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A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Stem cell therapies show promise for treating various diseases but face challenges in clinical use and require better monitoring techniques.

Versican is important for hair growth and could help find new hair regrowth treatments.

17β-estradiol lowers polyamine oxidase levels in breast cancer cells through estrogen receptor 2.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

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

Scientists developed tools to observe hair regeneration in real time and assess skin health, using glowing mice and light-controlled genes.

Researchers created a mouse cell line to study hair growth and test hair growth drugs.

miR-144-y and FOXO3 play key roles in skin and feather development in Zhedong White geese.

Vitamin C derivative reduces hair loss-related protein in cells.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

The same gene mutation can cause different symptoms in family members.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

Finasteride side effects in young men may be linked to specific gene variations.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Nonionic liposomes are the best for delivering genes to skin cells.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

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

The K14 promoter is more active in skin cells than the K5 promoter.