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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.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

IGFBP5 may be a potential target for Parkinson's treatment by reducing neuron death.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Dermal EZH2 controls skin cell development and hair growth in mice.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Egfl6 is not needed for zebrafish face development.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

TGF-β2 plays a key role in human hair growth and development.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

GhDET2 is crucial for cotton fiber growth.

A genetic variant linked to hair thinning in Japanese women was found.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

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

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Junctional proteins stabilize the inner root sheath and connect the companion layer in human hair.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.