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The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Targeting IL-15 may help treat Alopecia Areata.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

New mutations in the DSG4 gene cause a rare hair condition.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

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

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

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

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

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

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Disabling the FGF5 gene in sheep leads to longer wool.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.