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A specific protein in chicken embryos links early skin layers to feather development.

Researchers identified specific genes that are important for mouse skin cell development and healing.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The study found that expanded skin regenerates similarly to normal skin, with 77 genes playing a role in the process.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Researchers found a genetic region that influences the number of coat layers in dogs.

Sex hormones, especially estradiol, can change chicken feather shapes and colors.

Understanding and manipulating epigenetic changes can potentially lead to human organ regeneration therapies, but more research is needed to improve these methods and minimize risks.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

IL-36α helps grow new hair follicles and speeds up wound healing.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

A new botanical treatment improved hair growth and symptoms in lichen planopilaris patients.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Histone modification is key in treating chronic inflammatory skin diseases.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

The study provides insights into hair growth mechanisms in yaks.

Keratinocytes and adipose-derived stem cells can effectively heal difficult skin wounds.

EZH2 levels decrease as fetuses develop and are higher in adult skin, which may affect skin growth and repair.