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MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

Baicalin may help reduce excessive male hormone levels in PCOS.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Higher Galectin-3 levels are linked to insulin resistance and may predict androgenetic alopecia severity.

Two gene areas linked to male pattern baldness found, more research needed.

Transglutaminase activity is important for skin and is found in both mammals and birds.

A KRT32 gene variant causes loose anagen hair syndrome.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Topical immunotherapy for alopecia areata may work by creating immune cell clusters in the skin.

Modified laparoscopic sleeve gastrectomy effectively controls diabetes and treats obesity with minimal complications.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Researchers created a new mouse model for studying scleroderma.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

A specific genetic deletion in goats affects cashmere yield and thickness.

Retinoic acid changes skin cells to mucosal cells with goblet cells, needing TG2/Gh, Gbx1, and TGF-beta.