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The fuzzy gene is crucial for controlling hair growth cycles.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

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

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Stress stops hair growth in mice by causing early hair growth phase end and harmful inflammation through a specific nerve-related pathway.

Researchers found a new mutation causing total hair loss from birth.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

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

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

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

Mutations in the KRT85 gene cause hair and nail problems.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Prostaglandin E2 helps prevent hair loss from radiotherapy by protecting hair growth cells and aiding self-repair.

Telogen effluvium is a condition where hair falls out due to various factors like illness, stress, or nutrient deficiency.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

Hair loss from Telogen Effluvium usually gets better within 6 months after addressing the cause.

Stress can stop hair growth in mice, and treatments can reverse this effect.

Blocking BMP signaling causes hair loss and disrupts hair growth cycles.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Telogen effluvium is a common type of hair loss that can resolve on its own or become chronic, with treatment depending on early diagnosis.

Aryl hydrocarbon receptor overexpression found in miniaturized hair follicles in female hair loss.

Dexamethasone speeds up hair loss in mice, while cyclosporin A slows it down.

Roxithromycin, an antibiotic, can increase hair growth and might be used as a treatment for hair loss.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Chronic Telogen Effluvium may resolve after years and is diagnosed by examining the patient's history and clinical signs, with treatment aimed at underlying causes and possibly minoxidil.

Teloptosis is a key point in hair loss that could help in creating prevention-focused hair care strategies.

UVB radiation harms hair growth and health, causing cell death and other changes in human hair follicles.