Distribution of emerin during the cell cycle.

[1]  F. Muntoni,et al.  Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy , 1999, Nature Genetics.

[2]  S. Manilal,et al.  Colocalization of emerin and lamins in interphase nuclei and changes during mitosis. , 1998, Biochemical and biophysical research communications.

[3]  Crafford A. Harris,et al.  Detergent–salt resistance of LAP2α in interphase nuclei and phosphorylation‐dependent association with chromosomes early in nuclear assembly implies functions in nuclear structure dynamics , 1998, The EMBO journal.

[4]  Juliet A. Ellis,et al.  Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype. , 1998, Journal of cell science.

[5]  L. Cartegni,et al.  Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy. , 1997, Human molecular genetics.

[6]  Howard J. Worman,et al.  Nuclear Membrane Dynamics and Reassembly in Living Cells: Targeting of an Inner Nuclear Membrane Protein in Interphase and Mitosis , 1997, The Journal of cell biology.

[7]  L. Cartegni,et al.  Immunocytochemical detection of emerin within the nuclear matrix , 1997, Neuromuscular Disorders.

[8]  C. Maison,et al.  The inner nuclear membrane protein LAP1 forms a native complex with B‐type lamins and partitions with spindle‐associated mitotic vesicles , 1997, The EMBO journal.

[9]  S. Bione,et al.  X‐linked emery‐dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample , 1997, Annals of neurology.

[10]  S. Hofbauer,et al.  Preassembly of annulate lamellae in egg extracts inhibits nuclear pore complex formation, but not nuclear membrane assembly. , 1997, European journal of cell biology.

[11]  R. Foisner Dynamic organisation of intermediate filaments and associated proteins during the cell cycle , 1997, BioEssays : news and reviews in molecular, cellular and developmental biology.

[12]  Mark Fricker,et al.  Interphase Nuclei of Many Mammalian Cell Types Contain Deep, Dynamic, Tubular Membrane-bound Invaginations of the Nuclear Envelope , 1997, The Journal of cell biology.

[13]  K. Wilson,et al.  Nuclear envelope assembly after mitosis. , 1997, Trends in cell biology.

[14]  F. Muntoni,et al.  Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodies , 1997, Neuromuscular Disorders.

[15]  M. Dabauvalle,et al.  A biochemical and immunological comparison of nuclear and cytoplasmic pore complexes. , 1996, Journal of cell science.

[16]  G. Krohne,et al.  Characterization and quantitation of three B-type lamins in Xenopus oocytes and eggs: increase of lamin LI protein synthesis during meiotic maturation. , 1996, Journal of cell science.

[17]  S. Manilal,et al.  The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein. , 1996, Human molecular genetics.

[18]  V. Cordes,et al.  Cytoplasmic annulate lamellae in cultured cells: composition, distribution, and mitotic behavior , 1996, Cell and Tissue Research.

[19]  T. Tsukahara,et al.  Emerin deficiency at the nuclear membrane in patients with Emery-Dreif uss muscular dystrophy , 1996, Nature Genetics.

[20]  A. Ciccodicola,et al.  Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease. , 1995, Human molecular genetics.

[21]  S. Klauck,et al.  Identification of novel mutations in three families with Emery-Dreifuss muscular dystrophy. , 1995, Human molecular genetics.

[22]  D. Forbes,et al.  Nuclear pore complex assembly studied with a biochemical assay for annulate lamellae formation , 1995, The Journal of cell biology.

[23]  U. Aebi,et al.  Cloning of a cDNA for lamina‐associated polypeptide 2 (LAP2) and identification of regions that specify targeting to the nuclear envelope. , 1995, The EMBO journal.

[24]  E. Maestrini,et al.  Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy , 1994, Nature Genetics.

[25]  G. Krohne,et al.  Lamin-dependent nuclear envelope reassembly following mitosis: an argument. , 1994, Trends in cell biology.

[26]  J. Siekierka,et al.  Three distinct human thymopoietins are derived from alternatively spliced mRNAs. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[27]  R. Foisner,et al.  Integral membrane proteins and dynamic organization of the nuclear envelope. , 1994, Trends in cell biology.

[28]  R. Foisner,et al.  Integral membrane proteins of the nuclear envelope interact with lamins and chromosomes, and binding is modulated by mitotic phosphorylation , 1993, Cell.

[29]  N. Chaudhary,et al.  Stepwise reassembly of the nuclear envelope at the end of mitosis , 1993, The Journal of cell biology.

[30]  M. Ferguson-Smith,et al.  Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28. , 1993, Journal of medical genetics.

[31]  M. Rietschel,et al.  Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene , 1992, Neuromuscular Disorders.

[32]  M. Dabauvalle,et al.  Spontaneous assembly of pore complex-containing membranes ("annulate lamellae") in Xenopus egg extract in the absence of chromatin , 1991, The Journal of cell biology.

[33]  T. Y. Chen,et al.  Annulate lamellae: comparison of antigenic epitopes of annulate lamellae membranes with the nuclear envelope , 1988, The Journal of cell biology.

[34]  G. Reimer,et al.  Monoclonal autoantibody from a (New Zealand black x New Zealand white)F1 mouse and some human scleroderma sera target an Mr 34,000 nucleolar protein of the U3 RNP particle. , 1987, Arthritis and rheumatism.

[35]  P. Harper,et al.  Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome. , 1986, Journal of medical genetics.

[36]  G. Krohne,et al.  Involvement of nuclear lamins in postmitotic reorganization of chromatin as demonstrated by microinjection of lamin antibodies , 1986, The Journal of cell biology.

[37]  J. Kyhse-Andersen Electroblotting of multiple gels: a simple apparatus without buffer tank for rapid transfer of proteins from polyacrylamide to nitrocellulose. , 1984, Journal of biochemical and biophysical methods.

[38]  J. Vandekerckhove,et al.  Permanently proliferating rat vascular smooth muscle cell with maintained expression of smooth muscle characteristics, including actin of the vascular smooth muscle type , 1980, The Journal of cell biology.

[39]  R. Kornberg,et al.  An octamer of histones in chromatin and free in solution. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[40]  H. Worman,et al.  Nuclear lamin-binding proteins. , 1998, Sub-cellular biochemistry.

[41]  R. Goldman,et al.  The dynamic properties and possible functions of nuclear lamins. , 1995, International review of cytology.

[42]  R. Kessel Annulate lamellae: a last frontier in cellular organelles. , 1992, International review of cytology.

[43]  M. Dabauvalle,et al.  Assembly of nuclear pore complexes in Xenopus egg extract , 1991, Biology of the cell.