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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The HCR gene contributes to psoriasis risk.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

Two new gene clusters important for hair formation were found on human chromosome 11.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Low IRES/Cap translation is linked to higher stem cell potential.

Gene variation affects prostate issues and hair loss.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Two new gene clusters important for hair formation were found on human chromosome 11.

FOXN1 duplication can cause excessive hair growth.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

A new gene mutation linked to a skin condition was found in a Spanish family.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.