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  1. The combination of classical cytogenetics with molecular techniques represents a powerful approach for the comparative analysis of the genome, providing data for the systematic identification of chromosomal ho...

    Authors: Daniel Pacheco Bruschi, Miryan Rivera, Albertina Pimentel Lima, Ailín Blasco Zúñiga and Shirlei Maria Recco-Pimentel
    Citation: Molecular Cytogenetics 2014 7:22
  2. The chromosome preparation is a crucial step for obtaining satisfactory results in molecular cytogenetic researches. The preparation of plant chromosomes for molecular cytogenetic purposes remains a challenge ...

    Authors: Ilya Kirov, Mikhail Divashuk, Katrijn Van Laere, Alexander Soloviev and Ludmila Khrustaleva
    Citation: Molecular Cytogenetics 2014 7:21
  3. Although the link between brain aging and Alzheimer’s disease (AD) is a matter of debate, processes hallmarking cellular and tissue senescence have been repeatedly associated with its pathogenesis. Here, we ha...

    Authors: Yuri B Yurov, Svetlana G Vorsanova, Thomas Liehr, Alexei D Kolotii and Ivan Y Iourov
    Citation: Molecular Cytogenetics 2014 7:20
  4. Most previous studies of chromosomal mosaicism in IVF embryos were performed by fluorescence in situ hybridization (FISH) methods. While there are reports implicating chromosome aneuploidy in implantation failure...

    Authors: Veronica Novik, Emily B Moulton, Michael E Sisson, Shagun L Shrestha, Khoa D Tran, Harvey J Stern, Brian D Mariani and Wayne S Stanley
    Citation: Molecular Cytogenetics 2014 7:18
  5. Microdeletions of 14q22q23 have been associated with eye abnormalities and pituitary defects. Other phenotypic features in deletion carriers including hearing loss and response to growth hormone therapy are le...

    Authors: Sophie Brisset, Zuzana Slamova, Petra Dusatkova, Audrey Briand-Suleau, Karen Milcent, Corinne Metay, Martina Simandlova, Zdenek Sumnik, Lucie Tosca, Michel Goossens, Philippe Labrune, Elsa Zemankova, Jan Lebl, Gerard Tachdjian and Zdenek Sedlacek
    Citation: Molecular Cytogenetics 2014 7:17
  6. An ovotesticular disorder of sex development (OT-DSD) was rarely found in human. The mechanism causing such condition is poorly understood. We hereby reported a 11-year-old child with OT-DSD and a karyotype 46...

    Authors: Xin-Yi Xia, Wei-Ping Wang, Tian-Fu Li, Wei-Wei Li, Qiu-Yue Wu, Na Li, Cui Zhang, Hong-Liu Gao, Xiao-Jun Li and Ying-Xia Cui
    Citation: Molecular Cytogenetics 2014 7:16
  7. Chronic exposure of BTX (benzene, toluene, xylene) may lead to progressive degeneration of bone marrow, aplastic anemia and/or leukemia. In Brazil there is no self-service fuel in gas stations and attendants f...

    Authors: Fábio Santiago, Gilda Alves, Ubirani Barros Otero, Marianne Medeiros Tabalipa, Luciano Rios Scherrer, Nadezda Kosyakova, Maria Helena Ornellas and Thomas Liehr
    Citation: Molecular Cytogenetics 2014 7:15
  8. Whole arm t(9;13)(p11;p12) translocations are rare and have been described only a few times; all of the previously reported cases were familial.

    Authors: Ewa Wiland, Marta Olszewska, Andrew Georgiadis, Nataliya Huleyuk, Barbara Panasiuk, Danuta Zastavna, Svetlana A Yatsenko, Piotr Jedrzejczak, Alina T Midro, Alexander N Yatsenko and Maciej Kurpisz
    Citation: Molecular Cytogenetics 2014 7:14
  9. The Editors of Molecular Cytogenetics would like to thank all our reviewers who have contributed to the journal in volume 6 (2013).

    Authors: Thomas Liehr, Henry Heng and Yuri Yurov
    Citation: Molecular Cytogenetics 2014 7:11
  10. B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is characterized by recurrent genetic alterations including chromosomal translocations. The transcription factor PAX5, which is pivotal for B-cell commitmen...

    Authors: Dagmar Denk, Jutta Bradtke, Margit König and Sabine Strehl
    Citation: Molecular Cytogenetics 2014 7:13
  11. Meningiomas are mostly benign tumors which arise from the meninges. They are among the cytogenetically best-studied solid tumors, mostly displaying a normal karyotype or, as a typical primary aberration, monos...

    Authors: Cornelia Lerner, Ralf Ketter, Stefan Linsler, Wolfram Henn, Joachim Oertel and Steffi Urbschat
    Citation: Molecular Cytogenetics 2014 7:12
  12. Xq28 duplications, including MECP2 (methyl CpG-binding protein 2; OMIM 300005), have been identified in approximately 140 male patients presenting with hypotonia, severe developmental delay/intellectual disabilit...

    Authors: Francesca Novara, Alessandro Simonati, Federico Sicca, Roberta Battini, Simona Fiori, Annarita Contaldo, Lucia Criscuolo, Orsetta Zuffardi and Roberto Ciccone
    Citation: Molecular Cytogenetics 2014 7:10
  13. Polyploidy has been recognized for many years as an important hallmark of cancer cells. Polyploid cells can arise through cell fusion, endoreplication and abortive cell cycle. The inner nuclear membrane protein L...

    Authors: Shirley Oren Ben-Shoshan, Amos J Simon, Jasmine Jacob-Hirsch, Sigal Shaklai, Nurit Paz-Yaacov, Ninette Amariglio, Gideon Rechavi and Luba Trakhtenbrot
    Citation: Molecular Cytogenetics 2014 7:9
  14. The MCF7 (ER+/HER2-), T47D (ER+/HER2-), BT474 (ER+/HER2+) and SKBR3 (ER-/HER2+) breast cancer cell lines are widely used in breast cancer research as paradigms of the luminal and HER2 phenotypes. Although they...

    Authors: Milena Rondón-Lagos, Ludovica Verdun Di Cantogno, Caterina Marchiò, Nelson Rangel, Cesar Payan-Gomez, Patrizia Gugliotta, Cristina Botta, Gianni Bussolati, Sandra R Ramírez-Clavijo, Barbara Pasini and Anna Sapino
    Citation: Molecular Cytogenetics 2014 7:8
  15. Reported cases of “pure” duplication of the entire short arm of chromosome 16 (16p) are rare, with only 7 patients described in the literature. We report on a female infant with de novo 16p duplication localiz...

    Authors: Eva Maria Christina Schwaibold, Iris Bartels, Helmut Küster, Michael Lorenz, Peter Burfeind, Ronja Adam and Barbara Zoll
    Citation: Molecular Cytogenetics 2014 7:7

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