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Isabelle Draper

Showing results (21-30 of 26) with videos related to

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FEBS Letters|September 19, 2024
The splicing factor hnRNPL demonstrates conserved myocardial regulation across species and is altered in heart failureIsabelle Draper, Wanting Huang, Suchita Pande, et al.
The FEBS Journal|January 17, 2025
Effects of HMG CoA reductase (HMGCR) deficiency on skeletal muscle developmentMekala Gunasekaran, Hannah R Littel, Natalya M Wells, et al.
Biorxiv : the Preprint Server for Biology|June 21, 2024
Effects of HMGCR deficiency on skeletal muscle developmentMekala Gunasekaran, Hannah R Littel, Natalya M Wells, et al.
Acta Neuropathologica|January 4, 2024
Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated Alzheimer's diseaseAna Rita Agra Almeida Quadros, Zhaozhi Li, Xue Wang, et al.
Acta Neuropathologica|February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophyAndres Nascimento, Christine C Bruels, Sandra Donkervoort, et al.
American Journal of Human Genetics|April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
FEBS Letters|September 19, 2024
The splicing factor hnRNPL demonstrates conserved myocardial regulation across species and is altered in heart failureIsabelle Draper, Wanting Huang, Suchita Pande, et al.
The FEBS Journal|January 17, 2025
Effects of HMG CoA reductase (HMGCR) deficiency on skeletal muscle developmentMekala Gunasekaran, Hannah R Littel, Natalya M Wells, et al.
Biorxiv : the Preprint Server for Biology|June 21, 2024
Effects of HMGCR deficiency on skeletal muscle developmentMekala Gunasekaran, Hannah R Littel, Natalya M Wells, et al.
Acta Neuropathologica|January 4, 2024
Cryptic splicing of stathmin-2 and UNC13A mRNAs is a pathological hallmark of TDP-43-associated Alzheimer's diseaseAna Rita Agra Almeida Quadros, Zhaozhi Li, Xue Wang, et al.
Acta Neuropathologica|February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophyAndres Nascimento, Christine C Bruels, Sandra Donkervoort, et al.
American Journal of Human Genetics|April 16, 2021
A form of muscular dystrophy associated with pathogenic variants in JAG2Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Pageof 3