Browsing by Subject "Molecular genetics."

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Deregulated caveolin-1 and Hic-5 expression in mouse embryo fibroblasts lacking A-type lamin and homozygous for the N195K mutant form

Kamand, Lara Adnan. (2012)

Laminopathies are a group of genetic diseases which result from mutations or altered post translational processing of nuclear envelope (NE)-lamina proteins. Most of these disorders are caused by mutations in the LMNA gene ...
Hic-5 deregulation in lamin A-C and emerin - associated myopathies -

Daw, Ranim Houssam (2017)

In higher eukaryotes, the nuclear lamina – a meshwork of type V intermediate filaments – underlies and associates with the nuclear side of the inner nuclear membrane. It consists of 2 classes of proteins; (1) A-type lamins ...
Investigating the deregulation and bio-functional relevance of caveolin-1 in muscular laminopathies -

Diab El Harakeh, Dima Abed, (2015)

Laminopathies comprise a heterogeneous group of disorders arising from mutations or altered post translational processing of nuclear envelope (NE)-lamina proteins. The majority of these disorders are caused by inherited ...
Mutational analysis of HK022 nun basic domain binding to λ boxB reveals requirements distinct from λ N - by Caroline Sami Tawk.

Tawk, Caroline Sami. (2011)

Bacteriophage λ regulates the switch from immediate-early to delayed-early gene expression by the binding of N protein to nut (N-utilization) sites in two viral transcripts. The arginine-rich domain of N protein recognizes ...
The effect of lamin A-C loss or mutation on nuclear envelope proteomics and splicing factor deregulation in Emery-Dreifuss muscular dystrophy and dilated cardiomyopathy.

Zahr, Hind Camille (2019)

Mutations in the LMNA gene, which encodes for lamins A and C (lamin A-C) of the nuclear lamina, cause a wide array of tissue-specific pathologies, mostly affecting cardiac and skeletal muscle tissues. How mutations in a ...

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Browsing by Subject "Molecular genetics."

Browsing by Subject "Molecular genetics."

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