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C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Targeting CXXC5 and GSK-3β may help treat male pattern baldness.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Wnt5a overexpression alone doesn't cause psoriasis in mice but affects hair growth.

CUX1 boosts sheep hair cell growth and affects curl patterns.

Mouse models help target specific genes in lymphatic cells for research.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Twist2 is essential for proper skin healing and hair growth in developing mice.

Whn is essential for hair growth, and its malfunction causes hair loss.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

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

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

IL-1 receptor absence in mice leads to skin cysts and changes in immune response after UVB exposure.

Mouse Notch is important for determining cell roles in hair follicles.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

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

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.