| Year |
Citation |
Score |
| 2024 |
Wu W, Jin Q, Östlund C, Tanji K, Shin JY, Han J, Leu CS, Kushner J, Worman HJ. mTOR Inhibition Prolongs Survival and Has Beneficial Effects on Heart Function After Onset of Lamin A/C Gene Mutation Cardiomyopathy in Mice. Circulation. Heart Failure. e011110. PMID 38567527 DOI: 10.1161/CIRCHEARTFAILURE.123.011110 |
0.681 |
|
| 2024 |
Hernandez-Ono A, Zhao YP, Murray JW, Östlund C, Lee MJ, Shi A, Dauer WT, Worman HJ, Ginsberg HN, Shin JY. Dynamic regulation of hepatic lipid metabolism by torsinA and its activators. Jci Insight. PMID 38194265 DOI: 10.1172/jci.insight.175328 |
0.57 |
|
| 2023 |
Hernandez-Ono A, Zhao YP, Murray JW, Östlund C, Lee MJ, Shi A, Dauer WT, Worman HJ, Ginsberg HN, Shin JY. Functional interaction of torsinA and its activators in liver lipid metabolism. Biorxiv : the Preprint Server For Biology. PMID 37547008 DOI: 10.1101/2023.06.21.545957 |
0.579 |
|
| 2022 |
Östlund C, Hernandez-Ono A, Turk SJ, Dauer WT, Ginsberg HN, Worman HJ, Shin JY. Hepatocytes deficient in nuclear envelope protein lamina-associated polypeptide 1 are an ideal mammalian system to study intranuclear lipid droplets. Journal of Lipid Research. 100277. PMID 36100089 DOI: 10.1016/j.jlr.2022.100277 |
0.627 |
|
| 2022 |
Wang Y, Shilagardi K, Hsu T, Odinammadu KO, Maruyama T, Wu W, Lin CS, Damoci CB, Spear ED, Shin JY, Hsu W, Michaelis S, Worman HJ. Abolishing the prelamin A ZMPSTE24 cleavage site leads to progeroid phenotypes with near-normal longevity in mice. Proceedings of the National Academy of Sciences of the United States of America. 119. PMID 35197292 DOI: 10.1073/pnas.2118695119 |
0.609 |
|
| 2021 |
Shin JY, Worman HJ. Molecular Pathology of Laminopathies. Annual Review of Pathology. PMID 34672689 DOI: 10.1146/annurev-pathol-042220-034240 |
0.674 |
|
| 2021 |
Vignier N, Chatzifrangkeskou M, Pinton L, Wioland H, Marais T, Lemaitre M, Le Dour C, Peccate C, Cardoso D, Schmitt A, Wu W, Biferi MG, Naouar N, Macquart C, Beuvin M, ... ... Worman HJ, et al. The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies. Cell Reports. 36: 109601. PMID 34433058 DOI: 10.1016/j.celrep.2021.109601 |
0.645 |
|
| 2021 |
Kronenberg-Tenga R, Tatli M, Eibauer M, Wu W, Shin JY, Bonne G, Worman HJ, Medalia O. A lamin A/C variant causing striated muscle disease provides insights into filament organization. Journal of Cell Science. PMID 33536248 DOI: 10.1242/jcs.256156 |
0.653 |
|
| 2021 |
Dridi H, Wu W, Reiken SR, Ofer RM, Liu Y, Yuan Q, Sittenfeld L, Kushner J, Muchir A, Worman HJ, Marks AR. Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation. Human Molecular Genetics. PMID 33388782 DOI: 10.1093/hmg/ddaa278 |
0.688 |
|
| 2020 |
Marcelot A, Worman HJ, Zinn-Justin S. Protein structural and mechanistic basis of progeroid laminopathies. The Febs Journal. PMID 32799420 DOI: 10.1111/Febs.15526 |
0.452 |
|
| 2020 |
Lindenboim L, Zohar H, Worman HJ, Stein R. The nuclear envelope: target and mediator of the apoptotic process. Cell Death Discovery. 6: 29. PMID 32351716 DOI: 10.1038/S41420-020-0256-5 |
0.319 |
|
| 2019 |
Antoku S, Wu W, Joseph LC, Morrow JP, Worman HJ, Gundersen GG. ERK1/2 Phosphorylation of FHOD Connects Signaling and Nuclear Positioning Alternations in Cardiac Laminopathy. Developmental Cell. 51: 602-616.e12. PMID 31794718 DOI: 10.1016/J.Devcel.2019.10.023 |
0.501 |
|
| 2019 |
Muchir A, Worman HJ. Emery-Dreifuss muscular dystrophy: focal point nuclear envelope. Current Opinion in Neurology. 32: 728-734. PMID 31460960 DOI: 10.1097/Wco.0000000000000741 |
0.681 |
|
| 2019 |
Shin JY, Hernandez-Ono A, Fedotova T, Östlund C, Lee MJ, Gibeley SB, Liang CC, Dauer WT, Ginsberg HN, Worman HJ. Nuclear envelope-localized torsinA-LAP1 complex regulates hepatic VLDL secretion and steatosis. The Journal of Clinical Investigation. 130. PMID 31408437 DOI: 10.1172/Jci129769 |
0.63 |
|
| 2019 |
Östlund C, Chang W, Gundersen GG, Worman HJ. Pathogenic mutations in genes encoding nuclear envelope proteins and defective nucleocytoplasmic connections. Experimental Biology and Medicine (Maywood, N.J.). 1535370219862243. PMID 31299860 DOI: 10.1177/1535370219862243 |
0.455 |
|
| 2019 |
Wang Y, Shin JY, Nakanishi K, Homma S, Kim GJ, Tanji K, Joseph LC, Morrow JP, Stewart CL, Dauer WT, Worman HJ. Postnatal Development of Mice with Combined Genetic Depletions of Lamin A/C, Emerin and Lamina-associated Polypeptide 1. Human Molecular Genetics. PMID 31009944 DOI: 10.1093/Hmg/Ddz082 |
0.674 |
|
| 2019 |
Chang W, Wang Y, Luxton GWG, Östlund C, Worman HJ, Gundersen GG. Imbalanced nucleocytoskeletal connections create common polarity defects in progeria and physiological aging. Proceedings of the National Academy of Sciences of the United States of America. 116: 3578-3583. PMID 30808750 DOI: 10.1073/Pnas.1809683116 |
