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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 patients
Theodore 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 Diptera
Hajime 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 biosynthesis
James 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 locus
M 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 pathways
Yuhei 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 fear
Seth 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 mice
Daniela 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 rigidity
Robert 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 syndrome
V 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 FMR1
C Gunter, W Paradee, D C Crawford, et al.
Page
of 48
Search research articles
Search
Showing results (401-410 of 471) with videos related to
Sort By:
Page
of 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 patients
Theodore 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 Diptera
Hajime 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 biosynthesis
James 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 locus
M 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 pathways
Yuhei 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 fear
Seth 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 mice
Daniela 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 rigidity
Robert 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 syndrome
V 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 FMR1
C Gunter, W Paradee, D C Crawford, et al.
Page
of 48