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The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

A teenage girl with high androgen levels and PCOS developed a rare liver tumor, suggesting a possible link between high androgens and the tumor's growth.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

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

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

Researchers found that certain RNA molecules might play a role in the growth of Cashmere goat hair.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

Certain transporters are found in human hair follicles and may affect hair growth and loss.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

Potassium channel openers show promise for treating heart disease and other conditions, but more research is needed to fully understand their effects and safety.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

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

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

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

ATP increases melanin production in skin after UV exposure, with the P2X7 receptor being crucial for this process.

Finasteride improves hair growth and reduces hirsutism in women, but side effects and optimal dosages need further research.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A new gene mutation linked to a skin condition was found in a Spanish family.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

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

Finasteride helps hair growth by decreasing cell death in hair follicles.

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