S. E. C. Beersum : rechercher sur Z-Library

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1

Plant defence against nematodes is not mediated by changes in the soil microbial community

Susanne Wurst, Sander Van Beersum, Roel Wagenaar, Tanja Bakx-Schotman, Barbara Drigo, Ingar Janzik, Arnaud Lanoue, Wim H. Van Der Putten

Journal:

Functional Ecology

Année:

2009

Langue:

english

Fichier:

PDF, 382 KB

english, 2009

2

High-Pressure Gas Chromatography and Chromatography with Supercritical Fluids. I. The Effect of Pressure on Partition Coefficients in Gas-Liquid Chromatography with Carbon Dioxide as a Carrier Gas

Sie, S. T., Van Beersum, W., Rijnders, G. W. A.

Journal:

Separation Science

Année:

1966

Langue:

english

Fichier:

PDF, 1.10 MB

english, 1966

3

Plant Defence against Nematodes Is Not Mediated by Changes in the Soil Microbial Community

Susanne Wurst, Sander van Beersum, Roel Wagenaar, Tanja Bakx-Schotman, Barbara Drigo, Ingar Janzik, Arnaud Lanoue and Wim H. van der Putten

Journal:

Functional Ecology

Année:

2009

Langue:

english

Fichier:

PDF, 2.00 MB

english, 2009

4

Living apart together—bacterial volatiles influence methanotrophic growth and activity

Veraart, A. J., Garbeva, P., van Beersum, F., Ho, A., Hordijk, C. A., Meima-Franke, M., Zweers, A. J., Bodelier, P. L. E.

Journal:

The ISME Journal

Année:

2018

Langue:

english

Fichier:

PDF, 873 KB

english, 2018

5

Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: A new X-linked multiple congenital anomalies/mental retardation syndrome: Clinical description and molecular studies

Ben C. J. Hamel, Edwin C. M. Mariman, Sylvia E. C. van Beersum, Anneke M. J. Schoonbrood-Lenssen, Hans-Hilger Ropers

Journal:

American Journal of Medical Genetics Part A

Année:

1994

Langue:

english

Fichier:

PDF, 653 KB

english, 1994

6

Clinical and molecular studies in a large Dutch family with Noonan syndrome

Ineke Van Der Burgt, Ed Berends, Ed Lommen, Sylvia Van Beersum, Ben Hamel, Edwin Mariman

Journal:

American Journal of Medical Genetics Part A

Année:

1994

Langue:

english

Fichier:

PDF, 536 KB

english, 1994

7

Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies

Dr. E. C. M. Mariman, A. A. W. M. Gabreëls-Festen, S. E. C. van Beersum, L. J. Valentijn, F. Baas, P. A. Bolhuis, P. J. H. Jongen, H. H. Ropers, F. J. M. Gabreëls

Journal:

Annals of Neurology

Année:

1994

Langue:

english

Fichier:

PDF, 549 KB

english, 1994

8

Spurenanalyse mittels Gas/Feststoff-Chromatographie

F. H. Huyten, G. W. A. Rijnders, W. van Beersum

Journal:

Angewandte Chemie

Année:

1962

Langue:

german

Fichier:

PDF, 142 KB

german, 1962

9

Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies

E. C. M. Mariman, A. A. W. M. Gabreëls-Festen, S. E. C. Beersum, P. J. H. Jongen, E. Looij, F. Baas, P. A. Bolhuis, H. H. Ropers, F. J. M. Gabreëls

Journal:

Année:

1994

Langue:

english

Fichier:

PDF, 624 KB

english, 1994

10

Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1

Edwin C. M. Mariman, Anneke A. W. M. Gabreëls-Festen, Sylvia E. C. Beersum, Peter J. H. Jongen, Hans-Hilger Ropers, Fons J. M. Gabreëls

Journal:

Année:

1993

Langue:

english

Fichier:

PDF, 338 KB

english, 1993

11

Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q

E. C. M. Mariman, S. E. C. Beersum, C. W. R. J. Cremers, F. M. Baars, H. H. Ropers

Journal:

