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An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

The study identified key immune cell differences between mild and severe alopecia areata.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A rabbit gene important for hair development was identified and detailed.

The KRTAP36-2 gene in sheep affects wool yield.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

A rare genetic condition can mimic symptoms of other diseases, making diagnosis challenging.

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

Pax9 is crucial for proper tongue surface development and preventing skin-like changes.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.

Different genes affect hair length in yaks.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

SNP profiling allows personalized skincare treatments for better results and fewer side effects.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The SAM model helps understand aging and related diseases.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

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

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

Mutations in the HOXC13 gene cause hair and nail development issues.