0.348 |
|
| 2018 |
Nagy PL, Worman HJ. Next-Generation Sequencing and Mutational Analysis: Implications for Genes Encoding LINC Complex Proteins. Methods in Molecular Biology (Clifton, N.J.). 1840: 321-336. PMID 30141054 DOI: 10.1007/978-1-4939-8691-0_22 |
0.307 |
|
| 2018 |
Worman HJ, Michaelis S. Permanently Farnesylated Prelamin A, Progeria, and Atherosclerosis. Circulation. 138: 283-286. PMID 30012702 DOI: 10.1161/Circulationaha.118.034480 |
0.408 |
|
| 2018 |
Chatzifrangkeskou M, Yadin D, Marais T, Chardonnet S, Cohen-Tannoudji M, Mougenot N, Schmitt A, Crasto S, Di Pasquale E, Macquart C, Tanguy Y, Jebeniani I, Pucéat M, Morales Rodriguez B, Goldmann WH, ... ... Worman HJ, et al. Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation. Human Molecular Genetics. PMID 29878125 DOI: 10.1093/Hmg/Ddy215 |
0.702 |
|
| 2018 |
Choi JC, Wu W, Phillips E, Plevin R, Sera F, Homma S, Worman HJ. Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival. Human Molecular Genetics. PMID 29668927 DOI: 10.1093/Hmg/Ddy134 |
0.7 |
|
| 2017 |
Worman HJ. Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations. Biochemical Society Transactions. PMID 29196611 DOI: 10.1042/Bst20170236 |
0.52 |
|
| 2017 |
Le Dour C, Macquart C, Sera F, Homma S, Bonne G, Morrow JP, Worman HJ, Muchir A. Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene. Human Molecular Genetics. PMID 28069793 DOI: 10.1093/Hmg/Ddw389 |
0.671 |
|
| 2016 |
Wu W, Chordia MD, Hart BP, Kumarasinghe ES, Ji MK, Bhargava A, Lawlor MW, Shin JY, Sera F, Homma S, Muchir A, Khire UR, Worman HJ. Macrocyclic MEK1/2 inhibitor with efficacy in a mouse model of cardiomyopathy caused by lamin A/C gene mutation. Bioorganic & Medicinal Chemistry. PMID 28011205 DOI: 10.1016/J.Bmc.2016.12.014 |
0.784 |
|
| 2016 |
Le Dour C, Wu W, Béréziat V, Capeau J, Vigouroux C, Worman HJ. Extracellular Matrix Remodeling and Transforming Growth Factor-β Signaling Abnormalities Induced by Lamin A/C Variants that Cause Lipodystrophy. Journal of Lipid Research. PMID 27845687 DOI: 10.1194/Jlr.M071381 |
0.387 |
|
| 2016 |
Shin JY, Méndez-López I, Hong M, Wang Y, Tanji K, Wu W, Shugol L, Krauss RS, Dauer WT, Worman HJ. Lamina-associated polypeptide 1 is dispensable for embryonic myogenesis but required for postnatal skeletal muscle growth. Human Molecular Genetics. PMID 27798115 DOI: 10.1093/Hmg/Ddw368 |
0.647 |
|
| 2016 |
Chatzifrangkeskou M, Le Dour C, Wu W, Morrow JP, Joseph LC, Beuvin M, Sera F, Homma S, Vignier N, Mougenot N, Bonne G, Lipson KE, Worman HJ, Muchir A. ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene. Human Molecular Genetics. PMID 27131347 DOI: 10.1093/Hmg/Ddw090 |
0.685 |
|
| 2016 |
Wang Y, Lichter-Konecki U, Anyane-Yeboa K, Shaw JE, Lu JT, Östlund C, Shin JY, Clark LN, Gundersen GG, Nagy PL, Worman HJ. Mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder. Journal of Cell Science. PMID 27034136 DOI: 10.1242/Jcs.187302 |
0.657 |
|
| 2016 |
Wu W, Patel A, Kyöstilä K, Lohi H, Mladkova N, Kiryluk K, Sun X, Lefkowitch JH, Worman HJ, Gharavi AG. Genome-wide Association Study in Mice Identifies Loci Affecting Liver-related Phenotypes Including Sel1l Influencing Serum Bile Acids. Hepatology (Baltimore, Md.). PMID 26857093 DOI: 10.1002/Hep.28495 |
0.317 |
|
| 2016 |
Muchir A, Worman HJ. Targeting Mitogen-Activated Protein Kinase Signaling in Mouse Models of Cardiomyopathy Caused by Lamin A/C Gene Mutations. Methods in Enzymology. 568: 557-80. PMID 26795484 DOI: 10.1016/Bs.Mie.2015.07.028 |
0.723 |
|
| 2015 |
Herrada I, Samson C, Velours C, Renault L, Östlund C, Chervy P, Puchkov D, Worman HJ, Buendia B, Zinn-Justin S. Muscular Dystrophy Mutations Impair the Nuclear Envelope Emerin Self-assembly Properties. Acs Chemical Biology. PMID 26415001 DOI: 10.1021/Acschembio.5B00648 |
0.389 |
|
| 2015 |
Worman HJ, Schirmer EC. Nuclear membrane diversity: underlying tissue-specific pathologies in disease? Current Opinion in Cell Biology. 34: 101-12. PMID 26115475 DOI: 10.1016/J.Ceb.2015.06.003 |
0.391 |
|
| 2015 |
Chang W, Antoku S, Östlund C, Worman HJ, Gundersen GG. Linker of nucleoskeleton and cytoskeleton (LINC) complex-mediated actin-dependent nuclear positioning orients centrosomes in migrating myoblasts. Nucleus (Austin, Tex.). 6: 77-88. PMID 25587885 DOI: 10.1080/19491034.2015.1004947 |
0.33 |
|
| 2015 |
Chang W, Worman HJ, Gundersen GG. Accessorizing and anchoring the LINC complex for multifunctionality. The Journal of Cell Biology. 208: 11-22. PMID 25559183 DOI: 10.1083/Jcb.201409047 |
0.303 |
|
| 2014 |
Lindenboim L, Sasson T, Worman HJ, Borner C, Stein R. Cellular stress induces Bax-regulated nuclear bubble budding and rupture followed by nuclear protein release. Nucleus (Austin, Tex.). 5: 527-41. PMID 25482068 DOI: 10.4161/19491034.2014.970105 |
