Wim Hul: search on Z-Library

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1

Insights into the multifactorial causation of obesity by integrated genetic and epigenetic analysis

Diels, Sara, Vanden Berghe, Wim, Van Hul, Wim

Journal:

Obesity Reviews

Year:

2020

Language:

english

File:

PDF, 779 KB

english, 2020

2

Long-term effects of low-intensity exercise training on fat metabolism in weight-reduced obese men

Dorien P. van Aggel-Leijssen, Wim H. Saris, Gabby B. Hul, Marleen A. van Baak

Journal:

Year:

2002

Language:

english

File:

PDF, 140 KB

english, 2002

3

Paget's Disease of Bone: Evidence for Complex Pathogenetic Interactions

Pui Yan Jenny Chung, Wim Van Hul

Journal:

Seminars in Arthritis and Rheumatism

Year:

2012

Language:

english

File:

PDF, 1.35 MB

english, 2012

4

Congenital skeletal abnormalities: an introduction to the radiological semiology

Filip M. Vanhoenacker, Wim Van Hul, Jan Gielen, Arthur M. De Schepper

Journal:

European Journal of Radiology

Year:

2001

Language:

english

File:

PDF, 1.13 MB

english, 2001

5

The Effect of Low-Intensity Exercise Training on Fat Metabolism of Obese Women

Dorien P. van Aggel-Leijssen, Wim H. Saris, Anton J. Wagenmakers, Gabby B. Hul, Marleen A. van Baak

Journal:

Year:

2001

Language:

english

File:

PDF, 1.99 MB

english, 2001

6

A look behind the scenes: the risk and pathogenesis of primary osteoporosis

Hendrickx, Gretl, Boudin, Eveline, Van Hul, Wim

Journal:

Nature Reviews Rheumatology (formerly Nature Clinical Practice Rheumatology)

Year:

2015

Language:

english

File:

PDF, 490 KB

english, 2015

7

Common variants in the gene for the serotonin receptor 6 (HTR6) do not contribute to obesity

Armand V. Peeters, Sigri Beckers, An Verrijken, Peter Roevens, Pieter J. Peeters, Luc F. van Gaal, Wim van Hul

Journal:

Journal of Genetics

Year:

2010

Language:

english

File:

PDF, 149 KB

english, 2010

8

Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

Wim Wuyts, Wim Van Hul, Kristel De Boulle, Jan Hendrickx, Egbert Bakker, Filip Vanhoenacker, Florindo Mollica, Hermann-Josef Lüdecke, Bekir Sitki Sayli, Ugo E. Pazzaglia, Geert Mortier, Ben Hamel, Ern

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 327 KB

english, 1998

9

Localization of a Gene for Autosomal Dominant Osteopetrosis (Albers-Schönberg Disease) to Chromosome 1p21

Wim Van Hul, Jens Bollerslev, Jeppe Gram, Els Van Hul, Wim Wuyts, Olivier Benichou, Filip Vanhoenacker, Patrick J. Willems

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 260 KB

english, 1997

10

MECHANISMS IN ENDOCRINOLOGY: Genetic regulation of bone formation: from monogenic to complex bone disorders.

Boudin, Eveline, Van Hul, Wim

Journal:

European Journal of Endocrinology

Year:

2017

Language:

english

File:

PDF, 1.45 MB

english, 2017

11

Association Study and Mutation Analysis of Adiponectin Shows Association of Variants in APM1 with Complex Obesity in Women

Sigri Beckers, Armand V. Peeters, Fenna De Freitas, Ilse L. Mertens, Stijn L. Verhulst, Dominique Haentjens, Kristine N. Desager, Luc F. Van Gaal, Wim Van Hul

Journal:

Annals of Human Genetics

Year:

2009

Language:

english

File:

PDF, 242 KB

english, 2009

12

10.1038/12699

Warman, Matthew L., Hurvitz, Jennifer R., Suwairi, Wafaa M., Van Hul, Wim, El-Shanti, Hatem, Superti-Furga, Andrea, Roudier, Jean, Holderbaum, Daniel, Pauli, Richard M., Herd, J. Kenneth, Hul, Els Van

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 318 KB

english, 1999

13

The Effects of Increasing Serum Calcitriol on Energy and Fat Metabolism and Gene Expression

