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Items: 1 to 20 of 170

1.

Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route.

Abalı S, Tamura M, Turan S, Atay Z, Isguven P, Güran T, Haliloglu B, Baş S, Isojima T, Kitanaka S, Bereket A.

J Pediatr Endocrinol Metab. 2020 Feb 12. pii: /j/jpem.ahead-of-print/jpem-2019-0466/jpem-2019-0466.xml. doi: 10.1515/jpem-2019-0466. [Epub ahead of print]

PMID:
32049653
2.

Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector.

Okumura T, Horie Y, Lai CY, Lin HT, Shoda H, Natsumoto B, Fujio K, Kumaki E, Okano T, Ono S, Tanita K, Morio T, Kanegane H, Hasegawa H, Mizoguchi F, Kawahata K, Kohsaka H, Moritake H, Nunoi H, Waki H, Tamaru SI, Sasako T, Yamauchi T, Kadowaki T, Tanaka H, Kitanaka S, Nishimura K, Ohtaka M, Nakanishi M, Otsu M.

Stem Cell Res Ther. 2019 Jun 24;10(1):185. doi: 10.1186/s13287-019-1273-2.

3.

Familial dysalbuminemic hyperthyroxinemia in a 12-year-old girl.

Oda Y, Tamura M, Kitanaka S.

Pediatr Int. 2019 May;61(5):520-522. doi: 10.1111/ped.13839. Epub 2019 May 14. No abstract available.

PMID:
31087584
4.

[Rickets/Osteomalacia. Vitamin D dependency.]

Kitanaka S.

Clin Calcium. 2018;28(10):1343-1349. doi: CliCa181013431349. Japanese.

PMID:
30269116
5.

Pyridoxal 5'-phosphate and related metabolites in hypophosphatasia: Effects of enzyme replacement therapy.

Akiyama T, Kubota T, Ozono K, Michigami T, Kobayashi D, Takeyari S, Sugiyama Y, Noda M, Harada D, Namba N, Suzuki A, Utoyama M, Kitanaka S, Uematsu M, Mitani Y, Matsunami K, Takishima S, Ogawa E, Kobayashi K.

Mol Genet Metab. 2018 Sep;125(1-2):174-180. doi: 10.1016/j.ymgme.2018.07.006. Epub 2018 Jul 17.

PMID:
30049651
6.

Facet Joint Osteoarthritis Affects Spinal Segmental Motion in Degenerative Spondylolisthesis.

Kitanaka S, Takatori R, Arai Y, Nagae M, Tonomura H, Mikami Y, Inoue N, Ogura T, Fujiwara H, Kubo T.

Clin Spine Surg. 2018 Oct;31(8):E386-E390. doi: 10.1097/BSD.0000000000000674.

PMID:
29912734
7.

Identification of Lycopodium Alkaloids Produced by an Ultraviolet-Irradiated Strain of Paraboeremia, an Endophytic Fungus from Lycopodium serratum var. longipetiolatum.

Ishiuchi K, Hirose D, Suzuki T, Nakayama W, Jiang WP, Monthakantirat O, Wu JB, Kitanaka S, Makino T.

J Nat Prod. 2018 May 25;81(5):1143-1147. doi: 10.1021/acs.jnatprod.7b00627. Epub 2018 Apr 20.

PMID:
29676580
8.

Identification of Two Phenanthrene Derivatives from Australasian Allied Species in Genus Dendrobium.

Takamiya T, Kitamura S, Suzuki S, Shioda N, Matsuo Y, Murase K, Kaiho Y, Tsurumaki Y, Fujiwara Y, Sone M, Machida T, Matsumoto R, Miyamoto A, Hirose D, Furukawa M, Makino M, Matsuzaki K, Kitanaka S, Yukawa T, Iijima H.

Chem Pharm Bull (Tokyo). 2018 Jun 1;66(6):642-650. doi: 10.1248/cpb.c18-00076. Epub 2018 Apr 5.

9.

Incidence rate and characteristics of symptomatic vitamin D deficiency in children: a nationwide survey in Japan.

Kubota T, Nakayama H, Kitaoka T, Nakamura Y, Fukumoto S, Fujiwara I, Hasegawa Y, Ihara K, Kitanaka S, Koyama S, Kusuda S, Mizuno H, Nagasaki K, Oba K, Sakamoto Y, Takubo N, Shimizu T, Tanahashi Y, Hasegawa K, Tsukahara H, Yorifuji T, Michigami T, Ozono K.

