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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The search scheme SMRI is faster and more secure for retrieving encrypted data from the cloud.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Scientists successfully edited a goat's genes to grow more and longer cashmere hair.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

Researchers found a new mutation causing total hair loss from birth.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

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

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

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

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Rac1 is essential for proper hair structure and color.

Deleting the CRIF1 gene in mice disrupts skin and hair formation, certain proteins affect hair growth, a new compound may improve skin and hair health, blood cell-derived stem cells can create skin-like structures, and hair follicle stem cells come from embryonic cells needing specific signals for development.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Loss of keratin K2 causes skin problems and inflammation.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

MOF controls skin development by regulating genes for mitochondria and cilia.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Cells in hair follicles help create fat cells in the skin by releasing a protein called Sonic Hedgehog.