Manfred S. Wehnert: search on Z-Library

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1

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

Lucie Gueneau, Anne T. Bertrand, Jean-Philippe Jais, Mustafa A. Salih, Tanya Stojkovic, Manfred Wehnert, Maria Hoeltzenbein, Simone Spuler, Shinji Saitoh, Annie Verschueren, Christine Tranchant, Maud

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 1.06 MB

english, 2009

2

The LINC complex and human disease

Meinke, Peter, Nguyen, Thuy Duong, Wehnert, Manfred S.

Journal:

Biochemical Society Transactions

Year:

2011

Language:

english

File:

PDF, 251 KB

english, 2011

3

Contribution of SUN1 Mutations to the Pathomechanism in Muscular Dystrophies

Li, Ping, Meinke, Peter, Huong, Le Thi Thanh, Wehnert, Manfred, Noegel, Angelika A.

Journal:

Year:

2014

Language:

english

File:

PDF, 4.73 MB

english, 2014

4

Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy

Michal Vytopil, Enzo Ricci, Antonio Dello Russo, Frank Hanisch, Stephan Neudecker, Stephan Zierz, Roberta Ricotti, Laurence Demay, Pascale Richard, Manfred Wehnert, Gisèle Bonne, Luciano Merlini, Dani

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 79 KB

english, 2002

5

A muscle-specific DNase I-like gene in human Xq28

Parrish, Julia E., Ciccodicola, Alfredo, Wehnert, Manfred, Cox, Gerald F., Chen, Ellson, Nelson, David L.

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 3.34 MB

english, 1995

6

A rapid scanning strip for tri- and dinucleotide short tandem repeats

Wehnert, Manfred S., Matson, Robert S., Rampal, Jang B., Coassin, Peter J., Caskey, C.Thomas

Journal:

Nucleic Acids Research

Year:

1994

Language:

english

File:

PDF, 378 KB

english, 1994

7

Twenty-five novel mutations of the factor IX gene in haemophilia B

Karin Wulff, Winnie Schröder, Manfred Wehnert, Falko H. Herrmann

Journal:

Year:

1995

Language:

english

File:

PDF, 261 KB

english, 1995

8

Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutations

Lindsay J. Emerson, Mark R. Holt, Matthew A. Wheeler, Manfred Wehnert, Maddy Parsons, Juliet A. Ellis

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

2009

Language:

english

File:

PDF, 1.15 MB

english, 2009

9

Early onset of cardiomyopathy in two brothers with X-linked Emery–Dreifuss muscular dystrophy

Ülvi-Astra Talkop, Inga Talvik, Margit Sõnajalg, Hiljar Sibul, Anneli Kolk, Andres Piirsoo, Rolf Warzok, Karin Wulff, Manfred S Wehnert, Tiina Talvik

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 180 KB

english, 2002

10

Nesprins, but not sun proteins, switch isoforms at the nuclear envelope during muscle development

K. Natalie Randles, Le Thanh Lam, Caroline A. Sewry, Megan Puckelwartz, Denis Furling, Manfred Wehnert, Elizabeth M. McNally, Glenn E. Morris

Journal:

Developmental Dynamics

Year:

2010

Language:

english

File:

PDF, 1.56 MB

english, 2010

11

Nuclear protein import is reduced in cells expressing nuclear envelopathy-causing lamin A mutants

Albert Busch, Tilman Kiel, Wolfgang-M. Heupel, Manfred Wehnert, Stefan Hübner

Journal:

Experimental Cell Research

Year:

2009

Language:

english

File:

PDF, 1.20 MB

english, 2009

12

Isolation, Mapping, and Genomic Structure of an X-Linked Gene for a Subunit of Human Mitochondrial Complex I

Olga Zhuchenko, Manfred Wehnert, Jennifer Bailey, Zhong Sheng Sun, Cheng Chi Lee

Journal:

Year:

1996

Language:

english

File:

PDF, 489 KB

english, 1996

13

Mutations of the iduronate-2-sulfatase (IDS) gene in patients with hunter syndrome (mucopolysaccharidosis II)

Winnie Schröder, Karin Wulff, Manfred Wehnert, Günter Seidlitz, Falko H. Herrmann

Journal:

Year:

1994

Language:

english

File:

PDF, 351 KB

english, 1994

14

Reply to the letter by Kling et al.

