about
Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorderRecombinant core streptavidins. A minimum-sized core streptavidin has enhanced structural stability and higher accessibility to biotinylated macromolecules.Cloneless genomic DNA analysis: an efficient and simple methods for de novo genomic sequencing projects and gap filling.Advances in DNA diagnostics.Construction and characterization of a NotI linking library of human chromosome 21.Human Genome Project and cystic fibrosis--a symbiotic relationship.A DNA sequencing strategy that requires only five bases of known terminal sequence for priming.Streptavidin-based containment systems for genetically engineered microorganisms.The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomereHypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: a preliminary report.Advanced paternal age is a risk factor for schizophrenia in IraniansProbing the genetic population structure of Trypanosoma cruzi with polymorphic microsatellitesDifferential display of genome subsets containing specific interspersed repeats.Engineering subunit association of multisubunit proteins: a dimeric streptavidin.The Escherichia coli chromosome contains specific, unmethylated dam and dcm sitesEpigenetic and pharmacoepigenomic studies of major psychoses and potentials for therapeutics.Targeted cDNA differential display (TcDD).Substrate DNA and cofactor regulate the activities of a multi-functional restriction-modification enzyme, BcgI.An electrophoretic karyotype for Schizosaccharomyces pombe by pulsed field gel electrophoresis.A set of inter-Alu PCR markers for chromosome 21 generated from pulsed-field gel-fractionated NotI restriction fragments.Large-scale structure conservation along the entire long arm of human chromosome 21.Cloning and characterization of EagI YACs from human chromosome 21.A streptavidin mutant containing a cysteine stretch that facilitates production of a variety of specific streptavidin conjugates.Molecular engineering of streptavidinThe Experts at HadamarHigh polymorphism level of genomic sequences flanking insertion sites of human endogenous retroviral long terminal repeatsEvolving methods for single nucleotide polymorphism detection: Factor V Leiden mutation detection
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P50
description
researcher ORCID ID = 0000-0002-0346-8907
@en
wetenschapper
@nl
name
Cassandra L Smith
@ast
Cassandra L Smith
@en
Cassandra L Smith
@es
Cassandra L Smith
@nl
type
label
Cassandra L Smith
@ast
Cassandra L Smith
@en
Cassandra L Smith
@es
Cassandra L Smith
@nl
prefLabel
Cassandra L Smith
@ast
Cassandra L Smith
@en
Cassandra L Smith
@es
Cassandra L Smith
@nl
P106
P1153
7501659243
8082152000
P31
P496
0000-0002-0346-8907