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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.

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

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

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

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

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

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

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

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

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

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

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The 25Up study collected extensive data on mental disorders and related factors in Australian twins and siblings to investigate the genetics of psychiatric illnesses.

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 yeast found in a sea lion's skin lesion was almost identical to that on healthy skin, suggesting environmental factors may affect fungal growth and the cause of the lesion is unclear.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

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.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

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

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

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