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Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

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

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

A genetic variant linked to hair thinning in Japanese women was found.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

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

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

The research found specific genes that may cause longer hair in Tianzhu White Yak.

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

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

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

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.

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

A specific genetic deletion in goats affects cashmere yield and thickness.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

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.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

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.

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

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A mother's diet at conception can cause lasting genetic changes in her child.