Search Results - "DORLAND, L"

The F-BAR protein pacsin2 inhibits asymmetric VE-cadherin internalization from tensile adherens junctions by Dorland, Yvonne L., Malinova, Tsveta S., van Stalborch, Anne-Marieke D., Grieve, Adam G., van Geemen, Daphne, Jansen, Nicolette S., de Kreuk, Bart-Jan, Nawaz, Kalim, Kole, Jeroen, Geerts, Dirk, Musters, René J. P., de Rooij, Johan, Hordijk, Peter L., Huveneers, Stephan

“…Vascular homoeostasis, development and disease critically depend on the regulation of endothelial cell–cell junctions. Here we uncover a new role for the F-BAR…”
Get full text

Self-Assembled Fluorescent Organic Nanoparticles for Live-Cell Imaging by Fischer, Irén, Petkau-Milroy, Katja, Dorland, Yvonne L., Schenning, Albertus P. H. J., Brunsveld, Luc

“…Fluorescent, cell‐permeable, organic nanoparticles based on self‐assembled π‐conjugated oligomers with high absorption cross‐sections and high quantum yields…”
Get full text

Cell–cell junctional mechanotransduction in endothelial remodeling by Dorland, Yvonne L., Huveneers, Stephan

Get full text

Cell–cell junctional mechanotransduction in endothelial remodeling by Dorland, Yvonne L., Huveneers, Stephan

“…The vasculature is one of the most dynamic tissues that encounter numerous mechanical cues derived from pulsatile blood flow, blood pressure, activity of…”
Get full text

Prenatal and early postnatal treatment in 3-phosphoglycerate-dehydrogenase deficiency by de Koning, TJ, Klomp, LWJ, van Oppen, ACC, Beemer, FA, Dorland, L, van den Berg, IET, Berger, R

“…3-phosphoglycerate-dehydrogenase (3-PGDH) deficiency is an L-serine biosynthesis disorder, characterised by congenital microcephaly, severe psychomotor…”
Get full text

Expanding the clinical spectrum of 3-phosphoglycerate dehydrogenase deficiency by Tabatabaie, L, Klomp, L. W. J, Rubio-Gozalbo, M. E, Spaapen, L. J. M, Haagen, A. A. M, Dorland, L, de Koning, T. J

“…3-Phosphoglycerate dehydrogenase (3-PGDH) deficiency is considered to be a rare cause of congenital microcephaly, infantile onset of intractable seizures and…”
Get full text

Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy by Westermann, C.M, Dorland, L, Votion, D.M, de Sain-van der Velden, M.G.M, Wijnberg, I.D, Wanders, R.J.A, Spliet, W.G.M, Testerink, N, Berger, R, Ruiter, J.P.N, van der Kolk, J.H

“…Abstract The aim of the current study was to assess lipid metabolism in horses with atypical myopathy. Urine samples from 10 cases were subjected to analysis…”
Get full text

Decreased oxidative phosphorylation and PGAM deficiency in horses suffering from atypical myopathy associated with acquired MADD by Westermann, C.M., Dorland, L., van Diggelen, O.P., Schoonderwoerd, K., Bierau, J., Waterham, H.R., van der Kolk, J.H.

“…Earlier research on ten horses suffering from the frequently fatal disorder atypical myopathy showed that MADD (multiple acyl-CoA dehydrogenase deficiency) is…”
Get full text

Amino acid profile during exercise and training in Standardbreds by Westermann, C.M., Dorland, L., Wijnberg, I.D., de Sain-van der Velden, M.G.M., van Breda, E., Barneveld, A., de Graaf-Roelfsema, E., Keizer, H.A., van der Kolk, J.H.

“…The objective of this study is to assess the influence of acute exercise, training and intensified training on the plasma amino acid profile. In a 32-week…”
Get full text

Equine acquired multiple acyl-CoA dehydrogenase deficiency (MADD) in 14 horses associated with ingestion of Maple leaves (Acer pseudoplatanus) covered with European tar spot (Rhytisma acerinum) by van der Kolk, J.H., Wijnberg, I.D., Westermann, C.M., Dorland, L., de Sain-van der Velden, M.G.M., Kranenburg, L.C., Duran, M., Dijkstra, J.A., van der Lugt, J.J., Wanders, R.J.A., Gruys, E.

