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New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Researchers found 15 new genetic links to skin traits in Japanese women.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Antiandrogen therapy helps treat genetic hair loss.

Researchers found two new genetic variants linked to Alzheimer's disease.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

AGA is a genetic, hormonal hair loss treated with finasteride, minoxidil, and supplements, but new compounds are being developed.

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

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

The document explains the genetic causes and characteristics of inherited hair disorders.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

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

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

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.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

pCLCA2 protein may help maintain skin structure and function.

WWP2 is crucial for tooth development in mice.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.