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Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Certain gene variations increase the risk of alopecia areata in Koreans.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Acne is a common skin condition that can be influenced by diet, lifestyle, and hormones, and requires a treatment approach that includes psychological considerations.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Maintaining DNA integrity in stem cells is crucial to prevent aging and cancer.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

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

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

The circadian clock is crucial for tissue renewal and regeneration, affecting stem cell functions and having implications for health and disease.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Pregnancy can increase lupus activity, but careful planning and treatment can improve outcomes.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Stress hormone corticosterone blocks a growth factor to slow down hair stem cell activity and hair growth.

Muscles and nerves that cause goosebumps also help control hair growth.