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He Fu

Showing results (41-50 of 45) with videos related to

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Nature Communications|February 2, 2019
Marine biofilms constitute a bank of hidden microbial diversity and functional potentialWeipeng Zhang, Wei Ding, Yong-Xin Li, et al.
Nature Medicine|April 2, 2013
PPARβ/δ governs Wnt signaling and bone turnoverCarina 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 trialXinmiao 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 AcetylationKezhi Yan, Justine Rousseau, Rebecca Okashah Littlejohn, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 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 potentialWeipeng Zhang, Wei Ding, Yong-Xin Li, et al.
Nature Medicine|April 2, 2013
PPARβ/δ governs Wnt signaling and bone turnoverCarina 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 trialXinmiao 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 AcetylationKezhi Yan, Justine Rousseau, Rebecca Okashah Littlejohn, et al.
Pageof 5