 Tomozumi Takatani, Ph.D., M.D.
| Title | Research Fellow in Medicine (EXT) |
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| Institution | Joslin Diabetes Center |
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| Department | Medicine |
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| Address | Joslin Diabetes Center
Research - 4th Floor
One Joslin Place
Boston MA 02215
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| Phone | 617/309-2400 |
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 Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications.
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Nagasaka H, Okano Y, Kimura A, Mizuochi T, Sanayama Y, Takatani T, Nakagawa S, Hasegawa E, Hirano K, Mochizuki H, Ohura T, Ishige-Wada M, Usui H, Yorifuji T, Tsukahara H, Hirayama S, Ohtake A, Yamato S, Miida T. Oxysterol changes along with cholesterol and vitamin D changes in adult phenylketonuric patients diagnosed by newborn mass-screening. Clin Chim Acta. 2013 Feb 1; 416:54-9.
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Nagasaka H, Yorifuji T, Bandsma RH, Takatani T, Asano H, Mochizuki H, Takuwa M, Tsukahara H, Inui A, Tsunoda T, Komatsu H, Hiejima E, Fujisawa T, Hirano K, Miida T, Ohtake A, Taguchi T, Miwa I. Sustained high plasma mannose less sensitive to fluctuating blood glucose in glycogen storage disease type Ia children. J Inherit Metab Dis. 2013 Jan; 36(1):75-81.
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Hayashi H, Inamura K, Aida K, Naoi S, Horikawa R, Nagasaka H, Takatani T, Fukushima T, Hattori A, Yabuki T, Horii I, Sugiyama Y. AP2 adaptor complex mediates bile salt export pump internalization and modulates its hepatocanalicular expression and transport function. Hepatology. 2012 Jun; 55(6):1889-900.
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Ishikawa H, Kiyokawa T, Takatani T, Wen WG, Shozu M. Giant multilocular sex cord tumor with annular tubules associated with precocious puberty. Am J Obstet Gynecol. 2012 Jan; 206(1):e14-6.
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Kinoshita K, Minagawa M, Takatani T, Takatani R, Ohashi M, Kohno Y. Establishment of diagnosis by bisulfite-treated methylation-specific PCR method and analysis of clinical characteristics of pseudohypoparathyroidism type 1b. Endocr J. 2011; 58(10):879-87.
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Fujii K, Matsuo K, Takatani T, Uchikawa H, Kohno Y. Multiple cavitations in posterior reversible leukoencephalopathy syndrome associated with hemolytic-uremic syndrome. Brain Dev. 2012 Apr; 34(4):318-21.
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Nagasaka H, Tsukahara H, Takatani T, Sanayama Y, Takayanagi M, Ohura T, Sakamoto O, Ito T, Wada M, Yoshino M, Ohtake A, Yorifuji T, Hirayama S, Miida T, Fujimoto H, Mochizuki H, Hattori T, Okano Y. Cross-sectional study of bone metabolism with nutrition in adult classical phenylketonuric patients diagnosed by neonatal screening. J Bone Miner Metab. 2011 Nov; 29(6):737-43.
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Takatani T, Minagawa M, Takatani R, Kinoshita K, Kohno Y. AMP-activated protein kinase attenuates Wnt/ß-catenin signaling in human osteoblastic Saos-2 cells. Mol Cell Endocrinol. 2011 Jun 6; 339(1-2):114-9.
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Nagasaka H, Yorifuji T, Takatani T, Okano Y, Tsukahara H, Yanai H, Hirano K, Hui SP, Hirayama S, Ito T, Chiba H, Miida T. CD36 deficiency predisposing young children to fasting hypoglycemia. Metabolism. 2011 Jun; 60(6):881-7.
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Takatani T, Matsuo K, Kinoshita K, Takatani R, Minagawa M, Kohno Y. A novel missense mutation in the AVPR2 gene of a Japanese infant with nephrogenic diabetes insipidus. J Pediatr Endocrinol Metab. 2010 Apr; 23(4):415-8.
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Miwa I, Taguchi T, Asano H, Murata T, Yorifuji T, Nagasaka H, Takatani T. Low level of fasting plasma mannose in a child with glycogen storage disease type 0 (liver glycogen synthase deficiency). Clin Chim Acta. 2010 Jul 4; 411(13-14):998-9.
