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Showing results (1281-1290 of 2,138) with videos related to
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Journal of Experimental Child Psychology
|
April 5, 2025
From error to insight: Removing non-systematic responding data in the delay discounting task may introduce systematic bias
Brett W Gelino, Bryant M Stone, Geoffrey D Kahn, et al.
Journal of Biophotonics
|
October 25, 2018
Ultra-low background Raman sensing using a negative-curvature fibre and no distal optics
Stephanos Yerolatsitis, Fei Yu, Sarah McAughtrie, et al.
Diabetologia
|
March 26, 2014
GPR120 (FFAR4) is preferentially expressed in pancreatic delta cells and regulates somatostatin secretion from murine islets of Langerhans
Virginia M Stone, Shalinee Dhayal, Katy J Brocklehurst, et al.
Cancer
|
March 1, 2014
Disparity in perceptions of disease characteristics, treatment effectiveness, and factors influencing treatment adherence between physicians and patients with myelodysplastic syndromes
David P Steensma, Rami S Komrokji, Richard M Stone, et al.
ACS Case Reviews in Surgery
|
March 13, 2023
Early Prophylactic Gastrectomy for the Management of Gastric Adenomatous Proximal Polyposis Syndrome (GAPPS)
A C Salami, J M Stone, R H Greenberg, et al.
Circulation
|
September 5, 2002
Effect of treatment for Chlamydia pneumoniae and Helicobacter pylori on markers of inflammation and cardiac events in patients with acute coronary syndromes: South Thames Trial of Antibiotics in Myocardial Infarction and Unstable Angina (STAMINA)
Adam F M Stone, Michael A Mendall, Juan-Carlos Kaski, et al.
Molecular Vision
|
April 26, 2001
Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCR
W H Wang, L G McNatt, A R Shepard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 6, 2011
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes
Qihong Zhang, Darryl Nishimura, Seongjin Seo, et al.
American Journal of Human Genetics
|
June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United States
D F Barker, C J Pruchno, X Jiang, et al.
Ophthalmic Genetics
|
December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene
B Piguet, E Héon, F L Munier, et al.
Page
of 214
Search research articles
Search
Showing results (1281-1290 of 2,138) with videos related to
Sort By:
Page
of 214
Journal of Experimental Child Psychology
|
April 5, 2025
From error to insight: Removing non-systematic responding data in the delay discounting task may introduce systematic bias
Brett W Gelino, Bryant M Stone, Geoffrey D Kahn, et al.
Journal of Biophotonics
|
October 25, 2018
Ultra-low background Raman sensing using a negative-curvature fibre and no distal optics
Stephanos Yerolatsitis, Fei Yu, Sarah McAughtrie, et al.
Diabetologia
|
March 26, 2014
GPR120 (FFAR4) is preferentially expressed in pancreatic delta cells and regulates somatostatin secretion from murine islets of Langerhans
Virginia M Stone, Shalinee Dhayal, Katy J Brocklehurst, et al.
Cancer
|
March 1, 2014
Disparity in perceptions of disease characteristics, treatment effectiveness, and factors influencing treatment adherence between physicians and patients with myelodysplastic syndromes
David P Steensma, Rami S Komrokji, Richard M Stone, et al.
ACS Case Reviews in Surgery
|
March 13, 2023
Early Prophylactic Gastrectomy for the Management of Gastric Adenomatous Proximal Polyposis Syndrome (GAPPS)
A C Salami, J M Stone, R H Greenberg, et al.
Circulation
|
September 5, 2002
Effect of treatment for Chlamydia pneumoniae and Helicobacter pylori on markers of inflammation and cardiac events in patients with acute coronary syndromes: South Thames Trial of Antibiotics in Myocardial Infarction and Unstable Angina (STAMINA)
Adam F M Stone, Michael A Mendall, Juan-Carlos Kaski, et al.
Molecular Vision
|
April 26, 2001
Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCR
W H Wang, L G McNatt, A R Shepard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 6, 2011
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes
Qihong Zhang, Darryl Nishimura, Seongjin Seo, et al.
American Journal of Human Genetics
|
June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United States
D F Barker, C J Pruchno, X Jiang, et al.
Ophthalmic Genetics
|
December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene
B Piguet, E Héon, F L Munier, et al.
Page
of 214