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Stem Cell Research
|
December 19, 2024
Generation of a human induced pluripotent stem cell lines (UKJi003-A) from a patient with Fabry disease and healthy donor (UKJi004-A)
Mohamed M Bekhite, Sascha Hübner, Tom Kretzschmar, et al.
Current Genomics
|
April 3, 2018
Molecular Cytogenetic Analysis of One African and Five Asian Macaque Species Reveals Identical Karyotypes as in Mandrill
Wiwat Sangpakdee, Alongkoad Tanomtong, Arunrat Chaveerach, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 21, 2014
BAC-probes applied for characterization of fragile sites (FS)
Kristin Mrasek, Kathleen Wilhelm, Luciana G Quintana, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
March 8, 2012
Microdeletion and microduplication syndromes
Anja Weise, Kristin Mrasek, Elisabeth Klein, et al.
International Journal of Oncology
|
March 4, 2010
Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones
Kristin Mrasek, Christiane Schoder, Anne-Christin Teichmann, et al.
Journal of Cancer Research and Clinical Oncology
|
September 25, 2013
Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases
Nadine Aust, Silke Schüle, Annelore K Altendorf-Hofmann, et al.
International Journal of Oncology
|
June 6, 2007
Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R
Julia Rosenhahn, Anja Weise, Susanne Michel, et al.
Cell Cycle (Georgetown, Tex.)
|
September 4, 2016
S100A11 plays a role in homologous recombination and genome maintenance by influencing the persistence of RAD51 in DNA repair foci
Franziska Foertsch, Anna Szambowska, Anja Weise, et al.
Molecular Cytogenetics
|
January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
Sofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics
|
November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report
Emmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
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Search research articles
Search
Showing results (61-70 of 121) with videos related to
Sort By:
Page
of 13
Stem Cell Research
|
December 19, 2024
Generation of a human induced pluripotent stem cell lines (UKJi003-A) from a patient with Fabry disease and healthy donor (UKJi004-A)
Mohamed M Bekhite, Sascha Hübner, Tom Kretzschmar, et al.
Current Genomics
|
April 3, 2018
Molecular Cytogenetic Analysis of One African and Five Asian Macaque Species Reveals Identical Karyotypes as in Mandrill
Wiwat Sangpakdee, Alongkoad Tanomtong, Arunrat Chaveerach, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
September 21, 2014
BAC-probes applied for characterization of fragile sites (FS)
Kristin Mrasek, Kathleen Wilhelm, Luciana G Quintana, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
March 8, 2012
Microdeletion and microduplication syndromes
Anja Weise, Kristin Mrasek, Elisabeth Klein, et al.
International Journal of Oncology
|
March 4, 2010
Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones
Kristin Mrasek, Christiane Schoder, Anne-Christin Teichmann, et al.
Journal of Cancer Research and Clinical Oncology
|
September 25, 2013
Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases
Nadine Aust, Silke Schüle, Annelore K Altendorf-Hofmann, et al.
International Journal of Oncology
|
June 6, 2007
Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R
Julia Rosenhahn, Anja Weise, Susanne Michel, et al.
Cell Cycle (Georgetown, Tex.)
|
September 4, 2016
S100A11 plays a role in homologous recombination and genome maintenance by influencing the persistence of RAD51 in DNA repair foci
Franziska Foertsch, Anna Szambowska, Anja Weise, et al.
Molecular Cytogenetics
|
January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
Sofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics
|
November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report
Emmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
Page
of 13