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Udo Koehler

Showing results (1-10 of 26) with videos related to

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European Journal of Pediatrics|February 4, 2012
Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literatureBeate Schmidt, Floris Udink ten Cate, Michael Weiss, et al.
Fetal Diagnosis and Therapy|October 16, 2009
Single cell analysis of mutations in the APC geneVeronika Mayer, Ulrike Schoen, Elke Holinski-Feder, et al.
Biomedical Microdevices|January 9, 2009
Single particle adsorbing transfer systemDaniela Woide, Veronika Mayer, Thorsten Wachtmeister, et al.
Neuropediatrics|March 14, 2013
Generalized epilepsy in two patients with 5p duplicationGerhard Kluger, Udo Koehler, Teresa M Neuhann, et al.
Cytoskeleton (Hoboken, N.J.)|July 19, 2018
Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family studyKatharina Neubauer, Doris Boeckelmann, Udo Koehler, et al.
Cells|October 23, 2021
A Novel Likely Pathogenic Variant in the <i>BLOC1S5</i> Gene Associated with Hermansky-Pudlak Syndrome Type 11 and an Overview of Human BLOC-1 DeficienciesDoris Boeckelmann, Mira Wolter, Barbara Käsmann-Kellner, et al.
Molecular Cytogenetics|February 6, 2016
CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genesEmanuele G Coci, Udo Koehler, Thomas Liehr, et al.
Clinical Case Reports|November 21, 2018
Extending the critical regions for mutations in the non-coding gene <i>RNU4ATAC</i> in another patient with Roifman SyndromeAriane Hallermayr, Janine Graf, Udo Koehler, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|November 15, 2012
CD133 induces tumour-initiating properties in HEK293 cellsMartin Canis, Axel Lechner, Brigitte Mack, et al.
Blood Cells, Molecules & Diseases|March 13, 2017
Novel mutation in two brothers with Hermansky Pudlak syndrome type 3Kirstin Sandrock-Lang, Ingrid Bartsch, Nina Buechele, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
European Journal of Pediatrics|February 4, 2012
Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literatureBeate Schmidt, Floris Udink ten Cate, Michael Weiss, et al.
Fetal Diagnosis and Therapy|October 16, 2009
Single cell analysis of mutations in the APC geneVeronika Mayer, Ulrike Schoen, Elke Holinski-Feder, et al.
Biomedical Microdevices|January 9, 2009
Single particle adsorbing transfer systemDaniela Woide, Veronika Mayer, Thorsten Wachtmeister, et al.
Neuropediatrics|March 14, 2013
Generalized epilepsy in two patients with 5p duplicationGerhard Kluger, Udo Koehler, Teresa M Neuhann, et al.
Cytoskeleton (Hoboken, N.J.)|July 19, 2018
Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family studyKatharina Neubauer, Doris Boeckelmann, Udo Koehler, et al.
Cells|October 23, 2021
A Novel Likely Pathogenic Variant in the <i>BLOC1S5</i> Gene Associated with Hermansky-Pudlak Syndrome Type 11 and an Overview of Human BLOC-1 DeficienciesDoris Boeckelmann, Mira Wolter, Barbara Käsmann-Kellner, et al.
Molecular Cytogenetics|February 6, 2016
CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genesEmanuele G Coci, Udo Koehler, Thomas Liehr, et al.
Clinical Case Reports|November 21, 2018
Extending the critical regions for mutations in the non-coding gene <i>RNU4ATAC</i> in another patient with Roifman SyndromeAriane Hallermayr, Janine Graf, Udo Koehler, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|November 15, 2012
CD133 induces tumour-initiating properties in HEK293 cellsMartin Canis, Axel Lechner, Brigitte Mack, et al.
Blood Cells, Molecules & Diseases|March 13, 2017
Novel mutation in two brothers with Hermansky Pudlak syndrome type 3Kirstin Sandrock-Lang, Ingrid Bartsch, Nina Buechele, et al.
Pageof 3