Nijtmans, L.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

51

Mitochondrial assembly in yeast

Les A Grivell, Marta Artal-Sanz, Gertjan Hakkaart, Liesbeth de Jong, Leo G.J Nijtmans, Katinka van Oosterum, Michel Siep, Hans van der Spek

Journal:

Year:

1999

Language:

english

File:

PDF, 205 KB

english, 1999

52

Blue Native electrophoresis to study mitochondrial and other protein complexes

Leo G.J Nijtmans, Nadine S Henderson, Ian J Holt

Journal:

Year:

2002

Language:

english

File:

PDF, 205 KB

english, 2002

53

New perspectives on the assembly process of mitochondrial respiratory chain complex cytochrome c oxidase

Cristina Ugalde, Marieke J.H Coenen, Murtada H Farhoud, Stefanie Gilinsky, Werner J.H Koopman, Lambert P van den Heuvel, Jan A.M Smeitink, Leo G.J Nijtmans

Journal:

Year:

2002

Language:

english

File:

PDF, 349 KB

english, 2002

54

Iterative orthology prediction uncovers new mitochondrial proteins and identifies C12orf62 as the human ortholog of COX14, a protein involved in the assembly of cytochromecoxidase

Radek Szklarczyk, Bas FJ Wanschers, Thomas D Cuypers, John J Esseling, Moniek Riemersma, Mariël AM van den Brand, Jolein Gloerich, Edwin Lasonder, Lambert P van den Heuvel, Leo G Nijtmans, Martijn A H

Journal:

Year:

2012

Language:

english

File:

PDF, 880 KB

english, 2012

55

Human mitochondrial complex I assembly: A dynamic and versatile process

Rutger O. Vogel, Jan A.M. Smeitink, Leo G.J. Nijtmans

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2007

Language:

english

File:

PDF, 745 KB

english, 2007

56

Mitigation of NADH: Ubiquinone oxidoreductase deficiency by chronic Trolox treatment

Werner J.H. Koopman, Sjoerd Verkaart, Sjenet E. van Emst-de Vries, Sander Grefte, Jan A.M. Smeitink, Leo G.J. Nijtmans, Peter H.G.M. Willems

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2008

Language:

english

File:

PDF, 492 KB

english, 2008

57

S12.20 Delayed assembly kinetics of respiratory chain complex i in cybrids harbouring primary LHON mutations

Rosa Pello, Valerio Carelli, Andrea Martinuzzi, Leo Nijtmans, Miguel A. Martín, Jan Smeitink, Joaquín Arenas, Cristina Ugalde

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2008

Language:

english

File:

PDF, 65 KB

english, 2008

58

S9/2 Cause and consequence of altered mitochondrial dynamics in mitochondrial complex I deficiency

Werner J.H. Koopman, Leo G. Nijtmans, Jan A.M. Smeitink, Peter H.G.M. Willems

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2008

Language:

english

File:

PDF, 74 KB

english, 2008

59

A structure for the yeast prohibitin complex: Structure prediction and evidence from chemical crosslinking and mass spectrometry

Jaap W. Back, Marta Artal Sanz, Luitzen de Jong, Leo J. de Koning, Leo G.J. Nijtmans, Chris G. de Koster, Les A. Grivell, Hans van der Spek, Anton O. Muijsers

Journal:

Protein Science

Year:

2002

Language:

english

File:

PDF, 168 KB

english, 2002

60

Mammalian Mitochondrial Complex I: Biogenesis, Regulation, and Reactive Oxygen Species Generation

Koopman, Werner J.H., Nijtmans, Leo G.J., Dieteren, Cindy E.J., Roestenberg, Peggy, Valsecchi, Federica, Smeitink, Jan A.M., Willems, Peter H.G.M.

