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

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.

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

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.

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

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.

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

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

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.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Porphyra-334 may help reduce wrinkles and promote hair growth.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.