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Maria C Bolling

Showing results (31-40 of 34) with videos related to

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Human Molecular Genetics|November 28, 2022
PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosisIrma van de Beek, Iris E Glykofridis, Jan C Oosterwijk, et al.
Science Translational Medicine|July 22, 2021
Dynamic loading of human engineered heart tissue enhances contractile function and drives a desmosome-linked disease phenotypeJacqueline M Bliley, Mathilde C S C Vermeer, Rebecca M Duffy, et al.
Genes|January 13, 2021
Meta-Analysis of Mutations in <i>ALOX12B</i> or <i>ALOXE3</i> Identified in a Large Cohort of 224 PatientsAlrun Hotz, Julia Kopp, Emmanuelle Bourrat, et al.
The Journal of Investigative Dermatology|September 16, 2023
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar KeratodermaAnnemieke J M H Verkerk, Daniela Andrei, Mathilde C S C Vermeer, et al.
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Showing results (31-40 of 34) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 34 results.
Human Molecular Genetics|November 28, 2022
PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosisIrma van de Beek, Iris E Glykofridis, Jan C Oosterwijk, et al.
Science Translational Medicine|July 22, 2021
Dynamic loading of human engineered heart tissue enhances contractile function and drives a desmosome-linked disease phenotypeJacqueline M Bliley, Mathilde C S C Vermeer, Rebecca M Duffy, et al.
Genes|January 13, 2021
Meta-Analysis of Mutations in <i>ALOX12B</i> or <i>ALOXE3</i> Identified in a Large Cohort of 224 PatientsAlrun Hotz, Julia Kopp, Emmanuelle Bourrat, et al.
The Journal of Investigative Dermatology|September 16, 2023
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar KeratodermaAnnemieke J M H Verkerk, Daniela Andrei, Mathilde C S C Vermeer, et al.
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