Program and Schedule

Time

Program

Venue

November 7 (Friday)

0830-2100

Registration

King Hall Hotel

1900-2000

Welcome Reception
Chairs:
Yau-Huei Wei, President of ASMRM
Shusen Liu, President of Chinese-Mit

King Hall Hotel

Special Lectures (2000-2100)
Chairs: Hong-Kyu Lee, Min-xing Guan

King Hall Hotel

2000-2030

Eric A. Schon (New York)：Inheritance of human mitochondrial nucleoids (30 min)

King Hall Hotel

2030-2100

Erich Gnaiger (Insbrück): Mitochondrial respiratory capacity and control in skeletal and cardiac muscle - from mouse to humans (30 min)

King Hall Hotel

November 8 (Saturday)

0830-0900

Opening Ceremony
Chair: Yong Zhang

Library of TUS

Session I: Bioenergetics and Metabolism (0900-1030)
Chairs: Bernhard Kadenbach, Erich Gnaiger

Library of TUS

0900-0930

Armen Y. Mulkidjanian (Osnabrueck): Mechanisms of proton transfer along and across the energy converting membranes (30 min)

0930-1000

Michael R. Duchen (London)：Mitochondria as ATP consumers: the cell biology of the endogenous inhibitory protein, IF-1 (30 min)

1000-1030

Shusen Liu (Beijing): Experimental evidence for ΔpH surface component of Proton motive force,ΔpHS , in ATP synthesis and other ΔpHS -requirement processes of mitochondria (30 min)

1030-1050

Tea and Coffee break

Session II: ROS and Signaling-1 (1050-1200)
Chairs: Michael R. Duchen, Heping Chen

Library of TUS

1050-1120

Yau-Huei Wei (Taipei): The cross-talk between in the regulation of gene expression mitochondria and the nucleus during differentiation of human mesenchymal stem cells (30 min)

1120-1140

Hideyuki J. Majima (Kagoshima): ROS generated from mitochondria control Nrf2/Keap1 signaling (20 min)

1140-1200

Shey-Shing Sheu (New York)：Crosstalk signaling between Mitochondrial Ca2+, ROS, and morphology: Pharmacological and pathophysicological relevance (20 min)

1200-1210

Photo

1210-1300

Lunch time

Student Restaurant  

1300-1400

Poster Presentations

Library of TUS

Special Lectures (1400-1530)
Chairs: Yau-Huei Wei, Shusen Liu

Library of TUS

1400-1430

Douglas C. Wallace (California): A mitochondrial paradigm for metabolic and degenerative diseases, aging and cancer: Mitochondria as Qi (30 min)

1430-1500

Minxin Guan (Ohio/Wenzhou): Mitochondrial deafness (30 min)

1500-1530

Bernhard Kadenbach (Marburg): The role of cytochrome c oxidase in the generation of mitochondrial ROS and degenerative diseases (30 min)

Session III: ROS and Signaling-2 (1530-1630)
Chairs: David A. Hood , Armen Mulkidjanian

Library of TUS

1530-1550

Heping Chen and Zheng Ming (Beijing): A Flash of Insight into Mitochondrial Superoxide Production (20 min)

1550-1610

Youngmi Kim Pak (Seoul): Mitochondria control protein as a novel therapeutic target for metabolic syndrome (20 min)

1610-1630

Jianxing Xu (Beijing): Pay more attention to the nonphosphorylative respiration of mitochondria (20 min)

1630-1650

Tea and Coffee break

Session IV: Mitochondrial Dynamics and Movement (1650-1830)
Chairs: Anne N. Murphy, Youngmi Kim Pak

Library of TUS

1650-1720

Richard J. Youle (Bethesda): The Bcl-2 Family, mitochondria morphogenesis and apoptosis (30 min)

1720-1750

Quan Chen (Tianjin/Beijing): The ubiquitination of mitofusin regulates mitochondrial fusion and dynamics (30 min)

