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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

H19 boosts hair growth potential by activating Wnt signaling, possibly helping treat hair loss.

Type XIX Collagen is present in specific skin and hair cells during development.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

SRD5A2 methylation in blood can predict how well someone will respond to finasteride treatment.

Researchers found a non-functional sheep keratin gene due to mutations.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

The HCR gene contributes to psoriasis risk.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

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

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Keratin 19 helps identify skin stem cells, with its presence varying by body location, age, and culture stage.