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Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Insulin resistance is linked to PCOS and can lead to other health issues, but treatments like metformin can help manage symptoms.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The WIF1 gene is crucial for hair growth in Angora rabbits.

Hair growth can be influenced by manipulating keratin and growth factor genes.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

The vitamin D receptor can act without its usual activating molecule, affecting hair growth and skin cancer, but its full range of actions is not well understood.

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

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

The KRTAP36-2 gene in sheep affects wool yield.

Certain gene variations are linked to the thickness of cashmere goat hair.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.