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Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Two mouse mutations cause similar hair loss despite different skin changes.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

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

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

Porphyra-334 may help reduce wrinkles and promote hair growth.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Blue light promotes hair growth by interacting with specific receptors in hair follicles.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Fetal cells could improve skin repair with minimal scarring and are a potential ready-to-use solution for tissue engineering.

Mutations in the KRT85 gene cause hair and nail problems.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Male hormones like testosterone may make COVID-19 worse, and testing for sensitivity to these hormones could help predict how severe a patient's symptoms might be. Treatments that reduce these hormones are being explored.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

Accurate diagnosis and timely, tailored treatments improve outcomes in obstetrics and gynecology.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Androgenic alopecia, a common hair loss condition, is linked to changes in androgen metabolism and genetics, and can be treated with finasteride and minoxidil, but these treatments are only fully effective in 10% of patients.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.