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Sex hormones may affect COVID-19 severity, with men often faring worse, and targeting related pathways could offer treatment options.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

Alopecia patients struggle with emotions and stress, and improving emotional intelligence may help manage hair loss.

Different drug doses approved in Japan and the U.S. are not mainly due to different clinical responses, and ethnic factors should be considered in setting drug doses.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Red blood cell folate levels are reliable indicators of long-term folate status in alopecia areata patients.

Male children's genital development issues can be caused by genetic mutations or environmental factors affecting hormone action.

Hair loss patterns differ between males and females due to 5 master regulators and JAK-STAT signaling affects hair growth.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

Insufficient androgen action in male fetuses can cause genital development issues due to genetic mutations or environmental chemicals.

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

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

The interdigital gland of Vembur sheep shows sex-based differences in size and chemical makeup, possibly affecting communication and disease protection.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

ECM changes may play a role in hair loss, with differences between males and females.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Different races and genders have unique skin and hair issues, requiring specialized care and more research for effective treatment.