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High levels of male hormones and irregular periods best predict how well PCOS patients will respond to metformin treatment.

A specific gene mutation causes long hair in Angora rabbits.

Certain microRNAs are important for sheep hair follicle development and could help improve wool quality.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Adipose-derived stem cells help heal burns but need more research.

Mesenchymal stem cells could help treat aging-related diseases better than current methods.

Most children recovered from COVID-19 in 4 weeks, but some experienced long-term symptoms, especially older kids.

A gene mutation in Lama3 is linked to a common type of hair loss.

Stem cell therapies could be a promising alternative for hair loss treatment, but more research is needed to understand their full potential and safety.

DNA markers can help predict male pattern baldness, useful in criminal and missing person cases.

Alopecia areata needs more recognition and better treatment access in Latin America to improve patient care and outcomes.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

A mother's iron levels early in pregnancy can influence the DNA makeup of her child, potentially affecting the child's health.

Scalp melanoma is more common and easier to diagnose early in people with androgenetic alopecia due to sun damage.

The document summarized various dermatology studies and case reports.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

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

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Low serum complement levels in SLE patients don't always match with disease flares; monitoring C3 and C4 is useful, but cell-bound complement products might better indicate disease activity.

Mitochondrial therapy and platelet-rich plasma therapy both stimulated hair regrowth in aging mice, with mitochondrial therapy showing similar effectiveness to plasma therapy.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Vitamin D receptor helps control hair growth and could be used to treat certain skin tumors.

Vitamin D receptor may help protect against UV-induced skin cancer.