Hayashi, Masaharu

Production and function of monocyte chemoattractant protein-1 and other β-chemokines in murine glial cells

Hayashi, M., Luo, Y., Laning, J., Strieter, R. M., & Dorf, M. E. (1995) · Journal of Neuroimmunology

Neuroinflammation and Neurodegeneration MechanismsChemokine receptors and signaling

Cited by 226

Selective Depletion of Molecularly Defined Cortical Interneurons in Human Holoprosencephaly with Severe Striatal Hypoplasia

Fertuzinhos, S., Krsnik, Ž., Kawasawa, Y. I., Rašin, M.-R., Kwan, K. Y., Chen, J.-G., Judaš, M., Hayashi, M., & Šestan, N. (2009) · Cerebral Cortex

Neurogenesis and neuroplasticity mechanismsFetal and Pediatric Neurological Disorders

Cited by 106

Long-term melatonin treatment for the sleep problems and aberrant behaviors of children with neurodevelopmental disorders

Yuge, K., Nagamitsu, S., Ishikawa, Y., Hamada, I., Takahashi, H., Sugioka, H., Yotsuya, O., Mishima, K., Hayashi, M., & Yamashita, Y. (2020) · BMC Psychiatry

Circadian rhythm and melatoninSleep and related disorders

Cited by 57

Oxidative stress in developmental brain disorders

Hayashi, M., Miyata, R., & Tanuma, N. (2012) · Advances in Experimental Medicine and Biology

Metabolism and Genetic DisordersAntioxidant Activity and Oxidative Stress

Cited by 56

Nationwide survey of Cockayne syndrome in Japan: Incidence, clinical course and prognosis

Kubota, M., Ohta, S., Ando, A., Koyama, A., Terashima, H., Kashii, H., Hoshino, H., Sugita, K., & Hayashi, M. (2015) · Pediatrics International

Genomics and Rare DiseasesGenetic and rare skin diseases.

Cited by 50

A neuropathological study of a case of the prader-willi syndrome with an interstitial deletion of the proximal long arm of chromosome 15

Hayashi, M., Itoh, M., Kabasawa, Y., Hayashi, H., Satoh, J., & Morimatsu, Y. (1992) · Brain and Development

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 45