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A compound from brown algae boosts the production of a certain inflammatory substance in skin cells.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

OsUEV1B protein is essential for controlling phosphate levels in rice.

PADs are crucial for healthy skin and hair, and their imbalance can cause skin and hair disorders.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

A peptide known for reducing wrinkles also effectively inhibits an enzyme linked to skin inflammation and acne.

A certain gene variation can affect protein production and is linked to male pattern baldness.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

BBS7 is crucial for maintaining healthy gums by regulating important signaling pathways.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Id2 gene helps keep hair follicle stem cells inactive.

Inhibiting PDE8A may help treat hair loss by boosting fat cell growth and hair regeneration.