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New melanoma treatments can cause skin side effects, including skin cancer and rashes, but combining treatments may reduce these risks.

Acitretin is effective for severe psoriasis and can be used long-term due to no immunosuppression, but must be carefully monitored for side effects and is not for pregnant women.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Beta-sitosterol has potential health benefits but needs more research to fully understand its effects and improve its use in treatments.

Gene differences may affect baldness treatment response in Korean men.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Shrunken heads retain some facial features and hair characteristics, allowing for limited individual identification.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

People with Down's syndrome are more likely to have syringomas.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Human hair follicle stem cells can turn into multiple cell types but lose some of this ability after being grown in the lab for a long time.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

A hospital outbreak of catheter infections in calves was caused by a bacteria from a beef herd, leading to longer hospital stays, more drug use, and calf deaths.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.