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[New] L-Cysteine supplementation prevents liver transplantation in a patient with TRMU deficiency.

Research paper by Claudia C Soler-Alfonso, Nishita N Pillai, Erin E Cooney, Krupa R KR Mysore, Suzanne S Boyer, Fernando F Scaglia

Indexed on: 12 Feb '19

Published on: 12 Feb '19 in Molecular Genetics and Metabolism Reports

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[New] Mitochondrial RNA granules are critically dependent on mtDNA replication factors Twinkle and mtSSB.

Research paper by Fenna F Hensen, Alisa A Potter, Selma L SL van Esveld, Aleix A Tarrés-Solé, Arka A Chakraborty, Maria M Solà, Johannes N JN Spelbrink

Indexed on: 05 Feb '19

Published on: 05 Feb '19 in Nucleic acids research

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[New] Metabolic liver diseases presenting with neonatal cholestasis: at the crossroad between old and new paradigms

Research paper by Helena Moreira-Silva, Inês Maio; Anabela Bandeira; Esmeralda Gomes-Martins; Ermelinda Santos-Silva

Indexed on: 30 Jan '19

Published on: 28 Jan '19 in European Journal of Pediatrics

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[New] Mitochondrial unfolded protein response: a stress response with implications for fertility and reproductive aging.

Research paper by Emre E Seli, Tianren T Wang, Tamas L TL Horvath

Indexed on: 30 Jan '19

Published on: 30 Jan '19 in Fertility and Sterility®

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[New] Cereblon attenuates DNA damage-induced apoptosis by regulating the transcription-independent function of p53.

Research paper by Liang L Zhou, Guoqiang G Xu

Indexed on: 27 Jan '19

Published on: 27 Jan '19 in Cell Death & Disease

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[New] Evidence that growth hormone can improve mitochondrial function in oocytes from aged mice.

Research paper by Haiyan H Hou, Xi X Wang, Qi Q Yu, Hong-Yi HY Li, Shao-Jie SJ Li, Rui-Yi RY Tang, Zai-Xin ZX Guo, Ya-Qiong YQ Chen, Chun-Xiu CX Hu, Zhi-Juan ZJ Yang, Wen-Ke WK Zhang, Yan Y Qin

Indexed on: 23 Jan '19

Published on: 23 Jan '19 in Reproduction (Cambridge, England)

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[New] Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn's disease.

Research paper by Ravi R Patel, Lucia Lee LL Coulter, Joanna J Rimmer, Miles M Parkes, Patrick Francis PF Chinnery, Oscar O Swift

Indexed on: 17 Jan '19

Published on: 17 Jan '19 in BMC gastroenterology

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[New] ATM is activated by ATP depletion and modulates mitochondrial function through NRF1.

Research paper by Hei-Man HM Chow, Aifang A Cheng, Xuan X Song, Mavis R MR Swerdel, Ronald P RP Hart, Karl K Herrup

Indexed on: 16 Jan '19

Published on: 16 Jan '19 in The Journal of cell biology

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[New] Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far.

Research paper by Dario D Pacitti, Michelle M Levene, Caterina C Garone, Niranjanan N Nirmalananthan, Bridget E BE Bax

Indexed on: 11 Jan '19

Published on: 11 Jan '19 in Frontiers in genetics

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[New] Biomolecules, Vol. 9, Pages 15: Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

Research paper by Boel De Paepe

Indexed on: 10 Jan '19

Published on: 07 Jan '19 in Biomolecules

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[New] Transmission of Dysfunctional Mitochondrial DNA and Its Implications for Mammalian Reproduction.

Research paper by Kanokwan K Srirattana, Justin C JC St John

Indexed on: 09 Jan '19

Published on: 09 Jan '19 in Advances in anatomy, embryology, and cell biology

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[New] Reader response: Right Brain: Withholding treatment from a child with an epileptic encephalomyopathy

Research paper by Sethi N. K.

Indexed on: 07 Jan '19

Published on: 24 Dec '18 in Neurology

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[New] Editors' note: Right Brain: Withholding treatment from a child with an epileptic encephalomyopathy

Research paper by Ganesh, A, Galetta, S.

Indexed on: 07 Jan '19

Published on: 24 Dec '18 in Neurology

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[New] Mitochondrial Dysfunction in Type 2 Diabetes Mellitus: An Organ-Based Analysis.

