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SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

MOF controls skin development by regulating genes for mitochondria and cilia.

Hard α-keratin has a universal molecular structure with a specific superlattice arrangement.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Keratin gene clusters in humans and marsupials are similarly organized.

Dual TCR Treg cells are common in mouse tissues and vary by location.

The cuneate nucleus has two main neuron types: relay neurons and interneurons.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

Human hair keratins were cataloged, showing their roles in hair differentiation stages.

Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

Keratins are important for skin cell health and their problems can cause diseases.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Sebaceous glands help study fatty acid transporters and binding proteins.

The document introduced a new naming system for keratin-associated proteins to improve clarity and communication across species.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

Human hair has a new region with ordered filaments and the cuticle contains β-keratin sheets.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Basonuclin helps keratinocytes multiply and prevents them from fully maturing.

The study improved understanding of keratin fiber structure by showing consistent microfibril diameter but varying distances and electron density profiles.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.