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A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

Non-liganded Vitamin D Receptor is crucial for healthy skin and hair.

A new type of nerve cell involved in itch perception was discovered.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Changing YBX1 protein activity affects skin stem cell function and aging.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Neuregulin3 affects cell development in the skin and mammary glands.

Different enzymes are active in different parts of developing mouse organs.

RNase L suppresses regeneration in mammals.

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

The protein ER71/ETV2 helps regrow hair after chemotherapy by improving the growth of new blood vessels.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Estrogen and its receptors play a key role in hair growth, with differences between males and females.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

Vitamin D receptor mutations can cause alopecia by affecting hair growth genes.

Defective protein folding due to a mutation is key in ANE syndrome.

EDA is vital for bone and cartilage formation and could help treat skeletal disorders.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

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

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

A specific gene mutation causes a severe skin disorder in a family.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.