Journal:

Antioxidants & Redox Signaling

Year:

2010

Language:

english

File:

PDF, 11.33 MB

english, 2010

61

Ribosome profiling reveals features of normal and disease-associated mitochondrial translation

Rooijers, Koos, Loayza-Puch, Fabricio, Nijtmans, Leo G., Agami, Reuven

Journal:

Nature Communications

Year:

2013

Language:

english

File:

PDF, 1.69 MB

english, 2013

62

Mitochondrial complex III stabilizes complex I in the absence of NDUFS4 to provide partial activity

Calvaruso, M. A., Willems, P., van den Brand, M., Valsecchi, F., Kruse, S., Palmiter, R., Smeitink, J., Nijtmans, L.

Journal:

Human Molecular Genetics

Year:

2012

Language:

english

File:

PDF, 194 KB

english, 2012

63

Mutations in COA6 cause Cytochrome c Oxidase Deficiency and Neonatal Hypertrophic Cardiomyopathy

Baertling, Fabian, A.M. van den Brand, Mariel, Hertecant, Jozef L., Al-Shamsi, Aisha, P. van den Heuvel, Lambert, Distelmaier, Felix, Mayatepek, Ertan, Smeitink, Jan A., Nijtmans, Leo G.J., Rodenburg,

Journal:

Year:

2015

Language:

english

File:

PDF, 378 KB

english, 2015

64

TEFM (c17orf42) is necessary for transcription of human mtDNA

Minczuk, M., He, J., Duch, A. M., Ettema, T. J., Chlebowski, A., Dzionek, K., Nijtmans, L. G. J., Huynen, M. A., Holt, I. J.

Journal:

Nucleic Acids Research

Year:

2011

Language:

english

File:

PDF, 6.74 MB

english, 2011

65

Characterization of SURF-1 Expression and Surf-1p Function in Normal and Disease Conditions

Tiranti, V., Galimberti, C., Nijtmans, L., Bovolenta, S., Paola Perini, M., Zeviani, M.

Journal:

Human Molecular Genetics

Year:

1999

Language:

english

File:

PDF, 475 KB

english, 1999

66

[Topics in Current Genetics] Mitochondrial Function and Biogenesis Volume 8 || Function and dysfunction of the oxidative phosphorylation system

Nijtmans, Leo G.J.

Year:

2004

File:

PDF, 664 KB

2004

67

Endogenous Cytokinins in Flower Bud Forming Explants of Tobacco

VAN DER KRIEKEN, W. M., VAN ELDIK, G., NIJTMANS, L., CROES, A. F., WULLEMS, G. J.

Journal:

Journal of Experimental Botany

Year:

1991

Language:

english

File:

PDF, 357 KB

english, 1991

68

Encyclopedia of Life Sciences || Oxidative Phosphorylation System: Nuclear Genes and Genetic Disease

Year:

2001

Language:

english

File:

PDF, 258 KB

english, 2001

69

Identification of Mitochondrial Complex I Assembly Intermediates by Tracing Tagged NDUFS3 Demonstrates the Entry Point of Mitochondrial Subunits

Vogel, R. O., Dieteren, C. E. J., van den Heuvel, L. P. W. J., Willems, P. H. G. M., Smeitink, J. A. M., Koopman, W. J. H., Nijtmans, L. G. J.

Journal:

Journal of Biological Chemistry

Year:

2006

Language:

english

File:

PDF, 850 KB

english, 2006

70

Solute diffusion is hindered in the mitochondrial matrix

Dieteren, C. E. J., Gielen, S. C. A. M., Nijtmans, L. G. J., Smeitink, J. A. M., Swarts, H. G., Brock, R., Willems, P. H. G. M., Koopman, W. J. H.

Journal:

Proceedings of the National Academy of Sciences

Year:

2011

Language:

english

File:

PDF, 1.31 MB

english, 2011

71

Subunits of Mitochondrial Complex I Exist as Part of Matrix- and Membrane-associated Subcomplexes in Living Cells

Dieteren, C. E. J., Willems, P. H. G. M., Vogel, R. O., Swarts, H. G., Fransen, J., Roepman, R., Crienen, G., Smeitink, J. A. M., Nijtmans, L. G. J., Koopman, W. J. H.

