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

TCDD disrupts skin stem cells, causing skin issues like chloracne.

CRH promotes fat production in skin cells, affecting conditions like acne.

The Celsr1 gene is crucial for normal hair patterning in mice.

CHI3L1 and CXCL5 proteins help promote hair growth.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

CCC1 is essential for pH balance and normal cell function in plants.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Variation in the TCHH gene affects wool curliness in sheep.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

CDP is crucial for lung and hair follicle cell development.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

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

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

CNGC14 is crucial for calcium entry needed for root hair growth in plants.

A new one-step test can quickly identify skin cancer during surgery.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

CXCR2 in skin cells promotes tumor growth.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

CCL5 is important for the hair growth potential of human dermal papilla cells.