1 - 25 of 30 results for author:"Huynen M.A." in Literature citations
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| 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 oxidase. Szklarczyk R., Wanschers B.F., Cuypers T.D., Esseling J.J., Riemersma M., van den Brand M.A., Gloerich J., Lasonder E., van den Heuvel L.P., Nijtmans L.G. et al. Genome Biol. 13:RESEARCH0012.1-RESEARCH0012.14(2012) · UniProtKB (9) · Mapped (7) |
| C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translation. Wanschers B.F., Szklarczyk R., Pajak A., van den Brand M.A., Gloerich J., Rodenburg R.J., Lightowlers R.N., Nijtmans L.G., Huynen M.A. Nucleic Acids Res. 40:4040-4051(2012) · UniProtKB (1) |
| Analysis of genes regulated by the transcription factor LUMAN identifies ApoA4 as a target gene in dendritic cells. Sanecka A., Ansems M., van Hout-Kuijer M.A., Looman M.W., Prosser A.C., Welten S., Gilissen C., Sama I.E., Huynen M.A., Veltman J.A. et al. Mol. Immunol. 50:66-73(2012) · Mapped (4) |
| Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology. Jonckheere A.I., Huigsloot M., Lammens M., Jansen J., van den Heuvel L.P., Spiekerkoetter U., von Kleist-Retzow J.C., Forkink M., Koopman W.J., Szklarczyk R. et al. Mitochondrion 11:954-963(2011) · Mapped (2) |
| A mutation in C2orf64 causes impaired cytochrome c oxidase assembly and mitochondrial cardiomyopathy. Huigsloot M., Nijtmans L.G., Szklarczyk R., Baars M.J., van den Brand M.A., Hendriksfranssen M.G., van den Heuvel L.P., Smeitink J.A., Huynen M.A., Rodenburg R.J. Am. J. Hum. Genet. 88:488-493(2011) · UniProtKB (1) · Mapped (6) |
| The organellar genome and metabolic potential of the hydrogen-producing mitochondrion of Nyctotherus ovalis. de Graaf R.M., Ricard G., van Alen T.A., Duarte I., Dutilh B.E., Burgtorf C., Kuiper J.W., van der Staay G.W., Tielens A.G., Huynen M.A. et al. Mol. Biol. Evol. 28:2379-2391(2011) · UniProtKB (35) |
| NDUFB7 and NDUFA8 are located at the intermembrane surface of complex I. Szklarczyk R., Wanschers B.F., Nabuurs S.B., Nouws J., Nijtmans L.G., Huynen M.A. |
| 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., Huynen M.A., Holt I.J. Nucleic Acids Res. 39:4284-4299(2011) · UniProtKB (2) · Mapped (1) |
| Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus. Kouwenhoven E.N., van Heeringen S.J., Tena J.J., Oti M., Dutilh B.E., Alonso M.E., de la Calle-Mustienes E., Smeenk L., Rinne T., Parsaulian L. et al. PLoS Genet. 6:e1001065-e1001065(2010) · Mapped (11) |
| A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome. Richter R., Rorbach J., Pajak A., Smith P.M., Wessels H.J., Huynen M.A., Smeitink J.A., Lightowlers R.N., Chrzanowska-Lightowlers Z.M. EMBO J. 29:1116-1125(2010) · UniProtKB (2) |
| The alpha-kinase family: an exceptional branch on the protein kinase tree. Middelbeek J., Clark K., Venselaar H., Huynen M.A., van Leeuwen F.N. Cell. Mol. Life Sci. 67:875-890(2010) · Mapped (6) |
| The hydrogenosomes of Psalteriomonas lanterna. de Graaf R.M., Duarte I., van Alen T.A., Kuiper J.W., Schotanus K., Rosenberg J., Huynen M.A., Hackstein J.H. BMC Evol. Biol. 9:287-287(2009) · UniProtKB (8) |
| Expansion of the human mitochondrial proteome by intra- and inter-compartmental protein duplication. Szklarczyk R., Huynen M.A. Genome Biol. 10:R135-R135(2009) · Mapped (250) |
| The mitochondrial genomes of the ciliates Euplotes minuta and Euplotes crassus. de Graaf R.M., van Alen T.A., Dutilh B.E., Kuiper J.W., van Zoggel H.J., Huynh M.B., Gortz H.D., Huynen M.A., Hackstein J.H. BMC Genomics 10:514-514(2009) · UniProtKB (65) |
| Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease. Saada A., Vogel R.O., Hoefs S.J., van den Brand M.A., Wessels H.J., Willems P.H., Venselaar H., Shaag A., Barghuti F., Reish O. et al. Am. J. Hum. Genet. 84:718-727(2009) · UniProtKB (4) |
| Complex fate of paralogs. Szklarczyk R., Huynen M.A., Snel B. BMC Evol. Biol. 8:337-337(2008) · Mapped (46) |
| The iron-sulphur protein Ind1 is required for effective complex I assembly. Bych K., Kerscher S., Netz D.J.A., Pierik A.J., Zwicker K., Huynen M.A., Lill R., Brandt U., Balk J. |
| Identification of Nipsnap1 as a novel auxiliary protein inhibiting TRPV6 activity. Schoeber J.P., Topala C.N., Lee K.P., Lambers T.T., Ricard G., van der Kemp A.W., Huynen M.A., Hoenderop J.G., Bindels R.J. Pflugers Arch. 457:91-101(2008) · Mapped (9) |
| Reconstructing the evolution of the mitochondrial ribosomal proteome. Smits P., Smeitink J.A., van den Heuvel L.P., Huynen M.A., Ettema T.J. Nucleic Acids Res. 35:4686-4703(2007) · Mapped (79) |
| Development of the first marmoset-specific DNA microarray (EUMAMA): a new genetic tool for large-scale expression profiling in a non-human primate. Datson N.A., Morsink M.C., Atanasova S., Armstrong V.W., Zischler H., Schlumbohm C., Dutilh B.E., Huynen M.A., Waegele B., Ruepp A. et al. BMC Genomics 8:190-190(2007) · UniProtKB (593) |
| Molecular and biochemical analysis of the plastidic ADP-glucose transporter (ZmBT1) from Zea mays. Kirchberger S., Leroch M., Huynen M.A., Wahl M., Neuhaus H.E., Tjaden J. J. Biol. Chem. 282:22481-22491(2007) · UniProtKB (1) |
| YfhJ, a molecular adaptor in iron-sulfur cluster formation or a frataxin-like protein? Pastore C., Adinolfi S., Huynen M.A., Rybin V., Martin S., Mayer M., Bukau B., Pastore A. Structure 14:857-867(2006) · Mapped (1) |
| Deciphering the evolution and metabolism of an anammox bacterium from a community genome. Strous M., Pelletier E., Mangenot S., Rattei T., Lehner A., Taylor M.W., Horn M., Daims H., Bartol-Mavel D., Wincker P. et al. Nature 440:790-794(2006) · UniProtKB (4,495) |
| POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome. van Reeuwijk J., Janssen M., van den Elzen C., Beltran-Valero de Bernabe D., Sabatelli P., Merlini L., Boon M., Scheffer H., Brockington M., Muntoni F. et al. J. Med. Genet. 42:907-912(2005) · UniProtKB (1) · Mapped (2) |
| An anaerobic mitochondrion that produces hydrogen. Boxma B., de Graaf R.M., van der Staay G.W.M., van Alen T.A., Ricard G., Gabaldon T., van Hoek A.H.A.M., Moon-van der Staay S.Y., Koopman W.J.H., van Hellemond J.J. et al. Nature 434:74-79(2005) · UniProtKB (80) |