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Linea Melchior

Showing results (11-20 of 27) with videos related to

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BMC Cancer|January 12, 2020
P53, Somatostatin receptor 2a and Chromogranin A immunostaining as prognostic markers in high grade gastroenteropancreatic neuroendocrine neoplasmsKirstine Nielsen, Tina Binderup, Seppo W Langer, et al.
Neuromolecular Medicine|September 18, 2015
Association Study of CHRNA7 Promoter Variants with Sensory and Sensorimotor Gating in Schizophrenia Patients and Healthy Controls: A Danish Case-Control StudyBirgitte Bertelsen, Bob Oranje, Linea Melchior, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 30, 2013
Microduplication of 15q13.3 and Xq21.31 in a family with Tourette syndrome and comorbiditiesLinea Melchior, Birgitte Bertelsen, Nanette Mol Debes, et al.
American Journal of Physical Anthropology|April 13, 2007
mtDNA from hair and nail clarifies the genetic relationship of the 15th century Qilakitsoq Inuit mummiesM Thomas P Gilbert, Durita Djurhuus, Linea Melchior, et al.
Journal of Neuroendocrinology|August 20, 2021
Increase of Ki-67 index and influence on mortality in patients with neuroendocrine neoplasmsPernille Holmager, Seppo W Langer, Birgitte Federspiel, et al.
European Journal of Human Genetics : EJHG|February 20, 2014
Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndromeBirgitte Bertelsen, Linea Melchior, Lars R Jensen, et al.
Virchows Archiv : an International Journal of Pathology|March 16, 2024
Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLCLinea Melchior, Astrid Hirschmann, Paul Hofman, et al.
Psychiatry Research|January 18, 2015
A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHDBirgitte Bertelsen, Linea Melchior, Lars Riff Jensen, et al.
Journal of Medical Genetics|February 1, 2011
Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardationKaren Grønskov, Rebecca L Poole, Johanne M D Hahnemann, et al.
Experimental and Molecular Pathology|September 27, 2015
Multi-center evaluation of the novel fully-automated PCR-based Idylla™ BRAF Mutation Test on formalin-fixed paraffin-embedded tissue of malignant melanomaLinea Melchior, Morten Grauslund, Beatriz Bellosillo, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
BMC Cancer|January 12, 2020
P53, Somatostatin receptor 2a and Chromogranin A immunostaining as prognostic markers in high grade gastroenteropancreatic neuroendocrine neoplasmsKirstine Nielsen, Tina Binderup, Seppo W Langer, et al.
Neuromolecular Medicine|September 18, 2015
Association Study of CHRNA7 Promoter Variants with Sensory and Sensorimotor Gating in Schizophrenia Patients and Healthy Controls: A Danish Case-Control StudyBirgitte Bertelsen, Bob Oranje, Linea Melchior, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 30, 2013
Microduplication of 15q13.3 and Xq21.31 in a family with Tourette syndrome and comorbiditiesLinea Melchior, Birgitte Bertelsen, Nanette Mol Debes, et al.
American Journal of Physical Anthropology|April 13, 2007
mtDNA from hair and nail clarifies the genetic relationship of the 15th century Qilakitsoq Inuit mummiesM Thomas P Gilbert, Durita Djurhuus, Linea Melchior, et al.
Journal of Neuroendocrinology|August 20, 2021
Increase of Ki-67 index and influence on mortality in patients with neuroendocrine neoplasmsPernille Holmager, Seppo W Langer, Birgitte Federspiel, et al.
European Journal of Human Genetics : EJHG|February 20, 2014
Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndromeBirgitte Bertelsen, Linea Melchior, Lars R Jensen, et al.
Virchows Archiv : an International Journal of Pathology|March 16, 2024
Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLCLinea Melchior, Astrid Hirschmann, Paul Hofman, et al.
Psychiatry Research|January 18, 2015
A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHDBirgitte Bertelsen, Linea Melchior, Lars Riff Jensen, et al.
Journal of Medical Genetics|February 1, 2011
Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardationKaren Grønskov, Rebecca L Poole, Johanne M D Hahnemann, et al.
Experimental and Molecular Pathology|September 27, 2015
Multi-center evaluation of the novel fully-automated PCR-based Idylla™ BRAF Mutation Test on formalin-fixed paraffin-embedded tissue of malignant melanomaLinea Melchior, Morten Grauslund, Beatriz Bellosillo, et al.
Pageof 3