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Maja Dembic

Showing results (1-10 of 21) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|July 23, 2004
Multifluorescence labeling and colocalization analysesMassimo Riccio, Maja Dembic, Caterina Cinti, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|May 25, 2017
Pregnancy-associated plasma protein-A (PAPP-A) and the proform of the eosinophil major basic protein (ProMBP) are associated with increased risk of death in heart failure patientsMaja Dembic, Paula L Hedley, Christian Torp-Pedersen, et al.
Plos Genetics|April 24, 2018
Intronic PAH gene mutations cause a splicing defect by a novel mechanism involving U1snRNP binding downstream of the 5' splice siteAinhoa Martínez-Pizarro, Maja Dembic, Belén Pérez, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 20, 2020
Down-Regulation of CK2α Leads toUp-Regulation of the Cyclin-Dependent Kinase Inhibitor p27<sup>KIP1</sup> in Conditions Unfavorable for the Growth of Myoblast CellsBarbara Guerra, Maja Dembic, Mohammad A Siddiqui, et al.
Molecular Genetics and Genomics : MGG|December 1, 2022
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hipMaja Dembic, Lars van Brakel Andersen, Martin Jakob Larsen, et al.
Molecular Oncology|March 23, 2026
Somatic mutational landscape in von Hippel-Lindau familial hemangioblastomaMaja Dembic, Anne Nørremølle, Lilian Bomme Ousager, et al.
Molecular Genetics and Metabolism|September 6, 2016
The prevalent deep intronic c. 639+919 G>A GLA mutation causes pseudoexon activation and Fabry disease by abolishing the binding of hnRNPA1 and hnRNP A2/B1 to a splicing silencerBruno Palhais, Maja Dembic, Rugivan Sabaratnam, et al.
Pathology, Research and Practice|August 28, 2021
Synchronous detection of pancreatic adenocarcinoma and paraganglioma in a Whipple resection specimenTrine Aaquist, Maja Dembic, Mads Thomassen, et al.
Nucleic Acid Therapeutics|April 9, 2024
Splice-Switching Antisense Oligonucleotides Correct Phenylalanine Hydroxylase Exon 11 Skipping Defects and Rescue Enzyme Activity in PhenylketonuriaAinhoa Martínez-Pizarro, Mar Álvarez, Maja Dembic, et al.
Neurobiology of Disease|September 3, 2005
Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellumMassimo Riccio, Spartaco Santi, Maja Dembic, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|July 23, 2004
Multifluorescence labeling and colocalization analysesMassimo Riccio, Maja Dembic, Caterina Cinti, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|May 25, 2017
Pregnancy-associated plasma protein-A (PAPP-A) and the proform of the eosinophil major basic protein (ProMBP) are associated with increased risk of death in heart failure patientsMaja Dembic, Paula L Hedley, Christian Torp-Pedersen, et al.
Plos Genetics|April 24, 2018
Intronic PAH gene mutations cause a splicing defect by a novel mechanism involving U1snRNP binding downstream of the 5' splice siteAinhoa Martínez-Pizarro, Maja Dembic, Belén Pérez, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 20, 2020
Down-Regulation of CK2α Leads toUp-Regulation of the Cyclin-Dependent Kinase Inhibitor p27<sup>KIP1</sup> in Conditions Unfavorable for the Growth of Myoblast CellsBarbara Guerra, Maja Dembic, Mohammad A Siddiqui, et al.
Molecular Genetics and Genomics : MGG|December 1, 2022
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hipMaja Dembic, Lars van Brakel Andersen, Martin Jakob Larsen, et al.
Molecular Oncology|March 23, 2026
Somatic mutational landscape in von Hippel-Lindau familial hemangioblastomaMaja Dembic, Anne Nørremølle, Lilian Bomme Ousager, et al.
Molecular Genetics and Metabolism|September 6, 2016
The prevalent deep intronic c. 639+919 G>A GLA mutation causes pseudoexon activation and Fabry disease by abolishing the binding of hnRNPA1 and hnRNP A2/B1 to a splicing silencerBruno Palhais, Maja Dembic, Rugivan Sabaratnam, et al.
Pathology, Research and Practice|August 28, 2021
Synchronous detection of pancreatic adenocarcinoma and paraganglioma in a Whipple resection specimenTrine Aaquist, Maja Dembic, Mads Thomassen, et al.
Nucleic Acid Therapeutics|April 9, 2024
Splice-Switching Antisense Oligonucleotides Correct Phenylalanine Hydroxylase Exon 11 Skipping Defects and Rescue Enzyme Activity in PhenylketonuriaAinhoa Martínez-Pizarro, Mar Álvarez, Maja Dembic, et al.
Neurobiology of Disease|September 3, 2005
Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellumMassimo Riccio, Spartaco Santi, Maja Dembic, et al.
Pageof 3