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

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

miR-200a reduces goose fibroblast growth by targeting PITX2 in the Wnt pathway.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Matriptase is crucial for skin, hair, and immune cell health, and its imbalance can lead to cancer.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

Sex steroids affect the MafB gene differently in male and female hamsters.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

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

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

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

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

The role of 5α-reductase-3 in prostate cancer is unclear and needs more research.

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.