Niels Boon, Gabby B. J. Hul, Audrey Sicard, Eveline Kole, Elisa R. Van, Den Berg, Nathalie Viguerie, Dominique Langin, Wim H. M. Saris

Journal:

Year:

2006

Language:

english

File:

PDF, 152 KB

english, 2006

14

The Genetics of Low-Density Lipoprotein Receptor-Related Protein 5 in Bone: A Story of Extremes

Balemans, Wendy, Van Hul, Wim

Journal:

Year:

2007

Language:

english

File:

PDF, 209 KB

english, 2007

15

Sclerosing bone dysplasias

Boudin, Eveline, Van Hul, Wim

Journal:

Best Practice & Research Clinical Endocrinology & Metabolism

Year:

2018

Language:

english

File:

PDF, 606 KB

english, 2018

16

Molecular and clinical examination of an Italian DEFECT 11 family

Wuyts, Wim, Gennaro, Giancarlo Di, Bianco, Federico, Wauters, Jan, Morocutti, Cristoforo, Pierelli, Francesco, Bossuyt, Paul, Van Hul, Wim, Casali, Carlo

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 293 KB

english, 1999

17

Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

Sonya I. Haslam, Wim Van Hul, Antonio Morales-Piga, Wendy Balemans, J. L. San-Millan, Kiyoshi Nakatsuka, Patrick Willems, Neva E. Haites, Stuart H. Ralston

Journal:

Journal of Bone and Mineral Research

Year:

1998

Language:

english

File:

PDF, 183 KB

english, 1998

18

Identification of mutations in the NUCB2/nesfatin gene in children with severe obesity

Doreen Zegers, Sigri Beckers, Fenna de Freitas, Karen Jennes, Jasmijn K. Van Camp, Ilse L. Mertens, Kim Van Hoorenbeeck, Raoul P. Rooman, Kristine N. Desager, Guy Massa, Luc F. Van Gaal, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 417 KB

english, 2012

19

Novel SOST gene mutation in a sclerosteosis patient and her parents

Sanjay Kumar Bhadada, Ashu Rastogi, Ellen Steenackers, Eveline Boudin, Ashutosh Arya, Vandana Dhiman, Anil Bhansali, Wim Van Hul

Journal:

Year:

2013

Language:

english

File:

PDF, 647 KB

english, 2013

20

Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters

Hendrickx, Gretl, Boudin, Eveline, Fijałkowski, Igor, Nielsen, Torben Leo, Andersen, Marianne, Brixen, Kim, Van Hul, Wim

Journal:

Year:

2014

Language:

english

File:

PDF, 612 KB

english, 2014

21

PPARα gene expression correlates with severity and histological treatment response in patients with non-alcoholic steatohepatitis

Francque, Sven, Verrijken, An, Caron, Sandrine, Prawitt, Janne, Paumelle, Réjane, Derudas, Bruno, Lefebvre, Philippe, Taskinen, Marja-Riitta, Van Hul, Wim, Mertens, Ilse, Hubens, Guy, Van Marck, Eric,

Journal:

Journal of Hepatology

Year:

2015

Language:

english

File:

PDF, 965 KB

english, 2015

22

[ACM Press the 1st international conference - Orlando, Florida, United States (1993.01.04-1993.01.07)] Proceedings of the 1st international conference on Intelligent user interfaces - IUI '93 - Commenting on action

Claassen, Wim, Bos, Edwin, Huls, Carla, De Smedt, Koenraad

Year:

1993

Language:

english

File:

PDF, 803 KB

english, 1993

23

Monogenic and Complex Forms of Obesity: Insights from Genetics Reveal the Leptin-Melanocortin Signaling Pathway as a Common Player

Zegers, Doreen, Van Hul, Wim, Van Gaal, Luc F., Beckers, Sigri

Journal:

Critical Reviews in Eukaryotic Gene Expression

Year:

2012

Language:

english

File:

PDF, 688 KB

english, 2012

24

Spondylo-epi-metaphyseal dysplasia due to a homozygous missense mutation in the gene encoding Matrilin-3 (T120M)

Das, Liza, Dhiman, Vandana, Van Hul, Wim, Bhansali, Anil, Gogate, Yashpal, Steenackers, Ellen, Mortier, Geert, Bhadada, Sanjay Kumar

Journal:

Year:

2020

File:

PDF, 1.55 MB

2020

25

Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion

Wim Wuyts, Dominique Roland, Hermann-Josef Lüdecke, Jan Wauters, Martine Foulon, Wim Van Hul, Lionel Van Maldergem

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 235 KB

english, 2002

26

Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome

Guy Camp, Piet Stinissen, Wim Hul, Hubert Backhovens, Anita Wehnert, Antoon Vandenberge, Christine Broeckhoven

Journal:

Year:

1989

Language:

english

File:

PDF, 463 KB

english, 1989

27

Clinical and molecular analysis of nine families with Adams–Oliver syndrome

Verdyck, Pieter, Holder-Espinasse, Muriel, Hul, Wim Van, Wuyts, Wim

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 138 KB

english, 2003

28

An Autosomal Dominant High Bone Mass Phenotype in Association With Craniosynostosis in an Extended Family Is Caused by an LRP5 Missense Mutation

Mei Lan Kwee, Wendy Balemans, Erna Cleiren, Johan JP Gille, Frits Van Der Blij, Jan M Sepers, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2005

Language:

english

File:

PDF, 493 KB

english, 2005

29

A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene

Wendy Balemans, Erna Cleiren, Ulrike Siebers, Jürgen Horst, Wim Van Hul

Journal:

Year:

2005

Language:

english

File:

PDF, 1.23 MB

english, 2005

30

Sclerosing Bone Dysplasias: Leads Toward Novel Osteoporosis Treatments

Fijalkowski, Igor, Boudin, Eveline, Mortier, Geert, Van Hul, Wim

Journal:

Current Osteoporosis Reports

Year:

2014

Language:

english

File:

PDF, 427 KB

english, 2014

31

Novel LRP5 Missense Mutation in a Patient With a High Bone Mass Phenotype Results in Decreased DKK1-Mediated Inhibition of Wnt Signaling*

Wendy Balemans, Jean-Pierre Devogelaer, Erna Cleiren, Elke Piters, Emanuelle Caussin, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2007

Language:

english

File:

PDF, 1.87 MB

english, 2007

32

Missense Mutations in LRP5 Are Not a Common Cause of Idiopathic Osteoporosis in Adult Men

Patricia Crabbe, Wendy Balemans, Andy Willaert, Inge Van Pottelbergh, Erna Cleiren, Paul J Coucke, Minrong Ai, Stefan Goemaere, Wim Van Hul, Anne De Paepe, Jean-Marc Kaufman

Journal:

Journal of Bone and Mineral Research

Year:

2005

Language:

english

File:

PDF, 375 KB

english, 2005

33

A Contiguous Physical Map of the Pericentromeric Region of Chromosome 21q between D21Z1 and D21S13E

Wim Van Hul, Guy Van Camp, Lieven Stuyver, Jean M. Delabar, Melvin G. McInnis, Andrew C. Warren, Stylianos E. Antonarakis, Christine Van Broeckhoven

Journal:

Year:

1993

File:

PDF, 397 KB

1993

34

Single nucleotide polymorphisms in sFRP4 are associated with bone and body composition related parameters in Danish but not in Belgian men

Eveline Boudin, Elke Piters, Torben Leo Nielsen, Marianne Andersen, Greet Roef, Youri Taes, Kim Brixen, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 209 KB

english, 2012

35

Macrocephaly and sclerosis of the tubular bones in an isolated patient: a mild case of craniodiaphyseal dysplasia?

Janssens, Katrien, Thompson, Elizabeth, Vanhoenacker, Filip, Savarirayan, Ravi, Morris, Lloyd, Dobbie, Angus, Van Hul, Wim

Journal:

Clinical Dysmorphology

Year:

2003

Language:

english

File:

PDF, 209 KB

english, 2003

36

Fibrogenesis Imperfecta Ossium and Response to Human Growth Hormone: A Potential Therapy

Bhadada, Sanjay Kumar, Dhiman, Vandana, Mukherjee, Soham, Aggarwal, Sameer, Bal, Amanjit, Sukumar, Suja P., Sood, Ashwani, Sharma, Dinesh Chandra, Khandelwal, Niranjan, Bhansali, Anil, Van Hul, Wim, R

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2017

Language:

english

File:

PDF, 781 KB

english, 2017

37

First missense mutation in the SOST gene causing sclerosteosis by loss of sclerostin function