“…This case-series describes fourteen horses suspected of equine acquired multiple acyl-CoA dehydrogenase deficiency (MADD) also known as atypical myopathy of…”
Get full text

Nuclear shape, protrusive behaviour and in vivo retention of human bone marrow mesenchymal stromal cells is controlled by Lamin-A/C expression by Dorland, Yvonne L., Cornelissen, Anne S., Kuijk, Carlijn, Tol, Simon, Hoogenboezem, Mark, van Buul, Jaap D., Nolte, Martijn A., Voermans, Carlijn, Huveneers, Stephan

“…Culture expanded mesenchymal stromal cells (MSCs) are being extensively studied for therapeutic applications, including treatment of graft-versus-host disease,…”
Get full text

Cucurbit[8]uril Reactivation of an Inactivated Caspase‐8 Mutant Reveals Differentiated Enzymatic Substrate Processing by Dang, Dung T., van Onzen, Arthur H. A. M., Dorland, Yvonne L., Brunsveld, Luc

“…Caspase‐8 constructs featuring an N‐terminal FGG sequence allow for selective twofold recognition by cucurbit[8]uril, which leads to an increase of the…”
Get full text

Equine biochemical multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of rhabdomyolysis by Westermann, C.M., de Sain-van der Velden, M.G.M., van der Kolk, J.H., Berger, R., Wijnberg, I.D., Koeman, J.P., Wanders, R.J.A., Lenstra, J.A., Testerink, N., Vaandrager, A.B., Vianey-Saban, C., Acquaviva-Bourdain, C., Dorland, L.

“…Two horses (a 7-year-old Groninger warmblood gelding and a six-month-old Trakehner mare) with pathologically confirmed rhabdomyolysis were diagnosed as…”
Get full text

Rhabdomyolysis in early‐onset very long‐chain acyl‐CoA dehydrogenase deficiency despite normal glucose after fasting by Engbers, H. M., Dorland, L., De Sain, M. G. M., Eskes, P. F., Visser, G.

“…Summary A patient with very long‐chain acyl‐CoA dehydrogenase (VLCAD) deficiency presented in the neonatal period with hypoketotic hypoglycaemia and at the age…”
Get full text

Removal of chloroform from biodegradable therapeutic microspheres by radiolysis by Zielhuis, S.W., Nijsen, J.F.W., Dorland, L., Krijger, G.C., van het Schip, A.D., Hennink, W.E.

“…Radioactive holmium-166 loaded poly( l-lactic acid) microspheres are promising systems for the treatment of liver malignancies. These microspheres are loaded…”
Get full text

Congenital microcephaly and seizures due to 3‐phosphoglycerate dehydrogenase deficiency: Outcome of treatment with amino acids by De Koning, T. J., Duran, M., Maldergem, L. Van, Pineda, M., Dorland, L., Gooskens, R., Jaeken, J., Poll‐The, B. T.

“…Congenital microcephaly, intractable seizures and severe psycho‐motor retardation characterize 3‐phosphoglycerate dehydrogenase (3‐PGDH) deficiency, a disorder…”
Get full text

A Novel Disorder of N-Glycosylation Due to Phosphomannose Isomerase Deficiency by de Koning, T.J., Dorland, L., van Diggelen, O.P., Boonman, A.M.C., de Jong, G.J., van Noort, W.L., De Schryver, Jear, Duran, M., van den Berg, I.E.T., Gerwig, G.J., Berger, R., Poll-The, B.T.

“…Three siblings suffered from an unusual disorder of cyclic vomiting and congenital hepatic fibrosis. Serum transferrin isoelectric focusing showed increased…”
Get full text

Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy by Körver-Keularts, I. M. L. W., de Visser, M., Bakker, H. D., Wanders, R. J. A., Vansenne, F., Scholte, H. R., Dorland, L., Nicolaes, G. A. F., Spaapen, L. M. J., Smeets, H. J. M., Hendrickx, A. T. M., van den Bosch, B. J. C.

“…In a 28-year-old male with a mild mitochondrial myopathy manifesting as exercise intolerance and early signs of cardiomyopathy without muscle weakness or…”
Get full text

Ornithine aminotransferase deficiency: Diagnostic difficulties in neonatal presentation by Cleary, M. A., Dorland, L., Koning, T. J., Poll‐The, B. T., Duran, M., Mandell, R., Shih, V. E., Berger, R., Olpin, S. E., Besley, G. T. N.

“…Summary We describe two unrelated cases of ornithine aminotransferase (OAT) deficiency with rare neonatal presentation of hyperammonaemia. The diagnosis in the…”
Get full text

P.1.37 Proline affects brain function in 22q11DS children with the low-activity COMT158 allele by Vorstman, J.A.S, Turetsky, B.I, Dorland, L, Sprong, M, Emanuel, B.S, Kahn, R.S, de Sain, M, Engeland, H, Kemner, C, Beemer, F.A

Get full text