0.365 |
|
| 2014 |
Muchir A, Wu W, Sera F, Homma S, Worman HJ. Mitogen-activated protein kinase kinase 1/2 inhibition and angiotensin II converting inhibition in mice with cardiomyopathy caused by lamin A/C gene mutation. Biochemical and Biophysical Research Communications. 452: 958-61. PMID 25218145 DOI: 10.1016/J.Bbrc.2014.09.020 |
0.709 |
|
| 2014 |
Meinke P, Mattioli E, Haque F, Antoku S, Columbaro M, Straatman KR, Worman HJ, Gundersen GG, Lattanzi G, Wehnert M, Shackleton S. Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization. Plos Genetics. 10: e1004605. PMID 25210889 DOI: 10.1371/Journal.Pgen.1004605 |
0.458 |
|
| 2014 |
Worman HJ, Dauer WT. The nuclear envelope: an intriguing focal point for neurogenetic disease. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 11: 764-72. PMID 25119890 DOI: 10.1007/S13311-014-0296-8 |
0.408 |
|
| 2014 |
Shin JY, Le Dour C, Sera F, Iwata S, Homma S, Joseph LC, Morrow JP, Dauer WT, Worman HJ. Depletion of lamina-associated polypeptide 1 from cardiomyocytes causes cardiac dysfunction in mice. Nucleus (Austin, Tex.). 5: 260-459. PMID 24859316 DOI: 10.4161/Nucl.29227 |
0.683 |
|
| 2014 |
Choi JC, Worman HJ. Nuclear envelope regulation of signaling cascades. Advances in Experimental Medicine and Biology. 773: 187-206. PMID 24563349 DOI: 10.1007/978-1-4899-8032-8_9 |
0.64 |
|
| 2014 |
Shin JY, Dauer WT, Worman HJ. Lamina-associated polypeptide 1: protein interactions and tissue-selective functions. Seminars in Cell & Developmental Biology. 29: 164-8. PMID 24508913 DOI: 10.1016/J.Semcdb.2014.01.010 |
0.696 |
|
| 2014 |
Wu W, Iwata S, Homma S, Worman HJ, Muchir A. Depletion of extracellular signal-regulated kinase 1 in mice with cardiomyopathy caused by lamin A/C gene mutation partially prevents pathology before isoenzyme activation. Human Molecular Genetics. 23: 1-11. PMID 23933734 DOI: 10.1093/Hmg/Ddt387 |
0.723 |
|
| 2013 |
Shin JY, Méndez-López I, Wang Y, Hays AP, Tanji K, Lefkowitch JH, Schulze PC, Worman HJ, Dauer WT. Lamina-associated polypeptide-1 interacts with the muscular dystrophy protein emerin and is essential for skeletal muscle maintenance. Developmental Cell. 26: 591-603. PMID 24055652 DOI: 10.1016/J.Devcel.2013.08.012 |
0.656 |
|
| 2013 |
Muchir A, Kim YJ, Reilly SA, Wu W, Choi JC, Worman HJ. Inhibition of extracellular signal-regulated kinase 1/2 signaling has beneficial effects on skeletal muscle in a mouse model of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutation. Skeletal Muscle. 3: 17. PMID 23815988 DOI: 10.1186/2044-5040-3-17 |
0.757 |
|
| 2013 |
Bourgeois B, Gilquin B, Tellier-Lebègue C, Östlund C, Wu W, Pérez J, El Hage P, Lallemand F, Worman HJ, Zinn-Justin S. Inhibition of TGF-β signaling at the nuclear envelope: characterization of interactions between MAN1, Smad2 and Smad3, and PPM1A. Science Signaling. 6: ra49. PMID 23779087 DOI: 10.1126/Scisignal.2003411 |
0.363 |
|
| 2013 |
Worman HJ, Segil N. Nucleocytoplasmic connections and deafness. The Journal of Clinical Investigation. 123: 553-5. PMID 23348730 DOI: 10.1172/Jci67454 |
0.402 |
|
| 2013 |
Singh M, Hunt CR, Pandita RK, Kumar R, Yang CR, Horikoshi N, Bachoo R, Serag S, Story MD, Shay JW, Powell SN, Gupta A, Jeffery J, Pandita S, Chen BP, ... ... Worman HJ, et al. Lamin A/C depletion enhances DNA damage-induced stalled replication fork arrest. Molecular and Cellular Biology. 33: 1210-22. PMID 23319047 DOI: 10.1128/Mcb.01676-12 |
0.324 |
|
| 2013 |
Choi JC, Worman HJ. Reactivation of autophagy ameliorates LMNA cardiomyopathy. Autophagy. 9: 110-1. PMID 23044536 DOI: 10.4161/Auto.22403 |
0.676 |
|
| 2013 |
Kamradt M, Zou C, Liu L, Wang Y, Fitchev PP, Worman HJ, Crawford SE, Talamonti M, Gao Q. Abstract 331: Head and neck and skin squamous cell carcinoma developed in a BRCA2 knockout mouse model. Cancer Research. 73: 331-331. DOI: 10.1158/1538-7445.Am2013-331 |
0.301 |
|
| 2012 |
Choi JC, Wu W, Muchir A, Iwata S, Homma S, Worman HJ. Dual specificity phosphatase 4 mediates cardiomyopathy caused by lamin A/C (LMNA) gene mutation. The Journal of Biological Chemistry. 287: 40513-24. PMID 23048029 DOI: 10.1074/Jbc.M112.404541 |
0.791 |
|
| 2012 |
Frock RL, Chen SC, Da DF, Frett E, Lau C, Brown C, Pak DN, Wang Y, Muchir A, Worman HJ, Santana LF, Ladiges WC, Rabinovitch PS, Kennedy BK. Cardiomyocyte-specific expression of lamin a improves cardiac function in Lmna-/- mice. Plos One. 7: e42918. PMID 22905185 DOI: 10.1371/Journal.Pone.0042918 |
0.661 |
|
| 2012 |
Wang Y, Ostlund C, Choi JC, Swayne TC, Gundersen GG, Worman HJ. Blocking farnesylation of the prelamin A variant in Hutchinson-Gilford progeria syndrome alters the distribution of A-type lamins. Nucleus (Austin, Tex.). 3: 452-62. PMID 22895092 DOI: 10.4161/Nucl.21675 |
