Microbial proteinase inside human cells as anti-mitochondrial activity: A new virulence factor in infectious diseases?

بواسطة Bongaerts, Ger P.A., van den Heuvel, Lambert P.
الحاوية / القاعدة Med Hypotheses (2008)

Uremic Toxins Induce ET-1 Release by Human Proximal Tubule Cells, which Regulates Organic Cation Uptake Time-Dependently

بواسطة Schophuizen, Carolien M. S., Hoenderop, Joost G. J., Masereeuw, Rosalinde, van den Heuvel, Lambert P.
الحاوية / القاعدة Cells (2015)

Reconstructing the evolution of the mitochondrial ribosomal proteome

بواسطة Smits, Paulien, Smeitink, Jan A. M., van den Heuvel, Lambert P., Huynen, Martijn A., Ettema, Thijs J. G.
منشور في 2007

Analysis of CTNS gene transcripts in nephropathic cystinosis

بواسطة Taranta, Anna, Wilmer, Martijn J., van den Heuvel, Lambert P., Bencivenga, Paola, Bellomo, Francesco, Levtchenko, Elena N., Emma, Francesco
منشور في 2010

Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation

بواسطة de Laat, Paul, Koene, Saskia, van den Heuvel, Lambert P. W. J., Rodenburg, Richard J. T., Janssen, Mirian C. H., Smeitink, Jan A. M.
منشور في 2012

ATYPICAL HEMOLYTIC UREMIC SYNDROME AND GENETIC ABERRATIONS IN THE COMPLEMENT FACTOR H RELATED 5 GENE

بواسطة Westra, Dineke, Vernon, Katherine A., Volokhina, Elena B., Pickering, Matthew C., van de Kar, Nicole C.A.J., van den Heuvel, Lambert P.
منشور في 2012

The genetics of atypical hemolytic uremic syndrome

بواسطة Feitz, Wouter J. C., van de Kar, Nicole C. A. J., Orth-Höller, Dorothea, van den Heuvel, Lambert P. J. W., Licht, Christoph
الحاوية / القاعدة Med Genet (2018)

Therapeutic concentrations of calcineurin inhibitors do not deregulate glutathione redox balance in human renal proximal tubule cells

بواسطة Ramazani, Yasaman, Knops, Noël, Berlingerio, Sante Princiero, Adebayo, Oyindamola Christiana, Lismont, Celien, Kuypers, Dirk J., Levtchenko, Elena, van den Heuvel, Lambert P., Fransen, Marc
الحاوية / القاعدة PLoS One (2021)

Agrin Is a Major Heparan Sulfate Proteoglycan Accumulating in Alzheimer’s Disease Brain

بواسطة Verbeek, Marcel M., Otte-Höller, Irene, van den Born, Jacob, van den Heuvel, Lambert P. W. J., David, Guido, Wesseling, Pieter, de Waal, Robert M. W.
منشور في 1999

NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease

بواسطة Hoefs, Saskia J G, van Spronsen, Francjan J, Lenssen, Ellen W H, Nijtmans, Leo G, Rodenburg, Richard J, Smeitink, Jan A M, van den Heuvel, Lambert P
منشور في 2011

Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle

بواسطة Smits, Paulien, Antonicka, Hana, van Hasselt, Peter M, Weraarpachai, Woranontee, Haller, Wolfram, Schreurs, Marieke, Venselaar, Hanka, Rodenburg, Richard J, Smeitink, Jan A, van den Heuvel, Lambert P
منشور في 2011

Cell Biological Responses after Shiga Toxin-1 Exposure to Primary Human Glomerular Microvascular Endothelial Cells from Pediatric and Adult Origin

بواسطة Feitz, Wouter J. C., van Setten, Petra A., van der Velden, Thea J. A. M., Licht, Christoph, van den Heuvel, Lambert P. J. W., van de Kar, Nicole C. A. J.
الحاوية / القاعدة Int J Mol Sci (2021)

Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy

بواسطة Smits, Paulien, Saada, Ann, Wortmann, Saskia B, Heister, Angelien J, Brink, Maaike, Pfundt, Rolph, Miller, Chaya, Haas, Dorothea, Hantschmann, Ralph, Rodenburg, Richard J T, Smeitink, Jan A M, van den Heuvel, Lambert P
منشور في 2011

Characterization of anticoagulant heparinoids by immunoprofiling

بواسطة Wijnhoven, Tessa J., van de Westerlo, Els M., Smits, Nicole C., Lensen, Joost F., Rops, Angelique L., van der Vlag, Johan, Berden, Jo H., van den Heuvel, Lambert P., van Kuppevelt, Toin H.
منشور في 2007

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

بواسطة Szklarczyk, Radek, Wanschers, Bas FJ, Cuypers, Thomas D, Esseling, John J, Riemersma, Moniek, van den Brand, Mariël AM, Gloerich, Jolein, Lasonder, Edwin, van den Heuvel, Lambert P, Nijtmans, Leo G, Huynen, Martijn A
منشور في 2012

Analysis of 953 Human Proteins from a Mitochondrial HEK293 Fraction by Complexome Profiling

بواسطة Wessels, Hans J. C. T., Vogel, Rutger O., Lightowlers, Robert N., Spelbrink, Johannes N., Rodenburg, Richard J., van den Heuvel, Lambert P., van Gool, Alain J., Gloerich, Jolein, Smeitink, Jan A. M., Nijtmans, Leo G.
منشور في 2013

SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors

بواسطة Renkema, G Herma, Wortmann, Saskia B, Smeets, Roel J, Venselaar, Hanka, Antoine, Marion, Visser, Gepke, Ben-Omran, Tawfeg, van den Heuvel, Lambert P, Timmers, Henri J L M, Smeitink, Jan A, Rodenburg, Richard J T
الحاوية / القاعدة Eur J Hum Genet (2015)

First Successful Conception Induced by a Male Cystinosis Patient

بواسطة Veys, Koenraad R., D’Hauwers, Kathleen W., van Dongen, Angelique J. C. M., Janssen, Mirian C., Besouw, Martine T. P., Goossens, Ellen, van den Heuvel, Lambert P., Wetzels, Alex A. M. M., Levtchenko, Elena N.
الحاوية / القاعدة JIMD Rep (2017)

Primary Human Derived Blood Outgrowth Endothelial Cells: An Appropriate In Vitro Model to Study Shiga Toxin Mediated Damage of Endothelial Cells

بواسطة Feitz, Wouter J. C., van de Kar, Nicole C. A. J., Cheong, Ian, van der Velden, Thea J. A. M., Ortiz-Sandoval, Carolina G., Orth-Höller, Dorothea, van den Heuvel, Lambert P. J. W., Licht, Christoph
الحاوية / القاعدة Toxins (Basel) (2020)

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

بواسطة 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, Stefan, Smeitink, Jan A. M.
منشور في 2006