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Asli Silahtaroglu

Showing results (21-30 of 35) with videos related to

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Genes|October 29, 2025
<i>ROGDI</i>-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense VariantSopio Gverdtsiteli, Trine Bjørg Hammer, Xenia Hermann, et al.
Molecular and Cellular Neurosciences|January 1, 2018
Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease modelRegina Hertfelder Reynolds, Maria Hvidberg Petersen, Cecilie Wennemoes Willert, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 13, 2023
PRRT2 benign familial infantile seizures (BFIS) with atypical evolution to encephalopathy related to status epilepticus during sleep (ESES)Alberto Cossu, Joana L Santos, Giulia Galati, et al.
Nucleic Acids Research|December 26, 2007
Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liverJoacim Elmén, Morten Lindow, Asli Silahtaroglu, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2022
The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratioAnja Holm, Marie-Laure Possovre, Mojtaba Bandarabadi, et al.
Scientific Reports|December 22, 2017
Enrichment of megabase-sized DNA molecules for single-molecule optical mapping and next-generation sequencingJoanna M Łopacińska-Jørgensen, Jonas N Pedersen, Mads Bak, et al.
Psychiatric Genetics|August 24, 2013
An association study between the norepinephrine transporter gene and depressionHenriette N Buttenschøn, Iben S Jacobsen, Matias B Grynderup, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndromeAlina T Midro, Barbara Panasiuk, Zeynep Tümer, et al.
Neurobiology of Disease|October 16, 2014
Deficiency of the miR-29a/b-1 cluster leads to ataxic features and cerebellar alterations in miceAikaterini S Papadopoulou, Lutgarde Serneels, Tilmann Achsel, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Genes|October 29, 2025
<i>ROGDI</i>-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense VariantSopio Gverdtsiteli, Trine Bjørg Hammer, Xenia Hermann, et al.
Molecular and Cellular Neurosciences|January 1, 2018
Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease modelRegina Hertfelder Reynolds, Maria Hvidberg Petersen, Cecilie Wennemoes Willert, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 13, 2023
PRRT2 benign familial infantile seizures (BFIS) with atypical evolution to encephalopathy related to status epilepticus during sleep (ESES)Alberto Cossu, Joana L Santos, Giulia Galati, et al.
Nucleic Acids Research|December 26, 2007
Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liverJoacim Elmén, Morten Lindow, Asli Silahtaroglu, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2022
The evolutionarily conserved miRNA-137 targets the neuropeptide hypocretin/orexin and modulates the wake to sleep ratioAnja Holm, Marie-Laure Possovre, Mojtaba Bandarabadi, et al.
Scientific Reports|December 22, 2017
Enrichment of megabase-sized DNA molecules for single-molecule optical mapping and next-generation sequencingJoanna M Łopacińska-Jørgensen, Jonas N Pedersen, Mads Bak, et al.
Psychiatric Genetics|August 24, 2013
An association study between the norepinephrine transporter gene and depressionHenriette N Buttenschøn, Iben S Jacobsen, Matias B Grynderup, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndromeAlina T Midro, Barbara Panasiuk, Zeynep Tümer, et al.
Neurobiology of Disease|October 16, 2014
Deficiency of the miR-29a/b-1 cluster leads to ataxic features and cerebellar alterations in miceAikaterini S Papadopoulou, Lutgarde Serneels, Tilmann Achsel, et al.
Pageof 4