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No link found between specific genes and female pattern hair loss.

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

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Genetic variations affecting skin structure play a key role in severe acne.

MC4R gene variants not linked to female hair loss.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

The Drug Ontology was updated to better classify drugs for hypertension, malaria, and opioid abuse, and to allow for more accurate research queries.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

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

Androgens can cause hair growth in some areas and hair loss on the scalp.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Polycystic ovary syndrome, a disorder causing menstrual issues and infertility, can be treated with lifestyle changes, medication, herbal remedies, surgery, and assisted reproductive techniques like artificial insemination and IVF.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

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

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.

Mutations in the KRT85 gene cause hair and nail problems.

White piedra is a rare hair infection treated with oral and topical antifungals.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.