1750-1810

Young-Gyu Ko (Seoul): Mitochondria fuse sarcolemma during myogensis (20 min)

1810-1830

Yong Zhang (Tianjin): The physiological adaptation of mitochondrial fusion and fission to aging and exercise (20 min)

November 9 (Sunday)

Session V: Mitochondria and Health-1: Aging, disease and apoptosis (0830-1020)
Chairs: Yusaku Nakabeppu, Quan Chen

Library of TUS

0830-0900

Masashi Tanaka (Tokyo): Therapeutic potential of pyruvate for mitochondrial diseases (30 min)

0900-0920

Donald D. Newmeyer (California): Multiple mitochondrial events critical for cell death (20 min)

0920-0940

Christiaan Leeuwenburgh (Florida): Iron accumulation in the mitochondria with age (20 min)

0940-1000

Chung Y. Hsu (Taipei): Mitochondrial dysfunction in amyloid-induced cerebrovascular degeneration (20 min)

1000-1020

Yusaku Nakabeppu (Fukuoka): The mitochondrial toxin, 3-nitropropionic acid induces MUTYH-dependent striatal neurode generation with accumulation of 8-oxoguanine which is effectively suppressed by OGG1 and MTH1 (20 min)

1020-1050

Tea and Coffee break

Session VI: Mitochcondria and Health-2: mtDNA mutations (1050-1210)
Chairs: Eric A. Schon, Masashi Tanaka

Library of TUS

1050-1110

Jia Qu (Wenzhou): Clinical and genetic features of LHON in Chinese population (20 min)

1110-1130

Yidong Bai (San Antonio): A heteroplasmic, not homoplasmic, mitochondrial DNA mutation promotes tumorigenesis via alteration in reactive oxygen species generation and apoptosis (20 min)

1130-1250

Hsin-Chen Lee (Taipei): Mitochondrial DNA mutations in human cancers (20 min)

1150-1210

Yu Qi (Beijing): The study on human mitochondrial A3243G mutation in Chinese patients (20 min)

1210-1300

Lunch time
Workshop on “High-Resolution Respirometry”
Hosted by: Erich Gnaiger (Insbrück)

Student Restaurant/
Library

1300-1400

Poster Presentations

Library of TUS

Session VII: Mitochondria and Sports Medicine (1400-1510)
Chairs: Richard J. Youle , Yong Zhang

Library of TUS

1400-1430

David A. Hood (Toronto)：Mechanisms of mitochondrial biogenesis in muscle: effect of exercise and age (30 min)

1430-1450

Jiankang Liu (Xi’an): Mitochondrial dysfunction and biogenesis in endurance exercise: Effects of mitochondrial nutrients (20 min)

1450-1510

Shuzhe Ding (Shanghai): Role of exercise and hindlimb suspending on the gene expression of PDK4, CPT-1 and mitochondrial dynamin in skeletal muscle (20 min)

Session VIII: Mitochondrial Physiopathology & Pharmacology (1510-1620)
Chairs: Chung Y. Hsu, Lingjia Qian

Library of TUS

1510-1540

Hong Kyu Lee (Seoul): Mitochondrial dysfunction and enviromental toxins (30 min)

1540-1600

Anne N. Murphy (California): The outer mitochondrial membrane Fe-S protein mitoNEET: An alternative target of the insulin sensitizer pioglitazone? (20 min)

1600-1620

Jing Gao (Jiangsu): Novel oxadiazolo[3,4-d]pyrimidine nucleoside derivatives exhibited antitumor activities through NO-mediated mitochondrial dysfunction (20 min)

1620-1640

Tea and Coffee break

Selected Oral Presentations (1640-1800)

Library of TUS

Selected Oral Presentations : Basic Aspects
Chairs: Jiankang Liu, Yi-Dong Bai

Room 1

1640-1650

Xinmin Cao (Singapore): Identification of GRIM-19 as a functional subunit of mitochondrial respiratory chain Complex I and its function in the heart development

