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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Prolactin affects hair growth cycles and can cause early hair follicle regression.

AR-27 E-Chol siRNA can effectively regrow hair by reducing androgen receptor gene activity.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Genetically modified rats help reveal how vitamin D affects bone and skin health.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

RXR agonists may promote hair growth in humans.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Activating the GDNF-GFRα1-RET signaling pathway could potentially promote skin and limb regeneration in humans and could be used to treat hair loss and promote wound healing.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

KRT72 gene helps form hair.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

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

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A new treatment for hair loss shows promise with fewer side effects.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

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

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.