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  1. 1
    J. Woodman, T. Fara, M. Dzieciatkowska, M. Trejo, N. Luong, K. C. Hansen, P. C. Megee, Cell cycle-specific cleavage of Scc2 regulates its cohesin deposition activity, Proceedings of the National Academy of Sciences, 2014, 111, 19, 7060

    CrossRef

  2. 2
    Dale Dorsett, Judith A. Kassis, Checks and Balances between Cohesin and Polycomb in Gene Silencing and Transcription, Current Biology, 2014, 24, 11, R535

    CrossRef

  3. 3
    Ana Losada, Cohesin in cancer: chromosome segregation and beyond, Nature Reviews Cancer, 2014, 14, 6, 389

    CrossRef

  4. 4
    Christophe Decroos, Christine M. Bowman, Joe-Ann S. Moser, Karen E. Christianson, Matthew A. Deardorff, David W. Christianson, Compromised Structure and Function of HDAC8 Mutants Identified in Cornelia de Lange Syndrome Spectrum Disorders, ACS Chemical Biology, 2014, 9, 9, 2157

    CrossRef

  5. 5
    C. Baquero-Montoya, M.C. Gil-Rodríguez, M.E. Teresa-Rodrigo, M. Hernández-Marcos, G. Bueno-Lozano, I. Bueno-Martínez, S. Remeseiro, R. Fernández-Hernández, M. Bassecourt-Serra, M. Rodríguez de Alba, E. Queralt, A. Losada, B. Puisac, F.J. Ramos, J. Pié, Could a patient with SMC1A duplication be classified as a human cohesinopathy?, Clinical Genetics, 2014, 85, 5
  6. 6
    Elena Pavlidis, Gaetano Cantalupo, Sara Bianchi, Benedetta Piccolo, Francesco Pisani, Epileptic features in Cornelia de Lange syndrome: Case report and literature review, Brain and Development, 2014, 36, 10, 837

    CrossRef

  7. 7
    Alexander R. Ball, Yen-Yun Chen, Kyoko Yokomori, Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies, Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms, 2014, 1839, 3, 191

    CrossRef

  8. 8
    Baoshan Xu, Shuai Lu, Jennifer L Gerton, Roberts syndrome, Rare Diseases, 2014, 2, 1, e27743

    CrossRef

  9. 9
    Carolina Baquero-Montoya, María-Concepción Gil-Rodríguez, María Hernández-Marcos, María-Esperanza Teresa-Rodrigo, Alicia Vicente-Gabas, María-Luisa Bernal, Cesar-Horacio Casale, Gloria Bueno-Lozano, Inés Bueno-Martínez, Ethel Queralt, Olaya Villa, Cristina Hernando-Davalillo, Lluís Armengol, Paulino Gómez-Puertas, Beatriz Puisac, Angelo Selicorni, Feliciano J. Ramos, Juan Pié, Severe ipsilateral musculoskeletal involvement in a Cornelia de Lange patient with a novel NIPBL mutation, European Journal of Medical Genetics, 2014, 57, 9, 503

    CrossRef

  10. 10
    Libin Mei, Desheng Liang, Yanru Huang, Qian Pan, Lingqian Wu, Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndrome, Gene, 2014,

    CrossRef

  11. 11
    Francesca Telese, Amir Gamliel, Dorota Skowronska-Krawczyk, Ivan Garcia-Bassets, Michael G. Rosenfeld, “Seq-ing” Insights into the Epigenetics of Neuronal Gene Regulation, Neuron, 2013, 77, 4, 606

    CrossRef

  12. 12
    Katarzyna Kuleszewicz, Xiangwei Fu, Nobuaki R Kudo, Cohesin loading factor Nipbl localizes to chromosome axes during mammalian meiotic prophase, Cell Division, 2013, 8, 1, 12

    CrossRef

  13. 13
    Gunjan D. Mehta, Ravinder Kumar, Sanjeeva Srivastava, Santanu Kumar Ghosh, Cohesin: Functions beyond sister chromatid cohesion, FEBS Letters, 2013, 587, 15, 2299

    CrossRef

  14. 14
    Maha M. Eid, Samia A. Temtamy, Cytogenetic studies of chromosomal breakage diseases, Middle East Journal of Medical Genetics, 2013, 2, 1, 11

    CrossRef

  15. 15
    Alberto Verrotti, Sergio Agostinelli, Giovanni Prezioso, Giangennaro Coppola, Giuseppe Capovilla, Antonino Romeo, Pasquale Striano, Pasquale Parisi, Salvatore Grosso, Alberto Spalice, Thomas Foiadelli, Paolo Curatolo, Francesco Chiarelli, Salvatore Savasta, Epilepsy in patients with Cornelia de Lange syndrome: A clinical series, Seizure, 2013, 22, 5, 356

