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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

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

Portable point-of-care testing can improve quick and accurate genetic disorder detection.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The B2 genes are crucial for hair growth in rats.

Keratins are important for skin cell health and their problems can cause diseases.

Non-coding RNAs help control hair growth cycles in cashmere goats, suggesting ways to improve cashmere production.

Monilethrix is linked to a gene cluster on chromosome 12.

FoxN1 gene is crucial for proper thymus structure and normal skin appearance.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Hair follicles and urine cell pellets are promising for transcriptome studies due to consistent quality and useful expression profiles.

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

Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

NIPT can help detect potential maternal cancer, and GIPXplore can identify immune diseases in pregnancies.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

New LSS gene variants help understand congenital hypotrichosis 14 better.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.