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The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Pangenome analysis reveals key genes for pig adaptation and traits, aiding genetic improvement.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

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.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

Wnt/β-catenin signaling is crucial for cell fusion in placental development.

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

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

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

HOXC13 is essential for hair and nail development by regulating Foxn1.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The protein p21 is more abundant in normal skin cells than in melanoma cells and may help protect against melanoma, with UVB light affecting its levels.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Rac1 is crucial for normal hair structure and pigmentation.

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

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Specific keratin gene mutations can cause monilethrix.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.