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The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

Two mouse mutations cause similar hair loss despite different skin changes.

Certain immune markers may predict chemotherapy response in mesothelioma, and nivolumab is a tolerable and effective treatment for advanced non-small cell lung cancer.

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

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

NuMA-microtubule interactions are vital for proper skin structure formation and function.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

MOTILIPERM may help treat male infertility by reducing stress in cells.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

Mice can regenerate ear tissue without the p53 protein.

Mechanical stress causes ligament thickening through WISP-1 and Hedgehog signaling.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

Sebaceous glands help study fatty acid transporters and binding proteins.

Phospholipase C-δ1 is crucial for normal hair development.

OXI1 kinase is essential for plant defense and root hair growth in Arabidopsis.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

Stem cell-derived vesicles improve blood vessel growth in limbs.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Rac1 is crucial for normal hair structure and pigmentation.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.