1650-1700

Yingli Shang (Beijing): Targeted expression of the human uncoupling protein 2 (hUCP2) to mouse liver increases susceptibility to LPS induced acute liver injury

1700-1710

Xiaolin Gao (Beijing): The association analysis between maximal aerobic capability and sequence polymorphisms of mtDNA hypervariable region II

1710-1720

Jingjing Xu (Jiangsu): Mitochondrial regulation is involved in antitumor effects of novel 7-azaindirubin derivates

1720-1730

Shanjun Chen (Tampere): A cytoplasmic suppressor of tko25t

1730-1740

Young Min Cho (Seoul): Severely compromised mitochondrial function prompts mitochondrial transfer between cells by augmenting chemotaxis

1740-1750

Yu Xu (Chongqing): Effects of palmitic acid on activity of uncoupling proteins and proton leak of brain mitochondria in vitro from exposure to simulating high altitude hypoxia rats

1750-1800

Xingbo Zhao (Beijing): Exploring the history of pig domestication in East Asia: Evidence from ancient mtDNA data

Selected Oral Presentations: Clinical Aspects
Chairs: Yu Qi, Jing Gao

Room 2

1640-1650

Massoud Houshmand (Tehran): Complex I deficiency in Persian multiple sclerosis patients

1650-1700

Yinan Ma (Beijing): The Study of Mitochondrial A3243G Mutation in Different Tissues

1700-1710

Ji Zhang (California): Beyond insulin secretion: The role of mitochondrial phosphatase PTPMT1 in glucose and lipid homeostasis

1710-1720

Hui Zhao (Beijing): Influence on the super-sensitivity to aminoglycosides in a family with mitochondrial 12S rRNA mutation

1720-1730

Y. Whitney Yin (Austin): Structural basis for mitochondrial DNA polymerase implicated human diseases

1730-1740

Yasong Wu (Beijing): Alterations of HVⅡ region and the copy number of mitochondrial DNA in individuals with HIV/AIDS

1740-1750

Jianjuan Zhang (Wenzhou): A novel OPA1 mutation in a Chinese family with autosomal dominant optic atrophy

1750-1800

Mohammad Mehdi (Tehran): Mitochondrial ATPase 6 gene as a hot spot for Neurodegenerative disorders?

1830-2000

Closing Banquet

Sports Hotel
Restaurant

November 10 (Monday)

0900-1100

City Tour or Departure

Hotels

Timetable: 13:00-14:00 on November 8 and 9
Venue: Library of TUS

No.

Presentation Authors

Title

Session A：Mitochondria and Health Aging, Diseases and Cell Death

P-A01

Wei-Chien Hsu,et al.

Detection of somatic mitochondrial DNA mutations in different grades of human astrocytoma Tissues

P-A02

Ling-Wan Chang,et al.

Induced mitochondrial dysfunction and apoptosis of rat glioma cells by C6 ceramide

P-A03

Xinyue Chen,et al.

P53 reduced mitochondrial toxicity induced by AZT

P-A04

Chia-Wei Liou,et al.

Association between a Common mtDNA D-Loop Variant and Alteration of mtDNA Copy Number

P-A05

Chih-HaoWang, et al.

The role of mitochondria during differentiation of preadipocytes and insulin iInsensitivity of adipocytes with mitochondrial dysfunction

P-A06

Sheng-Hao Wang,
et al.

Cadmium-induced autophagy and apoptosis are mediated by a calcium signaling pathway

P-A07

Daojun Hong,et al.

Phenotype and clinical course of in a family with autosomal dominant progressive external ophthalmoplegia caused by a novel Twinkle mutation

P-A08

Jiang-Bin Feng,et al.

Spontaneous and Cobalt-60 irradiation-induced mtDNA 4934bp deletion in human blood samples

P-A09

Han-Wen Guo,et al.

Evaluation of NADH fluorescence lifetime as a photobiological measure in ALA-PDT

P-A10

Ji-feng Guo,et al.

