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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

BLMP-1 is important for regular molting and gene expression cycles in worms.

WNT10A is important for tissue development and linked to various human disorders.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

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

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Whn is essential for hair growth, and its malfunction causes hair loss.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Long non-coding RNAs affect feather growth in chickens in ways that don't follow traditional genetic rules.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

The protein ARA70/ELE1 is involved in male pattern baldness, and lower levels of its short form may lead to hair thinning.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A20 protein is crucial for normal skin and hair development.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

The naked mutation in mice causes hair loss and helps identify keratin genes.