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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Increased Toll-like receptors in blood cells may contribute to alopecia areata and could be a target for new treatments.

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

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

The lncRNA LOXL1-AS1 may help diagnose and treat androgenic alopecia.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

Obstructive sleep apnea can be hereditary and linked to a genetic mutation in the COL1A2 gene.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

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

Hyaluronan from Has2 is important for proper wound healing and hair follicle development.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Hairless gene not strongly linked to baldness.

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

Alopecia areata patients show increased inflammation and OX40 activation, suggesting a new treatment target.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

The visfatin GT genotype may increase the risk of Alopecia Areata.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

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