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Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Allopregnanolone changes gene expression in glioblastoma cells.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

MSC-protein helps regenerate gum tissue and bone.

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

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.

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.

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

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.

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

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

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

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

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.

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.

Miniaturized hairs stay connected to muscle in alopecia areata, allowing possible regrowth, but not in androgenetic alopecia.

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

Transplant success has improved with better immunosuppressive drugs and donor matching.

Patients with advanced breast cancer and high hormone receptor levels who had surgery for ovarian/pelvic metastases lived longer, especially if they had high estrogen receptor levels.

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

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

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

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Researchers found two genes that may explain why some Casertana pigs don't have hair.