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LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

Ritlecitinib shows promise in improving hair regrowth in adolescents with alopecia areata.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

Tiny particles from skin cells can help activate hair growth.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

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Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Epidermal neural crest stem cells from hair follicles can help repair nerve injuries.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

The index to ring finger ratio may indicate disease severity in female ankylosing spondylitis patients, but not in males.

A new treatment using a special gel with miR-665 reduces inflammation and helps hair regrow in alopecia areata.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Rac1 is crucial for normal hair structure and pigmentation.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

KLHL24-mutant stem cells help understand skin and heart disease.

Thymosin beta-4 promotes hair growth in mice.

Derinat helps extend hair growth by reducing harmful molecules in skin cells.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Three specific 4-azasteroid-2-oximes showed strong enzyme inhibition, but less than finasteride.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

SFRP-4 might be an early indicator of diabetes and hypertension in men with androgenic alopecia.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.