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Hair follicle bulge cells are important for hair survival and help heal the skin after injury, which might be relevant for understanding hidradenitis suppurativa.

Hirsutism greatly lowers the quality of life for Turkish women.

The HATMSC1 cell line from fat tissue can produce helpful factors for regenerative and immune therapies.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

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

Curved human hair has different structures on its convex and concave sides.

Human hair proteins have similar cysteine and glycine levels to skin proteins.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Hypochlorous acid spray improves wound healing and reduces redness and itching in hair transplant surgery.

Hairless protein can block vitamin D activation in skin cells.

HFMs can help study hair growth and test potential hair growth drugs.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Huaier helps hair grow back and repairs tissue after cancer treatment.

The girl has an inflammatory type of scarring hair loss.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The document helps doctors recognize and treat excessive hair growth in women.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

All women with significant unwanted hair growth have hormonal imbalances, often from polycystic ovary syndrome.

CARASIL can cause different symptoms even with the same genetic mutation.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

The document provides a method to prepare human scalp tissue for studying hair follicles at the single-cell level.