0.626 |
|
| 2012 |
Choi JC, Muchir A, Wu W, Iwata S, Homma S, Morrow JP, Worman HJ. Temsirolimus activates autophagy and ameliorates cardiomyopathy caused by lamin A/C gene mutation. Science Translational Medicine. 4: 144ra102. PMID 22837537 DOI: 10.1126/Scitranslmed.3003875 |
0.777 |
|
| 2012 |
Muchir A, Wu W, Choi JC, Iwata S, Morrow J, Homma S, Worman HJ. Abnormal p38α mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation. Human Molecular Genetics. 21: 4325-33. PMID 22773734 DOI: 10.1093/Hmg/Dds265 |
0.783 |
|
| 2012 |
Duarte-Rey C, Bogdanos D, Yang CY, Roberts K, Leung PS, Anaya JM, Worman HJ, Gershwin ME. Primary biliary cirrhosis and the nuclear pore complex. Autoimmunity Reviews. 11: 898-902. PMID 22487189 DOI: 10.1016/J.Autrev.2012.03.005 |
0.344 |
|
| 2012 |
Méndez-López I, Worman HJ. Inner nuclear membrane proteins: impact on human disease. Chromosoma. 121: 153-67. PMID 22307332 DOI: 10.1007/S00412-012-0360-2 |
0.455 |
|
| 2012 |
Attur M, Ben-Artzi A, Yang Q, Al-Mussawir HE, Worman HJ, Palmer G, Abramson SB. Perturbation of nuclear lamin A causes cell death in chondrocytes. Arthritis and Rheumatism. 64: 1940-9. PMID 22231515 DOI: 10.1002/Art.34360 |
0.357 |
|
| 2012 |
Muchir A, Reilly SA, Wu W, Iwata S, Homma S, Bonne G, Worman HJ. Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene. Cardiovascular Research. 93: 311-9. PMID 22068161 DOI: 10.1093/Cvr/Cvr301 |
0.708 |
|
| 2012 |
Worman HJ. Nuclear lamins and laminopathies. The Journal of Pathology. 226: 316-25. PMID 21953297 DOI: 10.1002/Path.2999 |
0.47 |
|
| 2012 |
Frock RL, Chen SC, Dai D, Frett E, Lau C, Brown C, Pak DN, Wang Y, Muchir A, Worman HJ, Santana LF, Ladiges WC, Rabinovitch PS, Kennedy BK. Correction: Cardiomyocyte-Specific Expression of Lamin A Improves Cardiac Function in Lmna−/−Mice Plos One. 7. DOI: 10.1371/Annotation/92Be6B32-D8E7-44C2-80A9-21097Ad27965 |
0.621 |
|
| 2011 |
Duband-Goulet I, Woerner S, Gasparini S, Attanda W, Kondé E, Tellier-Lebègue C, Craescu CT, Gombault A, Roussel P, Vadrot N, Vicart P, Ostlund C, Worman HJ, Zinn-Justin S, Buendia B. Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins. Experimental Cell Research. 317: 2800-13. PMID 21993218 DOI: 10.1016/J.Yexcr.2011.09.012 |
0.43 |
|
| 2011 |
Luxton GW, Gomes ER, Folker ES, Worman HJ, Gundersen GG. TAN lines: a novel nuclear envelope structure involved in nuclear positioning. Nucleus (Austin, Tex.). 2: 173-81. PMID 21818410 DOI: 10.4161/Nucl.2.3.16243 |
0.313 |
|
| 2011 |
Lu JT, Muchir A, Nagy PL, Worman HJ. LMNA cardiomyopathy: cell biology and genetics meet clinical medicine. Disease Models & Mechanisms. 4: 562-8. PMID 21810905 DOI: 10.1242/Dmm.006346 |
0.692 |
|
| 2011 |
Wu W, Muchir A, Shan J, Bonne G, Worman HJ. Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomyopathy caused by mutation in lamin A/C gene. Circulation. 123: 53-61. PMID 21173351 DOI: 10.1161/Circulationaha.110.970673 |
0.728 |
|
| 2011 |
Folker ES, Ostlund C, Luxton GW, Worman HJ, Gundersen GG. Lamin A variants that cause striated muscle disease are defective in anchoring transmembrane actin-associated nuclear lines for nuclear movement. Proceedings of the National Academy of Sciences of the United States of America. 108: 131-6. PMID 21173262 DOI: 10.1073/Pnas.1000824108 |
0.427 |
|
| 2010 |
Muchir A, Wu W, Worman HJ. Mitogen-activated protein kinase inhibitor regulation of heart function and fibrosis in cardiomyopathy caused by lamin A/C gene mutation. Trends in Cardiovascular Medicine. 20: 217-21. PMID 22293021 DOI: 10.1016/J.Tcm.2011.11.002 |
0.728 |
|
| 2010 |
Wang Y, Ostlund C, Worman HJ. Blocking protein farnesylation improves nuclear shape abnormalities in keratinocytes of mice expressing the prelamin A variant in Hutchinson-Gilford progeria syndrome. Nucleus (Austin, Tex.). 1: 432-9. PMID 21326826 DOI: 10.4161/Nucl.1.5.12972 |
0.438 |
|
| 2010 |
Muchir A, Worman HJ. Signaling defects and the nuclear envelope in progeria. Developmental Cell. 19: 355-6. PMID 20833355 DOI: 10.1016/J.Devcel.2010.08.019 |
0.652 |
|
| 2010 |
Kondé E, Bourgeois B, Tellier-Lebegue C, Wu W, Pérez J, Caputo S, Attanda W, Gasparini S, Charbonnier JB, Gilquin B, Worman HJ, Zinn-Justin S. Structural analysis of the Smad2-MAN1 interaction that regulates transforming growth factor-β signaling at the inner nuclear membrane. Biochemistry. 49: 8020-32. PMID 20715792 DOI: 10.1021/Bi101153W |
0.348 |
|
| 2010 |
Bruston F, Delbarre E, Ostlund C, Worman HJ, Buendia B, Duband-Goulet I. Loss of a DNA binding site within the tail of prelamin A contributes to altered heterochromatin anchorage by progerin. Febs Letters. 584: 2999-3004. PMID 20580717 DOI: 10.1016/J.Febslet.2010.05.032 |
