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Stem cells show promise for hair loss and skin treatments in aesthetics but need more research on safety and standard methods.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

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

Hair follicle stem cells can return to their original niche and help regenerate hair.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Dermal papilla cells are key for hair growth and color, influencing hair type and size, and their interaction with stem cells could help treat hair loss and color disorders.

Finasteride reduces PSA levels, terazosin doesn't affect them, and tracking prostate cancer in patients taking finasteride could be difficult.

Special proteins are important for skin balance, healing, and aging, and affect skin stem cells.

The review indicates that understanding of long COVID symptoms is still limited and better research is needed for diagnosis and treatment.

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.

Microneedling helps with hair loss, especially with 5% minoxidil, but more high-quality research is needed.

The skin's basement membrane is specially designed to support different types of connections between skin layers and hair follicles.

People with alopecia areata often have lower vitamin D levels than healthy people.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

There is no causal relationship between androgenetic alopecia and serum uric acid.

Skin organoids from stem cells can help study and treat skin issues but face some challenges.

Childhood sexual trauma, especially between ages 5-7, is linked to lower cortisol levels in adult hair, suggesting long-term stress response changes.

Topical corticosteroids are the main treatment for Erosive Pustular Dermatosis, but recurrence is common after stopping treatment.

The research mapped out the cell types and molecular processes involved in developing Cashmere goat hair follicles.

Ultrasound shows 96% of young men with erectile dysfunction after using finasteride have abnormal penile tissue.

The skin's dermal layer contains true stem cells with diverse functions and interactions that need more research to fully understand.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

New treatments focusing on immune pathways show promise for stubborn hair loss.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Finding functions for unknown GPCRs is hard but key for making new drugs.

Normal hair thickness varies by scalp area and a mix of hair thicknesses is typical in healthy individuals.