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Mammals might fail to regenerate not because they lack the right cells, but because of how cells respond to their surroundings, and changing this environment could enhance regeneration.

EVAL membranes help create cell structures that can regrow hair follicles.

Fat-derived stem cells, platelet-rich plasma, and biomaterials show promise for healing chronic skin wounds and improving soft tissue with few side effects.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

New methods to improve the healing abilities of mesenchymal stem cells for disease treatment are promising but need more research.

Oral retinoids can cause side effects ranging from mild to severe, including birth defects, and require careful monitoring and contraception.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

NSAIDs may not affect soft tissue healing but should be used carefully for bone fractures and more research is needed to understand sex differences in response.

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

Hair follicles are valuable for regenerative medicine and wound healing.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Androgens affect bone and fat cell development differently based on the cells' embryonic origin.

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

Systemic retinoids are effective for psoriasis but have side effects; benefits may outweigh risks, especially when reducing cancer risks from other treatments.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

The document concludes that careful surgical methods and choosing the right materials are key for successful scalp, skull, and frontal sinus reconstruction.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

The new FDA labeling rules provide more detailed drug safety information for pregnant and breastfeeding women, but more data is needed on the risks of many dermatologic drugs.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

New patents show progress in developing drugs targeting the Wnt pathway for diseases like cancer and hair loss.

Women with polycystic ovary syndrome have a higher risk of certain fractures.