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CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

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Human bone cells mainly produce a type 1 enzyme that may help regulate bone health.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Basal cell carcinomas need extra mutations to grow from small to large tumors.

Biglycan helps regulate hair growth and regeneration.

Mutations in the KRT16 gene can cause skin and nail disorders.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

Laminin-511 is crucial for early hair growth and maintaining important hair development signals.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Children with pituitary dwarfism have higher zinc and copper, lower manganese, and similar iron levels in hair compared to normal children.

Hirsutism in females is caused by high male hormones or sensitive hair follicles.

A mutation in mice causes hair loss and immune problems.

Endoglin is crucial for proper hair growth cycles and stem cell activation in mice.

Using human recombinant hyaluronidase in donor strip harvesting may improve the procedure.

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

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Idiopathic hirsutism causes excessive hair growth in women, can be treated with medication and hair removal, but cannot be fully reversed.

Nestin helps identify certain melanoma cells in nodular melanoma.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A woman had unusual hair growth on one side of her chin without a known cause.

BMP2 and BMP7 have opposite roles in feather formation.

Keratin 16 delays skin maturation and affects skin and hair development in mice.