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T Warren

Showing results (401-410 of 471) with videos related to

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Biorxiv : the Preprint Server for Biology|January 31, 2024
Mitochondrial ncRNA LDL-805 declines in alveolar epithelial type 2 cells of chronic obstructive pulmonary disease patientsTheodore L Mathuram, Yafei Su, Jonathan E Bard, et al.
Developmental Biology|September 5, 2006
Spook and Spookier code for stage-specific components of the ecdysone biosynthetic pathway in DipteraHajime Ono, Kim F Rewitz, Tetsuro Shinoda, et al.
Insect Biochemistry and Molecular Biology|September 8, 2004
Phantom encodes the 25-hydroxylase of Drosophila melanogaster and Bombyx mori: a P450 enzyme critical in ecdysone biosynthesisJames T Warren, Anna Petryk, Guillermo Marqués, et al.
Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.
Human Molecular Genetics|May 24, 2007
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathwaysYuhei Nishimura, Christa L Martin, Araceli Vazquez-Lopez, et al.
Frontiers in Behavioral Neuroscience|November 30, 2011
Versatility of fear-potentiated startle paradigms for assessing human conditioned fear extinction and return of fearSeth D Norrholm, Kemp M Anderson, Ilana W Olin, et al.
Developmental Cell|December 29, 2004
Fragile X protein functions with lgl and the par complex in flies and miceDaniela C Zarnescu, Peng Jin, Joerg Betschinger, et al.
British Journal of Pharmacology|December 3, 2023
Piezo1-mediated regulation of smooth muscle cell volume in response to enhanced extracellular matrix rigidityRobert T Johnson, Reesha Solanki, Finn Wostear, et al.
Cell|November 24, 2001
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndromeV Brown, P Jin, S Ceman, et al.
Human Molecular Genetics|November 13, 1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.
Pageof 48

Showing results (401-410 of 471) with videos related to

Sort By:
Pageof 48
Biorxiv : the Preprint Server for Biology|January 31, 2024
Mitochondrial ncRNA LDL-805 declines in alveolar epithelial type 2 cells of chronic obstructive pulmonary disease patientsTheodore L Mathuram, Yafei Su, Jonathan E Bard, et al.
Developmental Biology|September 5, 2006
Spook and Spookier code for stage-specific components of the ecdysone biosynthetic pathway in DipteraHajime Ono, Kim F Rewitz, Tetsuro Shinoda, et al.
Insect Biochemistry and Molecular Biology|September 8, 2004
Phantom encodes the 25-hydroxylase of Drosophila melanogaster and Bombyx mori: a P450 enzyme critical in ecdysone biosynthesisJames T Warren, Anna Petryk, Guillermo Marqués, et al.
Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.
Human Molecular Genetics|May 24, 2007
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathwaysYuhei Nishimura, Christa L Martin, Araceli Vazquez-Lopez, et al.
Frontiers in Behavioral Neuroscience|November 30, 2011
Versatility of fear-potentiated startle paradigms for assessing human conditioned fear extinction and return of fearSeth D Norrholm, Kemp M Anderson, Ilana W Olin, et al.
Developmental Cell|December 29, 2004
Fragile X protein functions with lgl and the par complex in flies and miceDaniela C Zarnescu, Peng Jin, Joerg Betschinger, et al.
British Journal of Pharmacology|December 3, 2023
Piezo1-mediated regulation of smooth muscle cell volume in response to enhanced extracellular matrix rigidityRobert T Johnson, Reesha Solanki, Finn Wostear, et al.
Cell|November 24, 2001
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndromeV Brown, P Jin, S Ceman, et al.
Human Molecular Genetics|November 13, 1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.
Pageof 48