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Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

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

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Keratin peptides can change hair shape gently without harsh chemicals.

Scientists improved an enzyme to better produce a hair growth-promoting chemical from an immunosuppressant.

Water and fatty acids affect hair's surface differently based on hair damage, and models can help understand hair-cosmetic interactions.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Insulin resistance and high male hormone levels are major causes of Polycystic Ovary Syndrome.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

P-selectin is not the only factor that prevents scarring in fetal wound healing in mice.

Mummy hair from the Taklamakan desert has calcium and phosphorus inside.

A genetic marker linked to a type of hair loss was found in most patients studied.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A new wound dressing with p-Coumaric acid helps heal diabetic wounds faster by reducing inflammation and promoting skin repair.

VB1953 gel significantly reduced acne and resistant bacteria in patients who didn't respond to clindamycin.

Certain genes may promote longer root hairs in plants when phosphorus is low.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Higher cortisol levels are linked to poor coping, while higher DHEA levels are linked to job confidence.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.