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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

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

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Researchers found genes linked to hair loss in male giant pandas.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Phospholipids help plant proteins move by regulating receptor interactions.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

The Gsdma3 gene is essential for normal hair development in mice.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

Deleting MPZL3 increases skin oil production and reduces body fat.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Activating TLR3 boosts autophagy gene expression in skin cells.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Key genes linked to hair growth and cancer were identified in hairless mice.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

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

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

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

PP2Acα is essential for proper hair and skin development.