المؤلفون: Chenxi Liu, Ruihua Huang, Guosheng Su, Liming Hou, Wuduo Zhou, Qian Liu, Zijian Qiu, Qingbo Zhao, Pinghua Li

المصدر: BMC Genomics, Vol 24, Iss 1, Pp 1-14 (2023)

مصطلحات موضوعية: Taihu Lake region pigs, Danish Large White pigs, Introgression, Fertility, NDUFS4 gene, Biotechnology, TP248.13-248.65, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2164

URL الوصول: https://doaj.org/article/affd689966f5412ba51180de8677574f

المؤلفون: Liu, Chenxi, Huang, Ruihua, Su, Guosheng, Hou, Liming, Zhou, Wuduo, Liu, Qian, Qiu, Zijian, Zhao, Qingbo^{Aff1, IDs1286402309860x_cor8}, Li, Pinghua^{Aff1, Aff2, IDs1286402309860x_cor9}

المصدر: BMC Genomics. 24(1)

المؤلفون: Mohammad Vafaee‐Shahi, Saeide Ghasemi, Mehran Beiraghi Toosi, Mahmoud Reza Ashrafi, Reza Shervin Badv, Ali Reza Tavasoli, Leila Tahernia

المصدر: Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)

مصطلحات موضوعية: gaze palsy, lactate, Leigh syndrome, mitochondria, NDUFS4 gene, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2050-0904

URL الوصول: https://doaj.org/article/58d33fd325714bb888c58f92bad9772c

المؤلفون: Chen, Qimei, Zeng, Yongqing, Wang, Hui, Yang, Lun, Yang, Yun, Zhu, Honglei, Shi, Yuan, Chen, Wei, Hu, Yanxia

المصدر: Molecular Biology Reports: An International Journal on Molecular and Cellular Biology. February 2013 40(2):1599-1608

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المؤلفون: Mar Tulinius, Niklas Darin, Kalliopi Sofou, Linda De Meirleir, Johanna Uusimaa, Charalampos Tzoulis, Pirjo Isohanni, Karin Naess, Elsebet Ostergaard, Irenaeus F.M. de Coo, Tuula Lönnqvist, Laurence A. Bindoff

المساهمون: Neurology, Reproduction and Genetics, Neurogenetics, Clinical sciences, Research Programme for Molecular Neurology, Research Programs Unit, Anu Wartiovaara / Principal Investigator, Clinicum, Children's Hospital, University of Helsinki, Lastenneurologian yksikkö, HUS Children and Adolescents

المصدر: Journal of Medical Genetics, 55(1), 21-27. BMJ Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Male, Cardiomyopathy, CHILDHOOD, CHILDREN, DNA, Mitochondrial/genetics, 0302 clinical medicine, ENCEPHALOMYOPATHY, 3123 Gynaecology and paediatrics, Leigh Disease/genetics, Genetics (clinical), Genetics, 1184 Genetics, developmental biology, physiology, Phenotype, Cohort, Female, medicine.symptom, Leigh Disease, medicine.medical_specialty, Mitochondrial DNA, Ataxia, DNA ABNORMALITIES, Mutation/genetics, Mitochondrial disease, Biology, DNA/genetics, MITOCHONDRIAL DISEASE, DNA, Mitochondrial, Central nervous system disease, 03 medical and health sciences, Internal medicine, medicine, Humans, Leigh disease, Genetic Association Studies, Cell Nucleus, CARDIOMYOPATHY, Genetic heterogeneity, CLINICAL-FEATURES, 3112 Neurosciences, Infant, DNA, medicine.disease, 030104 developmental biology, NDUFS4 GENE, Mutation, Cell Nucleus/metabolism, COMPLEX-I DEFICIENCY, 030217 neurology & neurosurgery, SURF1 GENE-MUTATIONS, Follow-Up Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e782b6beb24f12292c3fa670ed54b98f
https://hdl.handle.net/1765/104599

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المؤلفون: Papa, S., Scacco, S., Sardanelli, A.M., Petruzzella, V., Vergari, R., Signorile, A., Technikova-Dobrova, Z.

المصدر: Bioscience Reports. February 2002 22(1):3-16

المؤلفون: Papa, S., Sardanelli, A. M., Scacco, S., Petruzzella, V., Technikova-Dobrova, Z., Vergari, R., Signorile, A.

المصدر: Journal of Bioenergetics and Biomembranes. February 2002 34(1):1-10

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