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Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

CDP is crucial for lung and hair follicle cell development.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

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

Lamins are vital for cell survival, organ development, and preventing premature aging.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Whale genes show changes that help them live in water, like less hair and better flippers.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

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

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The Hairless gene is crucial for healthy skin and hair growth.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

FGF13 gene changes cause excessive hair growth in a rare condition.

New treatments for COVID-19 show promise, but more effective antiviral drugs are needed.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.