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Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

New treatments targeting immune pathways show promise for severe hair loss but need more research for safety and effectiveness.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

Using neurohormones to control keratin can lead to new skin disease treatments.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

The document concludes that understanding hair follicles requires more research using computational methods and an integrative approach, considering the current limitations in hair treatment products.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

Altered retinoid metabolism in cicatricial alopecia suggests a balanced vitamin A diet may prevent the condition.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

People with Lichen Planopilaris are more likely to have autoimmune diseases, especially Systemic Lupus Erythematosus, and less likely to have diabetes and some other common conditions.

The enzymes 5α-reductase and 3α/β-hydroxysteroid oxidoreductase help create brain-active substances from progesterone and testosterone, which could be used for treatment, but more research is needed to ensure their safety and effectiveness.

Metformin helps regulate menstrual cycles, induce ovulation, and improve pregnancy outcomes in women with PCOS.

Understanding and treating hair disorders in different ethnic groups requires knowledge of specific hair care practices and hair characteristics.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Low vitamin D levels are common in people with Alopecia Areata.

The Drug Ontology was updated to better classify drugs for hypertension, malaria, and opioid abuse, and to allow for more accurate research queries.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

People with certain types of alopecia have a slightly higher risk of cancer, especially thyroid, bladder, and prostate cancers.

Blocking adenosine A2B receptor may prevent or treat hearing loss.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

The RORα gene is active in different parts of cashmere goat hair follicles and may be influenced by melatonin, especially in December when hair growth changes.

Using special RNA to target a mutant gene fixed hair problems in mice.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Methotrexate side effects vary by race and sex.

Specific genes influence hair and cashmere growth in Laiwu black goats.

Chronic inflammatory skin diseases are caused by disrupted interactions between skin cells and immune cells.

Animal models, especially mice, are essential for advancing hair loss research and treatment.