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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 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.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Skin's uneven surface and hair follicles affect its stress and strain but don't change its overall strength, and help prevent the skin from peeling apart.

The symposium showed that stem cells are key for understanding and treating skin diseases and for developing new skin models and therapies.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Combining PRP with Minoxidil improves hair density and thickness more than Minoxidil alone.

Injectable treatments can effectively and safely improve hair growth in adults with androgenetic alopecia.