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Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

HLA-DRB5 and other genes may be linked to alopecia universalis.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

The document concludes that various treatments, including laser therapy, are effective for managing pseudofolliculitis barbae, especially in darker skin types.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Scientists found a gene in mice that causes early hearing loss.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

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

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.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Hair follicles can regrow in wounded adult mouse skin using a process like embryo development.

Keratins help protect cells, aid in cancer diagnosis, and influence cancer behavior and treatment.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

Testosterone is important for men's sexual function, may help some women's sexual desire, while other hormones and neurotransmitters also play complex roles in sexual behavior.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

The Rotterdam Study aims to understand various diseases in older adults.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.