Jiesheng Lu

发表

Exercise‐induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency

S. Dimauro, K. Park, Shin J Oh, 2006, Muscle & nerve.

Varying loads of the mitochondrial DNA A3243G mutation in different tissues: Implications for diagnosis

S. Dimauro, K. Engelstad, P. Kaufmann, 2004, American journal of medical genetics. Part A.

Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.

S. Dimauro, M. Mancuso, P. Kaufmann, 2005, Archives of neurology.

Identification of a novel D109Y mutation in Cu/Zn superoxide dismutase (sod1) gene associated with amyotrophic lateral sclerosis

H. Mitsumoto, P. Gordon, Jiesheng Lu, 2007, Journal of the Neurological Sciences.

Study of Mitochondrial DNA Mutations in Patients With Migraine With Prolonged Aura

S. Dimauro, S. Silberstein, W. Young, 2004, Headache.

The molecular basis of pyruvate carboxylase deficiency: mosaicism correlates with prolonged survival.

Hong Yang, Dong Wang, P. Briones, 2008, Molecular genetics and metabolism.

Egr-1, a master switch coordinating upregulation of divergent gene families underlying ischemic stress

Nigel Mackman, David M. Stern, Y. Zou, 2000, Nature Medicine.

Mitochondrial single nucleotide polymorphism genotyping by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using cleavable biotinylated dideoxynucleotides.

Jingyue Ju, Chunmei Qiu, James J Russo, 2012, Analytical biochemistry.

Hypoxia-associated Induction of Early Growth Response-1 Gene Expression*

Y. Zou, D. Pinsky, N. Mackman, 1999, The Journal of Biological Chemistry.

A novel POLG gene mutation in a patient with SANDO.

S. Dimauro, M. Hirano, B. Kurt, 2012, Journal of experimental and integrative medicine.

The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.

J. Ganesh, S. Dimauro, M. Hirano, 2008, Archives of neurology.

Ten-minute DNA Release Kits - A novel approach to obtain DNA easily in modern biological science

Yucui Zhu, Jiesheng Lu, Huaijie Zhu, 2006 .

Mutation in an mtDNA Protein-Coding Gene

S. Dimauro, M. Mansukhani, R. Chmait, 2013, Journal of child neurology.

A novel tRNAVal mitochondrial DNA mutation causing MELAS

S. Dimauro, A. Khandji, J. Willey, 2008, Journal of the Neurological Sciences.