[HTML][HTML] Causal relationship between the loss of RUNX3 expression and gastric cancer
QL Li, K Ito, C Sakakura, H Fukamachi, K Inoue, XZ Chi… - Cell, 2002 - cell.com
Runx3/Pebp2αC null mouse gastric mucosa exhibits hyperplasias due to stimulated
proliferation and suppressed apoptosis in epithelial cells, and the cells are resistant to growth-…
proliferation and suppressed apoptosis in epithelial cells, and the cells are resistant to growth-…
[PDF][PDF] The Hippo signaling pathway components Lats and Yap pattern Tead4 activity to distinguish mouse trophectoderm from inner cell mass
N Nishioka, K Inoue, K Adachi, H Kiyonari, M Ota… - Developmental cell, 2009 - cell.com
Outside cells of the preimplantation mouse embryo form the trophectoderm (TE), a process
requiring the transcription factor Tead4. Here, we show that transcriptionally active Tead4 can …
requiring the transcription factor Tead4. Here, we show that transcriptionally active Tead4 can …
Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog
…, T Fujita, T Furuichi, K Ito, K Inoue… - Genes & …, 2004 - genesdev.cshlp.org
The differentiation of mesenchymal cells into chondrocytes and chondrocyte proliferation
and maturation are fundamental steps in skeletal development. Runx2 is essential for …
and maturation are fundamental steps in skeletal development. Runx2 is essential for …
[HTML][HTML] Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease
M Khajavi, K Inoue, JR Lupski - European journal of human genetics, 2006 - nature.com
The nonsense-mediated decay (NMD) pathway is an mRNA surveillance system that typically
degrades transcripts containing premature termination codons (PTCs) in order to prevent …
degrades transcripts containing premature termination codons (PTCs) in order to prevent …
[HTML][HTML] 15-deoxy-Δ12,14-PGJ2 induces synoviocyte apoptosis and suppresses adjuvant-induced arthritis in rats
…, D Bishop-Bailey, K Inoue… - The Journal of …, 2000 - Am Soc Clin Investig
Peroxisome proliferator–activated receptors (PPARs) are members of the nuclear hormone
receptor superfamily and have a dominant regulatory role in adipocyte and monocyte …
receptor superfamily and have a dominant regulatory role in adipocyte and monocyte …
Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations
K Inoue, M Khajavi, T Ohyama, S Hirabayashi… - Nature …, 2004 - nature.com
The molecular mechanisms by which different mutations in the same gene can result in
distinct disease phenotypes remain largely unknown. Truncating mutations of SOX10 cause …
distinct disease phenotypes remain largely unknown. Truncating mutations of SOX10 cause …
[PDF][PDF] Polarity-dependent distribution of angiomotin localizes Hippo signaling in preimplantation embryos
Background In preimplantation mouse embryos, the first cell fate specification to the
trophectoderm or inner cell mass occurs by the early blastocyst stage. The cell fate is controlled by …
trophectoderm or inner cell mass occurs by the early blastocyst stage. The cell fate is controlled by …
Inhibition of human lung cancer cell growth by the peroxisome proliferator-activated receptor-γ agonists through induction of apoptosis
…, S Mukai, R Yamada, M Kohno, K Inoue… - Biochemical and …, 2000 - Elsevier
Peroxisome proliferator-activated receptors (PPARs), members of the nuclear hormone
receptors superfamily, have an important regulatory role in adipogenesis and inflammation. …
receptors superfamily, have an important regulatory role in adipogenesis and inflammation. …
Runx3 controls the axonal projection of proprioceptive dorsal root ganglion neurons
K Inoue, S Ozaki, T Shiga, K Ito, T Masuda… - Nature …, 2002 - nature.com
Dorsal root ganglion (DRG) neurons specifically project axons to central and peripheral
targets according to their sensory modality. The Runt-related genes Runx1 and Runx3 are …
targets according to their sensory modality. The Runt-related genes Runx1 and Runx3 are …
Molecular mechanisms for genomic disorders
K Inoue, JR Lupski - Annual review of genomics and human …, 2002 - annualreviews.org
▪ Abstract Genomic rearrangements play a major role in the pathogenesis of human genetic
diseases. Nonallelic homologous recombination (NAHR) between low-copy repeats (LCRs) …
diseases. Nonallelic homologous recombination (NAHR) between low-copy repeats (LCRs) …