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Nature Communications
|
February 2, 2019
Marine biofilms constitute a bank of hidden microbial diversity and functional potential
Weipeng Zhang, Wei Ding, Yong-Xin Li, et al.
Nature Medicine
|
April 2, 2013
PPARβ/δ governs Wnt signaling and bone turnover
Carina Scholtysek, Julia Katzenbeisser, He Fu, et al.
BMJ (Clinical Research Ed.)
|
March 20, 2026
Effect of a clinical decision support system on stroke care quality and outcomes in patients with acute ischaemic stroke (GOLDEN BRIDGE II): cluster randomised clinical trial
Xinmiao Zhang, Lingling Ding, Jing Jing, et al.
American Journal of Human Genetics
|
November 4, 2017
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures"
Chae Syng Lee, He Fu, Nissan Baratang, et al.
American Journal of Human Genetics
|
December 13, 2016
Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation
Kezhi Yan, Justine Rousseau, Rebecca Okashah Littlejohn, et al.
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Search research articles
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Showing results (41-50 of 45) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 45 results.
Nature Communications
|
February 2, 2019
Marine biofilms constitute a bank of hidden microbial diversity and functional potential
Weipeng Zhang, Wei Ding, Yong-Xin Li, et al.
Nature Medicine
|
April 2, 2013
PPARβ/δ governs Wnt signaling and bone turnover
Carina Scholtysek, Julia Katzenbeisser, He Fu, et al.
BMJ (Clinical Research Ed.)
|
March 20, 2026
Effect of a clinical decision support system on stroke care quality and outcomes in patients with acute ischaemic stroke (GOLDEN BRIDGE II): cluster randomised clinical trial
Xinmiao Zhang, Lingling Ding, Jing Jing, et al.
American Journal of Human Genetics
|
November 4, 2017
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures"
Chae Syng Lee, He Fu, Nissan Baratang, et al.
American Journal of Human Genetics
|
December 13, 2016
Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation
Kezhi Yan, Justine Rousseau, Rebecca Okashah Littlejohn, et al.
Page
of 5