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Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Vitiligo causes white skin patches and can lead to psychological stress.

Extracellular vesicles may effectively treat hair loss with minimal side effects.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Women with PCOS had higher SRAGE levels, possibly linked to BMI, not PCOS.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Hormonal treatments like birth control pills can improve acne in women with excess hair growth and hormone imbalances.

Understanding how melanocyte stem cells work could lead to new treatments for hair graying and skin pigmentation disorders.

Experts recommend using evidence-based methods to diagnose and treat hirsutism, focusing on symptoms and underlying causes.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Oral isotretinoin may slightly improve acne but increases the risk of side effects like dry lips and skin; more research is needed to understand its full risks and benefits.

The document concludes that more research is needed on treatments for hair loss in both men and women, especially on medication combinations and their benefits.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

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.

Tumescent fluid increases scalp hair angles, which may improve hair transplant results and reduce surgeon fatigue.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

Understanding skin structure and development helps diagnose and treat skin disorders.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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

Keratins are important for skin cell health and their problems can cause diseases.

Notch-related genes play a key role in the development and cycling of hair follicles.

Dr. Rochelle Torgerson says female-pattern hair loss is often hereditary, starts after puberty, and can be slowed with treatments like Minoxidil. It can also indicate other health issues.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Hair loss discovery causes stress; talking to dermatologists helps.