Search research articles
Contact Us
Filters
Showing results (651-660 of 1,144) with videos related to
Page
of 115
Sort By:
BMJ Public Health
|
March 6, 2026
Why ethics in social listening and infodemic management matters for public health
Giovanni Spitale, Federico Germani, Nikola Biller-Andorno, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP
|
June 21, 2005
New insights into the mechanism of imposex induction in the dogwhelk Nucella lapillus
M M Santos, L Filipe C Castro, M N Vieira, et al.
Lancet (London, England)
|
February 27, 1993
Environmental trichlorfon and cluster of congenital abnormalities
A E Czeizel, C Elek, S Gundy, et al.
Clinical Otolaryngology and Allied Sciences
|
April 14, 2000
Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)
H Kunst, H Marres, P Huygen, et al.
Gene
|
February 9, 2012
A novel Acetyl-CoA synthetase short-chain subfamily member 1 (Acss1) gene indicates a dynamic history of paralogue retention and loss in vertebrates
L Filipe C Castro, Monica Lopes-Marques, Jonathan M Wilson, et al.
Operative Dentistry
|
July 6, 2016
Six-month Follow-up of Cervical Composite Restorations Placed With a New Universal Adhesive System: A Randomized Clinical Trial
L S Lopes, F S Calazans, R Hidalgo, et al.
Journal of Thermal Biology
|
January 6, 2018
Using thermography as a diagnostic tool for omphalitis on newborn calves
C L Shecaira, C H Seino, J A Bombardelli, et al.
Environmental Health Perspectives
|
January 5, 2008
Mixtures of estrogenic chemicals enhance vitellogenic response in sea bass
Ana D Correia, Sandro Freitas, Martin Scholze, et al.
The Journal of Nutrition
|
October 15, 1998
Protein deficiency and nutritional recovery modulate insulin secretion and the early steps of insulin action in rats
M Q Latorraca, M A Reis, E M Carneiro, et al.
Gene
|
May 14, 2015
Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
F Pasutto, L Mauri, B Popp, et al.
Page
of 115
Search research articles
Search
Showing results (651-660 of 1,144) with videos related to
Sort By:
Page
of 115
BMJ Public Health
|
March 6, 2026
Why ethics in social listening and infodemic management matters for public health
Giovanni Spitale, Federico Germani, Nikola Biller-Andorno, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP
|
June 21, 2005
New insights into the mechanism of imposex induction in the dogwhelk Nucella lapillus
M M Santos, L Filipe C Castro, M N Vieira, et al.
Lancet (London, England)
|
February 27, 1993
Environmental trichlorfon and cluster of congenital abnormalities
A E Czeizel, C Elek, S Gundy, et al.
Clinical Otolaryngology and Allied Sciences
|
April 14, 2000
Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)
H Kunst, H Marres, P Huygen, et al.
Gene
|
February 9, 2012
A novel Acetyl-CoA synthetase short-chain subfamily member 1 (Acss1) gene indicates a dynamic history of paralogue retention and loss in vertebrates
L Filipe C Castro, Monica Lopes-Marques, Jonathan M Wilson, et al.
Operative Dentistry
|
July 6, 2016
Six-month Follow-up of Cervical Composite Restorations Placed With a New Universal Adhesive System: A Randomized Clinical Trial
L S Lopes, F S Calazans, R Hidalgo, et al.
Journal of Thermal Biology
|
January 6, 2018
Using thermography as a diagnostic tool for omphalitis on newborn calves
C L Shecaira, C H Seino, J A Bombardelli, et al.
Environmental Health Perspectives
|
January 5, 2008
Mixtures of estrogenic chemicals enhance vitellogenic response in sea bass
Ana D Correia, Sandro Freitas, Martin Scholze, et al.
The Journal of Nutrition
|
October 15, 1998
Protein deficiency and nutritional recovery modulate insulin secretion and the early steps of insulin action in rats
M Q Latorraca, M A Reis, E M Carneiro, et al.
Gene
|
May 14, 2015
Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
F Pasutto, L Mauri, B Popp, et al.
Page
of 115