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searching for Lamin B1 13 found (18 total)

alternate case: lamin B1

Laminopathy (3,435 words) [view diff] exact match in snippet view article find links to article

Some laminopathies however may lead to an early death, and mutations of lamin B1 (LMNB1 gene) may be lethal before or at birth. Patients with classical

Thymopoietin (1,434 words) [view diff] exact match in snippet view article find links to article

LAP2 plays a role in the regulation of nuclear architecture by binding lamin B1 and chromosomes. This interaction is regulated by phosphorylation during

Nuclear lamina (1,862 words) [view diff] exact match in snippet view article find links to article

filaments which can be categorized as either A-type (lamin A, C) or B-type (lamin B1, B2) according to homology of their DNA sequences, biochemical properties

Autosomal dominant leukodystrophy with autonomic disease (1,801 words) [view diff] exact match in snippet view article find links to article

duplication of the LMNB1 gene, this gene takes part in the production of the lamin B1 protein, which is essential for determining the nucleus' shape within the

Pelger–Huët anomaly (958 words) [view diff] exact match in snippet view article find links to article

myelodysplasia. In 2022, Reilly et al. showed that loss of LMNB1, the gene encoding lamin B1, is necessary and sufficient to cause pseudo-Pelger-Huet anomaly in neutrophils

Mir-23 microRNA precursor family (958 words) [view diff] exact match in snippet view article find links to article

PMC 2680038. PMID 19440340. Lin ST, Fu YH (2009). "miR-23 regulation of lamin B1 is crucial for oligodendrocyte development and myelination". Disease Models

Ying-Hui Fu (2,257 words) [view diff] exact match in snippet view article find links to article

phenotype back to individuals with an extra copy of nuclear laminar protein lamin B1 making ADLD one of the diseases named “laminopathies”. Sleep Science Award

RCE1 (474 words) [view diff] exact match in snippet view article find links to article

Hollinshead MS, Higbee NC, et al. (2003). "A carboxyl-terminal interaction of lamin B1 is dependent on the CAAX endoprotease Rce1 and carboxymethylation". J.

Louis Ptáček (1,413 words) [view diff] exact match in snippet view article find links to article

Saigoh K, Schiffmann R, Asahara H, Koeppen A, Hogan K, Ptáček LJ, Fu YH. Lamin B1 duplications cause autosomal dominant leukodystrophy. Nat Genet. 2006 Oct;

Cytotoxic T cell (3,852 words) [view diff] exact match in snippet view article find links to article

3, 6, and 7, leading to cleavage of death substrates such as lamin A, lamin B1, lamin B2, PARP (poly ADP ribose polymerase), and DNA-PKcs (DNA-activated

FAM227B (1,689 words) [view diff] exact match in snippet view article find links to article

Krishnamoorthy V, Parnaik VK (June 2018). "E3 ubiquitin ligase RNF123 targets lamin B1 and lamin-binding proteins". The FEBS Journal. 285 (12): 2243–2262. doi:10

Progeria (6,225 words) [view diff] exact match in snippet view article find links to article

is referred to as lamin A. In most mammalian cells, lamin A, along with lamin B1, lamin B2, and lamin C, makes up the nuclear lamina, which provides shape

MROH9 (2,166 words) [view diff] exact match in snippet view article find links to article

Krishnamoorthy V, Parnaik VK (June 2018). "E3 ubiquitin ligase RNF123 targets lamin B1 and lamin-binding proteins". The FEBS Journal. 285 (12): 2243–2262. doi:10