Search

everythinglearnresearchcommunity

for

Search:↓

Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

NK cells play a role in skin diseases like eczema and psoriasis.

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

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

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

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Notch signaling is essential for healthy skin and hair follicle maintenance.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

Methotrexate is not proven effective for inducing remission in ulcerative colitis.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Vitamin D is important for skin health and can help treat psoriasis, atopic dermatitis, and vitiligo.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

Fatp4 is crucial for healthy skin development and function.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

The vitamin D receptor can work without its usual activating molecule.