Journal:

Journal of Biological Chemistry

Year:

2008

Language:

english

File:

PDF, 1.08 MB

english, 2008

72

A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia

Szklarczyk, R., Wanschers, B. F. J., Nijtmans, L. G., Rodenburg, R. J., Zschocke, J., Dikow, N., van den Brand, M. A. M., Hendriks-Franssen, M. G. M., Gilissen, C., Veltman, J. A., Nooteboom, M., Koop

Journal:

Human Molecular Genetics

Year:

2013

Language:

english

File:

PDF, 394 KB

english, 2013

73

Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins

Schwab, Marina A., Sauer, Sven W., Okun, Jürgen G., Nijtmans, Leo G. J., Rodenburg, Richard J. T., van den Heuvel, Lambert P., Dröse, Stefan, Brandt, Ulrich, Hoffmann, Georg F., Ter Laak, Henk, Kölker

Journal:

Biochemical Journal

Year:

2006

Language:

english

File:

PDF, 366 KB

english, 2006

74

The Mitochondrial Prohibitin Complex Is Essential for Embryonic Viability and Germline Function in Caenorhabditis elegans

Sanz, M. A., Tsang, W. Y., Willems, E. M., Grivell, L. A., Lemire, B. D., van der Spek, H., Nijtmans, L. G. J.

Journal:

Journal of Biological Chemistry

Year:

2003

Language:

english

File:

PDF, 998 KB

english, 2003

75

ACAD9, a complex I assembly factor with a moonlighting function in fatty acid oxidation deficiencies

Nouws, J., te Brinke, H., Nijtmans, L. G., Houten, S. M.

Journal:

Human Molecular Genetics

Year:

2014

Language:

english

File:

PDF, 795 KB

english, 2014

76

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease

Pello, R., Martin, M. A., Carelli, V., Nijtmans, L. G., Achilli, A., Pala, M., Torroni, A., Gomez-Duran, A., Ruiz-Pesini, E., Martinuzzi, A., Smeitink, J. A., Arenas, J., Ugalde, C.

Journal:

Human Molecular Genetics

Year:

2008

Language:

english

File:

PDF, 582 KB

english, 2008

77

Impaired ATP Synthase Assembly Associated with a Mutation in the Human ATP Synthase Subunit 6 Gene

Nijtmans, L. G. J., Henderson, N. S., Attardi, G., Holt, I. J.

Journal:

Journal of Biological Chemistry

Year:

2001

Language:

english

File:

PDF, 850 KB

english, 2001

78

Subunit-specific Incorporation Efficiency and Kinetics in Mitochondrial Complex I Homeostasis

Dieteren, C. E. J., Koopman, W. J. H., Swarts, H. G., Peters, J. G. P., Maczuga, P., van Gemst, J. J., Masereeuw, R., Smeitink, J. A. M., Nijtmans, L. G. J., Willems, P. H. G. M.

Journal:

Journal of Biological Chemistry

Year:

2012

Language:

english

File:

PDF, 3.13 MB

english, 2012

79

A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy

Jonckheere, A I, Hogeveen, M, Nijtmans, L G J, van den Brand, M A M, Janssen, A J M, Diepstra, J H S, van den Brandt, F C A, van den Heuvel, L P, Hol, F A, Hofste, T G J, Kapusta, L, Dillmann, U, Sham

Journal:

Journal of Medical Genetics

Year:

2007

Language:

english

File:

PDF, 456 KB

english, 2007

80

Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome

Ostergaard, E., Rodenburg, R. J., van den Brand, M., Thomsen, L. L., Duno, M., Batbayli, M., Wibrand, F., Nijtmans, L.

