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Methylene blue staining effectively reveals detailed nerve structures in rat snouts.

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Activating androgen receptors in muscle can increase muscle mass and reduce fat.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Skin organoids can model tuberculosis infection and help test treatments.

Melanin granules can be expelled by exocytosis.

Sebaceous glands help study fatty acid transporters and binding proteins.

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

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Different hair follicles in the skin are innervated by unique combinations of mechanosensory neurons, crucial for touch sensation.

Mouse and human skin development share similar fibroblast timelines.

Lower levels of MYLK and CALD1 in bladder cancer and osteosarcoma are linked to worse survival rates.

Monilethrix hair issues are due to problems in the hair's internodes.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

Hair medullary cells in mammals vary in complexity, with humans having more structured cells similar to inner root sheath cells.

Amelanotic melanocytes from hair follicles are immature and likely don't transfer melanosomes to keratinocytes.

Trichoblastomas in aged house musk shrews show unique features and may involve serum amyloid A in inflammation.

Researchers found a way to make rat hair follicle cells start turning into motor neuron-like cells, but couldn't fully turn them into working motor neurons.

Human hair keratin scaffolds help repair injured muscles by breaking down and activating muscle cell growth.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Specific keratin gene mutations can cause monilethrix.

MTS24 marks a new type of skin cell that helps hair growth and repair.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.