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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

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

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

The study concluded that genetic mutations affect human hair diseases and identified key genes and pathways involved in hair growth and cycling.

Researchers found a genetic region that influences the number of coat layers in dogs.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Gene differences may affect baldness treatment response in Korean men.

Alisertib was found to be an effective and tolerable treatment for children with recurrent brain tumors.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

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

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Researchers identified specific genes that are important for mouse skin cell development and healing.