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Updated treatments for female hair loss include minoxidil, antiandrogens, hair transplants, and light therapy.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

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

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Different forms of FGF5 either promote or inhibit hair growth.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Adverse events in lung cancer treatments increase fear, anxiety, and depression, with newer therapies causing fewer side effects.

Activating β-catenin increases melanocytes and decreases Schwann cells.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.