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A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document concludes that managing side effects of MS therapies is crucial for treatment success and patient adherence.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

The triterpenoids from Ganoderma lucidum can block testosterone effects and may help treat enlarged prostate.

Hair loss gene found on chromosome 3q26.

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

Six new hair loss factors in men not linked to female hair loss.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Finasteride safely treats hair loss without harming hormones or reproduction, but may slightly reduce sexual function.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Indian Gooseberry has potential for cancer prevention and treatment and promotes hair growth.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Maintaining DNA integrity in stem cells is crucial to prevent aging and cancer.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

The PDGF/PDGFR pathway is a potential drug target with mixed success in treating various diseases, including some cancers and fibrosis.

Certain inhibitors slow down plant growth by causing early cell specialization without changing the cell development pattern.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The article concludes that while we understand a lot about how melanocytes age and how this can prevent cancer, there are still unanswered questions about certain pathways and genes involved.