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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.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

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

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Human hair follicle stem cells can be isolated using specific markers for potential therapeutic use.

Calcium reduces involucrin in rat hair bulbs but doesn't affect filaggrin and Kdap.

Androgen conjugates might be better indicators of skin sensitivity to hormones in women with excessive hair growth.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Engineered vesicles from macrophages help hair growth in mice and humans.

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.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Dutasteride may help shrink prostate cancer tumors.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Alopecia areata can be triggered by specific immune cells without genetic or environmental factors.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

The document is a detailed medical reference on skin and genetic disorders.

Men using steroids or finasteride to look more attractive may harm their fertility and sexual function, creating a paradox where they seem fit but may be less able to reproduce.

The model accurately predicts age from saliva and buccal cells for forensic use.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The document concludes that there have been significant improvements in diagnosing and treating skin diseases, including melanoma, with new techniques and therapies.

Human Schwann cells can be quickly made from hair follicle stem cells for nerve repair.