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Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

CAP7.1 is generally safe at 200 mg/m²/day, but can cause fatigue, nausea, hair loss, fever, and blood-related issues.

Researchers found a gene mutation responsible for a rare hair loss condition.

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

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

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Hair loss in androgenic alopecia patients is linked to changes in certain genes that control cell growth and death.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Researchers found a non-functional sheep keratin gene due to mutations.

Grasp protein helps maintain skin health after UVB exposure.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

The boy likely has a fungal infection causing hair loss.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

PPARγ signaling modulation can protect hair follicle stem cells from chemotherapy-induced damage.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Activating PPAR-γ signalling can protect hair follicle stem cells from damage caused by chemotherapy.

The BASP classification is a detailed and accurate way to categorize hair loss in both men and women.