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New treatments targeting skin stem cells show promise for skin repair, anti-aging, and cancer therapy.

Alopecia Areata is a complex, unpredictable autoimmune hair loss condition with limited treatment options and a significant psychological impact.

Activating NRF2 might help treat hair disorders by improving antioxidant defenses.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Using neurohormones to control keratin can lead to new skin disease treatments.

Different processes create patterns in skin and things like hair and feathers.

Hair follicle bulge cells don't help skin regrow after glucocorticoid damage; interfollicular epidermis cells do.

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

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

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Hormones and genes affect hair growth and male baldness.

Hairless gene not strongly linked to baldness.

Prolactin affects when mice shed and grow hair.

Rat dermal papilla cells have unique genes crucial for hair growth.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

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

Spironolactone might lower the chance of getting rosacea.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.