences
A J M Tack, P H Thrall, L G Barrett, et al.
European Journal of Endocrinology
|
May 31, 2011
Premature adrenarche: novel lessons from early onset androgen excess
Jan Idkowiak, Gareth G Lavery, Vivek Dhir, et al.
Jornal De Pediatria
|
December 4, 2003
[Report of a Brazilian patient with Wolfram Syndrome]
Paulo R G Zen, Louise L C Pinto, Ida V D Schwartz, et al.
Environmental Microbiology
|
February 4, 2021
Mixed infections alter transmission potential in a fungal plant pathogen
Luke G Barrett, Marcello Zala, Alexey Mikaberidze, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 20, 2014
A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects
Hakan Cangul, Veysel N Bas, Yaman Saglam, et al.
Page
of 44
Search research articles
Search
Showing results (271-280 of 439) with videos related to
Sort By:
Page
of 44
Vaccines
|
September 20, 2017
Targeting Host Cell Surface Nucleolin for RSV Therapy: Challenges and Opportunities
Peter Mastrangelo, Michael J Norris, Wenming Duan, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
May 8, 2015
Upregulation of UGT2B4 Expression by 3'-Phosphoadenosine-5'-Phosphosulfate Synthase Knockdown: Implications for Coordinated Control of Bile Acid Conjugation
Kathleen G Barrett, Hailin Fang, Daniela Cukovic, et al.
Andrology
|
April 29, 2025
Gonadal function in males with WFS1 spectrum disorder (Wolfram syndrome)-A European cohort perspective
Julia Rohayem, Olivia Cunningham, Denise Williams, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
September 24, 2004
Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature
S Iyer, M Korada, L Rainbow, et al.
American Journal of Veterinary Research
|
June 28, 2013
Evaluation of neutrophil apoptosis in horses with acute abdominal disease
Kathryn M Krista, Nathaniel A White, Jennifer G Barrett, et al.
Journal of Evolutionary Biology
|
August 22, 2012
Variation in infectivity and aggressiveness in space and time in wild host-pathogen systems: causes and consequences
A J M Tack, P H Thrall, L G Barrett, et al.
European Journal of Endocrinology
|
May 31, 2011
Premature adrenarche: novel lessons from early onset androgen excess
Jan Idkowiak, Gareth G Lavery, Vivek Dhir, et al.
Jornal De Pediatria
|
December 4, 2003
[Report of a Brazilian patient with Wolfram Syndrome]
Paulo R G Zen, Louise L C Pinto, Ida V D Schwartz, et al.
Environmental Microbiology
|
February 4, 2021
Mixed infections alter transmission potential in a fungal plant pathogen
Luke G Barrett, Marcello Zala, Alexey Mikaberidze, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 20, 2014
A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects
Hakan Cangul, Veysel N Bas, Yaman Saglam, et al.
Page
of 44