Endocr J. 2018 Jun 27;65(6):593-599. doi: 10.1507/endocrj.EJ18-0008. Epub 2018 Mar 10.

10.

A familial case of nail patella syndrome with a heterozygous in-frame indel mutation in the LIM domain of LMX1B.

Mukai M, Fujita H, Umegaki-Arao N, Sasaki T, Yasuda-Sekiguchi F, Isojima T, Kitanaka S, Amagai M, Kubo A.

J Dermatol Sci. 2018 Apr;90(1):90-93. doi: 10.1016/j.jdermsci.2017.12.010. Epub 2017 Dec 19.

PMID:
29290531
11.

3EZ, 20Ac-ingenol induces cell-specific apoptosis in cyclin D1 over-expression through the activation of ATR and downregulation of p-Akt.

Miyata S, Wang LY, Kitanaka S.

Leuk Res. 2018 Jan;64:46-51. doi: 10.1016/j.leukres.2017.08.007. Epub 2017 Aug 24.

PMID:
29179029
12.

Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia.

Tamura M, Ishizawa M, Isojima T, Özen S, Oka A, Makishima M, Kitanaka S.

Sci Rep. 2017 Jul 11;7(1):5102. doi: 10.1038/s41598-017-05081-x.

13.

Stereospecific inhibition of nitric oxide production in macrophage cells by flavanonols: Synthesis and the structure-activity relationship. Part 2.

Jiang WJ, Kitanaka S, Takamiya T, Iijima H.

Bioorg Med Chem. 2017 Aug 15;25(16):4277-4284. doi: 10.1016/j.bmc.2017.05.060. Epub 2017 Jun 15.

PMID:
28662961
14.

Vitamin D-Deficient Rickets in Japan.

Itoh M, Tomio J, Toyokawa S, Tamura M, Isojima T, Kitanaka S, Kobayashi Y.

Glob Pediatr Health. 2017 Jun 1;4:2333794X17711342. doi: 10.1177/2333794X17711342. eCollection 2017.

15.

Novel DHCR7 mutation in a case of Smith-Lemli-Opitz syndrome showing 46,XY disorder of sex development.

Tamura M, Isojima T, Kasama T, Mafune R, Shimoda K, Yasudo H, Tanaka H, Takahashi C, Oka A, Kitanaka S.

Hum Genome Var. 2017 May 11;4:17015. doi: 10.1038/hgv.2017.15. eCollection 2017.

16.

Steroid-resistant nephrotic syndrome as the initial presentation of nail-patella syndrome: a case of a de novo LMX1B mutation.

Nakata T, Ishida R, Mihara Y, Fujii A, Inoue Y, Kusaba T, Isojima T, Harita Y, Kanda C, Kitanaka S, Tamagaki K.

BMC Nephrol. 2017 Mar 23;18(1):100. doi: 10.1186/s12882-017-0516-7.

17.

Partial monosomy of 10p and duplication of another chromosome in two patients.

Ohta S, Isojima T, Mizuno Y, Kato M, Mimaki M, Seki M, Sato Y, Ogawa S, Takita J, Kitanaka S, Oka A.

Pediatr Int. 2017 Jan;59(1):99-102. doi: 10.1111/ped.13181.

PMID:
28102624
18.

Structure-activity relationship of the inhibitory effects of flavonoids on nitric oxide production in RAW264.7 cells.

Jiang WJ, Daikonya A, Ohkawara M, Nemoto T, Noritake R, Takamiya T, Kitanaka S, Iijima H.

Bioorg Med Chem. 2017 Jan 15;25(2):779-788. doi: 10.1016/j.bmc.2016.11.055. Epub 2016 Nov 29.

PMID:
27955927
19.

Chemical Compounds in Natural Medicines That Affect Macropharges and Adipocyte Cells.

Kitanaka S.

Yakugaku Zasshi. 2016;136(9):1195-216. doi: 10.1248/yakushi.16-00027. Review. Japanese.

20.

Spectrum of LMX1B mutations: from nail-patella syndrome to isolated nephropathy.

Harita Y, Kitanaka S, Isojima T, Ashida A, Hattori M.

Pediatr Nephrol. 2017 Oct;32(10):1845-1850. doi: 10.1007/s00467-016-3462-x. Epub 2016 Jul 23. Review.

PMID:
27450397

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