0.343 |
|
| 2010 |
Marji J, O'Donoghue SI, McClintock D, Satagopam VP, Schneider R, Ratner D, Worman HJ, Gordon LB, Djabali K. Defective lamin A-Rb signaling in Hutchinson-Gilford Progeria Syndrome and reversal by farnesyltransferase inhibition. Plos One. 5: e11132. PMID 20559568 DOI: 10.1371/Journal.Pone.0011132 |
0.453 |
|
| 2010 |
Wu W, Shan J, Bonne G, Worman HJ, Muchir A. Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene. Biochimica Et Biophysica Acta. 1802: 632-8. PMID 20388542 DOI: 10.1016/J.Bbadis.2010.04.001 |
0.73 |
|
| 2010 |
Worman HJ, Ostlund C, Wang Y. Diseases of the nuclear envelope. Cold Spring Harbor Perspectives in Biology. 2: a000760. PMID 20182615 DOI: 10.1101/Cshperspect.A000760 |
0.437 |
|
| 2010 |
Worman HJ, Foisner R. The nuclear envelope from basic biology to therapy. Biochemical Society Transactions. 38: 253-6. PMID 20074069 DOI: 10.1042/Bst0380253 |
0.385 |
|
| 2010 |
Worman HJ. Prelamin A prenylation and the treatment of progeria. Journal of Lipid Research. 51: 223-5. PMID 19965579 DOI: 10.1194/Jlr.E004366 |
0.439 |
|
| 2009 |
Dauer WT, Worman HJ. The nuclear envelope as a signaling node in development and disease. Developmental Cell. 17: 626-38. PMID 19922868 DOI: 10.1016/J.Devcel.2009.10.016 |
0.425 |
|
| 2009 |
Ostlund C, Folker ES, Choi JC, Gomes ER, Gundersen GG, Worman HJ. Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins. Journal of Cell Science. 122: 4099-108. PMID 19843581 DOI: 10.1242/Jcs.057075 |
0.575 |
|
| 2009 |
Ostlund C, Guan T, Figlewicz DA, Hays AP, Worman HJ, Gerace L, Schirmer EC. Reduction of a 4q35-encoded nuclear envelope protein in muscle differentiation. Biochemical and Biophysical Research Communications. 389: 279-83. PMID 19716805 DOI: 10.1016/J.Bbrc.2009.08.133 |
0.615 |
|
| 2009 |
Worman HJ, Fong LG, Muchir A, Young SG. Laminopathies and the long strange trip from basic cell biology to therapy. The Journal of Clinical Investigation. 119: 1825-36. PMID 19587457 DOI: 10.1172/Jci37679 |
0.69 |
|
| 2009 |
Verstraeten VL, Caputo S, van Steensel MA, Duband-Goulet I, Zinn-Justin S, Kamps M, Kuijpers HJ, Ostlund C, Worman HJ, Briedé JJ, Le Dour C, Marcelis CL, van Geel M, Steijlen PM, van den Wijngaard A, et al. The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress. Journal of Cellular and Molecular Medicine. 13: 959-71. PMID 19220582 DOI: 10.1111/J.1582-4934.2009.00690.X |
0.371 |
|
| 2009 |
Muchir A, Wu W, Worman HJ. Reduced expression of A-type lamins and emerin activates extracellular signal-regulated kinase in cultured cells. Biochimica Et Biophysica Acta. 1792: 75-81. PMID 19022376 DOI: 10.1016/J.Bbadis.2008.10.012 |
0.707 |
|
| 2009 |
Muchir A, Shan J, Bonne G, Lehnart SE, Worman HJ. Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins. Human Molecular Genetics. 18: 241-7. PMID 18927124 DOI: 10.1093/Hmg/Ddn343 |
0.729 |
|
| 2009 |
Muchir A, Wu W, Shan J, Bonne G, Worman H. G.P.15.06 Inhibition of c-Jun N-terminal kinases signaling to prevent cardiomyopathy caused by mutation in LMNA gene Neuromuscular Disorders. 19: 648-649. DOI: 10.1016/J.Nmd.2009.06.325 |
0.68 |
|
| 2008 |
Wang Y, Panteleyev AA, Owens DM, Djabali K, Stewart CL, Worman HJ. Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin. Human Molecular Genetics. 17: 2357-69. PMID 18442998 DOI: 10.1093/Hmg/Ddn136 |
0.392 |
|
| 2007 |
Worman HJ. Nuclear envelope protein autoantigens in primary biliary cirrhosis. Hepatology Research : the Official Journal of the Japan Society of Hepatology. 37: S406-11. PMID 17931195 DOI: 10.1111/J.1872-034X.2007.00227.X |
0.308 |
|
| 2007 |
Lüdtke A, Buettner J, Schmidt HH, Worman HJ. New PPARG mutation leads to lipodystrophy and loss of protein function that is partially restored by a synthetic ligand. Journal of Medical Genetics. 44: e88. PMID 17766367 DOI: 10.1136/Jmg.2007.050567 |
0.422 |
|
| 2007 |
Muchir A, Pavlidis P, Bonne G, Hayashi YK, Worman HJ. Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy. Human Molecular Genetics. 16: 1884-95. PMID 17567779 DOI: 10.1093/Hmg/Ddm137 |
0.725 |
|
| 2007 |
Worman HJ, Bonne G. "Laminopathies": a wide spectrum of human diseases. Experimental Cell Research. 313: 2121-33. PMID 17467691 DOI: 10.1016/J.Yexcr.2007.03.028 |
0.448 |
|
| 2007 |
Muchir A, Pavlidis P, Decostre V, Herron AJ, Arimura T, Bonne G, Worman HJ. Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy. The Journal of Clinical Investigation. 117: 1282-93. PMID 17446932 DOI: 10.1172/Jci29042 |
0.718 |
|
| 2007 |
Lüdtke A, Buettner J, Wu W, Muchir A, Schroeter A, Zinn-Justin S, Spuler S, Schmidt HH, Worman HJ. Peroxisome proliferator-activated receptor-gamma C190S mutation causes partial lipodystrophy. The Journal of Clinical Endocrinology and Metabolism. 92: 2248-55. PMID 17356052 DOI: 10.1210/Jc.2005-2624 |
