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A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

TRPS1 is crucial for bone, kidney, and hair follicle development.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

KRT72 gene helps form hair.

A new gene mutation causes a rare type of hair loss.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

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

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

BTNL2 helps protect hair follicles from immune attacks.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

ILC1-like cells can cause alopecia areata by themselves.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Whn is essential for hair growth, and its malfunction causes hair loss.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

A specific gene variation in goats is linked to better growth traits.

Common baldness is likely inherited through multiple genes, not just one.

β1 integrin may indicate and influence the severity of hair loss in androgenetic alopecia.

Removing SIX1 in fat cells reduces skin fibrosis.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.