Elke Piters, Cavit Culha, Martiene Moester, Rutger Van Bezooijen, Dirk Adriaensen, Thomas Mueller, Stella Weidauer, Karen Jennes, Fenna de Freitas, Clemens Löwik, Jean-Pierre Timmermans, Wim Van Hul,

Journal:

Year:

2010

Language:

english

File:

PDF, 520 KB

english, 2010

38

Association between polymorphisms of the Nesfatin gene, NUCB2, and obesity in men

Doreen Zegers, Sigri Beckers, Ilse L. Mertens, Luc F. Van Gaal, Wim Van Hul

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 255 KB

english, 2011

39

D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21

Warren, Andrew C., Petersen, Michael B., Van Hul, Wim, McInnis, Melvin G., Van Broeckhoven, Christine, Cox, Tara K., Chakravarti, Aravinda, Antonarakis, Stylianos E.

Journal:

Year:

1992

Language:

english

File:

PDF, 461 KB

english, 1992

40

Cover Image, Volume 170A, Number 6, June 2016

Bayat, Allan, Fijalkowski, Igor, Andersen, Tobias, Abdulmunem, Sura Azhar, van den Ende, Jenneke, Van Hul, Wim

Journal:

American Journal of Medical Genetics Part A

Year:

2016

File:

PDF, 350 KB

2016

41

Effect of β 1 - and β 2 -adrenergic stimulation on energy expenditure, substrate oxidation, and UCP3 expression in humans

Hoeks, Joris, van Baak, Marleen A., Hesselink, Matthijs K. C., Hul, Gabby B., Vidal, Hubert, Saris, Wim H. M., Schrauwen, Patrick

Journal:

American Journal of Physiology-Endocrinology and Metabolism

Year:

2003

Language:

english

File:

PDF, 303 KB

english, 2003

42

A novel frameshift mutation (1651ins5) in exon 10 of the CFTR gene can be misinterpreted as a ΔF508 mutation

Gino Delaere, Karel Stuer, Katrien Storm, Patrick J. Willems, Wim Van Hul

Journal:

Year:

1999

Language:

english

File:

PDF, 13 KB

english, 1999

43

Identification of genetic modifiers of monogenic (bone) diseases: New tools available, but with limitations

Journal:

Journal of Bone and Mineral Research

Year:

2011

Language:

english

File:

PDF, 48 KB

english, 2011

44

Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects

Wuyts, Wim, Waeber, Gerard, Meinecke, Peter, Schüler, Herdit, Goecke, Timm O, Hul, Wim Van, Bartsch, Oliver

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 175 KB

english, 2004

45

Mutation analysis ofWNT10Bin obese children, adolescents and adults

Camp, Jasmijn K., Zegers, Doreen, Verhulst, Stijn L., Hoorenbeeck, Kim, Massa, Guy, Verrijken, An, Desager, Kristine N., Gaal, Luc F., Hul, Wim, Beckers, Sigri

Journal:

Endocrine (Springer)

Year:

2013

Language:

english

File:

PDF, 230 KB

english, 2013

46

Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget’s Disease of Bone and Modifies the Age of Onset

De Ridder, Raphaël, Boudin, Eveline, Vandeweyer, Geert, Devogelaer, Jean-Pierre, Fransen, Erik, Mortier, Geert, Van Hul, Wim

Journal:

Calcified Tissue International

Year:

2019

Language:

english

File:

PDF, 905 KB

english, 2019

47

Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes

Wim Wuyts, Wim Van Hul

Journal:

Year:

2000

Language:

english

File:

PDF, 232 KB

english, 2000

48

Differential valine metabolism in adipose tissue of low and high fat-oxidizing obese subjects

Mandy Claessens, Wim H. M. Saris, Freek G. Bouwman, Chris T. A. Evelo, Gabby B. J. Hul, Ellen E. Blaak, Edwin C. M. Mariman

Journal:

PROTEOMICS - Clinical Applications

Year:

2007

Language:

english

File:

PDF, 363 KB

english, 2007

49

Extracellular Regulation of BMP Signaling in Vertebrates: A Cocktail of Modulators

Wendy Balemans, Wim Van Hul

Journal:

Developmental Biology

Year:

2002

Language:

english

File:

PDF, 537 KB

english, 2002

50

Sclerosing bone disorders: a lot of knowns but still some unknowns

Journal:

BoneKEy Reports

Year:

2012

Language:

english

File:

PDF, 205 KB

english, 2012

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