0.69 |
|
| 2007 |
Muchir A, Worman HJ. Emery-Dreifuss muscular dystrophy. Current Neurology and Neuroscience Reports. 7: 78-83. PMID 17217858 DOI: 10.1007/S11910-007-0025-3 |
0.72 |
|
| 2007 |
Muchir A, Pavlidis P, Decostre V, Herron A, Arimura T, Hayashi Y, Bonne G, Worman H. G.P.5.10 MAPK signaling pathway is commonly activated in hearts of mouse models of autosomal dominant and X-linked Emery–Dreifuss muscular dystrophy Neuromuscular Disorders. 17: 800. DOI: 10.1016/J.Nmd.2007.06.133 |
0.651 |
|
| 2006 |
Muchir A, Massart C, van Engelen BG, Lammens M, Bonne G, Worman HJ. Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins. Biochemical and Biophysical Research Communications. 351: 1011-7. PMID 17097067 DOI: 10.1016/J.Bbrc.2006.10.147 |
0.692 |
|
| 2006 |
Wang Y, Herron AJ, Worman HJ. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy. Human Molecular Genetics. 15: 2479-89. PMID 16825283 DOI: 10.1093/Hmg/Ddl170 |
0.459 |
|
| 2006 |
Caputo S, Couprie J, Duband-Goulet I, Kondé E, Lin F, Braud S, Gondry M, Gilquin B, Worman HJ, Zinn-Justin S. The carboxyl-terminal nucleoplasmic region of MAN1 exhibits a DNA binding winged helix domain. The Journal of Biological Chemistry. 281: 18208-15. PMID 16648637 DOI: 10.1074/Jbc.M601980200 |
0.326 |
|
| 2006 |
Worman HJ. Inner nuclear membrane and regulation of Smad-mediated signaling. Biochimica Et Biophysica Acta. 1761: 626-31. PMID 16574476 DOI: 10.1016/J.Bbalip.2006.02.010 |
0.403 |
|
| 2006 |
Ostlund C, Sullivan T, Stewart CL, Worman HJ. Dependence of diffusional mobility of integral inner nuclear membrane proteins on A-type lamins. Biochemistry. 45: 1374-82. PMID 16445279 DOI: 10.1021/Bi052156N |
0.392 |
|
| 2006 |
Boguslavsky RL, Stewart CL, Worman HJ. Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy. Human Molecular Genetics. 15: 653-63. PMID 16415042 DOI: 10.1093/Hmg/Ddi480 |
0.378 |
|
| 2006 |
Worman HJ, Gundersen GG. Here come the SUNs: a nucleocytoskeletal missing link. Trends in Cell Biology. 16: 67-9. PMID 16406617 DOI: 10.1016/J.Tcb.2005.12.006 |
0.404 |
|
| 2005 |
Lüdtke A, Heck K, Genschel J, Mehnert H, Spuler S, Worman HJ, Schmidt HH. Long-term treatment experience in a subject with Dunnigan-type familial partial lipodystrophy: efficacy of rosiglitazone. Diabetic Medicine : a Journal of the British Diabetic Association. 22: 1611-3. PMID 16241930 DOI: 10.1111/J.1464-5491.2005.01757.X |
0.303 |
|
| 2005 |
Worman HJ. Inner nuclear membrane and signal transduction. Journal of Cellular Biochemistry. 96: 1185-92. PMID 16211582 DOI: 10.1002/Jcb.20650 |
0.407 |
|
| 2005 |
Worman HJ, Courvalin JC. Nuclear envelope, nuclear lamina, and inherited disease. International Review of Cytology. 246: 231-79. PMID 16164970 DOI: 10.1016/S0074-7696(05)46006-4 |
0.479 |
|
| 2005 |
Paradisi M, McClintock D, Boguslavsky RL, Pedicelli C, Worman HJ, Djabali K. Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress. Bmc Cell Biology. 6: 27. PMID 15982412 DOI: 10.1186/1471-2121-6-27 |
0.427 |
|
| 2005 |
Worman HJ. Components of the nuclear envelope and their role in human disease. Novartis Foundation Symposium. 264: 35-42; discussion 42. PMID 15773746 DOI: 10.1002/0470093765.Ch4 |
0.461 |
|
| 2005 |
Broers JL, Kuijpers HJ, Ostlund C, Worman HJ, Endert J, Ramaekers FC. Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization. Experimental Cell Research. 304: 582-92. PMID 15748902 DOI: 10.1016/J.Yexcr.2004.11.020 |
0.416 |
|
| 2005 |
Ostlund C, Garcia-Carrasquillo RM, Belayew A, Worman HJ. Intracellular trafficking and dynamics of double homeodomain proteins. Biochemistry. 44: 2378-84. PMID 15709750 DOI: 10.1021/Bi047992W |
0.342 |
|
| 2005 |
Lin F, Morrison JM, Wu W, Worman HJ. MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-beta signaling. Human Molecular Genetics. 14: 437-45. PMID 15601644 DOI: 10.1093/Hmg/Ddi040 |
0.379 |
|
| 2004 |
Ostlund C, Worman HJ. Lamin-associated proteins. Methods in Cell Biology. 78: 829-59. PMID 15646641 DOI: 10.1016/S0091-679X(04)78029-2 |
0.386 |
|
| 2004 |
Gilchrist S, Gilbert N, Perry P, Ostlund C, Worman HJ, Bickmore WA. Altered protein dynamics of disease-associated lamin A mutants. Bmc Cell Biology. 5: 46. PMID 15596010 DOI: 10.1186/1471-2121-5-46 |
0.42 |
|
| 2004 |
Hutchison CJ, Worman HJ. A-type lamins: guardians of the soma? Nature Cell Biology. 6: 1062-7. PMID 15517000 DOI: 10.1038/Ncb1104-1062 |
0.36 |
|
| 2004 |
Muchir A, Worman HJ. The nuclear envelope and human disease. Physiology (Bethesda, Md.). 19: 309-14. PMID 15381760 DOI: 10.1152/Physiol.00022.2004 |
0.706 |
|
| 2004 |
Muchir A, Medioni J, Laluc M, Massart C, Arimura T, van der Kooi AJ, Desguerre I, Mayer M, Ferrer X, Briault S, Hirano M, Worman HJ, Mallet A, Wehnert M, Schwartz K, et al. Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations. Muscle & Nerve. 30: 444-50. PMID 15372542 DOI: 10.1002/Mus.20122 |
