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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Researchers created a new mouse model for studying scleroderma.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

Human melanocytes in skin and hair follicles don't express keratin 16 or 6 naturally.

Sox2-expressing cells can help grow hair and heal skin.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

GLI2 increases follistatin production in human skin cells.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

BST2 is highly expressed in certain immune cells in alopecia areata, suggesting a role in the disease.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Substance P helps hair growth by extending the growth phase and affecting certain growth factors.

SQSTM1 is linked to increased risk of alopecia areata.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

The research updated the skin cell profile, finding new skin cell markers and showing fibroblasts' key role in skin health.

Key genes and pathways influence wool traits in Merino sheep.

MPZL3 protein helps keep sebaceous gland size and cell growth in check.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

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