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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

Two new gene clusters important for hair formation were found on human chromosome 11.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

Hepatitis B virus exposure may be linked to increased risk of alopecia areata.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

The research found that chickenpox virus spreads in skin through blood then to skin cells, while shingles virus moves from nerves to hair follicle areas before infecting skin cells.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Hominis Placenta helps hair grow back by increasing cell growth and a specific growth factor.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

Certain genetic markers may increase or decrease prostate cancer risk.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Two new gene clusters important for hair formation were found on human chromosome 11.

Ribonucleotide excision repair is crucial to prevent skin cancer.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

Chicken feather gene mutation helps understand human hair disorders.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

Removing p16INK4a from skin cells can lead to faster and more clumped growth, which might help with hair growth.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Androgen receptor signaling causes early aging of cells important for hair growth by damaging their DNA.

VHL disease can cause early paragangliomas, needing lifelong monitoring.