0.702 |
|
| 2004 |
Worman HJ, Courvalin JC. How do mutations in lamins A and C cause disease? The Journal of Clinical Investigation. 113: 349-51. PMID 14755330 DOI: 10.1172/Jci20832 |
0.467 |
|
| 2003 |
Sharma GG, Hwang KK, Pandita RK, Gupta A, Dhar S, Parenteau J, Agarwal M, Worman HJ, Wellinger RJ, Pandita TK. Human heterochromatin protein 1 isoforms HP1(Hsalpha) and HP1(Hsbeta) interfere with hTERT-telomere interactions and correlate with changes in cell growth and response to ionizing radiation. Molecular and Cellular Biology. 23: 8363-76. PMID 14585993 DOI: 10.1128/Mcb.23.22.8363-8376.2003 |
0.325 |
|
| 2003 |
Worman HJ, Courvalin JC. Antinuclear antibodies specific for primary biliary cirrhosis. Autoimmunity Reviews. 2: 211-7. PMID 12848948 DOI: 10.1016/S1568-9972(03)00013-2 |
0.314 |
|
| 2003 |
Holt I, Ostlund C, Stewart CL, Man Nt, Worman HJ, Morris GE. Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo. Journal of Cell Science. 116: 3027-35. PMID 12783988 DOI: 10.1242/Jcs.00599 |
0.43 |
|
| 2003 |
Stierlé V, Couprie J, Ostlund C, Krimm I, Zinn-Justin S, Hossenlopp P, Worman HJ, Courvalin JC, Duband-Goulet I. The carboxyl-terminal region common to lamins A and C contains a DNA binding domain. Biochemistry. 42: 4819-28. PMID 12718522 DOI: 10.1021/Bi020704G |
0.321 |
|
| 2003 |
Ostlund C, Worman HJ. Nuclear envelope proteins and neuromuscular diseases. Muscle & Nerve. 27: 393-406. PMID 12661041 DOI: 10.1002/Mus.10302 |
0.453 |
|
| 2003 |
Favreau C, Dubosclard E, Ostlund C, Vigouroux C, Capeau J, Wehnert M, Higuet D, Worman HJ, Courvalin JC, Buendia B. 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. Experimental Cell Research. 282: 14-23. PMID 12490190 DOI: 10.1006/excr.2002.5669 |
0.322 |
|
| 2002 |
Worman HJ, Courvalin JC. The nuclear lamina and inherited disease. Trends in Cell Biology. 12: 591-8. PMID 12495848 DOI: 10.1016/S0962-8924(02)02401-7 |
0.444 |
|
| 2002 |
Krimm I, Ostlund C, Gilquin B, Couprie J, Hossenlopp P, Mornon JP, Bonne G, Courvalin JC, Worman HJ, Zinn-Justin S. The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy. Structure (London, England : 1993). 10: 811-23. PMID 12057196 DOI: 10.1016/S0969-2126(02)00777-3 |
0.415 |
|
| 2002 |
Hwang KK, Worman HJ. Gene regulation by human orthologs of Drosophila heterochromatin protein 1. Biochemical and Biophysical Research Communications. 293: 1217-22. PMID 12054505 DOI: 10.1016/S0006-291X(02)00377-7 |
0.347 |
|
| 2001 |
Holmer L, Worman HJ. Inner nuclear membrane proteins: functions and targeting. Cellular and Molecular Life Sciences : Cmls. 58: 1741-7. PMID 11766875 DOI: 10.1007/Pl00000813 |
0.369 |
|
| 2001 |
Hwang KK, Eissenberg JC, Worman HJ. Transcriptional repression of euchromatic genes by Drosophila heterochromatin protein 1 and histone modifiers. Proceedings of the National Academy of Sciences of the United States of America. 98: 11423-7. PMID 11562500 DOI: 10.1073/Pnas.211303598 |
0.366 |
|
| 2001 |
Wolff N, Gilquin B, Courchay K, Callebaut I, Worman HJ, Zinn-Justin S. Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy Febs Letters. 501: 171-176. PMID 11470279 DOI: 10.1016/S0014-5793(01)02649-7 |
0.45 |
|
| 2001 |
Laguri C, Gilquin B, Wolff N, Romi-Lebrun R, Courchay K, Callebaut I, Worman HJ, Zinn-Justin S. Structural characterization of the LEM motif common to three human inner nuclear membrane proteins Structure. 9: 503-511. PMID 11435115 DOI: 10.1016/S0969-2126(01)00611-6 |
0.345 |
|
| 2001 |
Ma J, Hwang KK, Worman HJ, Courvalin JC, Eissenberg JC. Expression and functional analysis of three isoforms of human heterochromatin-associated protein HP1 in Drosophila. Chromosoma. 109: 536-44. PMID 11305786 DOI: 10.1007/S004120000113 |
0.339 |
|
| 2001 |
Wilson KL, Benavente R, Burke B, Craigie R, Foisner R, Furukawa K, Gerace L, Goldman RD, Gruenbaum Y, Harris C, Hutchison CJ, Krohne G, Morris GE, Otto H, Simon AJ, ... Worman HJ, et al. Problems with LAP nomenclature. Nature Cell Biology. 3: E90. PMID 11283624 DOI: 10.1038/35070147 |
0.494 |
|
| 2000 |
Terjung B, Spengler U, Sauerbruch T, Worman HJ. 'Atypical p-ANCA' in IBD and hepatobiliary disorders react with a 50-kilodalton nuclear envelope protein of neutrophils and myeloid cell lines Gastroenterology. 119: 310-322. PMID 10930366 DOI: 10.1053/Gast.2000.9366 |
0.341 |
|
| 2000 |
Lin F, Blake DL, Callebaut I, Skerjanc IS, Holmer L, McBurney MW, Paulin-Levasseur M, Worman HJ. MAN1, an inner nuclear membrane protein that shares the LEM domain with lamina-associated polypeptide 2 and emerin Journal of Biological Chemistry. 275: 4840-4847. PMID 10671519 DOI: 10.1074/Jbc.275.7.4840 |
