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E Cottrell

Showing results (241-250 of 334) with videos related to

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American Journal of Medical Genetics. Part A|February 14, 2009
Atypical X-chromosome inactivation in an X;1 translocation patient demonstrating Xq28 functional disomyCatherine E Cottrell, Annemarie Sommer, Gail D Wenger, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|October 19, 2021
Targeted Therapy in a Young Adult With a Novel Epithelioid Tumor Driven by a PRRC2B-ALK FusionAjay Gupta, Huifei Liu, Kathleen M Schieffer, et al.
Neurobiology of Learning and Memory|July 16, 2016
Persistent increased PKMζ in long-term and remote spatial memoryChangchi Hsieh, Panayiotis Tsokas, Peter Serrano, et al.
Nucleic Acids Research|January 15, 2004
A real-time PCR assay for DNA-methylation using methylation-specific blockersSusan E Cottrell, Jürgen Distler, Nancy S Goodman, et al.
Pediatric Dermatology|December 29, 2021
KRIT1-positive hyperkeratotic cutaneous capillary venous malformationBayan Matarneh, Catherine E Cottrell, Samantha Choi, et al.
European Journal of Cancer (Oxford, England : 1990)|January 1, 1994
Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2N R Hall, G R Taylor, P J Finan, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 27, 2022
Alternative RNA splicing defects in pediatric cancers: new insights in tumorigenesis and potential therapeutic vulnerabilitiesA S Venkataramany, K M Schieffer, K Lee, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 29, 2017
Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathiesJoseph P Gaut, Sanjay Jain, John D Pfeifer, et al.
Cold Spring Harbor Molecular Case Studies|February 27, 2021
Clinical response to dabrafenib plus trametinib in a pediatric ganglioglioma with <i>BRAF</i> p.T599dup mutationKatherine E Miller, Kathleen M Schieffer, Olivia Grischow, et al.
Clinical Genetics|April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technologyC E Cottrell, J Mendell, M Hart-Kothari, et al.
Pageof 34

Showing results (241-250 of 334) with videos related to

Sort By:
Pageof 34
American Journal of Medical Genetics. Part A|February 14, 2009
Atypical X-chromosome inactivation in an X;1 translocation patient demonstrating Xq28 functional disomyCatherine E Cottrell, Annemarie Sommer, Gail D Wenger, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|October 19, 2021
Targeted Therapy in a Young Adult With a Novel Epithelioid Tumor Driven by a PRRC2B-ALK FusionAjay Gupta, Huifei Liu, Kathleen M Schieffer, et al.
Neurobiology of Learning and Memory|July 16, 2016
Persistent increased PKMζ in long-term and remote spatial memoryChangchi Hsieh, Panayiotis Tsokas, Peter Serrano, et al.
Nucleic Acids Research|January 15, 2004
A real-time PCR assay for DNA-methylation using methylation-specific blockersSusan E Cottrell, Jürgen Distler, Nancy S Goodman, et al.
Pediatric Dermatology|December 29, 2021
KRIT1-positive hyperkeratotic cutaneous capillary venous malformationBayan Matarneh, Catherine E Cottrell, Samantha Choi, et al.
European Journal of Cancer (Oxford, England : 1990)|January 1, 1994
Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2N R Hall, G R Taylor, P J Finan, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 27, 2022
Alternative RNA splicing defects in pediatric cancers: new insights in tumorigenesis and potential therapeutic vulnerabilitiesA S Venkataramany, K M Schieffer, K Lee, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 29, 2017
Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathiesJoseph P Gaut, Sanjay Jain, John D Pfeifer, et al.
Cold Spring Harbor Molecular Case Studies|February 27, 2021
Clinical response to dabrafenib plus trametinib in a pediatric ganglioglioma with <i>BRAF</i> p.T599dup mutationKatherine E Miller, Kathleen M Schieffer, Olivia Grischow, et al.
Clinical Genetics|April 13, 2011
Maternal uniparental disomy of chromosome 4 in a patient with limb-girdle muscular dystrophy 2E confirmed by SNP array technologyC E Cottrell, J Mendell, M Hart-Kothari, et al.
Pageof 34