Nishinakamura, Ryuichi

Sall1 is a transcriptional regulator defining microglia identity and function

Buttgereit, A., Lelios, I., Yu, X., Vrohlings, M., Krakoski, N. R., Gautier, E. L., Nishinakamura, R., Becher, B., & Greter, M. (2016) · Nature Immunology

Neuroinflammation and Neurodegeneration MechanismsNeurogenesis and neuroplasticity mechanisms

Cited by 570

Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development

Nishinakamura, R., Matsumoto, Y., Nakao, K., Nakamura, K., Sato, A., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., Scully, S., Lacey, D. L., et al. (2001) · Development

Renal and related cancersDevelopmental Biology and Gene Regulation

Cited by 358

The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development

Sakaki-Yumoto, M., Kobayashi, C., Sato, A., Fujimura, S., Matsumoto, Y., Takasato, M., Kodama, T., Aburatani, H., Asashima, M., Yoshida, N., et al. (2006) · Development

Developmental Biology and Gene RegulationCongenital heart defects research

Cited by 264

Sall4 regulates cell fate decision in fetal hepatic stem/progenitor cells

Oikawa, T., Kamiya, A., Kakinuma, S., Zeniya, M., Nishinakamura, R., Tajiri, H., & Nakauchi, H. (2009) · Gastroenterology

Liver physiology and pathologyDevelopmental Biology and Gene Regulation

Cited by 108

Sall4 Is Essential for Stabilization, But Not for Pluripotency, of Embryonic Stem Cells by Repressing Aberrant Trophectoderm Gene Expression

Yuri, S., Fujimura, S., Nimura, K., Takeda, N., Toyooka, Y., Fujimura, Y.-I., Aburatani, H., Ura, K., Koseki, H., Niwa, H., et al. (2009) · Stem Cells

Pluripotent Stem Cells ResearchDevelopmental Biology and Gene Regulation

Cited by 103

Sall4 controls differentiation of pluripotent cells independently of the Nucleosome Remodelling and Deacetylation (NuRD) complex

Miller, A., Ralser, M., Kloet, S. L., Loos, R., Nishinakamura, R., Bertone, P., Vermeulen, M., & Hendrich, B. (2016) · Development

Pluripotent Stem Cells ResearchDevelopmental Biology and Gene Regulation

Cited by 78

Mouse homolog of SALL1, a causative gene for Townes–Brocks syndrome, binds to A/T‐rich sequences in pericentric heterochromatin via its C‐terminal zinc finger domains

Yamashita, K., Sato, A., Asashima, M., Wang, P., & Nishinakamura, R. (2007) · Genes to Cells

Genomics and Chromatin DynamicsGenomic variations and chromosomal abnormalities

Cited by 52

Sall1 regulates cortical neurogenesis and laminar fate specification, implications for neural abnormalities in Townes Brocks Syndrome

Harrison, S. J., Nishinakamura, R., Jones, K. R., & Monaghan, A. P. (2011) · Disease Models & Mechanisms

Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene Regulation

Cited by 42

Sall4 regulates neuromesodermal progenitors and their descendants during body elongation in mouse embryos

Tahara, N., Kawakami, H., Chen, K. Q., Anderson, A., Yamashita Peterson, M., Gong, W., Shah, P., Hayashi, S., Nishinakamura, R., Nakagawa, Y., et al. (2019) · Development

Developmental Biology and Gene RegulationPluripotent Stem Cells Research

Cited by 35