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Some wound-healing cells can turn into fat cells around new hair growth in mice.

Epigenetic changes control how adult stem cells work and can lead to diseases like cancer if they go wrong.

Adult stem cells are important for tissue repair and have therapeutic potential, but more research is needed to fully use them.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Melanocyte stem cells are crucial for skin pigmentation and have potential in disease modeling and regenerative medicine.

The study showed that hair follicle stem cells can maintain and organize themselves in a lab setting, keeping their ability to renew and form hair and skin.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

The cornified cell envelope forms a protective barrier in skin and hair, using specific proteins and lipids to maintain effectiveness.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

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

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

BMP2 needs periosteal tissue to help regenerate mouse middle finger bones within a specific time.

The method quickly analyzes hair growth genes and shows that blocking Smo in skin cells stops hair growth.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

New models predict male pattern baldness better than old ones but still need improvement.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.