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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

FGF-1 causes spiral ganglion neurites to branch more.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

Pannexin 3 is important for bone formation and the development of bone cells.

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

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A specific gene mutation causes woolly hair and hair loss.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Disrupting the Sox21 gene in mice causes hair loss and regrowth cycles.

Citrullinated proteins from Porphyromonas gingivalis may contribute to rheumatoid arthritis.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Legumes use flavonoids to start a process with rhizobia for nitrogen fixation, involving specific genes and proteins.

Msx2 deficiency in mice leads to bone growth and organ development problems.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Arabidopsis plants adjust gene expression to maintain balance when auxin pathways are disrupted.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Cannabis has anti-inflammatory and antimicrobial properties, but more research is needed on its effects on plant and aquatic animal pathogens.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.