Manfred Wehnert, Winnie Schröder, Falko H. Herrmann

Journal:

Year:

1992

Language:

english

File:

PDF, 125 KB

english, 1992

15

Pre-Lamin A processing is linked to heterochromatin organization

Giovanna Lattanzi, Marta Columbaro, Elisabetta Mattioli, Vittoria Cenni, Daria Camozzi, Manfred Wehnert, Spartaco Santi, Massimo Riccio, Rosalba Del Coco, Nadir M. Maraldi, Stefano Squarzoni, Roland F

Journal:

Journal of Cellular Biochemistry

Year:

2007

Language:

english

File:

PDF, 283 KB

english, 2007

16

eLS || LiNC Complex and Human Genetic Muscular Disease

Wehnert, Manfred S

Year:

2001

Language:

english

File:

PDF, 413 KB

english, 2001

17

Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery–Dreifuss muscular dystrophy

Meinke, Peter, Schneiderat, Peter, Srsen, Vlastimil, Korfali, Nadia, Lê Thành, Phú, Cowan, Graeme J.M., Cavanagh, David R., Wehnert, Manfred, Schirmer, Eric C., Walter, Maggie C.

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 2.65 MB

english, 2015

18

Analyse des Verformungsverhaltens einer Hausmülldeponie

Markus Wehnert, Heiko P. Neher, Pieter A. Vermeer, Ludwig W. Zangl, Manfred Dzengel

Journal:

Year:

2005

Language:

german

File:

PDF, 496 KB

german, 2005

19

p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria

Janbernd Kirschner, Thomas Brune, Manfred Wehnert, Jonas Denecke, Christina Wasner, Anja Feuer, Thorsten Marquardt, Uwe-Peter Ketelsen, Peter Wieacker, Carsten G. Bönnemann, Rudolf Korinthenberg

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 141 KB

english, 2005

20

Mutations of theLMNAgene can mimic autosomal dominant proximal spinal muscular atrophy

Sabine Rudnik-Schöneborn, Elke Botzenhart, Thomas Eggermann, Jan Senderek, Benedikt G. H. Schoser, Rolf Schröder, Manfred Wehnert, Brunhilde Wirth, Klaus Zerres

Journal:

Year:

2007

Language:

english

File:

PDF, 284 KB

english, 2007

21

The Nuclear muscular dystrophies

Manfred S. Wehnert, Gisèle Bonne

Journal:

Seminars in Pediatric Neurology

Year:

2002

Language:

english

File:

PDF, 1.46 MB

english, 2002

22

Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription

Cristina Capanni, Vittoria Cenni, Elisabetta Mattioli, Patrizia Sabatelli, Andrea Ognibene, Marta Columbaro, Veena K Parnaik, Manfred Wehnert, Nadir M Maraldi, Stefano Squarzoni, Giovanna Lattanzi

Journal:

Experimental Cell Research

Year:

2003

Language:

english

File:

PDF, 700 KB

english, 2003

23

Distinct association of the nuclear pore protein Nup153 with A- and B-type lamins

Al-Haboubi, Teiba, Shumaker, Dale K., Köser, Joachim, Wehnert, Manfred, Fahrenkrog, Birthe

Journal:

Nucleus (Landes Bioscience)

Year:

2011

Language:

english

File:

PDF, 1.31 MB

english, 2011

24

Genomic structure and fine mapping of the two human filamin gene paraloguesFLNBandFLNCand comparative analysis of the filamin gene family

Christina Chakarova, Manfred S. Wehnert, Kerstin Uhl, Sadayappan Sakthivel, Hans-Peter Vosberg, Peter F. M. van der Ven, Dieter O. Fürst

Journal:

Year:

2000

Language:

english

File:

PDF, 2.15 MB

english, 2000

25

Expression of Lamin A Mutated in the Carboxyl-Terminal Tail Generates an Aberrant Nuclear Phenotype Similar to That Observed in Cells from Patients with Dunnigan-Type Partial Lipodystrophy and Emery-Dreifuss Muscular Dystrophy

Catherine Favreau, Emmanuelle Dubosclard, Cecilia, Ostlund, Corinne Vigouroux, Jacqueline Capeau, Manfred Wehnert, Dominique Higuet, Howard J. Worman, Jean-Claude Courvalin, Brigitte Buendia

