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A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Skin-derived precursors in hair follicles come from different origins but function similarly.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Polyamines help fix DNA damage accurately in cells.

Melatonin improves cashmere goat hair growth and quality by increasing antioxidants and reducing cell death.

In Brazil in 2018, the most common skin issues were acne, photoaging, and nonmelanoma skin cancer, with treatments often including topical medications and sunscreen.

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

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

Light therapy reduces scalp inflammation, boosts hair regrowth with Minoxidil 2%.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Light-based treatment, Photobiomodulation, shows promise for non-invasive skin therapy with few side effects.

Different combinations of human hair keratins affect how hair fibers form.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.