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

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

A new gene variant causes glucocorticoid resistance in a mother and son.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Hair loss gene found on chromosome 3q26.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Most hair follicle stem cells do not protect their DNA by dividing it unevenly.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A mutation in mice causes hair loss and immune problems.

A gene mutation in mice causes permanent hair loss and skin issues.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

New genes linked to male pattern baldness were found on chromosome 20p11.