المؤلفون: Chrifi, I. (Ihsane), Hermkens, D.M.A. (Dorien M. A.), Brandt, M.M. (Maarten), Van Dijk, C.G.M. (Christian G.M.), Bürgisser, P.E. (Petra), Haasdijk, R.A. (Remco), Pei, J. (Jiayi), Kamp, E. (Esther) van de, Zhu, C. (Changbin), Blonden, L. (Lau), Kros, J.M. (Johan), Duncker, D.J.G.M. (Dirk), Duckers, H.J. (Henricus), Cheng, C. (Caroline)

المصدر: Cardiovascular Research vol. 113 no. 14, pp. 1776-1788

مصطلحات موضوعية: Adherens junctions, Angiogenesis, Cgnl1, Focal adhesion, Ve-cadherin

وصف الملف: application/pdf

Relation: http://repub.eur.nl/pub/103945; urn:hdl:1765/103945

الاتاحة: http://repub.eur.nl/pub/103945
https://doi.org/10.1093/cvr/cvx175

المؤلفون: Veelen, W. (Wendy) van, Le, N.H. (Ngoc), Helvensteijn, W. (Werner), Blonden, L. (Lau), Theeuwes, J.J.M. (Myrte), Bakker, E.R.M. (Elvira), Franken, P.F. (Patrick), Gurp, L. (Léon) van, Meijlink, F. (Frits), Valk, M.A. (Martin) van der, Kuipers, E.J. (Ernst), Fodde, R. (Riccardo), Smits, M.J.M. (Ron)

المصدر: Gut (English Edition): an international journal of gastroenterology & hepatology vol. 60 no. 9, pp. 1204-1212

وصف الملف: application/pdf

Relation: http://repub.eur.nl/pub/22857; urn:hdl:1765/22857

الاتاحة: http://repub.eur.nl/pub/22857
https://doi.org/10.1136/gut.2010.233460

المؤلفون: Cheng, C.Y., Tempel, D., den Dekker, W.K., Haasdijk, R., Chrifi, I., Bos, F.L., Wagtmans, K., van de Kamp, E.H., Blonden, L., Biessen, E.A., Moll, F.L., Pasterkamp, G., Serruys, P.W., Schulte-Merker, S., Duckers, H.J.

المصدر: Cheng , C Y , Tempel , D , den Dekker , W K , Haasdijk , R , Chrifi , I , Bos , F L , Wagtmans , K , van de Kamp , E H , Blonden , L , Biessen , E A , Moll , F L , Pasterkamp , G , Serruys , P W , Schulte-Merker , S & Duckers , H J 2011 , ' Ets2 determines the inflammatory state of endothelial cells in advanced atherosclerotic lesions ' , Circulation Research , vol. 109 , no. 4 , pp. 382-395 . ....

وصف الملف: application/pdf

Relation: https://pure.knaw.nl/portal/en/publications/98b9f0ce-cc36-4603-a5e7-998e69b3213c

الاتاحة: https://pure.knaw.nl/portal/en/publications/98b9f0ce-cc36-4603-a5e7-998e69b3213c
https://doi.org/10.1161/CIRCRESAHA.111.243444
https://hdl.handle.net/20.500.11755/98b9f0ce-cc36-4603-a5e7-998e69b3213c
https://pure.knaw.nl/ws/files/486642/2011_Cheng_C_Circ_Res.pdf

المؤلفون: Heinonen, I.H.A. (Ilkka), Sorop, O. (Oana), Dalen, B.M. (Bas) van, Wüst, R.C.I. (Rob C. I.), Wouw, J. (Jens) van de, Beer, V.J. (Vincent Jacob) de, Octavia, Y. (Yanti), Duin, R.W.B. (Richard) van, Hoogstrate, Y. (Youri), Blonden, L. (Lau), Alkio, M. (Milla), Anttila, K. (Katja), Stubbs, A.P. (Andrew), Velden, J. (Jolanda) van der, Merkus, D. (Daphne), Duncker, D.J.G.M. (Dirk)