Mutation in DJ-1 induced cellular mitochondrial disfunction and oxidative stress associated with recessive parkinsonism

P-A11

Yu-Wen Huang,et al.

Mitochondrial point mutation significantly accumulate only in aged population

P-A12

Jung Hwan Hwang,
et al.

Pharmacological stimulation of NADH oxidation reverses metabolic syndrome

P-A13

Hyoung Kyu Kim,et al.

Tetrahydrobiopterin deficiency impaired cardiac mitochondria function

P-A14

Min Hee Lee,et al.

Translocation of BRAFV600E into mitochondria mediates anti-apoptosis and cellular energy metabolism

P-A15

June-Hyung Kim,et al.

Mitochondrial dysfunction and aerobic glycolysis in cancer cell invasion

P-A16

Kangsik Seo,et al.

Increased NAD+/NADH ratio promotes HIF-1α degradation and mitochondrial function in cancer cells

P-A17

Soung Jung Kim,et al.

Mitochondrial CRIF1 (mtCRIF1) deficiency compromises oxidative phosphorylation

P-A18

Chih-Hung Lee,et al.

Mitochondria role in the modulation of arsenic-elicited proliferative and apoptotic responses in human keratinocytes

P-A19

Wen-Yu Lee,et al.

Studies on the metabolic profiles of primary human skin fibroblasts from donors of different ages

P-A20

Mei-Chen Lo,et al.

Roles of autophagic cell death in AGEs- induced β-cell destruction

P-A21

Shi-Bei Wu,et al.

Hydrogen peroxide-induced alteration in the expression of antioxidant enzymes and acceleration of cellular senescence in skin fibroblasts of patients with MERRF syndrome

P-A22

Behnam Kamalidehghan,et al.

Investigation of MtDNA deletions in non-tumoral and tumoral cells in Gastric Cancer

P-A23

Yu-Ting Wu,et al.

Lysine Acetylation of Respiratory Enzyme Complex in Human Cells with Mitochondrial Dysfunction

P-A24

XiaoHua Liu,et al.

Damage of mitochondrial membrane induces myocardium injury in restraint stressed rats

P-A25

Yi-Fan Chen,et al.

Deficiency of Gret gene leads to premature ageing phenotype caused by a mitochondrial defect in mice

P-A26

Yongjun Luo,et al.

The ralationship between the Cox17 copy number variation and hypoxia adaptation

P-A27

Yuyun Xiong,et al.

Effects of asiatic acid on cell injury and improvement of motor deficit in a Drosophila model of Parkinson’s disease

P-A28

Yun Zhao,et al.

Hsp70 may protect the cardiomyocyte from stress-induced injury by inhibiting Fas- and mitochondria-mediated apoptosis

P-A29

Zhang Yao,et al.

A late-onset Leigh-syndrome patient caused by mitochondrial G13513A mutation

P-A30

Yumei Han,et al.

Muscular mitochondria biogenesis induced by endurance training in aged rat: Signaling regulation of Reactive Oxygen Species

P-A31

Huiling Huang,et al.

The study of mild hypothermia on the cerebral mitochondrial respiratory Function and proteomics following traumatic brain injury in rats

P-A32

Ziquan Liu,et al.

The physiological adaptation of mitochondrial fusion and fission to aging and endurance training in rat muscle

P-A33

Xinxing Wang,et al.

Expression of uncoupling protein 3 in mitochondria protects against stress induced myocardial injury: Based on proteomic study

P-A34

Xiaozhen Zhao,et al.

Effects of polygonatum oral liquid on hippocampal mitochondria ultrastructure and mitochondrial membrane potential in rats with vascular dementia

P-A35

Min Liang,et al.

The mitochondrial ND1 T3394C mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in two Chinese families

P-A36

Tang Xiao-Wen,et al.

Mitochondrial tRNAThr G15927A mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation

P-A37

Jianxin Lu,et al.

