Zobrazeno 1 - 10 of 33 pro vyhledávání: '"Carel Meijers"'
1
Completeness of pathology reports in stage II colorectal cancer
Autor: Jan N. M. IJzermans, W. J. Vles, Peter Paul L. O. Coene, Mike Kliffen, David D. E. Zimmerman, Michael Doukas, Stefan Büttner, Bettina E. Hansen, Zarina S. Lalmahomed, G. W. M. Tetteroo, J H Carel Meijers, Wietske W. Vrijland, Anneke A M van der Wurff, Robert R. J. Coebergh van den Braak, Rolf Torenbeek, Jan Willem T. Dekker, Ruth E M Fleischeuer
Publikováno v: Acta Chirurgica Belgica, 117(3), 181-187. Taylor & Francis Ltd
Introduction: The completeness of the pathological examination of resected colon cancer specimens is important for further clinical management. We reviewed the pathological reports of 356 patients regarding the five factors (pT-stage, tumor different
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7715519ddbe2f3b1eef7599b7d86eda
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2
Perturbations of Vascular Homeostasis and Aortic Valve Abnormalities in Fibulin-4 Deficient Mice
Autor: Loretha Myers, Carel Meijers, Harry C. Dietz, Roland Kanaar, Marcel Vermeij, George A. Garinis, Jeroen Essers, Dirk J. Duncker, Katsuhiro Hanada, Monique C. de Waard, Alex Maas, Maurice G.S. Kunen
Publikováno v: Circulation Research, 100(5), 738-746. Lippincott Williams & Wilkins
The Fibulins are a 6-member protein family hypothesized to function as intermolecular bridges that stabilize the organization of extracellular matrix structures. Here, we show that reduced expression of Fibulin-4 leads to aneurysm formation, dissecti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2431f186e739d9913f42394d672862b6
https://doi.org/10.1161/01.res.0000260181.19449.95
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3
Organization and chromosomal localization of the human ECEL1 (XCE) gene encoding a zinc metallopeptidase involved in the nervous control of respiration
Autor: Olivier Valdenaire, An Langeveld, Elisabeth Rohrbacher, Anja Schweizer, Carel Meijers
Publikováno v: Biochemical Journal, 346, 611-616. Portland Press, Ltd.
ECEL1 (endothelin-converting enzyme-like 1; previously known as XCE) is a putative zinc metalloprotease that was identified recently on the basis of its strong identity with endothelin-converting enzyme. Although the physiological function of ECEL1 i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c40ee0434e15962c1c48c0cacc4e13a
https://doi.org/10.1042/bj3460611
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4
RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gels systems
Autor: V. M. R. Heydendael, R. M. W. Hofstra, Charles H.C.M. Buys, Carel Meijers, Saskia M. Maas, Ying Wu, J.J. van den Ende, Jan Osinga, R.S.V.M. Severijnen, L.E. Siderius, Rein P. Stulp, Alice S. Brooks, P Elfferich, K.M. Bax
Publikováno v: Human mutation, 15(5), 418-429. Wiley-Liss Inc.