Research paper by Mark V MV Pinti, Garrett K GK Fink, Quincy A QA Hathaway, Andrya J AJ Durr, Amina A Kunovac, John M JM Hollander

Indexed on: 03 Jan '19

Published on: 03 Jan '19 in American journal of physiology. Endocrinology and metabolism

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[New] Histopathological liver findings in patients with hepatocerebral mitochondrial depletion syndrome with defined molecular basis.

Research paper by Maciej M Pronicki, Dorota D Piekutowska-Abramczuk, Dariusz D Rokicki, Katarzyna K Iwanicka-Pronicka, Wiesława W Grajkowska

Indexed on: 05 Dec '18

Published on: 05 Dec '18 in Polish journal of pathology : official journal of the Polish Society of Pathologists

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[New] Identification of an endemic Mediterranean brown trout mtDNA group within a highly perturbed aquatic system, the Llobregat River (NE Spain)

Research paper by M. Vera, C. Bouza; A. Casanova; S. Heras; P. Martínez; J. L. García-Marín

Indexed on: 03 Dec '18

Published on: 01 Jan '19 in Hydrobiologia

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[New] Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder.

Research paper by Christos C Chinopoulos, Spyros S Batzios, Lambertus P LP van den Heuvel, Richard R Rodenburg, Roel R Smeets, Hans R HR Waterham, Marjolein M Turkenburg, Jos P JP Ruiter, Ronald J A RJA Wanders, Judit J Doczi, Gergo G Horvath, Arpad A Dobolyi, Euthymia E Vargiami, Ron A RA Wevers, Dimitrios D Zafeiriou

Indexed on: 25 Nov '18

Published on: 25 Nov '18 in Molecular Genetics and Metabolism

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[New] Molecular Processes Connecting DNA Methylation Patterns with DNA Methyltransferases and Histone Modifications in Mammalian Genomes.

Research paper by Albert A Jeltsch, Julian J Broche, Pavel P Bashtrykov

Indexed on: 25 Nov '18

Published on: 25 Nov '18 in Genes

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[New] POLG-related disorders and their neurological manifestations.

Research paper by Shamima S Rahman, William C WC Copeland

Indexed on: 20 Nov '18

Published on: 20 Nov '18 in Nature Reviews Neurology

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[New] A homozygous variant in RRM2B is associated with severe metabolic acidosis and early neonatal death.

Research paper by Brent A BA Penque, Leila L Su, Jianghai J Wang, Weizhen W Ji, Allen A Bale, Frank F Luh, Robert K RK Fulbright, Uzair U Sarmast, Annalisa G AG Sega, Monica M Konstantino, Michele M Spencer-Manzon, Richard R Pierce, Yun Y Yen, Saquib A SA Lakhani

Indexed on: 16 Nov '18

Published on: 16 Nov '18 in European Journal of Medical Genetics

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[New] Nucleoside supplementation modulates mitochondrial DNA copy number in the dguok-/- zebrafish.

Research paper by Benjamin B Munro, Rita R Horvath, Juliane S JS Müller

Indexed on: 15 Nov '18

Published on: 15 Nov '18 in Human molecular genetics

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[New] Twinkle-Associated Mitochondrial DNA Depletion.

Research paper by Salma S Remtulla, Cam-Tu CT Emilie Nguyen, Chitra C Prasad, Craig C Campbell

Indexed on: 06 Nov '18

Published on: 06 Nov '18 in Pediatric Neurology

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[New] Mitochondrial Nucleoids: Superresolution microscopy analysis.

Research paper by Petr P Ježek, Tomáš T Špaček, Jan J Tauber, Vojtěch V Pavluch

Indexed on: 06 Nov '18

Published on: 06 Nov '18 in The International Journal of Biochemistry & Cell Biology

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[New] The mitochondrial inner membrane protein MPV17 prevents uracil accumulation in mitochondrial DNA

Research paper by Judith R. Alonzo, Chantel Venkataraman, Martha S. Field, Patrick J. Stover

Indexed on: 02 Nov '18

Published on: 01 Nov '18 in Journal of Biological Chemistry

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[New] Lower mitochondrial DNA content but not increased mutagenesis associates with decreased base excision repair activity in brains of AD subjects.