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Nagasaka H, Yorifuji T, Kobayashi K, Takikawa H, Komatsu H, Inui A, Fujisawa T, Miida T, Tsukahara H, Takatani T, Hayashi H. Favorable effect of 4-phenylacetate on liver functions attributable to enhanced bile salt export pump expression in ornithine transcarbamylase-deficient children. Mol Genet Metab. 2010 Jun; 100(2):123-8.
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Nagasaka H, Okano Y, Aizawa M, Miida T, Yorifuji T, Tajima G, Sakura N, Takatani T, Sanayama Y, Sugamoto K, Mayumi M, Kobayashi K, Hirano K, Takayanagi M, Tsukahara H. Altered metabolisms of mediators controlling vascular function and enhanced oxidative stress in asymptomatic children with congenital portosystemic venous shunt. Metabolism. 2010 Jan; 59(1):107-13.
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Watanabe Y, Inoue Y, Takatani T, Arai H, Yasuda T. Self-limited lupus-like presentation of human parvovirus B19 infection in a 1-year-old girl. Pediatr Int. 2009 Jun; 51(3):411-2.
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Nagasaka H, Yorifuji T, Momoi T, Yorifuji J, Hirano K, Ota A, Takatani T, Tsukahara H, Takayanagi M, Kobayashi K, Chiba H, Sato Y, Miida T. Lipoprotein profiles in children with two common cholesteryl ester transfer protein gene mutations, D442G and I14A, during the first year of life. Clin Chim Acta. 2009 Aug; 406(1-2):52-6.
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Nagasaka H, Tsukahara H, Yorifuji T, Miida T, Murayama K, Tsuruoka T, Takatani T, Kanazawa M, Kobayashi K, Okano Y, Takayanagi M. Evaluation of endogenous nitric oxide synthesis in congenital urea cycle enzyme defects. Metabolism. 2009 Mar; 58(3):278-82.
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Nagasaka H, Yorifuji T, Hirano K, Ota A, Toyama-Nakagawa Y, Takatani T, Tsukahara H, Kobayashi K, Takayanagi M, Inomata Y, Uemoto S, Miida T. Effects of bezafibrate on dyslipidemia with cholestasis in children with familial intrahepatic cholestasis-1 deficiency manifesting progressive familial intrahepatic cholestasis. Metabolism. 2009 Jan; 58(1):48-54.
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Takatani T, Arai H, Fujii K, Yasuda T, Kohno Y. A posterior fossa lipoma extending into the cervical spine and subcutaneous space via a cranium bifidum. Brain Dev. 2008 Oct; 30(9):603-5.
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Nagasaka H, Miida T, Hirano K, Ota A, Murayama K, Yorifuji T, Kobayashi K, Takatani T, Tsukahara H, Hui SP, Takayanagi M, Chiba H. Fluctuation of lipoprotein metabolism linked with bile acid-activated liver nuclear receptors in Alagille syndrome. Atherosclerosis. 2008 Jun; 198(2):434-40.
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Nagasaka H, Miida T, Hirano K, Ota A, Yorifuji T, Takatani T, Tsukahara H, Takayanagi M, Hui SP, Kobayashi K, Chiba H. Reduced apolipoprotein E-rich high-density lipoprotein level at birth is restored to the normal range in patients with familial hypercholesterolemia in the first year of life. J Clin Endocrinol Metab. 2008 Mar; 93(3):779-83.
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Nagasaka H, Hirano K, Ohtake A, Miida T, Takatani T, Murayama K, Yorifuji T, Kobayashi K, Kanazawa M, Ogawa A, Takayanagi M. Improvements of hypertriglyceridemia and hyperlacticemia in Japanese children with glycogen storage disease type Ia by medium-chain triglyceride milk. Eur J Pediatr. 2007 Oct; 166(10):1009-16.
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Nagasaka H, Yorifuji T, Murayama K, Kubota M, Kurokawa K, Murakami T, Kanazawa M, Takatani T, Ogawa A, Ogawa E, Yamamoto S, Adachi M, Kobayashi K, Takayanagi M. Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency. Eur J Pediatr. 2006 Sep; 165(9):618-24.
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