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Not having enough cystatin M/E protein causes less hair growth and dry skin.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

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

Skin grafts on mice can cause an immune response leading to hair loss, useful for studying human hair loss conditions.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Stump-tailed macaque best for researching hair loss causes and treatments.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

The guidelines suggest a detailed approach to diagnosing and treating lupus, with a focus on regular check-ups, personalized medicine, and a range of drug options for different cases.

Blocking the Wnt pathway could lead to new treatments for cancer and tissue repair but requires careful development to avoid side effects.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Both vitiligo and alopecia areata involve an immune response triggered by stress and specific genes, with treatments targeting this pathway showing potential.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Brain hormones significantly affect hair color and could potentially be used to prevent or reverse grey hair.

Maintaining the right amount of retinoic acid is crucial for healthy hair and skin.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

Ptprq has multiple forms that change during inner ear development.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Iron deficiency might contribute to hair loss in women.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.