Results 111 to 120 of about 2,672 (202)

Developmental and muscle-type-specific expression of mouse nebulin exons 127 and 128

open access: yes, 2006
The human nebulin gene includes 183 exons and four regions of alternative splicing. The mouse nebulin gene, with 166 exons, has a similar organization. Here we describe the expression patterns of one of the alternatively spliced regions of nebulin: exons
Aro, Mimmi   +4 more
core   +1 more source

The SH3 domain of nebulin binds selectively to type II peptides: theoretical prediction and experimental validation

open access: yes, 2002
Nebulin, a giant modular protein from muscle, is thought to act as a molecular ruler in sarcomere assembly. The C terminus of nebulin, located in the sarcomere Z-disk, comprises an SH3 domain, a module well known for its role in protein/protein ...
Temussi, PA   +31 more
core   +1 more source

A Circular RNA Generated from Nebulin (NEB) Gene Splicing Promotes Skeletal Muscle Myogenesis in Cattle as Detected by a Multi‐Omics Approach

open access: yesAdvanced Science
Cattle and the draught force provided by its skeletal muscle have been integral to agro‐ecosystems of agricultural civilization for millennia. However, relatively little is known about the cattle muscle functional genomics (including protein coding genes,
Kongwei Huang   +19 more
doaj   +1 more source

Alcohol Affects the Skeletal Muscle Proteins, Titin and Nebulin in Male and Female Rats

open access: yes, 2003
Alcoholic myopathy is characterized by decreased protein synthesis and contents resulting in atrophy of muscle fibers. We investigated the effect of alcohol on the cytoskeletal muscle proteins, nebulin and titin.
Hunter, R J   +13 more
core   +1 more source

Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathy

open access: yes, 1997
A locus for autosomal recessive nemaline myopathy (NEM2) has been assigned by linkage analysis to a 13-cM region between the markers D2S150 and D2S142 on 2q21.2-q22.
Millevoi, S.   +10 more
core  

Elucidating nebulin expression and function in health and disease [PDF]

open access: yes, 2019
The nemaline myopathies (NM) are a group of genetic muscle disorders, ranging in severity from severe, early lethal forms to milder muscle disorders with onset in childhood, sometimes presenting in adulthood.
Laitila, Jenni
core  

The application of quantitative SDS-PAGE method for measurement of extracellular recombinant scFv anti-p17 in crude protein

open access: yesJournal of Associated Medical Sciences, 2013
The quantitative determination of recombinant protein in crude protein is not commonly used because the protein is not in purified form. The Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was developed for quantitative determination
Kannaporn Intachai   +4 more
doaj  

NRAP reduction rescues sarcomere defects in nebulin-related nemaline myopathy. [PDF]

open access: yesHum Mol Genet, 2023
Casey JG   +5 more
europepmc   +1 more source

Common Ancestry from Southern Italy: Two Families with Dilated Cardiomyopathy Share the Same Homozygous Loss-of-Function Variant in <i>NRAP</i>. [PDF]

open access: yesGenes (Basel)
Onore ME   +12 more
europepmc   +1 more source

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