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Vitamin D receptor helps control hair growth genes in skin cells.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Using neurohormones to control keratin can lead to new skin disease treatments.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

White-tailed deer can get a hair loss condition that might make them more vulnerable to environmental threats.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Hair splitting and nail detachment are linked conditions.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Keratin mutations cause skin diseases and could lead to new treatments.

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

CD2 might be a new treatment target for patchy alopecia areata.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Hair diseases can have psychological effects and should be treated with a combination of psychosomatic care, therapy, and medication.

Epidermal stem cells could lead to new treatments for skin and hair disorders.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The document concludes that different types of hair loss have specific treatments, and early diagnosis is crucial for preventing permanent hair loss.

Different hair care practices and conditions affect African American hair and scalp health, requiring specialized knowledge for treatment.

The document concludes that accurate diagnosis and appropriate management are crucial for treating various hair disorders, which have significant psychological impacts.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

Six genetic conditions are often linked to complete scalp hair loss in children.

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