Search

everythinglearnresearchcommunity

for

Search:↓

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

A soluble factor in developing mouse whisker pads boosts nerve growth factor mRNA production.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Old C57BL/6 mice with unsynchronized hair cycles show less melanin in their spleens.

Exosome therapy may help treat diabetic nerve damage, but more research is needed.

The skin basement membrane is specialized for different tissue interactions, important for hair growth and attachment.

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

Specific keratin gene mutations can cause monilethrix.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

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

Neurosteroids regulate synaptic inhibition in the spinal cord and may help manage spinal pain.

A300 membranes help skin heal faster by promoting cell growth and repair.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Schizophrenia patients' stem cells show abnormal neuron development and mitochondrial issues.

Researchers developed a new method to clearly see and label hair proteins with minimal errors using advanced freezing and microscopy techniques.

Heterotypic cell contacts likely help hair matrix cells differentiate during mouse hair follicle development.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

Microencapsulation helps protect and track therapeutic cells, showing promise for treating various diseases, but more work is needed to improve the technology.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Solid-state NMR can effectively study keratin structure and treatment effects in fur.

Exosomes from umbilical cord stem cells help protect hair color and health under stress.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Sheet formation is key to macrofibril structure differences in wool.

Keratin hydrogel from human hair helps rats recover better from spinal cord injuries.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Adult spiny mice recover better from heart attacks than common lab mice.