المؤلفون: Cameron Young, Dominyka Batkovskyte, Miyuki Kitamura, Maria Shvedova, Yutaro Mihara, Jun Akiba, Wen Zhou, Anna Hammarsjö, Gen Nishimura, Shuichi Yatsuga, Giedre Grigelioniene, Tatsuya Kobayashi

المصدر: HGG Advances, Vol 4, Iss 1, Pp 100148- (2023)

مصطلحات موضوعية: mitochondria, TOM, translocase, TOMM7, skeletal dysplasia, lipoatrophy, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666247722000653; https://doaj.org/toc/2666-2477

URL الوصول: https://doaj.org/article/d0f69c7ad5b442daa8ce8c143d8685b9

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المؤلفون: Liya Liu, Lizhang Chen, Zhanzhan Li, Liang Li, Jian Qu, Jing Xue

المصدر: Iranian Journal of Public Health, Vol 43, Iss 10 (2014)

مصطلحات موضوعية: Dong nationality, Gene polymorphism, SNaPshot genotyping, TOMM7, Type 2 diabetes, Public aspects of medicine, RA1-1270

وصف الملف: electronic resource

Relation: https://ijph.tums.ac.ir/index.php/ijph/article/view/3886; https://doaj.org/toc/2251-6085; https://doaj.org/toc/2251-6093

URL الوصول: https://doaj.org/article/54a7668e28f74a14ace84df6285bc323

المؤلفون: Jessica A. Williams, Hong-Min Ni, Wen-Xing Ding

المصدر: Redox Biology
Redox Biology, Vol 4, Iss C, Pp 6-13 (2015)

مصطلحات موضوعية: PINK1, PTEN-induced putative kinase 1, Clinical Biochemistry, MFN2, Mitochondrial Degradation, Bcl2L1, Bcl-2 like 1, Cellular homeostasis, LIR, LC3-interacting region, Bioinformatics, Biochemistry, Mfn1, mitofusin 1, Miro, mitochondrial Rho GTPase, Mitochondrial Dynamics, 0302 clinical medicine, Mitophagy, MID49, mitochondrial dynamics protein of 49 kDa, MFN1, Homeostasis, SQSTM1, sequestosome 1, Fis1, mitochondrial fission 1, Mff, mitochondria fission factor, lcsh:QH301-705.5, FUNDC1, Fun14 domain containing 1, Cytoskeleton, PARL, presenilin-associatedrhomboid-like, Mammals, 0303 health sciences, lcsh:R5-920, UBA, ubiquitin-associated, MEFs, mouse embryonic fibroblasts, Graphical Review, Cell biology, Mitochondria, OPA1, optic atrophy 1, Hif-1, hypoxia-inducing factor 1, mitochondrial fusion, Usp30, ubiquitin-specific peptidase 30, Clec16a, C-type lectin domain family 16, member A, VDAC, voltage-dependent anion channel, HSPA1L, heat shock 70 kDa protein 1-like, Mitochondrial fission, lcsh:Medicine (General), FIS1, Bag4, Bcl2-associated athanogene 4, APAP, acetaminophen, Biology, Mitochondrial spheroids, Mfn2, mitofusin 2, 03 medical and health sciences, ROS, reactive oxygen species, TOMM20, translocase of outer mitochondrial membrane 20, PGAM5, phosphoglycerate mutase family member 5, Autophagy, LC3, microtubule-associated protein 1 light-chain 3, Animals, Humans, Drp1, dynamin-related protein 1, 030304 developmental biology, TOMM7, translocase of outer mitochondrial membrane 7, Parkin, Nrdp1, neuregulin receptor degradation protein 1, Organic Chemistry, Smurf1, Smad-specific E3 ubiquitin protein ligase 1, MDV, mitochondria-derived vesicles, SNPH, syntaphilin, lcsh:Biology (General), BNIP3, Bcl-2/adenovirus E1B 19 kDa protein-interacting protein 3, CCCP, m-chloro phenyl hydrazine, Lysosomes, 030217 neurology & neurosurgery, MUL1, mitochondrial ubiquitin ligase 1

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9371cc825dce4b8c2e502e65e96969ae
http://europepmc.org/articles/PMC4309858

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المؤلفون: Young C; Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA., Batkovskyte D; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm 17177, Sweden., Kitamura M; Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan., Shvedova M; Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA., Mihara Y; Department of Pathology, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan., Akiba J; Department of Diagnostic Pathology, Kurume University Hospital, Kurume, Fukuoka 830-0011, Japan., Zhou W; Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA., Hammarsjö A; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm 17177, Sweden.; Department of Clinical Genetics, Karolinska University Laboratory, Karolinska University Hospital, Stockholm 17176, Sweden., Nishimura G; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm 17177, Sweden.; Center for Intractable Disease, Saitama Medical University Hospital, Saitama, Japan., Yatsuga S; Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.; Department of Pediatrics, Faculty of Medicine, Fukuoka University, Fukuoka 814-0180, Japan., Grigelioniene G; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm 17177, Sweden.; Department of Clinical Genetics, Karolinska University Laboratory, Karolinska University Hospital, Stockholm 17176, Sweden.; Department of Clinical Genetics, and Department of Biomedical and Clinical Sciences, Linköping University, Linköping 58183, Sweden., Kobayashi T; Endocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

المصدر: HGG advances [HGG Adv] 2022 Oct 04; Vol. 4 (1), pp. 100148. Date of Electronic Publication: 2022 Oct 04 (Print Publication: 2023).

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101772885 Publication Model: eCollection Cited Medium: Internet ISSN: 2666-2477 (Electronic) Linking ISSN: 26662477 NLM ISO Abbreviation: HGG Adv

مواضيع طبية MeSH: Mitochondrial Membranes*/metabolism , Mitochondrial Diseases*/genetics, Mice ; Animals ; Carrier Proteins/metabolism ; Mitochondria/genetics ; Mitochondrial Precursor Protein Import Complex Proteins