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Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Specialized ribosomes affect aging in human skin cells.

Platelet-rich Plasma (PRP) helps treat hair loss effectively, especially when prepared using the double-spin method.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

MicroRNA-21 could help diagnose and treat skin fibrosis.

Different types of stem cells and their environments are key to skin repair and maintenance.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

Metformin has limited effectiveness for improving PCOS symptoms and lacks clear benefits, needing more research to confirm its efficacy.

There is no causal relationship between androgenetic alopecia and serum uric acid.

Systemic lupus erythematosus treatment can restore vision in patients with retinal artery occlusion.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.