Année:

1993

Langue:

english

Fichier:

PDF, 439 KB

english, 1993

12

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

E. C. M. Mariman, S. E. C. Beersum, C. W. R. J. Cremers, P. M. Struycken, H. H. Ropers

Journal:

Année:

1995

Langue:

english

Fichier:

PDF, 503 KB

english, 1995

13

The impact of soil organism composition and activated carbon on grass-legume competition

Susanne Wurst, Sander van Beersum

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 235 KB

english, 2009

14

Genetic Linkage Between the Collagen VII (COL7A1) Gene and the Autosomal Dominant Form of Dystrophic Epidermolysis Bullosa in Two Dutch Kindreds.

Gruis, Nelleke A., Bavinck, Jan N. Bouwes, Steijlen, Peter M., Van Der Schroeff, Jan G., Van Haeringen, Arie, Happle, Rudolf, Mariman, Edwin, Van Beersum, Sylvia E. C., Uitto, Jouni, Vermeer, Bert J.,

Journal:

The Journal of Investigative Dermatology

Année:

1992

Fichier:

PDF, 1.64 MB

1992

15

A mutation in the gene encoding the α2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)

Muragaki, Yasuteru, Mariman, Edwin C.M., van Beersum, Sylvia E.C., Perälä, Merja, van Mourik, Jan B.A., Warman, Matthew L., Olsen, Bjorn R., Hamel, Ben C.J.

Journal:

Nature Genetics

Année:

1996

Fichier:

PDF, 398 KB

1996

16

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Arts, Heleen H, Doherty, Dan, van Beersum, Sylvia E C, Parisi, Melissa A, Letteboer, Stef J F, Gorden, Nicholas T, Peters, Theo A, Märker, Tina, Voesenek, Krysta, Kartono, Aileen

Journal:

Nature Genetics

Année:

2007

Langue:

english

Fichier:

PDF, 565 KB

english, 2007

17

Uptake of cadmium, zinc, lead, and copper by earthworms near a zinc-smelting complex: Influence of soil pH and organic matter

W. Ma, Th. Edelman, I. van Beersum, Th. Jans

Journal:

Bulletin of Environmental Contamination and Toxicology

Année:

1983

Langue:

english

Fichier:

PDF, 180 KB

english, 1983

18

CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290

Nicholas T. Gorden, Heleen H. Arts, Melissa A. Parisi, Karlien L.M. Coene, Stef J.F. Letteboer, Sylvia E.C. van Beersum, Dorus A. Mans, Abigail Hikida, Melissa Eckert, Dana Knutzen, Abdulrahman F. Als

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 1.03 MB

english, 2008

19

Refined Genetic and Physical Localization of the Wagner Disease (WGN1) Locus and the Genes CRTL1 and CSPG2 to a 2- to 2.5-cM Region of Chromosome 5q14.3

Rahat Perveen, Niki Hart-Holden, Michael J. Dixon, Wojtek Wiszniewski, Alan E. Fryer, Han G. Brunner, Alfred J.L.H. Pinkners, Sylvie E.C. van Beersum, Graeme C.M. Black

Journal:

Année:

1999

Langue:

english

Fichier:

PDF, 134 KB

english, 1999

20

Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes

Frans A. Hol, Marga T. Schepens, Sylvia E.C. van Beersum, Elena Redolfi, Maurizio Affer, Paolo Vezzoni, Ben C.J. Hamel, Pamela S. Karnes, Edwin C.M. Mariman, Ileana Zucchi

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 111 KB

english, 2000

21

Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27

Hans van Bokhoven, Martin Jung, Arie P.T. Smits, Sylvia van Beersum, Franz Rüschendorf, Maurice van Steensel, Monique Veenstra, Joep H.A.M. Tuerlings, Edwin C.M. Mariman, Han G. Brunner, Thomas F. Wie

Journal:

The American Journal of Human Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 793 KB

english, 1999

22

p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation

Hans van Bokhoven, Ben C.J. Hamel, Mike Bamshad, Eugenio Sangiorgi, Fiorella Gurrieri, Pascal H.G. Duijf, Kaate R.J. Vanmolkot, Ellen van Beusekom, Sylvia E.C. van Beersum, Jacopo Celli, Gerard F.M. M

Journal:

The American Journal of Human Genetics

Année:

2001

Langue:

english

Fichier:

PDF, 244 KB

english, 2001

23

Mutations in the Human TBX4 Gene Cause Small Patella Syndrome

Ernie M.H.F. Bongers, Pascal H.G. Duijf, Sylvia E.M. van Beersum, Jeroen Schoots, Albert van Kampen, Andreas Burckhardt, Ben C.J. Hamel, František Lošan, Lies H. Hoefsloot, Helger G. Yntema, Nine V.A.

Journal:

The American Journal of Human Genetics

Année:

2004

Langue:

english

Fichier:

PDF, 2.40 MB

english, 2004

24

C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome

Arts, H. H., Bongers, E. M. H. F., Mans, D. A., van Beersum, S. E. C., Oud, M. M., Bolat, E., Spruijt, L., Cornelissen, E. A. M., Schuurs-Hoeijmakers, J. H. M., de Leeuw, N., Cormier-Daire, V., Brunne

Journal:

Journal of Medical Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 634 KB

english, 2011

25

A Mutation in COL9A2 Causes Multiple Epiphyseal Dysplasia (EDM2)

Yasuteru Muragaki, Edwin C. M. Mariman, Sylvia E. C. Van Beersum, Merja PerÄLÄ, Jan B. A. Van Mourik, Matthew L. Warman, Ben C. J. Hamel, Bjorn R. Olsen

Journal:

Annals of the New York Academy of Sciences

Année:

1996

Langue:

english

Fichier:

PDF, 401 KB

english, 1996

26

Scrutinizing ciliopathies by unravelling the ciliary interactome

J van Reeuwijk, K Boldt, DA Mans, Y Texier, SE van Beersum, SJ Letteboer…

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 78 KB

english, 2012

27

A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 gene

Brunner, Han G., van Beersum, Sylvia E.C., Warman, Matt L., Olsen, Bjorn R., Ropers, Hans-Hilger, Mariman, Edwin C.M.

Journal:

Human Molecular Genetics

Année:

1994

Langue:

english

Fichier:

PDF, 381 KB

english, 1994

28

Altered Regulation of Platelet-Derived Growth Factor receptor-α Gene-Transcription in vitro by Spina Bifida-Associated Mutant Pax1 Proteins

Paul H. L. J. Joosten, Frans A. Hol, Sylvia E. C. Van Beersum, Heiko Peters, Ben C. J. Hamel, Gijs B. Afink, Everardus J. J. Van Zoelen and Edwin C. M. Mariman

Journal:

Proceedings of the National Academy of Sciences

Année:

1998

Langue:

english

Fichier:

PDF, 1.23 MB

english, 1998

29

Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina

Eblimit, A., Nguyen, T.-M. T., Chen, Y., Esteve-Rudd, J., Zhong, H., Letteboer, S., Van Reeuwijk, J., Simons, D. L., Ding, Q., Wu, K. M., Li, Y., Van Beersum, S., Moayedi, Y., Xu, H., Pickard, P., Wan

Journal:

Human Molecular Genetics

Année:

2015

Langue:

english

Fichier:

PDF, 2.57 MB

english, 2015

30

Altered regulation of platelet-derived growth factor receptor- gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins

Joosten, P. H. L. J., Hol, F. A., van Beersum, S. E. C., Peters, H., Hamel, B. C. J., Afink, G. B., van Zoelen, E. J. J., Mariman, E. C. M.

Journal:

Proceedings of the National Academy of Sciences

Année:

1998

Langue:

english

Fichier:

PDF, 223 KB

english, 1998

31

Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations

Roepman, R., Letteboer, S. J. F., Arts, H. H., van Beersum, S. E. C., Lu, X., Krieger, E., Ferreira, P. A., Cremers, F. P. M.

