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Minoxidil decreases LH expression, while hydralazine has mixed effects on prolyl and lysyl hydroxylase activities.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

BAF200 is essential for proper heart and coronary artery formation.

The document concludes that treating tough skin disease in lupus involves sun protection, steroids, antimalarials, and various other therapies chosen based on individual risks and benefits.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

New treatments for lupus show promise, but more research is needed, especially for children.

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.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

The document concludes that the hCG protocol may help in obesity treatment and could be scientifically justified, but more research is needed.

New technologies help us better understand how skin microbes affect skin diseases.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

No genetic link between prostaglandins and hair loss found.

Certain bacteria can boost lentil growth and improve soil used for farming.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

The Itpr3 gene causes a specific hair pattern in mice.