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The conclusion is that in the Indian subcontinent, socioeconomic status, stress, and family structure affect the severity of alopecia areata, and its psychological impact is generally mild or moderate.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Kids with alopecia areata may experience more stress but not necessarily feel more anxious or depressed than others.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

More adolescent girls in urban areas of India have Polycystic Ovary Syndrome compared to those in rural areas.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Diet changes can protect against harmful environmental effects on fetal development.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

Selective breeding can enhance immunity in dairy cattle.

Insulin resistance is linked to PCOS and can lead to other health issues, but treatments like metformin can help manage symptoms.

Sox6 is important in heart and kidney health, affecting diseases like diabetes, heart disease, and high blood pressure.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

The document concludes that blocking the internal pathways that create androgens might help treat cancers that depend on sex hormones.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

TRPV4 helps cells repair tissue and reduce scarring by controlling calcium levels.

Male and female pattern hair loss have different molecular pathways, suggesting unique treatment targets for each sex.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

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

The B2 genes are crucial for hair growth in rats.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

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

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Mutations in hKAP1 genes may cause hereditary hair disorders.