Journal:

Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 234 KB

english, 2011

81

Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assembly

Hornig-Do, Hue-Tran, Tatsuta, Takashi, Buckermann, Angela, Bust, Maria, Kollberg, Gittan, Rötig, Agnes, Hellmich, Martin, Nijtmans, Leo, Wiesner, Rudolf J

Journal:

The EMBO Journal

Year:

2012

Language:

english

File:

PDF, 2.35 MB

english, 2012

82

Human NADH:ubiquinone oxidoreductase deficiency: radical changes in mitochondrial morphology?

Koopman, W. J. H., Verkaart, S., Visch, H. J., van Emst-de Vries, S., Nijtmans, L. G. J., Smeitink, J. A. M., Willems, P. H. G. M.

Journal:

AJP Cell Physiology

Year:

2007

Language:

english

File:

PDF, 338 KB

english, 2007

83

NUBPL mutations in patients with complex I deficiency and a distinct MRI pattern

Kevelam, S. H., Rodenburg, R. J., Wolf, N. I., Ferreira, P., Lunsing, R. J., Nijtmans, L. G., Mitchell, A., Arroyo, H. A., Rating, D., Vanderver, A., van Berkel, C. G. M., Abbink, T. E. M., Heutink, P

Journal:

Year:

2013

Language:

english

File:

PDF, 622 KB

english, 2013

84

Cerebellar Hypoplasia in Respiratory Chain Dysfunction

Lincke, C., van den Bogert, C., Nijtmans, L., Wanders, R., Tamminga, P., Barth, P.

Journal:

Neuropediatrics

Year:

1996

Language:

english

File:

PDF, 661 KB

english, 1996

85

Cell Biological Consequences of Mitochondrial NADH: Ubiquinone Oxidoreductase Deficiency

Smeitink, Jan, van den Heuvel, Lambert, Koopman, Werner, Nijtmans, Leo, Ugalde, Cristina, Willems, Peter

Journal:

Current Neurovascular Research

Year:

2004

Language:

english

File:

PDF, 77 KB

english, 2004

86

Increased mitochondrial ATP production capacity in brain of healthy mice and a mouse model of isolated complex I deficiency after isoflurane anesthesia

Manjeri, Ganesh R., Rodenburg, Richard J., Blanchet, Lionel, Roelofs, Suzanne, Nijtmans, Leo G., Smeitink, Jan A., Driessen, Jacques J., Koopman, Werner J. H., Willems, Peter H.

Journal:

Journal of Inherited Metabolic Disease

Year:

2016

Language:

english

File:

PDF, 488 KB

english, 2016

87

Mitochondrial Complex V Expression and Activity in Cystinotic Fibroblasts

Wilmer, Martijn J, van den Heuvel, Lambertus P, Rodenburg, Richard J, Vogel, Rutger O, Nijtmans, Leo G, Monnens, Leo A, Levtchenko, Elena N

Journal:

Pediatric Research

Year:

2008

Language:

english

File:

PDF, 309 KB

english, 2008

88

C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translation

Wanschers, B. F. J., Szklarczyk, R., Pajak, A., van den Brand, M. A. M., Gloerich, J., Rodenburg, R. J. T., Lightowlers, R. N., Nijtmans, L. G., Huynen, M. A.

Journal:

Nucleic Acids Research

Year:

2012

Language:

english

File:

PDF, 7.55 MB

english, 2012

89

Unraveling the complexity of mitochondrial complex I assembly: A dynamic process

Sánchez-Caballero, Laura, Guerrero-Castillo, Sergio, Nijtmans, Leo

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2016

Language:

english

File:

PDF, 1.16 MB

english, 2016

90

Complex I assembly: a puzzling problem

Vogel, Rutger, Nijtmans, Leo, Ugalde, Cristina, van den Heuvel, Lambert, Smeitink, Jan

Journal:

Current Opinion in Neurology

Year:

2004

Language:

english

File:

PDF, 129 KB

english, 2004

91

Solute diffusion is hindered in the mitochondrial matrix

Cindy E. J. Dieteren, Stan C. A. M. Gielen, Leo G. J. Nijtmans, Jan A. M. Smeitink, Herman G. Swarts, Roland Brock, Peter H. G. M. Willems and Werner J. H. Koopman

