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Hormones and sex affect potassium channel gene expression in electric fish, influencing their communication signals.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

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

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

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

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

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.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

Mouse skin can produce and process serotonin, with variations depending on hair cycle, body location, and mouse strain.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

A specific gene change in APCDD1 increases the risk of hair loss.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Epidermal stem cells create and maintain skin structures like hair and nails through specific signaling pathways and vary by location and function.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.