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The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The first in-prison dermatology clinic in the U.S. faced challenges and found certain skin conditions common among inmates, with rare cases of serious skin cancer.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

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

The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

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

Rosacea is a skin condition with unclear causes, classified into four subtypes.

Msx2 deficiency in mice leads to bone growth and organ development problems.

The woman has a rare, harmless skin condition specific to pregnancy that causes itchy bumps and will go away after she gives birth.

Vitamin D is crucial for skin health and managing skin diseases.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

Lambs fed a liquid diet showed abnormal wool and skin, which improved with more B-vitamins, suggesting a link to B-vitamin deficiency.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

The project created a standardized system for classifying skin lesions in lab rats and mice.

The document says that there are treatments for hair and nail diseases.

Hair and nail changes can indicate health issues, including cancer and side effects from cancer treatments.

Psychotropic drugs can cause hair loss or excessive hair growth.

Chemotherapy causes hair loss by damaging hair follicles and stem cells, with more research needed for prevention and treatment.

Children's hair grows in different types from before birth through puberty, with growth rates and characteristics varying by age, sex, and race.

Cedrol from Platycladus orientalis leaves may promote hair growth effectively, especially in female mice.

A hair strand caused a rare case of limb strangulation in a teenage girl with autism, and the condition is not always linked to child abuse.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

The most common causes of hair loss in children in South-East Nigeria are fungal infections and alopecia areata.

The document explains how to identify different hair problems using a microscope.