Journal:

Proceedings of the National Academy of Sciences

Year:

2011

Language:

english

File:

PDF, 1.48 MB

english, 2011

92

Abnormal cardiolipin and phosphatidylglycerol remodeling in barth syndrome

Vreken, P, Valianpour, F, LA, Grivell, LG, Nijtmans, RJA, Wanders, PG, Barth

Journal:

Biochemical Society Transactions

Year:

2001

Language:

english

File:

PDF, 131 KB

english, 2001

93

The Assembly Pathway of Mitochondrial Respiratory Chain Complex I

Guerrero-Castillo, Sergio, Baertling, Fabian, Kownatzki, Daniel, Wessels, Hans J., Arnold, Susanne, Brandt, Ulrich, Nijtmans, Leo

Journal:

Cell Metabolism

Year:

2016

Language:

english

File:

PDF, 3.73 MB

english, 2016

94

Mutations in mitochondrial complex I assembly factor NDUFAF3 cause Leigh syndrome

Baertling, Fabian, Sánchez-Caballero, Laura, Timal, Sharita, van den Brand, Mariël AM, Ngu, Lock Hock, Distelmaier, Felix, Rodenburg, Richard JT, Nijtmans, Leo GJ

Journal:

Molecular Genetics and Metabolism

Year:

2017

Language:

english

File:

PDF, 555 KB

english, 2017

95

Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive

Baertling, Fabian, Al-Murshedi, Fathiya, Sánchez-Caballero, Laura, Al-Senaidi, Khalfan, Joshi, Niranjan P, Venselaar, Hanka, van den Brand, Mariël AM, Nijtmans, Leo GJ, Rodenburg, Richard JT

Journal:

Year:

2017

Language:

english

File:

PDF, 1.29 MB

english, 2017

96

NDUFAF4 variants are associated with Leigh syndrome and cause a specific mitochondrial complex I assembly defect

Baertling, Fabian, Sánchez-Caballero, Laura, van den Brand, Mariël A M, Wintjes, Liesbeth T, Brink, Maaike, van den Brandt, Frans A, Wilson, Callum, Rodenburg, Richard J T, Nijtmans, Leo G J

Journal:

European Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 580 KB

english, 2017

97

A Heterozygous NDUFV1 Variant Aggravates Mitochondrial Complex I Deficiency in a Family with a Homoplasmic ND1 Variant

Baertling, Fabian, Sánchez-Caballero, Laura, van den Brand, Mariël A.M., Distelmaier, Felix, Janssen, Mirian C.H., Rodenburg, Richard J.T., Smeitink, Jan A.M., Nijtmans, Leo G.J.

Journal:

The Journal of Pediatrics

Year:

2018

Language:

english

File:

PDF, 1.15 MB

english, 2018

98

Corrigendum to “Mitigation of NADH:ubiquinone oxidoreductase deficiency by chronic Trolox treatment” [Biochimica et Biophysica Acta 1777/7–8 (2008) 853–859]

Koopman, Werner J.H., Verkaart, Sjoerd, van Emst-de Vries, Sjenet E., Grefte, Sander, Smeitink, Jan A.M., Nijtmans, Leo G.J., Willems, Peter H.G.M.

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2018

Language:

english

File:

PDF, 127 KB

english, 2018

99

Corrigendum to âSuperoxide production is inversely related to complex I activity in inherited complex I deficiencyâ [Biochim Biophys Acta. 1772 (3) (2007) 373â381]

Verkaart, Sjoerd, Koopman, Werner J.H., van Emst-de Vries, Sjenet E., Nijtmans, Leo G.J., van den Heuvel, Lambertus W.P.J., Smeitink, Jan A.M., Willems, Peter H.G.M.

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

2020

File:

PDF, 1.38 MB

2020