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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Low-dose radiation therapy may improve brain function in some Alzheimer's patients and is generally well-tolerated.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

Innate lymphoid cells help control skin bacteria by regulating sebaceous glands.

Dlx3 is essential for hair growth and regeneration.

Vitamin D receptor helps control hair growth and could be used to treat certain skin tumors.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

SkQ1 antioxidant improved health and lifespan in mice.

Low selenium levels can extend lifespan but worsen health issues.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

No link found between new male baldness genes and female hair loss.