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FEBS Letters
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September 19, 2024
The splicing factor hnRNPL demonstrates conserved myocardial regulation across species and is altered in heart failure
Isabelle Draper, Wanting Huang, Suchita Pande, et al.
The FEBS Journal
|
January 17, 2025
Effects of HMG CoA reductase (HMGCR) deficiency on skeletal muscle development
Mekala 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 development
Mekala 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 disease
Ana Rita Agra Almeida Quadros, Zhaozhi Li, Xue Wang, et al.
Acta Neuropathologica
|
February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy
Andres 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 JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
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Search research articles
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Showing results (21-30 of 26) with videos related to
Sort By:
Page
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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 failure
Isabelle Draper, Wanting Huang, Suchita Pande, et al.
The FEBS Journal
|
January 17, 2025
Effects of HMG CoA reductase (HMGCR) deficiency on skeletal muscle development
Mekala 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 development
Mekala 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 disease
Ana Rita Agra Almeida Quadros, Zhaozhi Li, Xue Wang, et al.
Acta Neuropathologica
|
February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy
Andres 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 JAG2
Sandra Coppens, Alison M Barnard, Sanna Puusepp, et al.
Page
of 3