Search Results - "Mariman, E. C. M."

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

“…Background/objective: Weight loss is often followed by weight regain after the dietary intervention (DI). Cellular stress is increased in adipose tissue of…”
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Heritability and genetic etiology of habitual physical activity: a twin study with objective measures by 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

“…Twin studies with objective measurements suggest habitual physical activity (HPA) are modestly to highly heritable, depending on age. We aimed to confirm or…”
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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 by 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

“…Background: The postprandial responses in (an)orexigenic hormones and feelings of hunger are characterized by large inter-individual differences. Food intake…”
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Susceptibility to spina bifida; an association study of five candidate genes by MORRISON, K., PAPAPETROU, C., HOL, F. A., MARIMAN, E. C. M., LYNCH, S. A., BURN, J., EDWARDS, Y. H.

“…Clues regarding candidate genes which influence susceptibility to spina bifida and anencephaly come from the identification of folate-associated risk factors…”
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Circulating ACE is a predictor of weight loss maintenance not only in overweight and obese women, but also in men by 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

“…BACKGROUND: Circulating angiotensin-converting enzyme (ACE) was identified as a predictor of weight loss maintenance in overweight/obese women of the Diogenes…”
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Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1 : evidence for genetic heterogeneity by MARIMAN, E. C. M, VAN BEERSUM, S. E. C, CREMERS, C. W. R. J, STRUYCKEN, P. M, ROPERS, H. H

“…Autosomal, dominantly inherited, non-chromaffin paragangliomas are tumors of the head and neck region occurring with a frequency of 1:30,000. Genomic…”
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Nutrigenomics in perspective by Mariman, E C M

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

“…Epigenetic phenomena are changes in phenotype that are due to resetting of gene expression under the influence of the environment or genetic factors without…”
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Decreased methylene tetrahydrofolate reductase activity due to the 677C→T mutation in families with spina bifida offspring by 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

“…Periconceptional folate intake reduces both the occurrence and recurrence risk of neural tube defects. Plasma homocysteine levels can be elevated in mothers of…”
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Biallelic expression of the H19 and IGF2 genes in human testicular germ cell tumors by van Gurp, R J, Oosterhuis, J W, Kalscheuer, V, Mariman, E C, Looijenga, L H

“…Genomic imprinting, resulting in the nonequivalence of expression of homologue genes depending on their parental origin, is an important determinant of the…”
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No evidence for paternal mtDNA transmission to offspring or extra-embryonic tissues after ICSI by 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.

“…There is a risk that ICSI may increase the transmission of mtDNA diseases to children born after this technique. Knowledge of the fate and transmission of…”
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Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV by RUBIO-GOZALBO, M. E, RUITENBEEK, W., SMEITINK, J. A. M, BENTLAGE, H. A. C. M, SCHÄGGER, H, SENGERS, R. C. A, TRIJBELS, J. M. F, TER LAAK, H. J, MARIMAN, E. C. M, BAKKER, M. M, DE JAGER, J

“…An infant with severe deficiency of complex III combined with less severe deficiencies of complexes I, II and IV of the mitochondrial respiratory chain in…”
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Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2 by LIGTENBERG, M. J. L, HOGERVORST, F. B. L, VOS, E. M. A. W, WIGBOUT, G, STRUYCKEN, P. M, MENKO, F. H, RUTGERS, E. J. T, HOEFSLOOT, E. H, MARIMAN, E. C. M, BRUNNER, H. G, VAN'T VEER, L. J, WILLEMS, H. W, ARTS, P. J. W, BRINK, G, HAGEMAN, S, BOSGOED, E. A. J, VAN DER LOOIJ, E, ROOKUS, M. A, DEVILEE, P

“…For families with a small number of cases of breast and/or ovarian cancer, limited data are available to predict the likelihood of genetic predisposition due…”
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Results of genetic testing : when confidentiality conflicts with a duty to warn relatives by LEUNG, Wai-Ching, MARIMAN, E. C. M, VAN DER WOUDEN, Johannes C, VAN AMERONGEN, Henk, WEIJER, Charles

“…As [Wilson]'s disease is autosomal recessive in inheritance, both [Martin] and [Alison] have a 1 in 4 risk of having the disease. The disease is treatable in…”
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Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q by MARIMAN, E. C. M, VAN BEERSUM, S. E. C, CREMERS, C. W. R. J, VAN BAARS, F. M, ROPERS, H. H

“…The gene for autosomal, dominantly inherited, non-chromaffin paragangliomas has previously been mapped at 11q23-qter by linkage analysis of a single family. In…”
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Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies by MARIMAN, E. C. M, GABREËLS-FESTEN, A. A. W. M, VAN BEERSUM, S. E. C, JONGEN, P. J. H, VAN DE LOOIJ, E, BAAS, F, BOLHUIS, P. A, ROPERS, H. H, GABREËLS, F. J. M

“…Hereditary neuropathy with liability to pressure palsies (HNPP) is a disorder of the peripheral nervous system, the cause of which has recently been identified…”
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Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood by KREMER, H, HAMEL, B. C. J, VAN DEN HELM, B, ARTS, W. F. M, DE WIJS, I. J, SISTERMANS, E. A, ROPERS, H.-H, MARIMAN, E. C. M

“…Linkage analysis is described in a family with X-linked mental retardation, ataxia, weakness, floppiness, delayed motor development, absence of deep tendon…”
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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 Puberty1 by Kremer, H, Martens, J. W. M, van Reen, M, Verhoef-Post, M, Wit, J. M, Otten, B. J, Drop, S. L. S, Delemarre-van de Waal, H. A, Pombo-Arias, M, De Luca, F, 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, Brunner, H. G

“…Herein, we report mutation analysis of the LH receptor gene in 17 males with LH-independent precocious puberty, of which 8 were familial and 9 had a negative…”
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Clustering of Anophthalmia and Microphthalmia: No Clustering Has Been Found-But a Link Seems to Exist with Population Density by Mariman, E. C. M.

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

“…Periconceptional folate supplementation reduces the risk of neural-tube defects. We studied the frequency of the 677C-->T mutation in the…”
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