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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.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

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

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

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

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.

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

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

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

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 certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

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.

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.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

The conclusion is that hair loss in women is caused by a mix of hormonal, environmental, and genetic factors, and treatments should target these various causes.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Gene regulation could revolutionize hair color by altering pigmentation from within.