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Inka Praulich

Showing results (1-10 of 10) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
Array-CGH in childhood MDSMarcel Tauscher, Inka Praulich, Doris Steinemann
European Journal of Haematology|March 31, 2012
Patient-specific analysis of FLT3 internal tandem duplications for the prognostication and monitoring of acute myeloid leukemiaJoanna Schiller, Inka Praulich, Cristiano Krings Rocha, et al.
Molecular Cytogenetics|April 5, 2011
A rare case of t(11;22) in a mantle cell lymphoma like B-cell neoplasia resulting in a fusion of IGL and CCND1: case reportCristiano Krings Rocha, Inka Praulich, Iris Gehrke, et al.
British Journal of Haematology|March 21, 2009
Mutation analysis of the HAX1 gene in childhood myelodysplastic syndromeDoris Steinemann, Inka Praulich, Noreen Otto, et al.
Haematologica|May 13, 2010
Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?Doris Steinemann, Marcel Tauscher, Inka Praulich, et al.
Haematologica|December 18, 2009
Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1Doris Steinemann, Larissa Arning, Inka Praulich, et al.
Genes, Chromosomes & Cancer|July 1, 2010
Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGHInka Praulich, Marcel Tauscher, Gudrun Göhring, et al.
British Journal of Haematology|August 19, 2011
Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemiaTim Ripperger, Marcel Tauscher, Inka Praulich, et al.
Molecular Cytogenetics|July 30, 2014
Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patientTereza Jancuskova, Radek Plachy, Lucie Zemankova, et al.
Clinical Genetics|February 26, 2022
Phenotypic spectrum of BLM- and RMI1-related Bloom syndromeIpek Ilgin Gönenc, Nursel H Elcioglu, Carolina Martinez Grijalva, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
Array-CGH in childhood MDSMarcel Tauscher, Inka Praulich, Doris Steinemann
European Journal of Haematology|March 31, 2012
Patient-specific analysis of FLT3 internal tandem duplications for the prognostication and monitoring of acute myeloid leukemiaJoanna Schiller, Inka Praulich, Cristiano Krings Rocha, et al.
Molecular Cytogenetics|April 5, 2011
A rare case of t(11;22) in a mantle cell lymphoma like B-cell neoplasia resulting in a fusion of IGL and CCND1: case reportCristiano Krings Rocha, Inka Praulich, Iris Gehrke, et al.
British Journal of Haematology|March 21, 2009
Mutation analysis of the HAX1 gene in childhood myelodysplastic syndromeDoris Steinemann, Inka Praulich, Noreen Otto, et al.
Haematologica|May 13, 2010
Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?Doris Steinemann, Marcel Tauscher, Inka Praulich, et al.
Haematologica|December 18, 2009
Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1Doris Steinemann, Larissa Arning, Inka Praulich, et al.
Genes, Chromosomes & Cancer|July 1, 2010
Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGHInka Praulich, Marcel Tauscher, Gudrun Göhring, et al.
British Journal of Haematology|August 19, 2011
Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemiaTim Ripperger, Marcel Tauscher, Inka Praulich, et al.
Molecular Cytogenetics|July 30, 2014
Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patientTereza Jancuskova, Radek Plachy, Lucie Zemankova, et al.
Clinical Genetics|February 26, 2022
Phenotypic spectrum of BLM- and RMI1-related Bloom syndromeIpek Ilgin Gönenc, Nursel H Elcioglu, Carolina Martinez Grijalva, et al.
Pageof 1