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Betamethasone dipropionate reduced skin thickness, fish oil increased it, and combined treatment had no significant effect.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Melatonin makes cashmere grow earlier and more by increasing certain gene activity in goats.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

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

The most common skin problems in polycystic ovarian disease are hirsutism and acne, and managing these symptoms is key for treatment.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Adenosine receptors could be promising targets for treating inflammatory skin diseases like psoriasis.

PRP helps skin heal, possibly through special cells called telocytes.

Most women with PCOS have insulin resistance, especially those with phenotype B.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Basement membrane changes are crucial for hair follicle development.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

Softer hydrogels help wounds heal better with less scarring.

Nanomaterials can significantly improve wound healing and future treatments may include smart, real-time monitoring.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

A new therapy for a skin blistering condition has not been developed yet.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.