Journal:

Proceedings of the National Academy of Sciences

Année:

2005

Langue:

english

Fichier:

PDF, 650 KB

english, 2005

32

Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33

Gabreels-Festen, A., van Beersum, S., Eshuis, L., LeGuern, E., Gabreels, F., van Engelen, B., Mariman, E.

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Année:

1999

Langue:

english

Fichier:

PDF, 178 KB

english, 1999

33

Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth disease

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.,

Journal:

Année:

1996

Langue:

english

Fichier:

PDF, 1.60 MB

english, 1996

34

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Schmidts, Miriam, Hou, Yuqing, Cortés, Claudio R., Mans, Dorus A., Huber, Celine, Boldt, Karsten, Patel, Mitali, van Reeuwijk, Jeroen, Plaza, Jean-Marc, van Beersum, Sylvia E. C., Yap, Zhi Min, Letteb

Journal:

Nature Communications

Année:

2015

Langue:

english

Fichier:

PDF, 1.46 MB

english, 2015

35

The Interaction of CCDC104/BARTL1 with Arl3 and Implications for Ciliary Function

Lokaj, Mandy, Kösling, Stefanie K., Koerner, Carolin, Lange, Sven M., van Beersum, Sylvia E.C., van Reeuwijk, Jeroen, Roepman, Ronald, Horn, Nicola, Ueffing, Marius, Boldt, Karsten, Wittinghofer, Alfr

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 3.96 MB

english, 2015

36

An organelle-specific protein landscape identifies novel diseases and molecular mechanisms

Boldt, Karsten, van Reeuwijk, Jeroen, Lu, Qianhao, Koutroumpas, Konstantinos, Nguyen, Thanh-Minh T., Texier, Yves, van Beersum, Sylvia E. C., Horn, Nicola, Willer, Jason R., Mans, Dorus A., Dougherty,

Journal:

Nature Communications

Année:

2016

Langue:

english

Fichier:

PDF, 2.02 MB

english, 2016

37

Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Schmidts, Miriam, Hou, Yuqing, Cortés, Claudio R., Mans, Dorus A., Huber, Celine, Boldt, Karsten, Patel, Mitali, van Reeuwijk, Jeroen, Plaza, Jean-Marc, van Beersum, Sylvia E. C., Yap, Zhi Min, Letteb

Journal:

Nature Communications

Année:

2016

Langue:

english

Fichier:

PDF, 131 KB

english, 2016

38

Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa

Nguyen, Thanh-Minh T, Hull, Sarah, Roepman, Ronald, van den Born, L Ingeborgh, Oud, Machteld M, de Vrieze, Erik, Hetterschijt, Lisette, Letteboer, Stef J F, van Beersum, Sylvia E C, Blokland, Ellen A,

Journal:

Journal of Medical Genetics

Année:

2017

Langue:

english

Fichier:

PDF, 1.85 MB

english, 2017

39

PDZD7 connects the Usher protein complex to the intraflagellar transport machinery

E De Vrieze,L Creemers,N Sorusch,M Gorris,J Van Reeuwijk,S Van Beersum…

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 290 KB

english, 2015

40

Systematic exploration of the ciliary protein landscape by large-scale affinity proteomics

Boldt, K, Van Reeuwijk, J, Lu, Q, Koutroumpas, K, Horn, N, Beersum, S, Texier, Y, Nguyen, TM, Willer, JR, Katsanis, N, Képès, F, Russell, RB, Ueffing, M, Roepman, R

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 252 KB

english, 2015

41

The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking

Bachmann-Gagescu, Ruxandra, Dona, Margo, Hetterschijt, Lisette, Tonnaer, Edith, Peters, Theo, de Vrieze, Erik, Mans, Dorus A., van Beersum, Sylvia E. C., Phelps, Ian G., Arts, Heleen H., Keunen, Jan E

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 12.73 MB

english, 2015