Journal:

Experimental Cell Research

Year:

2003

Language:

english

File:

PDF, 363 KB

english, 2003

26

Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy

Maria Hoeltzenbein, Thomas Karow, Joern A Zeller, Rolf Warzok, Karin Wulff, Marlies Zschiesche, Falko H Herrmann, Wolfgang Große-Heitmeyer, Manfred S Wehnert

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 155 KB

english, 1999

27

Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophy

Karin Wulff, Julia E. Parrish, Falko H. Herrmann, Manfred Wehnert

Journal:

Year:

1997

Language:

english

File:

PDF, 150 KB

english, 1997

28

Structural gene aberrations in mucopolysaccharidosis II (Hunter)

Manfred Wehnert, John J. Hopwood, Winnie Schröder, Falko H. Herrmann

Journal:

Year:

1992

Language:

english

File:

PDF, 435 KB

english, 1992

29

Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family

Coucke, Paul, Vits, Lleve, Camp, Guy Van, Serville, Francoise, Lyonnet, Stanislas, Kenwrick, Susan, Rosenthal, André, Wehnert, Manfred, Munnich, Arnold, Willems, Patrick J.

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 1.81 MB

english, 1994

30

LINC complex alterations in DMD and EDMD/CMT fibroblasts

Surayya Taranum, Eva Vaylann, Peter Meinke, Sabu Abraham, Liu Yang, Sascha Neumann, Iakowos Karakesisoglou, Manfred Wehnert, Angelika A. Noegel

Journal:

European Journal of Cell Biology

Year:

2012

Language:

english

File:

PDF, 3.15 MB

english, 2012

31

60th ENMC International Workshop: Non X-linked Emery–Dreifuss Muscular Dystrophy, 5–7 June 1998, Naarden, The Netherlands

Manfred Wehnert, Francesco Muntoni

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 52 KB

english, 1999

32

Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation

Türk, Matthias, Wehnert, Manfred, Schröder, Rolf, Chevessier, Frédéric

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 560 KB

english, 2013

33

Identification of mutational hot spots inLMNAencoding lamin A/C in patients with familial dilated cardiomyopathy

Andreas Perrot, Shwan Hussein, Volker Ruppert, Hartmut H. J. Schmidt, Manfred S. Wehnert, Nguyen Thuy Duong, Maximilian G. Posch, Anna Panek, Rainer Dietz, Ingrid Kindermann, Michael Böhm, Aleksandra

Journal:

Basic Research in Cardiology

Year:

2009

Language:

english

File:

PDF, 396 KB

english, 2009

34

Isolation of chromosome-specific genes by reciprocal probing of arrayed cDNA and cosmid libraries

Lee, Cheng Chi, Yazdani, Ali, Wehnert, Manfred, Zhao, ZhaoYang, Lindsay, Elizabeth A., Bailey, Jennifer, Coolbaugh, Mary I., Couch, Lisa, Xiong, Mengli, Chinault, A.Craig, Baldini, Antonio, Caskey, C.

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 4.25 MB

english, 1995

35

Immunohistochemistry on a panel of Emery–Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology

Le Thanh, Phu, Meinke, Peter, Korfali, Nadia, Srsen, Vlastimil, Robson, Michael I., Wehnert, Manfred, Schoser, Benedikt, Sewry, Caroline A., Schirmer, Eric C.

Journal:

Neuromuscular Disorders

Year:

2017

Language:

english

File:

PDF, 824 KB

english, 2017

36

Restrictive dermopathy: a rare laminopathy

Marc Thill, Thuy Duong Nguyen, Manfred Wehnert, Dorothea Fischer, Ingrid Hausser, Susanne Braun, Christian Jackisch

Journal:

Archives of Gynecology and Obstetrics

Year:

2008

Language:

english

File:

PDF, 455 KB

english, 2008

37

Restrictive dermopathy—a lethal congenital laminopathy. Case report and review of the literature

Paulo Morais, Sofia Magina, Maria do Céu Ribeiro, Manuela Rodrigues, José Manuel Lopes, Huong Le Thi Thanh, Manfred Wehnert, Hercília Guimarães

Journal:

