Yokota I - Search Results

1

A unique mutation in the vitamin D receptor gene in three Japanese patients with vitamin D-dependent rickets type II: utility of single-strand conformation polymorphism analysis for heterozygous carrier detection.

Saijo T, Ito M, Takeda E, Huq AH, Naito E, Yokota I, Sone T, Pike JW, Kuroda Y. Saijo T, et al. Among authors: yokota i. Am J Hum Genet. 1991 Sep;49(3):668-73. Am J Hum Genet. 1991. PMID: 1652893 Free PMC article.

2

Three novel SURF-1 mutations in Japanese patients with Leigh syndrome.

Ogawa Y, Naito E, Ito M, Yokota I, Saijo T, Shinahara K, Kuroda Y. Ogawa Y, et al. Among authors: yokota i. Pediatr Neurol. 2002 Mar;26(3):196-200. doi: 10.1016/s0887-8994(01)00382-4. Pediatr Neurol. 2002. PMID: 11955926

3

Clinical and biochemical findings in parents of children with vitamin D-dependent rickets Type II.

Yokota I, Takeda E, Ito M, Kobashi H, Saijo T, Kuroda Y. Yokota I, et al. J Inherit Metab Dis. 1991;14(2):231-40. doi: 10.1007/BF01800596. J Inherit Metab Dis. 1991. PMID: 1653381

4

25-Hydroxyvitamin D-24-hydroxylase in phytohemagglutinin-stimulated lymphocytes: intermediate bioresponse to 1,25-dihydroxyvitamin D3 of cells from parents of patients with vitamin D-dependent rickets type II.

Takeda E, Yokota I, Ito M, Kobashi H, Saijo T, Kuroda Y. Takeda E, et al. Among authors: yokota i. J Clin Endocrinol Metab. 1990 Apr;70(4):1068-74. doi: 10.1210/jcem-70-4-1068. J Clin Endocrinol Metab. 1990. PMID: 2156884

5

Pyruvate dehydrogenase deficiency caused by a four-nucleotide insertion in the E1 alpha subunit gene.

Naito E, Ito M, Yokota I, Matsuda J, Yara A, Kuroda Y. Naito E, et al. Among authors: yokota i. Hum Mol Genet. 1994 Jul;3(7):1193-4. doi: 10.1093/hmg/3.7.1193. Hum Mol Genet. 1994. PMID: 7981697 No abstract available.

6

Vitamin D-dependent rickets type II: regulation of human osteocalcin gene expression in cells with defective vitamin D receptors by 1,25-dihydroxyvitamin D-3, retinoic acid, and triiodothyronine.

Takeda E, Miyamoto K, Kubota M, Minami H, Yokota I, Saijo T, Naito E, Ito M, Kuroda Y. Takeda E, et al. Among authors: yokota i. Biochim Biophys Acta. 1994 Nov 29;1227(3):195-9. doi: 10.1016/0925-4439(94)90095-7. Biochim Biophys Acta. 1994. PMID: 7986828

7

Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency.

Naito E, Ito M, Yokota I, Saijo T, Ogawa Y, Kuroda Y. Naito E, et al. Among authors: yokota i. J Neurol Sci. 2002 Sep 15;201(1-2):33-7. doi: 10.1016/s0022-510x(02)00187-9. J Neurol Sci. 2002. PMID: 12163191

8

Thiamine-responsive pyruvate dehydrogenase deficiency in two patients caused by a point mutation (F205L and L216F) within the thiamine pyrophosphate binding region.

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Ogawa Y, Kitamura S, Takada E, Horii Y, Kuroda Y. Naito E, et al. Among authors: yokota i. Biochim Biophys Acta. 2002 Oct 9;1588(1):79-84. doi: 10.1016/s0925-4439(02)00142-4. Biochim Biophys Acta. 2002. PMID: 12379317 Free article.

9

Screening for disorders of pyruvate metabolism by measuring the ratio of the rates of lactate production and pyruvate decarboxylation in cultured skin fibroblasts.

Kuroda Y, Kawakami I, Kobashi H, Naito E, Ito M, Saijo T, Yokota I, Takeda E. Kuroda Y, et al. Among authors: yokota i. Clin Chim Acta. 1991 May 31;199(1):17-22. doi: 10.1016/0009-8981(91)90004-v. Clin Chim Acta. 1991. PMID: 1934498

10

Effect of long-term treatment with massive doses of 1 alpha-hydroxyvitamin D3 on calcium-phosphate balance in patients with vitamin D-dependent rickets type II.

Takeda E, Yokota I, Saijo T, Kawakami I, Ito M, Kuroda Y. Takeda E, et al. Among authors: yokota i. Acta Paediatr Jpn. 1990 Feb;32(1):39-43. doi: 10.1111/j.1442-200x.1990.tb00782.x. Acta Paediatr Jpn. 1990. PMID: 2158205

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