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A mutation in the VDR gene affects hair cycling without needing ligand binding.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

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

Genomic prediction can improve breeding strategies for Korean Sapsaree dogs.

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

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, and antioxidants may help treat hair loss.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

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Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

DGAT1 enzyme is crucial for healthy skin and hair by regulating retinoid levels.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

Hsc70 protein may influence hair growth by responding to androgens.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

SCD1 is crucial for skin health and overall energy balance.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

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

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

Dermatologists should consider alpha-gal syndrome in patients with unexplained chronic skin issues.