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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

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

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

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

Hair loss treatments work better with lifestyle changes.

Research on Hutchinson-Gilford progeria syndrome could help understand normal aging and heart disease.

Scarless healing is complex and influenced by genetics and environment, while better understanding could improve scar treatment.

The paper suggests that hair loss might be caused by skull growth, not just DHT's effect on hair follicles, and calls for more research.

The research identifies genes linked to wool quality in sheep and provides insights to improve wool production.

New treatments and strategies are needed for Alopecia Areata, focusing on immune response and better trial designs.

Psoriasis involves immune and genetic factors, and understanding these can improve treatments.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

Hypothyroidism may cause certain types of hair loss.

Skin aging reflects overall body aging and can indicate internal health conditions.

Studying rare genetic disorders can help us understand and treat common diseases better.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

FPHL is a common, age-related, genetic hair loss with unclear causes and limited treatment options.

Advancements in hair follicle culture have led to better understanding and potential treatments for hair loss.

Female pattern hair loss in women is caused by hormones and genetics, leading to hair thinning, with various treatments available.

Some maize lines resist stalk rot better due to specific genes and enzyme activities.

The Gsdma3 gene is essential for normal hair development in mice.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

Minoxidil promotes hair growth but exact mechanism is unknown.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

Methotrexate is a key, cost-effective drug for skin conditions, but requires careful monitoring for side effects.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.