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The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

Researchers found a gene mutation responsible for a rare hair loss condition.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

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

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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 SOSTDC1 gene is crucial for determining sheep wool type.

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

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

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

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Melatonin affects gene expression in goat hair follicles, potentially increasing cashmere production.