Hattori S - Search Results

1

Arrhythmia induced by spatiotemporal overexpression of calreticulin in the heart.

Hattori K, Nakamura K, Hisatomi Y, Matsumoto S, Suzuki M, Harvey RP, Kurihara H, Hattori S, Yamamoto T, Michalak M, Endo F. Hattori K, et al. Among authors: hattori s. Mol Genet Metab. 2007 Jul;91(3):285-93. doi: 10.1016/j.ymgme.2007.02.003. Epub 2007 May 4. Mol Genet Metab. 2007. PMID: 17482496

2

Isolation, tissue localization, and cellular characterization of progenitors derived from adult human salivary glands.

Sato A, Okumura K, Matsumoto S, Hattori K, Hattori S, Shinohara M, Endo F. Sato A, et al. Among authors: hattori s, hattori k. Cloning Stem Cells. 2007 Summer;9(2):191-205. doi: 10.1089/clo.2006.0054. Cloning Stem Cells. 2007. PMID: 17579552

3

Intracellular distribution of the Wilson's disease gene product (ATPase7B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease.

Nagano K, Nakamura K, Urakami KI, Umeyama K, Uchiyama H, Koiwai K, Hattori S, Yamamoto T, Matsuda I, Endo F. Nagano K, et al. Among authors: hattori s. Hepatology. 1998 Mar;27(3):799-807. doi: 10.1002/hep.510270323. Hepatology. 1998. PMID: 9500710

4

A mouse model of renal tubular injury of tyrosinemia type 1: development of de Toni Fanconi syndrome and apoptosis of renal tubular cells in Fah/Hpd double mutant mice.

Sun MS, Hattori S, Kubo S, Awata H, Matsuda I, Endo F. Sun MS, et al. Among authors: hattori s. J Am Soc Nephrol. 2000 Feb;11(2):291-300. doi: 10.1681/ASN.V112291. J Am Soc Nephrol. 2000. PMID: 10665936

5

Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuria.

Nakazato H, Yoshimuta J, Karashima S, Matsumoto S, Endo F, Matsuda I, Hattori S. Nakazato H, et al. Among authors: hattori s. Kidney Int. 1999 Jan;55(1):63-70. doi: 10.1046/j.1523-1755.1999.00231.x. Kidney Int. 1999. PMID: 9893114 Free article.

6

Complete rescue of lethal albino c14CoS mice by null mutation of 4-hydroxyphenylpyruvate dioxygenase and induction of apoptosis of hepatocytes in these mice by in vivo retrieval of the tyrosine catabolic pathway.

Endo F, Kubo S, Awata H, Kiwaki K, Katoh H, Kanegae Y, Saito I, Miyazaki J, Yamamoto T, Jakobs C, Hattori S, Matsuda I. Endo F, et al. Among authors: hattori s. J Biol Chem. 1997 Sep 26;272(39):24426-32. doi: 10.1074/jbc.272.39.24426. J Biol Chem. 1997. PMID: 9305902 Free article.

7

Another autosomal recessive form of focal glomerulosclerosis with neurological findings.

Nakazato H, Hattori S, Karashima S, Kawano T, Seguchi S, Kanahori M, Endo F. Nakazato H, et al. Among authors: hattori s. Pediatr Nephrol. 2002 Jan;17(1):16-9. doi: 10.1007/s004670200003. Pediatr Nephrol. 2002. PMID: 11793129

8

In situ evaluation of podocin in normal and glomerular diseases.

Horinouchi I, Nakazato H, Kawano T, Iyama K, Furuse A, Arizono K, Machida J, Sakamoto T, Endo F, Hattori S. Horinouchi I, et al. Among authors: hattori s. Kidney Int. 2003 Dec;64(6):2092-9. doi: 10.1046/j.1523-1755.2003.00303.x. Kidney Int. 2003. PMID: 14633131 Free article.

9

Identification of a single base insertion in the COL4A5 gene in Alport syndrome.

Nakazato H, Hattori S, Matsuura T, Koitabashi Y, Endo F, Matsuda I. Nakazato H, et al. Among authors: hattori s. Kidney Int. 1993 Nov;44(5):1091-6. doi: 10.1038/ki.1993.353. Kidney Int. 1993. PMID: 8264140 Free article.

10

Membranoproliferative glomerulonephritis in congenital portosystemic shunt without liver cirrhosis.

Karashima S, Hattori S, Nakazato H, Awata H, Seguchi S, Ikeda S, Sera Y, Endo F. Karashima S, et al. Among authors: hattori s. Clin Nephrol. 2000 Mar;53(3):206-11. Clin Nephrol. 2000. PMID: 10749300

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