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21 . Academic Journal
Intrahepatic venous anastomosis formation of the right liver in living donor liver transplantation: Evaluations by Doppler ultrasonography and pulse-inversion ultrasonography with Levovist
저자
by
Kaneko, T
;
Sugimoto, H
;
Hirota, M
;
Kure, S
;
Kiuchi, T
, et al.
소스
SURGERY
; JUL 2005, 138 1, p21-p27, 7p.
Full Text (ScienceDirect)
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27 . Academic Journal
A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem
저자
by
Boneh, A
;
Korman, SH
;
Sato, K
;
Kanno, J
;
Matsubara, Y
, et al.
소스
JOURNAL OF HUMAN GENETICS
; MAY 2005, 50 5, p230-p234, 5p.
Scopus
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27 . Academic Journal
Mild glycine encephalopathy (NKH) in a large kindred due to a silent exonic GLDC splice mutation
저자
by
Flusser, H
;
Korman, SH
;
Sato, K
;
Matsubara, Y
;
Galil, A
, et al.
소스
NEUROLOGY
; APR 26 2005, 64 8, p1426-p1430, 5p.
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27 . Academic Journal
Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia
저자
by
Niihori, T
;
Aoki, Y
;
Ohashi, H
;
Kurosawa, K
;
Kondoh, T
, et al.
소스
JOURNAL OF HUMAN GENETICS
; APR 2005, 50 4, p192-p202, 11p.
Scopus
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27 . Academic Journal
Intrahepatic circulatory time analysis of an ultrasound contrast agent in liver cirrhosis
저자
by
Hirota, M
;
Kaneko, T
;
Sugimoto, H
;
Kure, S
;
Inoue, S
, et al.
소스
LIVER INTERNATIONAL
; APR 2005, 25 2, p337-p342, 6p.
Scopus
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27 . Academic Journal
Electrophysiological and histopathological characteristics of progressive atrioventricular block accompanied by familial dilated cardiomyopathy caused by a novel mutation of lamin A/C gene
저자
by
Otomo, J
;
Kure, S
;
Shiba, T
;
Karibe, A
;
Shinozaki, T
, et al.
소스
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
; FEB 2005, 16 2, p137-p145, 9p.
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27 . Academic Journal
Significant association between nonsyndromic oral clefts and arylhydrocarbon receptor nuclear translocator (ARNT)
저자
by
Kayano, S
;
Suzuki, Y
;
Kanno, K
;
Aoki, Y
;
Kure, S
, et al.
소스
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
; SEP 15 2004, 130A 1, p40-p44, 5p.
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27 . Academic Journal
Wild-type phenylalanine hydroxylase activity is enhanced by tetrahydrobiopterin supplementation in vivo: an implication for therapeutic basis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency
저자
by
Kure, S
;
Sato, K
;
Fujii, K
;
Aoki, Y
;
Suzuki, Y
, et al.
소스
MOLECULAR GENETICS AND METABOLISM
; SEP-OCT 2004, 83 1-2, p150-p156, 7p.
Full Text (ScienceDirect)
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27 . Academic Journal
Identification of polymorphisms in the promoter region of the human NRF2 gene
저자
by
Yamamoto, T
;
Yoh, K
;
Kobayashi, A
;
Ishii, Y
;
Kure, S
, et al.
소스
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
; AUG 11 2004, 321 1, p72-p79, 8p.
Full Text (ScienceDirect)
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27 . Academic Journal
Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B-12-responsive methylmalonic acidemia: identification of a prevalent MMAA mutation
저자
by
Yang, X
;
Sakamoto, O
;
Matsubara, Y
;
Kure, S
;
Suzuki, Y
, et al.
소스
MOLECULAR GENETICS AND METABOLISM
; AUG 2004, 82 4, p329-p333, 5p.
Full Text (ScienceDirect)
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