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Results 1 - 20 of 413  for Central Connecticut State University

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1
Mitochondrion.
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Journal
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Mitochondrion.

Mitochondria Research Society.

Shannon, Ireland : Elsevier Science Ireland ©2001-

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2
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Initial Experiences with Proton MR Spectroscopy in Treatment Monitoring of Mitochondrial Encephalopathy

Lee, Seung-Koo ; Kim, Jinna ; Kim, Heung Dong ; Lee, Joon Soo ; Lee, Young Mock

Yonsei Medical Journal, 2010, Vol.51(5), p.672-675 [Peer Reviewed Journal]

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3
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Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family

Kullar, Peter J ; Gomez - Duran, Aurora ; Gammage, Payam A ; Garone, Caterina ; Minczuk, Michal ; Golder, Zoe ; Wilson, Janet ; Montoya, Julio ; Häkli, Sanna ; Kärppä, Mikko ; Horvath, Rita ; Majamaa, Kari ; Chinnery, Patrick F

Brain, 2018, Vol. 141(1), pp.55-62 [Peer Reviewed Journal]

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4
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Disease progression in patients with single, large-scale mitochondrial DNA deletions

Grady, John P ; Campbell, Georgia ; Ratnaike, Thiloka ; Blakely, Emma L ; Falkous, Gavin ; Nesbitt, Victoria ; Schaefer, Andrew M ; Mcnally, Richard J ; Gorman, Grainne S ; Taylor, Robert W ; Turnbull, Doug M ; Mcfarland, Robert

Brain, 2014, Vol. 137(2), pp.323-334 [Peer Reviewed Journal]

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5
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Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases

Papa, Sergio ; Rasmo, Domenico De ; Technikova-Dobrova, Zuzana ; Panelli, Damiano ; Signorile, Anna ; Scacco, Salvatore ; Petruzzella, Vittoria ; Papa, Francesco ; Palmisano, Giuseppe ; Gnoni, Antonio ; Micelli, Loris ; Sardanelli, Anna Maria

FEBS Letters, 09 March 2012, Vol.586(5), pp.568-577 [Peer Reviewed Journal]

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6
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Microangiopathy in the cerebellum of patients with mitochondrial DNA disease

Lax, Nichola Z ; Pienaar, Ilse S ; Reeve, Amy K ; Hepplewhite, Philippa D ; Jaros, Evelyn ; Taylor, Robert W ; Kalaria, Raj N ; Turnbull, Doug M

Brain, 2012, Vol. 135(6), pp.1736-1750 [Peer Reviewed Journal]

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7
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What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

Neeve, Vivienne C. M ; Samuels, David C ; Bindoff, Laurence A ; Van Den Bosch, Bianca ; Van Goethem, Gert ; Smeets, Hubert ; Lombès, Anne ; Jardel, Claude ; Hirano, Michio ; Dimauro, Salvatore ; De Vries, Maaike ; Smeitink, Jan ; Smits, Bart W ; De Coo, Ireneus F. M ; Saft, Carsten ; Klopstock, Thomas ; Keiling, Bianca - Cortina ; Czermin, Birgit ; Abicht, Angela ; Lochmüller, Hanns ; Hudson, Gavin ; Gorman, Grainne G ; Turnbull, Doug M ; Taylor, Robert W ; Holinski - Feder, Elke ; Chinnery, Patrick F ; Horvath, Rita

Brain, 2012, Vol. 135(12), pp.3614-3626 [Peer Reviewed Journal]

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8
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Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson’s disease

Fitzgerald, Julia C ; Zimprich, Alexander ; Carvajal Berrio, Daniel A ; Schindler, Kevin M ; Maurer, Brigitte ; Schulte, Claudia ; Bus, Christine ; Hauser, Anne - Kathrin ; Kübler, Manuela ; Lewin, Rahel ; Bobbili, Dheeraj Reddy ; Schwarz, Lisa M ; Vartholomaiou, Evangelia ; Brockmann, Kathrin ; Wüst, Richard ; Madlung, Johannes ; Nordheim, Alfred ; Riess, Olaf ; Martins, L. Miguel ; Glaab, Enrico ; May, Patrick ; Schenke - Layland, Katja ; Picard, Didier ; Sharma, Manu ; Gasser, Thomas ; Krüger, Rejko

Brain, 2017, Vol. 140(9), pp.2444-2459 [Peer Reviewed Journal]

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9
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Pluripotent Stem Cells for Uncovering the Role of Mitochondria in Human Brain Function and Dysfunction

