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Jennelle C Hodge

Showing results (1-10 of 53) with videos related to

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Human Molecular Genetics|September 26, 2007
Genetic heterogeneity among uterine leiomyomata: insights into malignant progressionJennelle C Hodge, Cynthia C Morton
Journal of Clinical Pathology|May 10, 2020
Non-fusion mutations in endometrial stromal sarcomas: what is the potential impact on tumourigenesis through cell cycle dysregulation?Snehal B Patel, Colin McCormack, Jennelle C Hodge
Journal of the American Academy of Dermatology|February 10, 2015
The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarrayJennifer L Hand, Cassandra K Runke, Jennelle C Hodge
Molecular Carcinogenesis|January 13, 2006
Lysophosphatidic acid stimulates PC-3 prostate cancer cell Matrigel invasion through activation of RhoA and NF-kappaB activityYoung Sun Hwang, Jennelle C Hodge, Neela Sivapurapu, et al.
Cancer Genetics|December 4, 2018
Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2)Jennelle C Hodge, David Bosler, Lauren Rubinstein, et al.
Cytogenetic and Genome Research|December 14, 2022
Genotype-Phenotype Correlation of Distal 2q37 DeletionsAiko Iwata-Otsubo, Kahlen R Darr, Wilfredo Torres-Martinez, et al.
The Journal of Molecular Diagnostics : JMD|May 8, 2016
Molecular Cytogenetic Analysis of JAZF1, PHF1, and YWHAE in Endometrial Stromal Tumors: Discovery of Genetic Complexity by Fluorescence in Situ HybridizationJennelle C Hodge, Patrick P Bedroske, Kathryn E Pearce, et al.
Cancer Research|March 22, 2003
Requirement of RhoA activity for increased nuclear factor kappaB activity and PC-3 human prostate cancer cell invasionJennelle C Hodge, Jeffrey Bub, Sushma Kaul, et al.
Cytogenetic and Genome Research|February 3, 2021
Two Patients with Complex Rearrangements Suggestive of Germline ChromoanagenesisPriyanka Arya, Jennelle C Hodge, Peggy A Matlock, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
In-frame multi-exon deletion of SMC1A in a severely affected female with Cornelia de Lange SyndromeNicole Hoppman-Chaney, Jin Sung Jang, Jin Jen, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|September 26, 2007
Genetic heterogeneity among uterine leiomyomata: insights into malignant progressionJennelle C Hodge, Cynthia C Morton
Journal of Clinical Pathology|May 10, 2020
Non-fusion mutations in endometrial stromal sarcomas: what is the potential impact on tumourigenesis through cell cycle dysregulation?Snehal B Patel, Colin McCormack, Jennelle C Hodge
Journal of the American Academy of Dermatology|February 10, 2015
The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarrayJennifer L Hand, Cassandra K Runke, Jennelle C Hodge
Molecular Carcinogenesis|January 13, 2006
Lysophosphatidic acid stimulates PC-3 prostate cancer cell Matrigel invasion through activation of RhoA and NF-kappaB activityYoung Sun Hwang, Jennelle C Hodge, Neela Sivapurapu, et al.
Cancer Genetics|December 4, 2018
Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2)Jennelle C Hodge, David Bosler, Lauren Rubinstein, et al.
Cytogenetic and Genome Research|December 14, 2022
Genotype-Phenotype Correlation of Distal 2q37 DeletionsAiko Iwata-Otsubo, Kahlen R Darr, Wilfredo Torres-Martinez, et al.
The Journal of Molecular Diagnostics : JMD|May 8, 2016
Molecular Cytogenetic Analysis of JAZF1, PHF1, and YWHAE in Endometrial Stromal Tumors: Discovery of Genetic Complexity by Fluorescence in Situ HybridizationJennelle C Hodge, Patrick P Bedroske, Kathryn E Pearce, et al.
Cancer Research|March 22, 2003
Requirement of RhoA activity for increased nuclear factor kappaB activity and PC-3 human prostate cancer cell invasionJennelle C Hodge, Jeffrey Bub, Sushma Kaul, et al.
Cytogenetic and Genome Research|February 3, 2021
Two Patients with Complex Rearrangements Suggestive of Germline ChromoanagenesisPriyanka Arya, Jennelle C Hodge, Peggy A Matlock, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
In-frame multi-exon deletion of SMC1A in a severely affected female with Cornelia de Lange SyndromeNicole Hoppman-Chaney, Jin Sung Jang, Jin Jen, et al.
Pageof 6