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You searched for: Author/Creator Nakajima, Yoko

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1. A novel homozygous variant in MICOS13/QIL1 causes hepato‐encephalopathy with mitochondrial DNA depletion syndrome. Issue 10 (4th August 2020)

2. Application of electrical resistivity to assess subsurface geological and hydrological conditions at post‐tin mining sites in Indonesia. (3rd February 2020)

3. Clinical, biochemical and molecular analysis of 13 Japanese patients with β‐ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation. Issue 5 (14th February 2014)

4. Decreased expression of interferon‐stimulated genes in B cells of patients with chronic hepatitis C during interferon‐free therapy potentially suggests the eradication of hepatitis C virus in the B cells: A cohort study. Issue 3 (15th July 2020)

5. Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β‐ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation. Issue 6 (12th August 2014)

6. Establishment and directed differentiation of induced pluripotent stem cells from glycogen storage disease type Ib patient. (28th October 2013)

7. Evaluation of subclinical chronic sun damage in the skin via the detection of long‐lasting ultraweak photon emission. Issue 6 (17th May 2021)

9. Impact of DPYD, DPYS, and UPB1 gene variations on severe drug‐related toxicity in patients with cancer. Issue 9 (20th July 2020)

10. Kinetic and molecular orbital analyses of dicarboxylic acylcarnitine methylesterification show that derivatization may affect the screening of newborns by tandem mass spectrometry. Issue 1 (1st January 2016)