Human Mutation, 15, 5, pp. 418-29
Human Mutation, 15, 418-29
Hirschsprung disease (HSCR) is a congenital disorder characterised by intestinal obstruction due to an absence of intramural ganglia along variable lengths of the intestine. RET is the major gene involved in HSCR. Mutations in the GDNF gene, and enco
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1272af64cabdf4bb99db7a6c651c1b90
https://hdl.handle.net/2066/184611
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5
The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients
Autor: Laurens G. Wilming, Angelique L. C. T. van Rijswijk, Frank Grosveld, C. A. Sylvia Snoeren, Carel Meijers
Publikováno v: Human Molecular Genetics, 6(2), 247-258. Oxford University Press
A wide spectrum of birth defects is caused by deletions of the DiGeorge syndrome chromosomal region at 22q11. Characteristic features include cranio-facial, cardiac and thymic malformations, which are thought to arise from disturbances in the interac
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b83d5aaebf89b0681f53d4aadc52021e
https://doi.org/10.1093/hmg/6.2.247
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7
Ablation of various regions within the avian vagal neural crest has differential effects on ganglion formation in the fore-, mid- and hindgut
Autor: Carel Meijers, Marjo J. H. Peters-Van Der Sanden, Adriana Gittenberger-De Groot, Dick Tibboel, Margaret L. Kirby, Maarten P. Mulder
Publikováno v: Developmental Dynamics. 196:183-194
The vagal neural crest adjacent to the first seven somites gives rise to both ganglionic and ectomesenchymal derivatives. Ganglionic derivatives are the neurons and supportive cells of the enteric nervous system (ENS), cardiac, and dorsal root gangli
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::418288d761a8e0a300b265953bf6ea61
https://doi.org/10.1002/aja.1001960305
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8
Microscopic localisation of protoporphyrin IX in normal mouse skin after topical application of 5-aminolevulinic acid or methyl 5-aminolevulinate
Autor: Dominic J. Robinson, Angelique van der Ploeg-van den Heuvel, Carel Meijers, Henriëtte S. de Bruijn, Henricus J. C. M. Sterenborg
Publikováno v: Journal of photochemistry and photobiology. B, Biology, 92(2), 91-97. Elsevier
Journal of Photochemistry and Photobiology B-Biology, 92(2), 91-97. Elsevier
Light fractionation does not enhance the response to photodynamic therapy (PDT) after topical methyl-aminolevulinate (MAL) application, whereas it is after topical 5-aminolevulinic acid (ALA). The differences in biophysical and biochemical characteri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0bdeb621954ffaa8f9f77a96921799e
https://pubmed.ncbi.nlm.nih.gov/18571933
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9
Constipation as the Presenting Symptom in De Novo Multiple Endocrine Neoplasia Type 2B
Autor: Carel Meijers, R. M. W. Hofstra, E. Van Der Harst, Hajo A. Bruining, J. C. Molenaar, R.R. de Krijger, Alice S. Brooks
Publikováno v: Pediatrics, 102(2), 405-408. AMER ACAD PEDIATRICS
Pediatrics, 102, 405-408. American Academy of Pediatrics
* Abbreviations: MEN 2 = : multiple endocrine neoplasia type 2 • MTC = : medullary thyroid carcinoma • PCR = : polymerase chain reaction • IND B = : intestinal neuronal dysplasia type B Multiple endocrine neoplasia type 2 (MEN 2) comprises thre
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab586464399b8af52750b74378592a67
https://doi.org/10.1542/peds.102.2.405
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10
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)
Autor: Gita Tan-Sindhunata, Charles H.C.M. Buys, Aravinda Chakravarti, Robert M. W. Hofstra, Carel Meijers, Rein P. Stulp, Jan Osinga, Ying Wu, Erik J. Kamsteeg, Misha Angrist, Conny M.A. van Ravenswaaij-Arts, Danielle Majoor-Krakauer
Publikováno v: Nature Genetics, 12, pp. 445-447
Nature Genetics, 12(4), 445-447. Nature Publishing Group
Nature Genetics, 12, 4, pp. 445-447
Nature Genetics, 12, 445-447
Hofstra, R M W, Osinga, J, Tan-Sindhunata, G, Wu, Y, Kamsteeg, E J, Stulp, R P, Van Ravenswaaij-Arts, C, Majoor-Krakauer, D, Angrist, M, Chakravarti, A, Meijers, C & Buys, C H C M 1996, ' A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) ', Nature Genetics, vol. 12, no. 4, pp. 445-447 . https://doi.org/10.1038/ng0496-445
Hirschsprung disease (HSCR) or colonic aganglionosis is a congenital disorder characterized by an absence of intramural ganglia along variable lengths of the colon resulting in intestinal obstruction. The incidence of HSCR is 1 in 5,000 live births.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470367cbde44beed553638dee1f9530d
https://hdl.handle.net/2066/23620
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