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Certain gene variations may increase the risk of hair loss in Egyptians.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

The visfatin GT genotype may increase the risk of Alopecia Areata.

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

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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

Testosterone replacement is recommended for men with low testosterone levels and symptoms of hypogonadism.

Curcuma aeruginosa rhizome extracts show potential as anticancer agents, with varying effectiveness against breast cancer cells.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Explosions don't stop hair proteins from being used to identify people.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Hair protein analysis might help identify a person's ethnicity, sex, and age in forensics.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Autophagy is crucial for normal sebaceous gland function and sebum composition.