Searching for "From "Glycosyltransferase" to "Congenital Muscular Dystrophy" Integrating Knowledge from NCBI Entrez Gene and the Gene Ontology." – sorted by Relevance.
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From “Glycosyltransferase ” to “Congenital Muscular Dystrophy”: Integrating Knowledge from NCBI
- . / Glycosyltransferase to Congenital Muscular Dystrophy: Integrating Knowledge from NCBI Entrez Gene and Gene Ontology
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Congenital Muscular Dystrophy with Rigid Spine Syndrome: A Clinical, Pathological, Radiological
- Congenital Muscular Dystrophy with Rigid Spine Syndrome: A Clinical, Pathological, Radiological
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Aqueous Humor Flow and Flare in Patients With Myotonic Dystrophy
- . Brubaker Purpose. Myotonic dystrophy is an autosomal dominant form of muscular dystrophy associated with a
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Glycosyltransferase efficiently controls phenylpropanoid pathway
- . Results The substrate specificity The glycosyltransferase gene used in this study was isolated from
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Prediction of Glycan Structures from Glycosyltransferase Expression Profiles
- structures from the expression data of human glycosyltransferase genes. This is a first attempt
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The Association for Research in Ophthalmology and The National Society for the Prevention of Blindness
- April 1968 Volume 7, Number 2 INVESTIGATIVE OPHTHALMOLOGY Symposium on congenital anomalies
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A Preliminary Report on Answering Complex Queries related to Drug Discovery using Answer Set Programming
- for glycosyltransferase is given. The query above requires integration of NCBI Entrez Gene (EG) and the Gene Ontology (GO
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O-fucosyltransferase 1 to Notch signaling
- cancers and congenital syndromes. Notch signaling is influenced by two conserved glycosyltransferases, O
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Fold recognition analysis of glycosyltransferase families: further members of structural
- glycosyltransferase SpsA from Bacillus subtilis (Figure 1) (Charnock and Davies, 1999; Tarbouriech et al., 2001
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Trends in hospitalizations for diagnosed congenital
- been published [2,3]. The number of US infants experiencing symptoms from congenital CMV infections
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