0.373 |
|
| 1999 |
Barton RM, Worman HJ. Prenylated prelamin A interacts with Narf, a novel nuclear protein Journal of Biological Chemistry. 274: 30008-30018. PMID 10514485 DOI: 10.1074/Jbc.274.42.30008 |
0.371 |
|
| 1999 |
Minc E, Allory Y, Worman HJ, Courvalin JC, Buendia B. Localization and phosphorylation of HP1 proteins during the cell cycle in mammalian cells Chromosoma. 108: 220-234. PMID 10460410 DOI: 10.1007/S004120050372 |
0.345 |
|
| 1998 |
Ye Q, Barton RM, Worman HJ. Nuclear lamin-binding proteins. Sub-Cellular Biochemistry. 31: 587-610. PMID 9932507 |
0.418 |
|
| 1998 |
Holmer L, Pezhman A, Worman HJ. The human lamin B receptor/sterol reductase multigene family Genomics. 54: 469-476. PMID 9878250 DOI: 10.1006/Geno.1998.5615 |
0.367 |
|
| 1997 |
Lin F, Worman HJ. Expression of nuclear lamins in human tissues and cancer cell lines and transcription from the promoters of the lamin A/C and B1 genes Experimental Cell Research. 236: 378-384. PMID 9367621 DOI: 10.1006/Excr.1997.3735 |
0.335 |
|
| 1997 |
Ellenberg J, Siggia ED, Moreira JE, Smith CL, Presley JF, Worman HJ, Lippincott-Schwartz J. Nuclear membrane dynamics and reassembly in living cells: Targeting of an inner nuclear membrane protein in interphase and mitosis Journal of Cell Biology. 138: 1193-1206. PMID 9298976 DOI: 10.1083/Jcb.138.6.1193 |
0.307 |
|
| 1997 |
Worman HJ. Molecular biological methods in diagnosis and treatment of liver diseases Clinical Chemistry. 43: 1476-1486. PMID 9265898 DOI: 10.1093/Clinchem/43.8.1476 |
0.316 |
|
| 1997 |
Ye Q, Callebaut I, Pezhman A, Courvalin JC, Worman HJ. Domain-specific interactions of human HP1-type chromodomain proteins and inner nuclear membrane protein LBR. The Journal of Biological Chemistry. 272: 14983-9. PMID 9169472 DOI: 10.1074/Jbc.272.23.14983 |
0.499 |
|
| 1997 |
Courvalin JC, Worman HJ. Nuclear envelope protein autoantibodies in primary biliary cirrhosis Seminars in Liver Disease. 17: 79-90. PMID 9089913 DOI: 10.1055/S-2007-1007185 |
0.365 |
|
| 1996 |
Favreau C, Worman HJ, Wozniak RW, Frappier T, Courvalin JC. Cell cycle-dependent phosphorylation of nucleoporins and nuclear pore membrane protein Gp210 Biochemistry. 35: 8035-8044. PMID 8672508 DOI: 10.1021/Bi9600660 |
0.363 |
|
| 1996 |
Ye Q, Worman HJ. Interaction between an integral protein of the nuclear envelope inner membrane and human chromodomain proteins homologous to Drosophila HP1. The Journal of Biological Chemistry. 271: 14653-6. PMID 8663349 DOI: 10.1074/Jbc.271.25.14653 |
0.523 |
|
| 1996 |
Lin F, Noyer CM, Ye Q, Courvalin JC, Worman HJ. Autoantibodies from patients with primary biliary cirrhosis recognize a region within the nucleoplasmic domain of inner nuclear membrane protein LBR. Hepatology (Baltimore, Md.). 23: 57-61. PMID 8550049 DOI: 10.1002/Hep.510230109 |
0.484 |
|
| 1995 |
Soullam B, Worman HJ. Signals and structural features involved in integral membrane protein targeting to the inner nuclear membrane Journal of Cell Biology. 130: 15-27. PMID 7790369 DOI: 10.1083/Jcb.130.1.15 |
0.356 |
|
| 1995 |
Ye Q, Worman HJ. Protein-protein interactions between human nuclear lamins expressed in yeast. Experimental Cell Research. 219: 292-8. PMID 7628545 DOI: 10.1006/Excr.1995.1230 |
0.524 |
|
| 1995 |
Lin F, Worman HJ. Structural organization of the human gene (LMNB1) encoding nuclear lamin B1 Genomics. 27: 230-236. PMID 7557986 DOI: 10.1006/Geno.1995.1036 |
0.368 |
|
| 1994 |
Ye Q, Worman HJ. Primary structure analysis and lamin B and DNA binding of human LBR, an integral protein of the nuclear envelope inner membrane. The Journal of Biological Chemistry. 269: 11306-11. PMID 8157662 |
0.433 |
|
| 1992 |
Courvalin JC, Segil N, Blobel G, Worman HJ. The lamin B receptor of the inner nuclear membrane undergoes mitosis-specific phosphorylation and is a substrate for p34cdc2-type protein kinase. The Journal of Biological Chemistry. 267: 19035-8. PMID 1326541 |
0.473 |
|
| 1990 |
Worman HJ, Evans CD, Blobel G. The lamin B receptor of the nuclear envelope inner membrane: a polytopic protein with eight potential transmembrane domains. The Journal of Cell Biology. 111: 1535-42. PMID 2170422 |
0.469 |
|
| 1990 |
Courvalin JC, Lassoued K, Worman HJ, Blobel G. Identification and characterization of autoantibodies against the nuclear envelope lamin B receptor from patients with primary biliary cirrhosis. The Journal of Experimental Medicine. 172: 961-7. PMID 2167346 DOI: 10.1084/Jem.172.3.961 |
0.448 |
|
| 1988 |
Worman HJ, Yuan J, Blobel G, Georgatos SD. A lamin B receptor in the nuclear envelope. Proceedings of the National Academy of Sciences of the United States of America. 85: 8531-4. PMID 2847165 DOI: 10.1073/Pnas.85.22.8531 |
0.436 |
|
| Show low-probability matches. |
