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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

A new mouse mutation causes skin and hair defects due to a gene change.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

LSD1 is crucial for regenerating hair cells in zebrafish.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

pbn-STAC effectively finds strategies for cellular reprogramming using deep reinforcement learning.

VILLIN4 helps root hair growth by organizing actin with calcium.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

Identifying specific genes helps improve goat breeding for better traits like growth and milk production.

The Tyrolean Iceman had mostly Anatolian farmer ancestry and traits like darker skin and a risk for certain health issues.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

RNA delivery is best for in-body use, while RNP delivery is good for outside-body use. Both methods are expected to greatly impact future treatments.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

Orai1 protein is crucial for tooth development and affects enamel thickness and mineralization.

Promising treatments for EBS include anti-inflammatory drugs, antibiotics, creams, mTOR inhibitors, and gene editing, but more trials are needed.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Ten miRNAs may play key roles in starting secondary hair follicle development in sheep foetuses.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Forensic DNA phenotyping faces challenges like inconsistent terms and limited genetic knowledge.