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Weiqun Yu

Showing results (31-40 of 35) with videos related to

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American Journal of Physiology. Renal Physiology|April 11, 2014
Spontaneous voiding by mice reveals strain-specific lower urinary tract function to be a quantitative genetic traitWeiqun Yu, Cheryl Ackert-Bicknell, John D Larigakis, et al.
American Journal of Physiology. Renal Physiology|April 24, 2015
Evaluation of voiding assays in mice: impact of genetic strains and sexDale E Bjorling, Zunyi Wang, Chad M Vezina, et al.
Biophysical Journal|September 18, 2014
Hypercompliant apical membranes of bladder umbrella cellsJohn C Mathai, Enhua H Zhou, Weiqun Yu, et al.
Function (Oxford, England)|July 11, 2024
Deletion of Mechanosensory β1-integrin From Bladder Smooth Muscle Results in Voiding Dysfunction and Tissue RemodelingWeiqun Yu, Bryce MacIver, Lanlan Zhang, et al.
American Journal of Human Genetics|November 12, 2019
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor MutationsNina Mann, Franziska Kause, Erik K Henze, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
American Journal of Physiology. Renal Physiology|April 11, 2014
Spontaneous voiding by mice reveals strain-specific lower urinary tract function to be a quantitative genetic traitWeiqun Yu, Cheryl Ackert-Bicknell, John D Larigakis, et al.
American Journal of Physiology. Renal Physiology|April 24, 2015
Evaluation of voiding assays in mice: impact of genetic strains and sexDale E Bjorling, Zunyi Wang, Chad M Vezina, et al.
Biophysical Journal|September 18, 2014
Hypercompliant apical membranes of bladder umbrella cellsJohn C Mathai, Enhua H Zhou, Weiqun Yu, et al.
Function (Oxford, England)|July 11, 2024
Deletion of Mechanosensory β1-integrin From Bladder Smooth Muscle Results in Voiding Dysfunction and Tissue RemodelingWeiqun Yu, Bryce MacIver, Lanlan Zhang, et al.
American Journal of Human Genetics|November 12, 2019
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor MutationsNina Mann, Franziska Kause, Erik K Henze, et al.
Pageof 4