European Journal of Pediatrics

Year:

2009

Language:

english

File:

PDF, 275 KB

english, 2009

38

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution

Capanni, Cristina, Squarzoni, Stefano, Cenni, Vittoria, D’Apice, Maria Rosaria, Gambineri, Alessandra, Novelli, Giuseppe, Wehnert, Manfred, Pasquali, Renato, Maraldi, Nadir M., Lattanzi, Giovanna

Journal:

Year:

2012

Language:

english

File:

PDF, 1.80 MB

english, 2012

39

A new marker at DXS 115 useful for carrier detection in hemophilia A

Manfred Wehnert, Winnie Schröder, Falko H. Herrmann

Journal:

Year:

1990

Language:

english

File:

PDF, 251 KB

english, 1990

40

Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene

Sebastian Kandert, Manfred Wehnert, Clemens R. Müller, Brigitte Buendia, Marie-Christine Dabauvalle

Journal:

European Journal of Cell Biology

Year:

2009

Language:

english

File:

PDF, 905 KB

english, 2009

41

Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery–Dreifuss muscular dystrophy

Maggie C. Walter, Thomas N. Witt, Beate Schlotter Weigel, Peter Reilich, Pascale Richard, Dieter Pongratz, Gisèle Bonne, Manfred S. Wehnert, Hanns Lochmüller

Journal:

Neuromuscular Disorders

Year:

2005

Language:

english

File:

PDF, 215 KB

english, 2005

42

Lamin A/C assembly defects in Emery–Dreifuss muscular dystrophy can be regulated by culture medium composition

Ian Holt, Nguyen thi Man, Manfred Wehnert, Glenn E. Morris

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 189 KB

english, 2006

43

World distribution of factor V Leiden mutation

MoniekP.M. de Maat, Cornelis Kluft, Jo̸rgen Jespersen, Jo̸rgen Gram, Winnie Schröder, Manuela Koessling, Karin Wulff, Manfred Wehnert, FalkoH. Herrmann, S. Fouéré, F. Guibal, P. Morel, D. Gou, A. Naip

Journal:

Year:

1996

Language:

english

File:

PDF, 329 KB

english, 1996

44

Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization

Meinke, Peter, Mattioli, Elisabetta, Haque, Farhana, Antoku, Susumu, Columbaro, Marta, Straatman, Kees R., Worman, Howard J., Gundersen, Gregg G., Lattanzi, Giovanna, Wehnert, Manfred, Shackleton, Sue

Journal:

Year:

2014

Language:

english

File:

PDF, 1.95 MB

english, 2014

45

Myofiber Degeneration in Autosomal Dominant Emery–Dreifuss Muscular Dystrophy (AD-EDMD) (LGMD1B)

Michel Mittelbronn, Frank Hanisch, Marc Gleichmann, Mechthild Stötter, Rudolf Korinthenberg, Manfred Wehnert, Gisèle Bonne, Sabine Rudnik-Schöneborn, Antje Bornemann

Journal:

Brain Pathology

Year:

2006

Language:

english

File:

PDF, 655 KB

english, 2006

46

Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25

Meuleman, Jan, Kuhlenbäumer, Gregor, Schirmacher, Anja, Wehnert, Manfred, De Jonghe, Peter, De Vriendt, Els, Young, Peter, Airaksinen, Eila, Pou-Serradell, Adolfo, Prats, José-Maria

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 287 KB

english, 1999

47

Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats

Reiner, Orly, Carrozzo, Romeo, Shen, Ying, Wehnert, Manfred, Faustinella, Fabrizia, Dobyns, William B., Caskey, C. Thomas, Ledbetter, David H.

Journal:

Year:

1993

File:

PDF, 793 KB

1993

48

Lamin A Ser404 Is a Nuclear Target of Akt Phosphorylation in C2C12 Cells

Cenni, Vittoria, Bertacchini, Jessika, Beretti, Francesca, Lattanzi, Giovanna, Bavelloni, Alberto, Riccio, Massimo, Ruzzene, Maria, Marin, Oriano, Arrigoni, Giorgio, Parnaik, Veena, Wehnert, Manfred,

Journal:

Journal of Proteome Research

Year:

2008

Language:

english

File:

PDF, 4.60 MB

english, 2008

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