Mitochondrial DNA and diabetes

P-A38

Jingzhang Ji,et al.

Screening for Variations in Mitochondrial ND6 Gene of type 2 diabetes mellitus People in Zhejiang Province

P-A39

Jingzhang Ji,et al.

Screening for Variations in Mitochondrial COⅡ Gene of type 2 diabetes mellitus People in Zhejiang Province

P-A40

Aifen Yang,et al.

Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation

P-A41

Fuxin Zhao,et al.

Clinical and Genetic Features of LHON is associated with the mitochondrial ND6 T14484C mutation in Chinese families

P-A42

Ji-feng Guo,et al.

Mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial disfunction and oxidative stress associated with recessive parkinsonism

P-A43

Yu-Wen Li,et al.

Detection of changes on mitochondrial gene expression induced by Cobalt-60 gamma-rays

P-A44

Yong Yan Li,et al.

Maternally inherited aminoglycoside-induced and nonsyndromic deafness May be associated with the novel A856G,A14692G mutations in the mitochondrial Genes

P-A45

Chein-Ju Lin,et al.

Anti-carcinogenic mechanism of temozolomide in malignant glioma through mitochondria-mediated cell death

P-A46

Qing-Jie Liu,et al.

Detection and confirmation of two novel mitochondrial DNA deletions in human lymphoblastoid cell line irradiated by cobalt-60 gamma rays

P-A47

Wei Ye,et al.

Molecular analysis on mitochondrial genes MTATP6 and MTATP8 in Chinese type 2 diabetes mellitus patients

P-A48

Hyun-Jung Koo,et al.

Microarray analysis of neuroprotective effects of Moutan cortex extract in SH-SY5Y cells

P-A49

Hossein Soltanzadeh,et al.

Analysis of the CAG repeat and A467T and W748S POLG mutations in Iranian patients With Multiple sclerosis

P-A50

Juan Wang,et al.

Exploring the action of artemisinin in a yeast model

P-A51

Mohammad Mehdi Heidari,et al.

Complex I and ATP content deficiency in Lymphocytes from Friedreich's ataxia

P-A52

Massoud Houshmand,et al.

Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with friedreichis ataxia

P-A53

Massoud Houshmand,et al.

Do mitochondrial DNA haplogroups play a role in susceptibility to tuberculosis?

P-A54

Massoud Houshmand,et al.

Investigation of genetic background polymorphism and mtDNA common Deletion in Parkinson's diseases

P-A55

Ghamarsoltan Dorraj,et al.

Lack of association of mitochondrial A3243G tRNALeu mutation in Iranian patients with type 2 diabetes

P-A56

Mehri Khatami,et al.

A large-scale mitochondrial DNA deletion in Iranian patients with arrhythmia disorders (Long QT Syndrome)

P-A57

Mohammad Hossein Salehi ,et al.

Low sperm motility due to mitochondrial DNA multiple deletions

P-A58

Farzaneh Fesahat,
et al.

Do haplogroups H and U Act to increase the penetrance of Alzheimer’s Disease?

P-A59

S.M.Seyedhassani,
et al.

Role of mitochondria in repeated pregnancy loss

P-A60

Ali Mohammad Ahadi,et al.

An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?

P-A61

Mohammad Mehdi Heidari,et al.

A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich’s ataxia

P-A62

Maryam Montazeri,
et al.

Investigation of polymorphisms in non-coding region of human mitochondrial DNA in 31 Iranian hypertrophic cardiomyopathy (HCM) patients

P-A63

Mehri Khatami,et al.

Accumulation of mitochondrial genome variations in persian LQTS patients: Could be as risk factor?

P-A64

Massoud Houshmand,et al.

Role of mitochondria in Ataxia-Telangiectasia: Investigation of mitochondrial deletions and Haplogroups

P-A65

Bibi Nasim Hosseini,
et al.

