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Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Low-penetration genes might help personalize colorectal cancer prevention.

Mutations in specific llama genes may affect fiber quality for textiles.

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

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

A 50 mg non-loading dose of ritlecitinib is safe for adults and adolescents.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Melatonin affects when and how certain genes work during the different stages of goat hair growth.

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

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Robertsonian translocation can cause recurrent miscarriages.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Spt4 and Spt6 are essential for fat cell development.

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

QLT0267 stops hair follicle cell growth and movement.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.