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Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Found new possible treatments for hair loss.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The research helps in creating genetically modified animals to study hair growth.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

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

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Variation in the TCHH gene affects wool curliness in sheep.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Obesity affects skin health, causing conditions like acanthosis nigricans and may require different treatment approaches.