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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Different types of stem cells help maintain and heal skin.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Epigenetic mechanisms control skin development by regulating gene expression.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Certain gene variations increase the risk of alopecia areata in Koreans.

Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Certain skin proteins can form anchoring structures without the protein AMACO.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.