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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Meis2 is essential for touch sensation and nerve function in mice.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new mouse mutation causes skin and hair defects due to a gene change.

Defects in certain proteins cause major heart abnormalities during early development.

Collagen XVII is important for cell functions and its absence can worsen cancer outcomes.

A new gene variant causes curly coats in some dog breeds.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

MOF controls skin development by regulating genes for mitochondria and cilia.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Id2 gene helps keep hair follicle stem cells inactive.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Certain genes are crucial for feather development in Wannan chickens.