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Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Key genes linked to hair growth and cancer were identified in hairless mice.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The SOSTDC1 gene is crucial for determining sheep wool type.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Alopecia Areata has no guaranteed treatment for hair regrowth, but options like corticosteroids and minoxidil are used, with future research focusing on genetic and immune therapies.

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.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

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

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.