Research paper by Daniela T DT Soltys, Carolina P M CPM Pereira, Fernanda T FT Rowies, José M JM Farfel, Lea T LT Grinberg, Claudia K CK Suemoto, Renata E P REP Leite, Roberta D RD Rodriguez, Nolan G NG Ericson, Jason H JH Bielas, Nadja C NC Souza-Pinto

Indexed on: 26 Oct '18

Published on: 26 Oct '18 in Neurobiology of Aging

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[New] Phenotypic expansion in DDX3X - a common cause of intellectual disability in females.

Research paper by Xia X Wang, Jennifer E JE Posey, Jill A JA Rosenfeld, Carlos A CA Bacino, Fernando F Scaglia, LaDonna L Immken, Jill M JM Harris, Scott E SE Hickey, Theresa M TM Mosher, Anne A Slavotinek, Jing J Zhang, Joke J Beuten, Magalie S MS Leduc, Weimin W He, Francesco F Vetrini, et al.

Indexed on: 24 Oct '18

Published on: 24 Oct '18 in Annals of Clinical and Translational Neurology

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[New] Mitochondrial DNA content of peripheral blood mononuclear cells in ART untreated & stavudine/zidovudine treated HIV-1-infected patients

Research paper by Dhakshinamoorthy Subashini, Thongadi Ramesh Dinesha, Rao B Srirama, Jayaseelan Boobalan, Selvamuthu Poongulali, Devaraj A Chitra, Sarvode N Mothi, Sunil Suhas Solomon, Shanmugam Saravanan, Suniti Solomon, Pachamuthu Balakrishnan

Indexed on: 22 Oct '18

Published on: 19 Oct '18 in Indian journal of medical sciences

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[New] Spice-derived phenolic, malabaricone B induces mitochondrial damage in lung cancer cells via a p53-independent pathway.

Research paper by Mrityunjay M Tyagi, Biswanath B Maity, Bhaskar B Saha, Ajay Kumar AK Bauri, Mahesh M Subramanian, Subrata S Chattopadhyay, Birija Sankar BS Patro

Indexed on: 16 Oct '18

Published on: 16 Oct '18 in Food & Function

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[New] Autophagy determines mtDNA copy number dynamics during starvation.

Research paper by Tania Catarina TC Medeiros, Martin M Graef

Indexed on: 12 Oct '18

Published on: 12 Oct '18 in Autophagy

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[New] MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathy.

Research paper by Matthias M Baumann, Herbert H Schreiber, Beate B Schlotter-Weigel, Wolfgang N WN Löscher, Rolf R Stucka, Daniela D Karall, Tim M TM Strom, Peter P Bauer, Birgit B Krabichler, Christine C Fauth, Dieter D Glaeser, Jan J Senderek

Indexed on: 10 Oct '18

Published on: 10 Oct '18 in Clinical Genetics

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3630 results for

Mitochondrial DNA depletion

Showing Results 1-30

Can't find what you're looking for? Suggest a paper to be added

[New] L-Cysteine supplementation prevents liver transplantation in a patient with TRMU deficiency.

[New] Mitochondrial RNA granules are critically dependent on mtDNA replication factors Twinkle and mtSSB.

[New] Metabolic liver diseases presenting with neonatal cholestasis: at the crossroad between old and new paradigms

[New] Mitochondrial unfolded protein response: a stress response with implications for fertility and reproductive aging.

[New] Cereblon attenuates DNA damage-induced apoptosis by regulating the transcription-independent function of p53.

[New] Evidence that growth hormone can improve mitochondrial function in oocytes from aged mice.

[New] Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn's disease.

[New] ATM is activated by ATP depletion and modulates mitochondrial function through NRF1.

[New] Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far.

[New] Biomolecules, Vol. 9, Pages 15: Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

[New] Transmission of Dysfunctional Mitochondrial DNA and Its Implications for Mammalian Reproduction.

[New] Reader response: Right Brain: Withholding treatment from a child with an epileptic encephalomyopathy

[New] Editors' note: Right Brain: Withholding treatment from a child with an epileptic encephalomyopathy

[New] Mitochondrial Dysfunction in Type 2 Diabetes Mellitus: An Organ-Based Analysis.

[New] Histopathological liver findings in patients with hepatocerebral mitochondrial depletion syndrome with defined molecular basis.

