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Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Seborrheic dermatitis is influenced by diet, genetics, and psychological factors.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Finasteride reduces prostate size and PSA levels in young patients.

Disulfide bonds in keratin fibers break more easily under stress, especially when wet, affecting fiber strength.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Hypothyroidism may cause certain types of hair loss.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Different hair loss types need accurate diagnosis for proper treatment.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

The skin's ability to produce hormones is linked to various skin conditions, and better understanding this process could lead to new treatments.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Non-coding RNAs help control hair growth in cashmere goats.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

The document concludes that diagnosing and treating hair loss is complex and requires understanding its psychological effects and underlying causes, while also calling for more research and new treatments.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.