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CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Ets2 gene is crucial for placental development in mice.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Blocking mTORC1 reduces skin tumor growth in mice.

A new mouse model effectively mimics vitiligo for research and drug testing.

Scientists made a mouse that can be made to lose hair and then grow it back.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Knocking out certain genes in mice helps understand skin and hair growth problems.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.