المصدر: Scientific Reports vol. 10 no. 1

وصف الملف: application/pdf

Relation: https://repub.eur.nl/pub/129401; urn:hdl:1765/129401

الاتاحة: https://repub.eur.nl/pub/129401
https://doi.org/10.1038/s41598-020-68637-4

المؤلفون: Breuning, M H, Snijdewint, F G, Brunner, H, Verwest, A, Ijdo, J W, Saris, J J, Dauwerse, J G, Blonden, L, Keith, T, Callen, D F

مصطلحات موضوعية: Research Article

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/27/10/603; http://dx.doi.org/10.1136/jmg.27.10.603

الاتاحة: http://jmg.bmj.com/cgi/content/short/27/10/603
https://doi.org/10.1136/jmg.27.10.603

المؤلفون: Ho, M F, Monaco, A P, Blonden, L A, van Ommen, G J, Affara, N A, Ferguson-Smith, M A, Lehrach, H

مصطلحات موضوعية: Genetic Markers, Male, X Chromosome, Genetic Linkage, Kell Blood-Group System, Chromosome Fragility, Restriction Mapping, Chromosome Mapping, Nucleic Acid Hybridization, DNA, Syndrome, Granulomatous Disease, Chronic, Muscular Dystrophies, Electrophoresis, Gel, Pulsed-Field, Blotting, Southern, Humans, Dinucleoside Phosphates, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d5cca6392057611071c9dbedcdd32e41
https://ora.ox.ac.uk/objects/uuid:54a2af22-066e-461f-9a21-67bc9e702ff1

المؤلفون: Ho, M, Monaco, A, Blonden, L, van Ommen, G, Affara, N, Ferguson-Smith, M, Lehrach, H

Relation: https://ora.ox.ac.uk/objects/uuid:54a2af22-066e-461f-9a21-67bc9e702ff1

الاتاحة: https://ora.ox.ac.uk/objects/uuid:54a2af22-066e-461f-9a21-67bc9e702ff1

المؤلفون: Roth, S, Franken, Patrick, Veelen, Wendy, Blonden, L, Raghoebir, Lalini, Beverloo, Berna, Drunen, E, Kuipers, Ernst, Rottier, Robbert, Fodde, Riccardo, Smits, R

المصدر: Roth , S , Franken , P , Veelen , W , Blonden , L , Raghoebir , L , Beverloo , B , Drunen , E , Kuipers , E , Rottier , R , Fodde , R & Smits , R 2009 , ' Generation of a Tightly Regulated Doxycycline-Inducible Model for Studying Mouse Intestinal Biology ' , Genesis , vol. 47 , no. 1 , pp. 7-13 . https://doi.org/10.1002/dvg.20446

مصطلحات موضوعية: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC021303, name=EMC MGC-02-13-03, /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC029601, name=EMC MGC-02-96-01, /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM042001, name=EMC MM-04-20-01

الاتاحة: https://pure.eur.nl/en/publications/e7e59dfb-d9c7-4e75-bd69-5e225161fa42
https://doi.org/10.1002/dvg.20446
http://hdl.handle.net/1765/24083

المؤلفون: Breuning, M. H., Snijdewint, F. G. M., Brunner, H., Verwest, A., Ijdo, J. W., Saris, J. J., Dauwerse, J. G., Blonden, L., Keith, T., Callen, D. F., Hyland, V. J., Xiao, G. H., Scherer, G., Higgs, D. R., Harris, P., Bachner, L., Reeders, S. T., Gregory Germino, Pearson, P. L., Ommen, G. J. B.

المساهمون: Pediatrics, Clinical Genetics, Cardiology, Health Services Management & Organisation (HSMO), Pharmacy

المصدر: Scopus-Elsevier
Journal of Medical Genetics, 27(10), 603-613. BMJ Publishing Group

