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The Arabidopsis rhd2 mutant is more sensitive to drought because of changes in cell membrane proteins and cell structure.

HPV8 E6 gene causes growth of certain skin stem cells.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

Scalp melanoma is often diagnosed late in people with hair loss, leading to worse outcomes.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

The 14-3-3σ gene is essential for preventing hair loss.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

Lack of cystatin M/E causes thin hair and dry skin.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

A hormone affects hair growth, certain molecules may prevent skin damage, a skin disease is linked to immune cells, glycerol helps skin hydration, and psoriasis treatment trials need improvement.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

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

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Disrupting natural body clocks increases the risk of developing type 2 diabetes.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

Understanding intermediate filaments helps explain hair health and related diseases.

Moles may stop growing because of cell cooperation, not just because of aging cells.

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

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.