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Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

lncRNAs may regulate hair follicle development in Hu sheep.

Hidradenitis suppurativa is a chronic skin disorder linked to genetics, lifestyle, and immune issues, treatable with medications and surgery.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

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

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Certain genes are linked to the risk of developing Alopecia Areata.

The HPV type 11 region activates hair-specific gene expression in mice.

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

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Hair follicle stem cell transplants can reverse liver cirrhosis by blocking harmful cell activation.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

HLD10 can include increased body hair and Mongolian spots.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

A genetic marker linked to a type of hair loss was found in most patients studied.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Ocu-miR-205 helps control hair growth in Rex rabbits by affecting cell processes and signaling pathways.

A specific gene mutation causes sparse, brittle hair in a family.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

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

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

The PML protein helps prevent skin cancer in mice.

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

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.