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The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

A20 protein is crucial for normal skin and hair development.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

Alopecia areata involves immune response and gene changes affecting hair loss.

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

Different hair loss types need accurate diagnosis for proper treatment.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

CDP is crucial for lung and hair follicle cell development.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.

FFA's causes may include environmental triggers and genetic factors.

Zinc can both inhibit and stimulate mouse hair growth, and might help recover hair after chemotherapy.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

Hair follicle culture helps develop new treatments for hair loss.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Hairless gene not strongly linked to baldness.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Low zinc levels may be linked to the return of gynecologic cancers.

Terbinafine can cause hair loss.