مصطلحات موضوعية: Adult, Genetic Markers, Male, Genetic Linkage, Locus (genetics), Biology, urologic and male genital diseases, Translocation, Genetic, Chromosome 16, Gene mapping, Genetic linkage, Genetics, Polycystic kidney disease, medicine, Humans, Family, Genetics (clinical), Genes, Dominant, Recombination, Genetic, Polycystic Kidney Diseases, PKD1, medicine.disease, female genital diseases and pregnancy complications, Genetic marker, Cosmid, Female, DNA Probes, Chromosomes, Human, Pair 16, Polymorphism, Restriction Fragment Length, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b883bc94694a60057b51d8fa0465669
https://pure.eur.nl/en/publications/fa628752-1cea-405c-b292-87bc53ff9a79

المؤلفون: van Veelen, W., Le, N.H., Helvensteijn, W., Blonden, L., Theeuwes, M., Bakker, E.R., Franken, P.F., van Gurp, L., Meijlink, F., van der Valk, M.A., Kuipers, E.J., Fodde, R., Smits, R.E.H.M.

المصدر: Gut vol.60 (2011) nr.9 p.1204-1212 [ISSN 0017-5749]

مصطلحات الفهرس: Artikel, Article

URL: https://pure.knaw.nl/portal/en/publications/101b9133-ebee-4ba2-9237-2dc1ad6eea2a

المؤلفون: Veelen, Wendy, Le, Hang, Helvensteijn, Werner, Blonden, L, Theeuwes, M, Bakker, Elvira, Franken, Patrick, van Gurp, L (Léon), Meijlink, F, Valk, MA, Kuipers, Ernst, Fodde, Riccardo, Smits, R

المصدر: Veelen , W , Le , H , Helvensteijn , W , Blonden , L , Theeuwes , M , Bakker , E , Franken , P , van Gurp , L , Meijlink , F , Valk , MA , Kuipers , E , Fodde , R & Smits , R 2011 , ' Beta-catenin tyrosine 654 phosphorylation increases Wnt signalling and intestinal tumorigenesis ' , Gut , vol. 60 , no. 9 , pp. 1204-1212 .

مصطلحات الفهرس: dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM032401; name=EMC MM-03-24-01, dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM042001; name=EMC MM-04-20-01, article

URL: https://pure.eur.nl/en/publications/23f60801-fde9-4c86-9da3-2a9b0d0bc50a

المؤلفون: Ried, T., Mahler, V., Vogt, P., Blonden, L., van Ommen, G. J. B., Cremer, T., Cremer, M.

المصدر: Human Genetics ; volume 85, issue 6, page 581-586 ; ISSN 0340-6717 1432-1203

الاتاحة: http://dx.doi.org/10.1007/bf00193578
http://link.springer.com/content/pdf/10.1007/BF00193578.pdf
http://link.springer.com/article/10.1007/BF00193578/fulltext.html
http://link.springer.com/content/pdf/10.1007/BF00193578

المؤلفون: Cremers, F P, van de Pol, D J, Wieringa, B, Collins, F S, Sankila, E M, Siu, V M, Flintoff, W F, Brunsmann, F, Blonden, L A, Ropers, H H

المصدر: Proceedings of the National Academy of Sciences of the United States of America; October 1989, Vol. 86 Issue: 19 p7510-7514, 5p

المؤلفون: Koenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Müller, C. R., Lindlöf, M., Kaariainen, H., La Chapelle, A., Kiuru, A., Savontaus, M. -L, Gilgenkrantz, H., Récan, D., Chelly, J., Kaplan, J. -C, Angela Elvira Covone, Archidiacono, N., Romeo, G., Liechti-Gailati, S., Schneider, V., Braga, S., Moser, H., Darras, B. T., Murphy, R., Francke, U., Chen, J. D., Morgan, G., Denton, M., Greenberg, C. R., Wrogemann, K., Blonden, L. A. J., Paassen, H. M. B., Ommen, G. J. B., Kunkel, L. M.

المصدر: Scopus-Elsevier

مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Reading Frames, Adolescent, Transcription, Genetic, Restriction Mapping, Deoxyribonuclease HindIII, Exons, Original Articles, musculoskeletal system, Muscular Dystrophies, Dystrophin, Mutation, Humans, Chromosome Deletion, Cloning, Molecular, Child, DNA Probes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9c1399124e0babfff3a37912cb22fbb2
https://pubmed.ncbi.nlm.nih.gov/2491009