Investigation on mtDNA deletions and twinkle gene mutation (G1423C) in Iranian patients with chronic progressive external opthalmoplagia

P-A66

Afshar Jafari,et al.

Effect of aerobic exercise training on mtDNA deletion in soleus muscle of trained and untrained Wistar rats

P-A67

Mansoureh Akouchekian,et al.

Appearance of large scale mitochondrial DNA deletion in human colorectal cancer and analysis of mitochondrial haplogroups in colorectal cancer

Session B: Mitochondria and Sports Medicine

P-B01

Timon Cheng-Yi Liu

Inhibition of Mitochondrial Functions and its Applications

P-B02

Fengyang Wang,et al.

Study on association between lactate threshold, free radicals threshold and mitochondria

P-B03

Dan S. Radut

Mitochondrial research in the sport &exercise medicine

P-B04

Jie Li,et al.

The effect of different methods of hypoxia training on Activities of respiratory Chain in mitochondria from mice’s Skeletal Muscle

P-B05

Zhengzhong Zeng,
et al.

Different transport mechanisms of 8-Oxoguanine DNA glycosylase (OGG1) in skeletal muscle of old rats by Exercises and Caloric Restriction

P-B06

Jinting Qu,et al.

Rapidly Up-regulated UCP3 induced by Acute Exercise: A Possible Role of UCP Pool in Skeletal Muscle

P-B07

Hai Bo,et al.

Endurance training attenuates the bioenergetics alterations of rat skeletal muscle mitochondria submitted to acute hypoxia

Session C: Mitochondrial Movement and Dynamics

P-C01

Yin-Chiu Chen,et al.

Oxidative stress and post-translational modifications of microtubules underlie defective morphology, distribution, and motility of mitochondria in MERRF syndrome

P-C02

Heng-Lu Nieh,et al.

Effects of methylglyoxal on mitochondrial morphology changes

P-C03

Yong-Hak Seo,et al.

Mitochondrial mass increase: A potential link between mitochondrial elongation and respiratory defects

P-C04

Junqin Hao,et al.

The influence of exercise and calorie restriction on the mitochondrial fusion and fission of the skeletal muscle in old rats

Session D: Mitochondrial Physiopathology and Pharmacology

P-D01

Junze Liu,et al.

The roles of UCPs in regulating cerebral mitochondrial ATP synthesis during hypoxia exposure

P-D02

Ronald Ma,et al.

Identification of a novel mutation in Succinate Dehydrogenase in a 21-year old woman presenting with hypertension and proteinuria during pregnancy

P-D03

Won Sun Park,et al.

The mitochondrial Ca2+-activated K+ channel activator, NS 1619 inhibits L-type Ca2+ channels in rat ventricular myocytes

P-D04

Chen Xia,et al.

Changes of uncoupling proteins activity and efficiency of oxidative phosphorylation in hypoxic exposed rat brain mitochondrial

P-D05

Yi-Chien Wu,et al.

The Role of RXR-α in mitochondria biogenesis of human U87MG astrocytoma cells

P-D06

Yuan Zhang,et al.

Mitochondria-nucleus Translocation of Mitofilin in Apoptosis

P-D07

Yun Hyi Ku,et al.

Glucagon-Like Peptide 1 Increases Mitochondrial Biogenesis and Function in INS-1 Cells

P-D08

Sun Young Ahn ,et al.

Mitochondrial dysfunction enhances the migration of vascular smooth muscle cell via suppression of Akt phosphorylation

P-D09

Zhenyu Zhang,et al.

Different Response to the Acute and Severe Hypoxia in Two Populations of the Migratory Locusts

Session E: mtDNA Mutations and Evolution

P-E01

Yutaka Nishigaki,et al.

A new comprehensive diagnosing system for mitochondrial DNA mutations using suspension array technology

P-E02

Yu Ding,et al.

The Mitochondrial tRNAGlu A14693G Mutation May Influence the Phenotypic Manifestation of Deafness-Associated 12S rRNA A1555G Mutation in a Chinese Family

P-E03

Shirin Jamshidi,et al.

