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

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.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

S100A3 protein is crucial for hair shaft formation in mice.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

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

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

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

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

Scientists found a gene in mice that causes early hearing loss.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Chromosomal differences affect how muscle cells respond to testosterone.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

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

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.