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TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

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

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Notch/RBP-J signaling is crucial for proper placement and timing of melanocyte development in hair follicles.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Basement membrane changes are crucial for hair follicle development.

Quick diagnosis and biotin treatment can dramatically improve biotinidase deficiency symptoms.

Vitamin D receptor helps control hair growth genes in skin cells.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

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

FLCN helps control iron levels in cells.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

KLHL24-mutant stem cells help understand skin and heart disease.

Bubble microneedles deliver drugs quickly and effectively through the skin and mouth.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Lack of KSR1 stops certain skin tumors in mice.

Metformin/dopamine-derived carbon dots help heal bacteria-infected wounds faster.