Masako Yanazawa
Mitsubishi Group (Japan)(JP)Institute of Life Sciences(IN)
Publications by Year
Research Areas
Developmental Biology and Gene Regulation, Alzheimer's disease research and treatments, Genetics and Neurodevelopmental Disorders, Neuroscience and Neuropharmacology Research, Epigenetics and DNA Methylation
Most-Cited Works
- → Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans(2002)704 cited
- → Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra- and periocular mesoderm and right pulmonary isomerism(1999)460 cited
- → Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation(2004)327 cited
- → Expression of a novel aristaless related homeobox gene ‘Arx’ in the vertebrate telencephalon, diencephalon and floor plate(1997)179 cited
- → Isolation and Characterization of Patient-derived, Toxic, High Mass Amyloid β-Protein (Aβ) Assembly from Alzheimer Disease Brains(2009)172 cited
- → Expression patterns of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation(1997)138 cited
- → Na, K-ATPase α3 is a death target of Alzheimer patient amyloid-β assembly(2015)135 cited
- → Arxhomeobox gene is essential for development of mouse olfactory system(2005)109 cited
- → Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice(2009)93 cited
- → Expression of inhibin α-subunit gene during mouse gametogenesis(1990)26 cited