Search

everythinglearnresearchcommunity

for

Search:↓

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Vitamin D receptor is crucial for skin wound healing.

Hataedock treatment improved skin health and reduced atopic dermatitis symptoms by enhancing the skin barrier and reducing inflammation.

Too much Smad7 changes skin and hair development by breaking down a protein called β-catenin, leading to more oil glands and fewer hair follicles.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

Ptprq has multiple forms that change during inner ear development.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

The Wnt/β-catenin pathway helps tissue regeneration but can also cause fibrosis, and drugs that inhibit this pathway may aid in healing skin and heart tissues.

Fetal skin heals without scarring due to unique cells and processes not present in adult skin healing.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Epidermal keratinocytes start wound healing and inflammation after schistosome infection.

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

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.

Adult esophageal cells can start to become like skin cells, with a key pathway influencing this change.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The study found a link between the severity of Lichen Planopilaris seen by doctors and the details seen under a microscope, and created a new way to measure this severity.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

The method increases stem-like cells for better skin regeneration.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Skin cells called dermal fibroblasts are important for skin growth, hair growth, and wound healing.

Understanding how baby skin heals without scars could help develop treatments for adults to heal wounds without leaving scars.