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Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

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

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Children generally have milder SARS symptoms than adults, with good outcomes and no deaths reported, but long-term effects are unclear.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

STK11 gene polymorphism does not predict metformin response in PCOS.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Mutant mice help researchers understand hair growth and related genetic factors.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

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

Genetically modified plants could be an important source of omega-3 fats to meet global needs.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Genetically modifying a bacteria and changing its growth conditions significantly increased the production of a chemical called dipicolinic acid.