| Transcriptional coactivator with PDZ-binding motif is essential for normal alveolarization in mice. Mitani A., Nagase T., Fukuchi K., Aburatani H., Makita R., Kurihara H.
Am. J. Respir. Crit. Care Med. 180:326-338(2009) · Mapped (14) |
| Thyroid transcription factor-1 inhibits transforming growth factor-beta-mediated epithelial-to-mesenchymal transition in lung adenocarcinoma cells. Saito R.A., Watabe T., Horiguchi K., Kohyama T., Saitoh M., Nagase T., Miyazono K.
Cancer Res. 69:2783-2791(2009) · Mapped (2) |
| The novel protein complex with SMARCAD1/KIAA1122 binds to the vicinity of TSS. Okazaki N., Ikeda S., Ohara R., Shimada K., Yanagawa T., Nagase T., Ohara O., Koga H.
J. Mol. Biol. 382:257-265(2008) · Mapped (6) |
| Smurf1 directly targets hPEM-2, a GEF for Cdc42, via a novel combination of protein interaction modules in the ubiquitin-proteasome pathway. Yamaguchi K., Ohara O., Ando A., Nagase T.
Biol. Chem. 389:405-413(2008) · Mapped (12) |
| Multiple renal cysts, urinary concentration defects, and pulmonary emphysematous changes in mice lacking TAZ. Makita R., Uchijima Y., Nishiyama K., Amano T., Chen Q., Takeuchi T., Mitani A., Nagase T., Yatomi Y., Aburatani H. et al.
Am. J. Physiol. Renal Physiol. 294:F542-53(2008) · Mapped (29) |
| Heterotrimeric G protein betagamma subunits stimulate FLJ00018, a guanine nucleotide exchange factor for Rac1 and Cdc42. Ueda H., Nagae R., Kozawa M., Morishita R., Kimura S., Nagase T., Ohara O., Yoshida S., Asano T.
J. Biol. Chem. 283:1946-1953(2008) · UniProtKB (1) · Mapped (39) |
| Calcitonin gene-related peptide mediates acid-induced lung injury in mice. Aoki-Nagase T., Nagase T., Oh-Hashi Y., Kurihara Y., Yamaguchi Y., Yamamoto H., Nagata T., Kurihara H., Ouchi Y.
Respirology 12:807-813(2007) · Mapped (4) |
| The induction of H3K9 methylation by PIWIL4 at the p16Ink4a locus. Sugimoto K., Kage H., Aki N., Sano A., Kitagawa H., Nagase T., Yatomi Y., Ohishi N., Takai D.
Biochem. Biophys. Res. Commun. 359:497-502(2007) · UniProtKB (2) · Mapped (7) |
| Adrenomedullin insufficiency increases allergen-induced airway hyperresponsiveness in mice. Yamamoto H., Nagase T., Shindo T., Teramoto S., Aoki-Nagase T., Yamaguchi Y., Hanaoka Y., Kurihara H., Ouchi Y.
J. Appl. Physiol. 102:2361-2368(2007) · Mapped (2) |
| Solution structure of the SWIRM domain of human histone demethylase LSD1. Tochio N., Umehara T., Koshiba S., Inoue M., Yabuki T., Aoki M., Seki E., Watanabe S., Tomo Y., Hanada M. et al.
Structure 14:457-468(2006) · UniProtKB (1) |
| Absence of leukotriene B4 receptor 1 confers resistance to airway hyperresponsiveness and Th2-type immune responses. Terawaki K., Yokomizo T., Nagase T., Toda A., Taniguchi M., Hashizume K., Yagi T., Shimizu T.
J. Immunol. 175:4217-4225(2005) · Mapped (3) |
| Temporal change in mKIAA gene expression during the early stage of retinoic acid-induced neurite outgrowth. Imai K., Kawai M., Tada M., Nagase T., Ohara O., Koga H.
Gene 364:114-122(2005) · Mapped (3) |
| Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder. Hashimoto K., Kato Z., Nagase T., Shimozawa N., Kuwata K., Omoya K., Li A., Matsukuma E., Yamamoto Y., Ohnishi H. et al.
Pediatr. Res. 58:263-269(2005) · Mapped (2) |
| Angiogenesis within the developing mouse neural tube is dependent on sonic hedgehog signaling: possible roles of motor neurons. Nagase T., Nagase M., Yoshimura K., Fujita T., Koshima I.
Genes Cells 10:595-604(2005) · Mapped (3) |
| Alternative splice variants encoding unstable protein domains exist in the human brain. Homma K., Kikuno R.F., Nagase T., Ohara O., Nishikawa K.
J. Mol. Biol. 343:1207-1220(2004) · UniProtKB (14) |
| Prediction of the coding sequences of mouse homologues of FLJ genes: the complete nucleotide sequences of 110 mouse FLJ-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries. Okazaki N., Kikuno R., Ohara R., Inamoto S., Koseki H., Hiraoka S., Saga Y., Kitamura H., Nakagawa T., Nagase T. et al.
DNA Res. 11:127-135(2004) · UniProtKB (48) |
| Prediction of the coding sequences of mouse homologues of KIAA gene: IV. The complete nucleotide sequences of 500 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries. Okazaki N., Kikuno R., Ohara R., Inamoto S., Koseki H., Hiraoka S., Saga Y., Seino S., Nishimura M., Kaisho T. et al.
DNA Res. 11:205-218(2004) · UniProtKB (476) · Mapped (3) |
| The CAP-Gly domain of CYLD associates with the proline-rich sequence in NEMO/IKKgamma. Saito K., Kigawa T., Koshiba S., Sato K., Matsuo Y., Sakamoto A., Takagi T., Shirouzu M., Yabuki T., Nunokawa E. et al.
Structure 12:1719-1728(2004) · Mapped (8) |
| Voltage-gated sodium channel expressed in cultured human smooth muscle cells: involvement of SCN9A. Jo T., Nagata T., Iida H., Imuta H., Iwasawa K., Ma J., Hara K., Omata M., Nagai R., Takizawa H. et al.
FEBS Lett. 567:339-343(2004) · UniProtKB (1) |
| Platelet-activating factor receptor develops airway hyperresponsiveness independently of airway inflammation in a murine asthma model. Ishii S., Nagase T., Shindou H., Takizawa H., Ouchi Y., Shimizu T.
J. Immunol. 172:7095-7102(2004) · Mapped (2) |
| Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene. Shimozawa N., Tsukamoto T., Nagase T., Takemoto Y., Koyama N., Suzuki Y., Komori M., Osumi T., Jeannette G., Wanders R.J. et al.
Hum. Mutat. 23:552-558(2004) · UniProtKB (1) · Mapped (2) |
| CRM1-dependent, but not ARE-mediated, nuclear export of IFN-alpha1 mRNA. Kimura T., Hashimoto I., Nagase T., Fujisawa J.
J. Cell. Sci. 117:2259-2270(2004) · Mapped (4) |
| Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes. Nagase T., Shimozawa N., Takemoto Y., Suzuki Y., Komori M., Kondo N.
Biochim. Biophys. Acta 1671:26-33(2004) · Mapped (28) |
| Phosphorylation of clock protein PER1 regulates its circadian degradation in normal human fibroblasts. Miyazaki K., Nagase T., Mesaki M., Narukawa J., Ohara O., Ishida N.
Biochem. J. 380:95-103(2004) · UniProtKB (2) · Mapped (31) |
| Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. Shimozawa N., Nagase T., Takemoto Y., Suzuki Y., Kondo N.
Adv. Exp. Med. Biol. 544:71-71(2003) · Mapped (2) |
in Literature Citations
