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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 451 to 455 of 455

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Cell type-specific integrin variants with alternative alpha chain cytoplasmic domains.
Tamura RN, Cooper HM, Collo G, Quaranta V
(1991) Proc Natl Acad Sci U S A 88: 10183-7
MeSH Terms: Amino Acid Sequence, Animals, Base Sequence, Cell Line, Cloning, Molecular, Cricetinae, Cytoplasm, Gene Expression, Genetic Variation, Humans, Immunoblotting, Integrins, Macromolecular Substances, Molecular Sequence Data, Oligodeoxyribonucleotides, Polymerase Chain Reaction, RNA, Messenger, Sequence Homology, Nucleic Acid
Added March 27, 2014
1 Communities
1 Members
0 Resources
18 MeSH Terms
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP
(1991) Cell 65: 905-14
MeSH Terms: Alleles, Amino Acid Sequence, Base Sequence, Blotting, Northern, Brain, Cosmids, DNA, Exons, Fragile X Mental Retardation Protein, Fragile X Syndrome, Gene Library, Gene Rearrangement, Genetic Variation, Humans, Molecular Sequence Data, Nerve Tissue Proteins, Oligonucleotide Probes, Polymerase Chain Reaction, RNA, RNA-Binding Proteins, Recombination, Genetic, Repetitive Sequences, Nucleic Acid, Restriction Mapping, Translocation, Genetic, X Chromosome
Added February 20, 2014
0 Communities
1 Members
0 Resources
25 MeSH Terms
Apolipoprotein B gene mutations affecting cholesterol levels.
Farese RV, Linton MF, Young SG
(1992) J Intern Med 231: 643-52
MeSH Terms: Apolipoproteins B, Cholesterol, Gene Expression Regulation, Genetic Variation, Humans, Hypobetalipoproteinemias, Mutation
Added May 27, 2014
0 Communities
1 Members
0 Resources
7 MeSH Terms
Relationship between platelet monoamine oxidase B activity and alleles at the MAOB locus.
Girmen AS, Baenziger J, Hotamisligil GS, Konradi C, Shalish C, Sullivan JL, Breakefield XO
(1992) J Neurochem 59: 2063-6
MeSH Terms: Adult, Alleles, Base Sequence, Blood Platelets, Chromosome Mapping, Enzyme Activation, Genetic Variation, Humans, Male, Middle Aged, Molecular Sequence Data, Monoamine Oxidase, Polymorphism, Genetic
Added May 27, 2014
0 Communities
1 Members
0 Resources
13 MeSH Terms
Interaction of human fibrinogen with staphylococci: presence of a binding region on normal and abnormal fibrinogen variants and fibrinogen derivatives.
Hawiger J, Hammond DK, Timmons S, Budzynski AZ
(1978) Blood 51: 799-812
MeSH Terms: Binding Sites, Cations, Divalent, Fibrinogen, Fibrinolysin, Genetic Variation, Humans, Hydrogen Bonding, Hydrogen-Ion Concentration, Iodine Radioisotopes, Peptides, Polymers, Staphylococcus
Added December 10, 2013
0 Communities
1 Members
0 Resources
12 MeSH Terms