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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

CE-PTG detects early hair follicle issues in balding areas, helping measure male hair loss.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

Hair restoration techniques and new cell sources improve hair loss treatments.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Androstanediol glucuronide is a reliable marker for hirsutism in women.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

PCOS may have evolved as an advantage in past environments with food scarcity.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

The document concludes that various treatments, including laser therapy, are effective for managing pseudofolliculitis barbae, especially in darker skin types.

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.

Early onset baldness in men may indicate a condition similar to PCOS, linked to heart disease, diabetes, and prostate issues.

Macrophages are essential for successful skin growth in reconstructive surgery.

Certain drugs change freshwater snail shells to a "banana" shape.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.

Skin varies in thickness, color, and features due to complex genetic and cellular processes.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Vitamin D may help reduce antibody levels in men with autoimmune thyroiditis and early-onset androgenic alopecia, but has no significant impact on thyroid function.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Human hair follicle cells can grow hair when put into mouse skin if they stay in contact with mouse cells.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

Excluding alopecia and mucous membrane components from the CLASI-A score reduces its effectiveness in capturing important disease activity.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.