Detalhe da pesquisa
1.
Rapid Mobilization Reveals a Highly Engraftable Hematopoietic Stem Cell.
Cell
; 172(1-2): 191-204.e10, 2018 01 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29224778
2.
The frequencies of very long-chain acyl-CoA dehydrogenase deficiency genetic variants in Japan have changed since the implementation of expanded newborn screening.
Mol Genet Metab
; 136(1): 74-79, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35400565
3.
Kangaroo mother care alters chromogranin A and perfusion index in preterm babies.
Pediatr Int
; 63(1): 53-59, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32542824
4.
Validation of Liquid Chromatography-Tandem Mass Spectrometry-Based 5-Plex Assay for Mucopolysaccharidoses.
Int J Mol Sci
; 21(6)2020 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32188102
5.
Survivin Is Required for Mouse and Human Bone Marrow Mesenchymal Stromal Cell Function.
Stem Cells
; 36(1): 123-129, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29067757
6.
Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases.
J Hum Genet
; 62(9): 809-814, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28515471
7.
Clinical Features of Carnitine Deficiency Secondary to Pivalate-Conjugated Antibiotic Therapy.
J Pediatr
; 173: 183-7, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27059912
8.
Fatal pulmonary arterial hypertension in an infant girl with incontinentia pigmenti.
Pediatr Int
; 58(5): 394-396, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27173419
9.
Internal tandem duplication mutations in FLT3 gene augment chemotaxis to Cxcl12 protein by blocking the down-regulation of the Rho-associated kinase via the Cxcl12/Cxcr4 signaling axis.
J Biol Chem
; 289(45): 31053-65, 2014 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25237195
10.
Metabolic disease in 10 patients with sudden unexpected death in infancy or acute life-threatening events.
Pediatr Int
; 57(3): 348-53, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25919294
11.
[A case of pancreatic neuroendocrine tumor presenting with main pancreatic duct invasion].
Nihon Shokakibyo Gakkai Zasshi
; 112(1): 86-93, 2015 Jan.
Artigo
em Japonês
| MEDLINE | ID: mdl-25744924
12.
Blockade of prostaglandin E2 signaling through EP1 and EP3 receptors attenuates Flt3L-dependent dendritic cell development from hematopoietic progenitor cells.
Blood
; 119(7): 1671-82, 2012 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22110249
13.
Ectopic neuroblastoma in monozygotic twins with different ages of onset: possible twin-to-twin metastasis in utero with distinct genetic alterations after birth.
J Pediatr Hematol Oncol
; 36(2): 166-8, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23669722
14.
Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1.
Anal Bioanal Chem
; 405(4): 1345-51, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23143007
15.
Therapy-related Ph+ leukemia after both bone marrow and mesenchymal stem cell transplantation for hypophosphatasia.
Pediatr Int
; 55(3): e52-5, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23782379
16.
The magnitude of CXCR4 signaling regulates resistance to quizartinib in FLT3/ITD+ cells via RUNX1.
Leuk Res
; 124: 106983, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36473282
17.
Clinical and molecular aspects of Japanese children with medium chain acyl-CoA dehydrogenase deficiency.
Mol Genet Metab
; 107(1-2): 237-40, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22796001
18.
Bezafibrate can be a new treatment option for mitochondrial fatty acid oxidation disorders: evaluation by in vitro probe acylcarnitine assay.
Mol Genet Metab
; 107(1-2): 87-91, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22841441
19.
Internal tandem duplication mutations in FLT3 gene augment chemotaxis to Cxcl12 protein by blocking the down-regulation of Rho-associated kinase via the Cxcl12/Cxcr4 signaling axis.
J Biol Chem
; 290(47): 28356, 2015 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-26590297
20.
Clinical and molecular investigation of 19 Japanese cases of glutaric acidemia type 1.
Mol Genet Metab
; 102(3): 343-8, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21176883