Zink, Annika ; Priller, Josef ; Prigione, Alessandro

Journal of Molecular Biology, 30 March 2018, Vol.430(7), pp.891-903 [Peer Reviewed Journal]

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10
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Prospective study of POLG mutations presenting in children with intractable epilepsy: Prevalence and clinical features

Uusimaa, Johanna ; Gowda, Vasantha ; Mcshane, Anthony ; Smith, Conrad ; Evans, Julie ; Shrier, Annie ; Narasimhan, Manisha ; O' Rourke, Anthony ; Rajabally, Yusuf ; Hedderly, Tammy ; Cowan, Frances ; Fratter, Carl ; Poulton, Joanna

Epilepsia, June 2013, Vol.54(6), pp.1002-1011 [Peer Reviewed Journal]

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11
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Epigenetics, epidemiology and mitochondrial DNA diseases

Chinnery, Patrick F ; Elliott, Hannah R ; Hudson, Gavin ; Samuels, David C ; Relton, Caroline L

International Journal of Epidemiology, 2012, Vol. 41(1), pp.177-187 [Peer Reviewed Journal]

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12
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Small fibre neuropathy in mitochondrial diseases explored with sudoscan

Luigetti, Marco ; Primiano, Guido ; Cuccagna, Cristina ; Bernardo, Daniela ; Sauchelli, Donato ; Vollono, Catello ; Servidei, Serenella

Clinical Neurophysiology, August 2018, Vol.129(8), pp.1618-1623 [Peer Reviewed Journal]

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13
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Prevalence of neurogenetic disorders in the North of England.

Bargiela, David ; Yu-Wai-Man, Patrick ; Keogh, Michael ; Horvath, Rita ; Chinnery, Patrick Francis ;Apollo - University of Cambridge Repository; Apollo - University of Cambridge Repository

Apollo - University of Cambridge Repository 2015

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14
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Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies

La Morgia, Chiara ; Ross - Cisneros, Fred N ; Sadun, Alfredo A ; Hannibal, Jens ; Munarini, Alessandra ; Mantovani, Vilma ; Barboni, Piero ; Cantalupo, Gaetano ; Tozer, Kevin R ; Sancisi, Elisa ; Salomao, Solange R ; Moraes, Milton N ; Moraes - Filho, Milton N ; Heegaard, Steffen ; Milea, Dan ; Kjer, Poul ; Montagna, Pasquale ; Carelli, Valerio

Brain, 2010, Vol. 133(8), pp.2426-2438 [Peer Reviewed Journal]

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15
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Method of carrier-free delivery of therapeutic RNA importable into human mitochondria: Lipophilic conjugates with cleavable bonds

Dovydenko, Ilya ; Tarassov, Ivan ; Venyaminova, Alya ; Entelis, Nina

Biomaterials, January 2016, Vol.76, pp.408-417 [Peer Reviewed Journal]

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16
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Metabolic Regulation of the Ultradian Oscillator Hes1 by Reactive Oxygen Species

Ventre, Simona ; Indrieri, Alessia ; Fracassi, Chiara ; Franco, Brunella ; Conte, Ivan ; Cardone, Luca ; Di Bernardo, Diego

Journal of Molecular Biology, 22 May 2015, Vol.427(10), pp.1887-1902 [Peer Reviewed Journal]

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17
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Mitochondrial transgene expression via an artificial mitochondrial DNA vector in cells from a patient with a mitochondrial disease

Ishikawa, Takuya ; Somiya, Kana ; Munechika, Reina ; Harashima, Hideyoshi ; Yamada, Yuma

Journal of Controlled Release, 28 March 2018, Vol.274, pp.109-117 [Peer Reviewed Journal]

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18
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The Parent Experience of Caring for a Child with Mitochondrial Disease

Senger, Brenda A ; Ward, Linda D ; Barbosa-Leiker, Celestina ; Bindler, Ruth C

Journal of Pediatric Nursing, January 2016, Vol.31(1), pp.32-41 [Peer Reviewed Journal]

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19
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Complex I spectrophotometric assay in cultured cells: Detailed analysis of key factors

Oliveira, Kátia Klug ; Kiyomoto, Beatriz Hitomi ; Rodrigues, Andresa De Santi ; Tengan, Célia Harumi

Analytical Biochemistry, 01 April 2013, Vol.435(1), pp.57-59 [Peer Reviewed Journal]

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20
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Strokes in mitochondrial diseases

N V Pizova

Nevrologiâ, Nejropsihiatriâ, Psihosomatika, 01 June 2012, Vol.4(2), pp.73-78 [Peer Reviewed Journal]

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