Adipocyte extracellular matrix composition, dynamics and role in obesity von Mariman, Edwin C. M, Wang, Ping

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Weight loss-induced cellular stress in subcutaneous adipose tissue and the risk for weight regain in overweight and obese adults von Roumans, N J T, Vink, R G, Bouwman, F G, Fazelzadeh, P, van Baak, M A, Mariman, E C M

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Circulating ACE is a predictor of weight loss maintenance not only in overweight and obese women, but also in men von Wang, P, Holst, C, Wodzig, W K W H, Andersen, M R, Astrup, A, van Baak, M A, Larsen, T M, Jebb, S A, Kafatos, A, Pfeiffer, A F H, Martinez, J A, Handjieva-Darlenska, T, Kunesova, M, Viguerie, N, Langin, D, Saris, W H M, Mariman, E C M

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Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida von van der Put, N.M.J., Trijbels, F.J.M., van den Heuvel, L.P., Blom, H.J., Steegers-Theunissen, R.P.M., Eskes, T.K.A.B., Mariman, E.C.M., den Heyer, M., Frosst, P., Rozen, R.

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Heritability and genetic etiology of habitual physical activity: a twin study with objective measures von Gielen, M, Westerterp-Plantenga, M. S, Bouwman, F. G, Joosen, A. M. C. P, Vlietinck, R, Derom, C, Zeegers, M. P, Mariman, E. C. M, Westerterp, K. R

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Localization of the gene for Cowden disease to chromosome 10q22-23 von Nelen, M.R, Padberg, G.W, Peeters, E.A.J, Lin, A.Y, Helm, B. van den, Frants, R.R, Goulon, V, Goldstein, A.M, Reen, M.M.M van, Eastern, D.F, Eeles, R.A, Hodgson, S, Mulvihill, J.J, Murday, V.A, Tucker, M.A, Mariman, E.C.M, Starink, T.M, Ponder, B.A.J, Ropers, H.H, Kremer, H, Longy, M, Eng, C

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SNP analyses of postprandial responses in (an)orexigenic hormones and feelings of hunger reveal long-term physiological adaptations to facilitate homeostasis von Hoed, M. den, Smeets, A.J.P.G, Veldhorst, M.A.B, Nieuwenhuizen, A.G, Bouwman, F.G, Heidema, A.G, Mariman, E.C.M, Westerterp-Plantenga, M.S, Westerterp, K.R

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Epigenetic Manifestations in Diet-Related Disorders von Mariman, E.C.M.

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A mutation in the gene encoding the α2 chain of the fibril-associated collagen IX, COL9A2 , causes multiple epiphyseal dysplasia (EDM2) von Muragaki, Yasuteru, Warman, Matthew L, van Beersum, Sylvia E.C, Mariman, Edwin C.M, Hamel, Ben C.J, Perälä, Merja, van Mourik, Jan B.A, Olsen, Bjorn R

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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease von GABREËLS-FESTEN, A. A. W. M, HOOGENDIJK, J. E, VAN ENGELEN, B. G. M, VAN BROECKHOVEN, C, MARIMAN, E. C. M, MEIJERINK, P. H. S, GABREËLS, F. J. M, BOLHUIS, P. A, VAN BEERSUM, S, KULKENS, T, NELIS, E, JENNEKENS, F. G. I, DE VISSER, M

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Decreased methylene tetrahydrofolate reductase activity due to the 677C→T mutation in families with spina bifida offspring von VAN DER PUT, N. M. J, VAN DEN HEUVEL, L. P, STEEGERS-THEUNISSEN, R. P. M, TRIJBELS, F. J. M, ESKES, T. K. A. B, MARIMAN, E. C. M, DEN HEYER, M, BLOM, H. J

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No evidence for paternal mtDNA transmission to offspring or extra-embryonic tissues after ICSI von Marchington, D.R., Scott Brown, M.S.G., Lamb, V.K., van Golde, R.J.T., Kremer, J.A.M., Tuerlings, J.H.A.M., Mariman, E.C.M., Balen, A.H., Poulton, J.

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Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth disease von Gabreels-Festen, A A. W.M, Hoogendijk, J E, Meijerink, P H.S, Gabreels, F J.M, Bolhuis, P A, van Beersum, S, Kulkens, T, Nelis, E, Jennekens, F G.I, de Visser, M, van Engelen, B G.M, Van Broeckhoven, C, Mariman, E C.M

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Hereditary neuropathy with liability to pressure palsies : Phenotypic differences between patients with the common deletion and a pmp22 frame shift mutation von LENSSEN, P. P. A, GABREËLS-FESTEN, A. A. W. M, VALENTIJN, L. J, JONGEN, P. J. H, VAN BEERSUM, S. E. C, VAN ENGELEN, B. G. M, VAN WENSEN, P. J. M, BOLHUIS, P. A, GABREËLS, F. J. M, MARIMAN, E. C. M

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Spina bifida and genetic factors related to myo-inositol, glucose, and zinc von Groenen, P.M.W, Klootwijk, R, Schijvenaars, M.M.V.A.P, Straatman, H, Mariman, E.C.M, Franke, B, Steegers-Theunissen, R.P.M

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Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1 : evidence for genetic heterogeneity von MARIMAN, E. C. M, VAN BEERSUM, S. E. C, CREMERS, C. W. R. J, STRUYCKEN, P. M, ROPERS, H. H

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A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male lh-independent precocious puberty von KREMERT, H, MARTENS, J. W. M, POTAU, N, BUCKLER, J. M. H, JANSEN, M, PARKS, J. S, LATIF, H. A, MOLL, G. W, EPPING, W, SAGGESE, G, MARIMAN, E. C. M, THEMMEN, A. P. N, VAN REEN, M, BRUNNER, H. G, VERHOEF-POST, M, WIT, J. M, OTTEN, B. J, DROP, S. L. S, DE WAAL, H. A. D.-V, POMBO-ARIAS, M, DE LUCA, F

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Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency von RUBIO-GOZALBO, M. E, SMEITINK, J. A. M, RUITENBEEK, W, LAAK, T, MULLAART, R. A, SCHUELKE, M, MARIMAN, E. C. M, SENGERS, R. C. A, GABREËLS, F. J. M

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Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2 von Ligtenberg, M J L, Hogervorst, F B L, Willems, H W, Arts, P J W, Brink, G, Hageman, S, Bosgoed, E A J, Looij, E Van der, Rookus, M A, Devilee, P, Vos, E M A W, Wigbout, G, Struycken, P M, Menko, F H, Rutgers, E J Th, Hoefsloot, E H, Mariman, E C M, Brunner, H G, Veer, L J Van’t

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Clustering of anophthalmia and microphthalmia von Mariman, E C M

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