[New] Identification of an endemic Mediterranean brown trout mtDNA group within a highly perturbed aquatic system, the Llobregat River (NE Spain)

[New] Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder.

[New] Molecular Processes Connecting DNA Methylation Patterns with DNA Methyltransferases and Histone Modifications in Mammalian Genomes.

[New] POLG-related disorders and their neurological manifestations.

[New] A homozygous variant in RRM2B is associated with severe metabolic acidosis and early neonatal death.

[New] Nucleoside supplementation modulates mitochondrial DNA copy number in the dguok-/- zebrafish.

[New] Twinkle-Associated Mitochondrial DNA Depletion.

[New] Mitochondrial Nucleoids: Superresolution microscopy analysis.

[New] The mitochondrial inner membrane protein MPV17 prevents uracil accumulation in mitochondrial DNA

[New] Lower mitochondrial DNA content but not increased mutagenesis associates with decreased base excision repair activity in brains of AD subjects.

[New] Phenotypic expansion in DDX3X - a common cause of intellectual disability in females.

[New] Mitochondrial DNA content of peripheral blood mononuclear cells in ART untreated & stavudine/zidovudine treated HIV-1-infected patients

[New] Spice-derived phenolic, malabaricone B induces mitochondrial damage in lung cancer cells via a p53-independent pathway.

[New] Autophagy determines mtDNA copy number dynamics during starvation.

[New] MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathy.

3630 results for

Mitochondrial DNA depletion

Showing Results 1-30

Can't find what you're looking for? Suggest a paper to be added

[New] L-Cysteine supplementation prevents liver transplantation in a patient with TRMU deficiency.

[New] Mitochondrial RNA granules are critically dependent on mtDNA replication factors Twinkle and mtSSB.

[New] Metabolic liver diseases presenting with neonatal cholestasis: at the crossroad between old and new paradigms

[New] Mitochondrial unfolded protein response: a stress response with implications for fertility and reproductive aging.

[New] Cereblon attenuates DNA damage-induced apoptosis by regulating the transcription-independent function of p53.

[New] Evidence that growth hormone can improve mitochondrial function in oocytes from aged mice.

[New] Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn's disease.

[New] ATM is activated by ATP depletion and modulates mitochondrial function through NRF1.

[New] Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far.

[New] Biomolecules, Vol. 9, Pages 15: Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

[New] Transmission of Dysfunctional Mitochondrial DNA and Its Implications for Mammalian Reproduction.

[New] Reader response: Right Brain: Withholding treatment from a child with an epileptic encephalomyopathy

[New] Editors' note: Right Brain: Withholding treatment from a child with an epileptic encephalomyopathy

[New] Mitochondrial Dysfunction in Type 2 Diabetes Mellitus: An Organ-Based Analysis.

[New] Histopathological liver findings in patients with hepatocerebral mitochondrial depletion syndrome with defined molecular basis.

[New] Identification of an endemic Mediterranean brown trout mtDNA group within a highly perturbed aquatic system, the Llobregat River (NE Spain)

[New] Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder.

[New] Molecular Processes Connecting DNA Methylation Patterns with DNA Methyltransferases and Histone Modifications in Mammalian Genomes.

[New] POLG-related disorders and their neurological manifestations.

[New] A homozygous variant in RRM2B is associated with severe metabolic acidosis and early neonatal death.

[New] Nucleoside supplementation modulates mitochondrial DNA copy number in the dguok-/- zebrafish.

[New] Twinkle-Associated Mitochondrial DNA Depletion.

[New] Mitochondrial Nucleoids: Superresolution microscopy analysis.

[New] The mitochondrial inner membrane protein MPV17 prevents uracil accumulation in mitochondrial DNA

[New] Lower mitochondrial DNA content but not increased mutagenesis associates with decreased base excision repair activity in brains of AD subjects.

[New] Phenotypic expansion in DDX3X - a common cause of intellectual disability in females.

[New] Mitochondrial DNA content of peripheral blood mononuclear cells in ART untreated & stavudine/zidovudine treated HIV-1-infected patients

[New] Spice-derived phenolic, malabaricone B induces mitochondrial damage in lung cancer cells via a p53-independent pathway.

[New] Autophagy determines mtDNA copy number dynamics during starvation.

[New] MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathy.

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