    CrossRef

  16. 16
    Cristina Gervasini, Chiara Picinelli, Jacopo Azzollini, Daniela Rusconi, Maura Masciadri, Anna Cereda, Cinzia Marzocchi, Giuseppe Zampino, Angelo Selicorni, Romano Tenconi, Silvia Russo, Lidia Larizza, Palma Finelli, Genomic imbalances in patients with a clinical presentation in the spectrum of Cornelia de Lange syndrome, BMC Medical Genetics, 2013, 14, 1, 41

    CrossRef

  17. 17
    Cristina Gervasini, Ilaria Parenti, Chiara Picinelli, Jacopo Azzollini, Maura Masciadri, Anna Cereda, Angelo Selicorni, Silvia Russo, Palma Finelli, Lidia Larizza, Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotype, European Journal of Medical Genetics, 2013, 56, 3, 138

    CrossRef

  18. 18
    Linda Mannini, Francesco Cucco, Valentina Quarantotti, Ian D. Krantz, Antonio Musio, Mutation Spectrum and Genotype–Phenotype Correlation in Cornelia de Lange Syndrome, Human Mutation, 2013, 34, 12
  19. 19
    María Carretero, Miguel Ruiz-Torres, Miriam Rodríguez-Corsino, Isabel Barthelemy, Ana Losada, Pds5B is required for cohesion establishment and Aurora B accumulation at centromeres, The EMBO Journal, 2013, 32, 22
  20. 20
    A.M.W. Coppus, People with intellectual disability: What do we know about adulthood and life expectancy?, Developmental Disabilities Research Reviews, 2013, 18, 1
  21. 21
    Silvia Remeseiro, Ana Cuadrado, Shimako Kawauchi, Anne L. Calof, Arthur D. Lander, Ana Losada, Reduction of Nipbl impairs cohesin loading locally and affects transcription but not cohesion-dependent functions in a mouse model of Cornelia de Lange Syndrome, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2013, 1832, 12, 2097

    CrossRef

  22. 22
    Babu V Sajesh, Zelda Lichtensztejn, Kirk J McManus, Sister chromatid cohesion defects are associated with chromosome instability in Hodgkin lymphoma cells, BMC Cancer, 2013, 13, 1, 391

    CrossRef

  23. 23
    Miri Zinder-Cohen, David Karasik, Itay Onn, Structural maintenance of chromosome complexes and bone development: the beginning of a wonderful relationship?, BoneKEy Reports, 2013, 2,

    CrossRef

  24. 24
    Zhen Shen, The origin recognition complex in human diseases, Bioscience Reports, 2013, 33, 3, 475

    CrossRef

  25. 25
    Chiara Barboni, Anna Cereda, Milena Mariani, Cristina Gervasini, Paola Ajmone, Andrea Biondi, Angelo Selicorni, A new report of Cornelia de Lange syndrome associated with split hand and feet, American Journal of Medical Genetics Part A, 2012, 158A, 11
  26. 26
    Silvia Remeseiro, Ana Cuadrado, Gonzalo Gómez-López, David G Pisano, Ana Losada, A unique role of cohesin-SA1 in gene regulation and development, The EMBO Journal, 2012, 31, 9
  27. 27
    A. M. Muehlmann, M. H. Lewis, Abnormal repetitive behaviours: shared phenomenology and pathophysiology, Journal of Intellectual Disability Research, 2012, 56, 5
  28. 28
    Zhe Zhang, Jinglan Liu, Maninder Kaur, Ian D. Krantz, Characterization of DNA methylation and its association with other biological systems in lymphoblastoid cell lines, Genomics, 2012, 99, 4, 209

    CrossRef

  29. 29
    Silvia Remeseiro, Ana Cuadrado, María Carretero, Paula Martínez, William C Drosopoulos, Marta Cañamero, Carl L Schildkraut, María A Blasco, Ana Losada, Cohesin-SA1 deficiency drives aneuploidy and tumourigenesis in mice due to impaired replication of telomeres, The EMBO Journal, 2012, 31, 9
  30. 30
    Jolanta Wierzba, María Gil-Rodríguez, Anna Polucha, Beatriz Puisac, María Arnedo, María Teresa-Rodrigo, Dorota Winnicka, Fausto G Hegardt, Feliciano J Ramos, Janusz Limon, Juan Pié, Cornelia de Lange syndrome with NIPBL mutation and mosaic Turner syndrome in the same individual, BMC Medical Genetics, 2012, 13, 1, 43

    CrossRef

  31. You have free access to this content31
    Akihiro Morita, Kumiko Nakahira, Taeko Hasegawa, Kaoru Uchida, Yoshihito Taniguchi, Shunichi Takeda, Atsushi Toyoda, Yoshiyuki Sakaki, Atsuko Shimada, Hiroyuki Takeda, Itaru Yanagihara, Establishment and characterization of Roberts syndrome and SC phocomelia model medaka (Oryzias latipes), Development, Growth & Differentiation, 2012, 54, 5
  32. 32
    Laura J. Paul, Philip R. Cohen, Razelle Kurzrock, Eyelash trichomegaly: review of congenital, acquired, and drug-associated etiologies for elongation of the eyelashes, International Journal of Dermatology, 2012, 51, 6
  33. 33
    Roy Rajan, James R. Benke, Antonie D. Kline, Howard P. Levy, Amy Kimball, Tiffany L. Mettel, Emily F. Boss, Stacey L. Ishman, Insomnia in Cornelia de Lange Syndrome, International Journal of Pediatric Otorhinolaryngology, 2012, 76, 7, 972

