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Metformin works better for adolescent girls with PCOS who have certain genetic variations.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Personalized treatments for hair loss are becoming more effective by using genetic information.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Treatments for common hair loss include minoxidil, finasteride, and hair transplantation.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Skin varies in thickness, color, and features due to complex genetic and cellular processes.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

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.

Men with more advanced male pattern baldness have a higher risk of prostate cancer and more severe disease.

aPKCλ is essential for hair follicle stem cell maintenance and wound healing.

Scientists developed tools to observe hair regeneration in real time and assess skin health, using glowing mice and light-controlled genes.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

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

The conclusion is that PCOS is caused by ovarian sensitivity to hormones and disrupted hormone control, possibly due to ovarian factors, and more research is needed.

Female Pattern Hair Loss affects women's self-esteem and needs more research for better treatment.

Hormones and genetics affect hair growth and patterns, with some changes reversible and others not.

Vitiligo causes white skin patches and is linked to autoimmune issues.

Insulin resistance contributes to hormone imbalances in many women with polycystic ovary syndrome.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Whale genes show changes that help them live in water, like less hair and better flippers.

The document concludes that various treatments, including laser therapy, are effective for managing pseudofolliculitis barbae, especially in darker skin types.

The document concludes that diagnosing PCOS in teenagers is difficult and should focus on specific hormone levels and menstrual irregularities, while also considering treatment for symptoms and related health issues.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.