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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

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

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

FGF5 gene mutations cause long hair in domestic cats.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

The study found key genes and pathways involved in cashmere goat hair growth stages.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

17β-estradiol can reduce inflammation in the skin.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Disabling the FGF5 gene in sheep leads to longer wool.

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

FGF13 gene changes cause excessive hair growth in a rare condition.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Tiny particles from brain cells help hair grow by targeting a specific hair growth pathway.

Notch signaling disruptions can cause various skin diseases.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

VDR regulation varies by tissue and is crucial for its biological functions.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.