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

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

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

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

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

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

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

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

RNA can be extracted from horsehair roots for analysis.

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

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

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.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

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.

Certain metabolites can either protect against or increase the risk of hair loss.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.