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Dr. Rodney Sinclair uses a detailed grading system to diagnose female pattern hair loss, recommends daily spironolactone and minoxidil for treatment, and believes genetics play a role in the condition.

Hormonal interactions, especially involving DHT and estrogen, play a key role in BPH development and treatment.

Low androgen levels might delay prostate cancer but could lead to more aggressive, therapy-resistant cancers.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The vitamin D receptor can work without its usual activating molecule.

Skin wounds can create fat cells that help regenerate hair follicles, with BMP signaling playing a crucial role in this process.

The document concludes that signs of male and female pattern baldness include uneven hair thickness, yellow spots, skin discoloration around hair follicles, more thin and soft hairs, and many hair follicles with just one hair.

Sebaceous glands can heal and regenerate after injury using their own stem cells and help from hair follicle cells.

Men with high genetic risk for Polycystic Ovary Syndrome (PCOS) have increased chances of obesity, type 2 diabetes, heart disease, and hair loss, showing PCOS risk factors can affect both genders.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

Researchers developed a new method to clearly see and label hair proteins with minimal errors using advanced freezing and microscopy techniques.

Trichoscopy effectively diagnoses and assesses the severity of androgenetic alopecia.

The conclusion is that future trials should report specific details about the PRP composition to better understand its effects on urologic conditions.

Two patients with lupus had an unusual type of hair loss not typical for the disease.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The twins' condition is unique and doesn't match any known syndromes.

Mitochondrial reactive oxygen species are essential for skin and hair development.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Scientists successfully edited a goat's genes to grow more and longer cashmere hair.

Trichoscopy is useful for detecting and monitoring androgenetic alopecia.

Trichoscopy, a hair loss evaluation technique, found that people with Androgenetic Alopecia have more thin hairs, yellow dots, and perifollicular discoloration than healthy individuals.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

Methotrexate is a promising and safe treatment for severe alopecia areata, with better results when combined with corticosteroids.

COVID-19 patients often experience hair loss and scalp pain, which may be related to the severity of their infection and treatment drugs.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

A specific gene mutation causes congenital hair loss.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

Silymarin and metformin together most improved hormone levels and ovulation in women with PCOS.