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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

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

A new gene mutation linked to a skin condition was found in a Spanish family.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

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

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

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

A specific genetic deletion in goats affects cashmere yield and thickness.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

CCC1 is essential for ion balance and proper plant cell function.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A specific gene mutation causes woolly hair and hair loss.

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

New genetic mutations causing hair loss were found in a Chinese family.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A mutation in the KRTHB5 gene causes hair and nail issues.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

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

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.