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CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

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

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Fat-related cells are important for initiating hair growth.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

Stem cells and their surrounding environment in hair follicles work closely together, affecting hair growth and having implications for cancer and tissue regeneration.

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

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The Hairless gene is crucial for healthy skin and hair growth.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Most clinicians follow discharge guidelines, many lupus patients don't use sunscreen regularly, dithranol is effective for psoriasis, biopsy methods should be based on lesion type, voriconazole may raise skin cancer risk, a new scale can help diagnose female hair loss early, and most melanomas may develop from existing moles.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

Mitochondrial dysfunction is linked to various skin conditions and could be a target for treatments.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

The symposium concluded that understanding the molecular mechanisms of skin aging could lead to better clinical practices and treatments.

Enzymes called PADIs play a key role in hair growth and loss.

Scalp melanoma, a deadly skin cancer, is often found late due to its hard-to-see location, especially in older men. Early detection, possible treatments, and the role of hairdressers in spotting it early are discussed. More research is needed to improve detection and treatment.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

CD4+ skin cells may be precursors to basal cell carcinoma.