    CrossRef

  34. 34
    Adam R. Leman, Eishi Noguchi, Local and global functions of Timeless and Tipin in replication fork protection, Cell Cycle, 2012, 11, 21, 3945

    CrossRef

  35. 35
    Qiulian Zhong, Desheng Liang, Jing Liu, Jinjie Xue, Lingqian Wu, Mutation Analysis in Chinese Patients with Cornelia de Lange Syndrome, Genetic Testing and Molecular Biomarkers, 2012, 16, 9, 1130

    CrossRef

  36. 36
    Dale Dorsett, Lena Ström, The Ancient and Evolving Roles of Cohesin in Gene Expression and DNA Repair, Current Biology, 2012, 22, 7, R240

    CrossRef

  37. 37
    Ana Cuadrado, Silvia Remeseiro, Gonzalo Gómez-López, David G. Pisano, Ana Losada, The specific contributions of cohesin-SA1 to cohesion and gene expression, Cell Cycle, 2012, 11, 12, 2233

    CrossRef

  38. 38
    V. Kanellopoulos, C. Iavazzo, C. Tzanatou, E. Papadakis, K. Tassis, A case of third trimester diagnosis of Cornelia de Lange syndrome, Archives of Gynecology and Obstetrics, 2011, 283, 1, 59

    CrossRef

  39. 39
    M Al-Owain, AM Alazami, FS Alkuraya, An autosomal recessive syndrome of severe cognitive impairment, dysmorphic facies and skeletal abnormalities maps to the long arm of chromosome 17, Clinical Genetics, 2011, 80, 5
  40. 40
    Rose C. Stavinoha, Antonie D. Kline, Howard P. Levy, Amy Kimball, Tiffany L. Mettel, Stacey L. Ishman, Characterization of sleep disturbance in Cornelia de Lange Syndrome, International Journal of Pediatric Otorhinolaryngology, 2011, 75, 2, 215

    CrossRef

  41. 41
    Richard Chien, Weihua Zeng, Alexander R. Ball, Kyoko Yokomori, Cohesin: a critical chromatin organizer in mammalian gene regulation, Biochemistry and Cell Biology, 2011, 89, 5, 445

    CrossRef

  42. 42
    Jeremy Turk, Jill Hoddell, Jo Moss, Kate Woodcock, Chris Oliver, Further refinement of the nature of the communication impairment in Cornelia de Lange syndrome, Advances in Mental Health and Intellectual Disabilities, 2011, 5, 4, 15

    CrossRef

  43. 43
    Thomas P. Slavin, Kevin Kuruvilla, Christine A. Curtis, Laurie A. Christ, Anna L. Mitchell, Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: Genotype–phenotype correlations, American Journal of Medical Genetics Part A, 2011, 155, 3
  44. 44
    Louise S Bicknell, Ernie M H F Bongers, Andrea Leitch, Stephen Brown, Jeroen Schoots, Margaret E Harley, Salim Aftimos, Jumana Y Al-Aama, Michael Bober, Paul A J Brown, Hans van Bokhoven, John Dean, Alaa Y Edrees, Murray Feingold, Alan Fryer, Lies H Hoefsloot, Nikolaus Kau, Nine V A M Knoers, James MacKenzie, John M Opitz, Pierre Sarda, Alison Ross, I Karen Temple, Annick Toutain, Carol A Wise, Michael Wright, Andrew P Jackson, Mutations in the pre-replication complex cause Meier-Gorlin syndrome, Nature Genetics, 2011, 43, 4, 356

    CrossRef

  45. 45
    Matthew G Guenther, Transcriptional control of embryonic and induced pluripotent stem cells, Epigenomics, 2011, 3, 3, 323

    CrossRef

  46. 46
    Andrew J. Wood, Aaron F. Severson, Barbara J. Meyer, Condensin and cohesin complexity: the expanding repertoire of functions, Nature Reviews Genetics, 2010, 11, 6, 391

    CrossRef

  47. 47
    V Denes, M Pilichowska, A Makarovskiy, G Carpinito, P Geck, Loss of a cohesin-linked suppressor APRIN (Pds5b) disrupts stem cell programs in embryonal carcinoma: an emerging cohesin role in tumor suppression, Oncogene, 2010, 29, 23, 3446

    CrossRef

  48. 48
    P Castronovo, A Delahaye-Duriez, C Gervasini, J Azzollini, F Minier, S Russo, M Masciadri, A Selicorni, A Verloes, L Larizza, Somatic mosaicism in Cornelia de Lange syndrome: a further contributor to the wide clinical expressivity?, Clinical Genetics, 2010, 78, 6
  49. 49
    Mauro Longoni, Meaghan K Russell, Barbara R Pober, Molecular Genetics of Congenital Diaphragmatic Hernia, eLS,