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Showing results (521-530 of 603) with videos related to

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European Journal of Neurology|October 1, 2022
Central nervous system cavernous malformations: cross-sectional study assessing rebleeding risk after a second haemorrhageAlejandro N Santos, Laurèl Rauschenbach, Hanah Hadice Gull, et al.
Scientific Reports|September 19, 2023
Natural course of cerebral and spinal cavernous malformations: a complete ten-year follow-up studyAlejandro N Santos, Laurèl Rauschenbach, Hanah H Gull, et al.
Peerj|August 31, 2017
RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancersVan L T Hoang, Lisa N Tom, Xiu-Cheng Quek, et al.
European Journal of Endocrinology|February 22, 2017
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursSunita M C De Sousa, Mark J McCabe, Kathy Wu, et al.
Bioorganic & Medicinal Chemistry Letters|July 28, 2019
Novel SAR for quinazoline inhibitors of EHMT1 and EHMT2Ruben Leenders, Remco Zijlmans, Bart van Bree, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
International Journal of Molecular Sciences|February 11, 2023
Perinatal Obesity Sensitizes for Premature Kidney Aging SignalingJaco Selle, Katrin Bohl, Katja Höpker, et al.
European Journal of Neurology|November 5, 2022
Small intracranial aneurysms of the anterior circulation: A negligible risk?Thiemo Florin Dinger, Jonas Peschke, Mehdi Chihi, et al.
Disease Models & Mechanisms|February 26, 2015
Modeling autosomal recessive cutis laxa type 1C in mice reveals distinct functions for Ltbp-4 isoformsInsa Bultmann-Mellin, Anne Conradi, Alexandra C Maul, et al.
Neurology|May 31, 2022
Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisRyan L Davis, Kishore R Kumar, Clare Puttick, et al.
Pageof 61

Showing results (521-530 of 603) with videos related to

Sort By:
Pageof 61
European Journal of Neurology|October 1, 2022
Central nervous system cavernous malformations: cross-sectional study assessing rebleeding risk after a second haemorrhageAlejandro N Santos, Laurèl Rauschenbach, Hanah Hadice Gull, et al.
Scientific Reports|September 19, 2023
Natural course of cerebral and spinal cavernous malformations: a complete ten-year follow-up studyAlejandro N Santos, Laurèl Rauschenbach, Hanah H Gull, et al.
Peerj|August 31, 2017
RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancersVan L T Hoang, Lisa N Tom, Xiu-Cheng Quek, et al.
European Journal of Endocrinology|February 22, 2017
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursSunita M C De Sousa, Mark J McCabe, Kathy Wu, et al.
Bioorganic & Medicinal Chemistry Letters|July 28, 2019
Novel SAR for quinazoline inhibitors of EHMT1 and EHMT2Ruben Leenders, Remco Zijlmans, Bart van Bree, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
International Journal of Molecular Sciences|February 11, 2023
Perinatal Obesity Sensitizes for Premature Kidney Aging SignalingJaco Selle, Katrin Bohl, Katja Höpker, et al.
European Journal of Neurology|November 5, 2022
Small intracranial aneurysms of the anterior circulation: A negligible risk?Thiemo Florin Dinger, Jonas Peschke, Mehdi Chihi, et al.
Disease Models & Mechanisms|February 26, 2015
Modeling autosomal recessive cutis laxa type 1C in mice reveals distinct functions for Ltbp-4 isoformsInsa Bultmann-Mellin, Anne Conradi, Alexandra C Maul, et al.
Neurology|May 31, 2022
Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisRyan L Davis, Kishore R Kumar, Clare Puttick, et al.
Pageof 61