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Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The new matrix improves skin regeneration and graft performance.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Certain gene variations are linked to the thickness of cashmere goat hair.

SOX9 is essential for the development of various organs and hair follicles.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

FGF5 gene mutations cause long hair in domestic cats.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

Disabling the FGF5 gene in sheep leads to longer wool.

Human hair loss may have evolved to help increase brain size.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

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

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

Many men misuse oral contraceptive pills for things like hair growth and muscle gain.

Self-assembling RADA16-I hydrogels with bioactive peptides significantly improve wound healing.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

UV exposure reduced hair shine in mice, but minoxidil helped restore it.

Skin stem cells in hair follicles are important for touch sensation.