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PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

A new mutation in mice causes crooked whiskers and messy hair.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

LIPH mutations cause woolly hair in some Chinese people.

Lack of TrkC receptor delays hair follicle development.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

KAP6 genes are conserved across species and active in hair follicles.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

ILK is essential for skin development, pigmentation, and healing.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

PKM2 is a promising target for heart repair and regeneration.

New treatments targeting specific genes show promise for treating keratin disorders.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

CNGC14 is crucial for calcium entry needed for root hair growth in plants.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

The KRTAP22-2 gene in sheep does not significantly affect wool traits.