Phylogenetic relationship in Iranian west Balitoridae(fishes) for Genus and Species detection with mitochondrial cytochrome b and D-loop genes

P-E04

Jindan Wang,et al.

Clinical evaluation and Sequence analysis of the Complete Mitochondrial genome of one very low Penetrance Chinese pedigree with Hearing Loss Carrying the 12S rRNA T1095C Mutation

P-E05

Qingfeng Yan,et al.

Nuclear modifier gene MTO2 modulates the phenotypic expression of mitochondrial DNA　paromomycin resistance mutation

P-E06

Young-Kyoung Lee,
et al.

Mitochondrial dysfunction is associated with mtDNA damage and mtOGG1 down-expression in human hepatocellular carcinoma cells

P-E07

Meixia Yuan,et al.

The mitochondrial ND4 G11696A mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in Chinese families

P-E08

Zhao xia Wang,et al.

Clinical, radiological, pathological studies in a patient with mtDNA G13513A mutation induced MELAS/Leigh overlap syndrome

P-E09

Seyed Ali Alemohammad,et al.

Distribution of mitochondrial DNA intergenic COII/tRNALYS 9 bp deletion in Iranian populations

P-E10

Shirin Jamshidi,et al.

Study of genetic variation in spring and autumn migratory form of Iranian endangered Salmo trutta caspius with two mitochondrial genes

P-E11

Nooshin Aflakian,et al.

Chromosome Y and mtDNA polymorphism among Pars ethnicity and Iranian Arabs, more mobility of men than women in ancient Persia

P-E12

Seyed Ali Ghorashi,
et al.

Phylogenetic analysis of anemone fishes of the Persian Gulf using mtDNA sequences

Session F: ROS and Signaling

P-F01

Guo Li,et al.

MR findings in Leigh Syndrome with SURF-1 gene 604G→C mutations

P-F02

Hyun-Jung Jung,et al.

Involvement of GSK3 inactivation in TGF β1-induced mitochondrial dysfunction

P-F03

Chun-Yi Liu,et al.

Involvement of PKCδ and ERK1/2 Signalling in Sensitivity to UV-induced Apoptosis of Human Cells Harboring 4,977 bp-Deleted mtDNA

P-F04

Zhongping Cao,et al.

ROS preconditioning protects PC12 cells against death induced by hypoxia

Session G: Others

P-G01

Bing Wen,et al.

ETFDH gene mutation as the molecular basis of riboflavin responsive lipid storage myopathy

P-G02

Heng-Lu Nieh,et al.

Proteomic analysis of glycogen synthase kinase 3-associated mitochondrial proteins

P-G03

Hsing-Wen Wang,
et al.

The use of NADH as a noninvasive optical biomarker in detecting mitochondrial function during stem cell differentiation and staurosporine-induced apoptosis

P-G04

Shu-Han Hsu,et al.

Effects of hypoxia on osteogenic differentiation of human mesenchymal stem cells

P-G05

Chen-Sung Lin, et al.

Oxidative damage and slteration in mitochondrial DNA Copy number in the esophageal muscle with their relationships to hOGG1 polymorphism

P-G06

RCW Ma,et al.

Meseneteric fat is the main determinant of cardiovascular risk in women with polycystic ovary syndrome

P-G07

Min Li,et al.

Polymorphisms analysis of mitochondrial cytochrome b gene in Chinese type 2 diabetes mellitus patients

Session H: Bioenergetics and Metabolism

P-H01

Tong Xie, et al

ATP synthesis of mitochondrial inner membrane coupled with high energized protons on membrane surface, ΔpH S measured by inserted fluorescent probe of 4-MU C-11

P-H02

Nie Jinlei, et al

New evidence for hypothesis of “Reactive Oxygen Cycle” with the Q Cycle and the proton cycle in the respiratory chain of mitochondria in exercise animal model