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  • Publication: CTBP1 and CTBP2 mutations underpinning neurological . . .
    C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a significant role during vertebrate neurodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes We screened different databases (PubMed, Scopus, Google Scholar, LILACS) by systematically searching journals and checking
  • De novo CTBP1 variant is associated with decreased mitochondrial . . .
    We describe a young woman presenting an early-onset, progressive neurodegenerative disorder with decreased mitochondrial complex I and IV activities in skeletal muscle Using WES, we identified a recurrent pathogenic de novo heterozygous CTBP1 variant previously associated with an early-onset neurologic disorder 8 We highlight the challenges of variant prioritization in a patient who was
  • CTBP1 and CTBP2 mutations underpinning neurological disorders: a . . .
    C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a significant role during vertebrate neurodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes We screened different
  • CTBP1 and CTBP2 mutations underpinning neurological disorders: a . . .
    C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a significant role during vertebrate neurodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes We screened different
  • CTBP1 and CTBP2 mutations underpinning neurological disorders: a . . .
    Abstract C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a significant role during vertebrate neu-rodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes
  • Using the Allen Brain Cell Atlas of the Human Brain to Gain . . . - MDPI
    Neurodegenerative disorders have been shown to be associated with the early onset of neurodevelopmental abnormalities during childhood or embryonic development Mutations that cause neurodevelopmental defects can lead to the development of an ‘at-risk normal brain’ susceptible to intrinsic and extrinsic factors, possibly leading to clinical manifestations of neurological disorders at an
  • CTBP1 and CTBP2 mutations underpinning neurological disorders: a . . .
    Abstract C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a significant role during vertebrate neu-rodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes
  • CTBP1 and CTBP2 mutations underpinning neurological disorders: a . . .
    C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a significant role during vertebrate neurodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes We screened different databases (PubMed, Scopus, Google Scholar, LILACS) by systematically searching journals and checking
  • CTBP1 and CTBP2 mutations underpinning neurological disorders: a . . .
    C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a significant role during vertebrate neurodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes
  • CTBP1 C-terminal binding protein 1 [Homo sapiens (human)] - Gene - NCBI
    CTBP1 and CTBP2 mutations underpinning neurological disorders: a systematic review
  • CTBP1 C-terminal binding protein 1 [ (human)]
    CTBP1 and CTBP2 mutations underpinning neurological disorders: a systematic review NADH NAD (+) binding and linked tetrameric assembly of the oncogenic transcription factors CtBP1 and CtBP2
  • CTBP2 C-terminal binding protein 2 [Homo sapiens (human)] - Gene - NCBI
    CTBP1 and CTBP2 mutations underpinning neurological disorders: a systematic review
  • Abstract 1426 CTBP1 Mutation Affects Neurodevelopment
    The C-terminal binding proteins (CtBP1 and CtBP2) are highly conserved and expressed in vertebrates CtBPs are co-repressors that bind to various chromatin-modifying factors and DNA binding repressors at the promoter regions of target genes through a protein interaction interface (PXDLS-binding cleft)
  • CTBP1 and CTBP2 mutations underpinning neurological disorders: a . . .
    ABSTRACT: Abstract C-terminal binding proteins (CtBP1 2) are transcriptional coregulators that play a signifcant role during vertebrate neu rodevelopment This systematic review aims to identify case reports with genetic variants in CTBP1 and CTBP2 associated with brain development syndromes We screened diferent databases (PubMed, Scopus, Google Scholar, LILACS) by systematically searching





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