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au.\*:("CARLOCK, L. R")

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NMDA receptor overstimulation triggers a prolonged wave of immediate early gene expression : Relationship to excitotoxicitySHAN, Y; CARLOCK, L. R; WALKER, P. D et al.Experimental neurology (Print). 1997, Vol 144, Num 2, pp 406-415, issn 0014-4886Article

Chromosomal localization of human gene for histidyl-RNA synthetase: clustering of genes encoding aminoacyl-tRNA synthetases on human chromosome 5WASMUTH, J. J; CARLOCK, L. R.Somatic cell and molecular genetics. 1986, Vol 12, Num 5, pp 513-517, issn 0740-7750Article

Immediate early gene activation during the initial phases of the excitotoxic cascadeWALKER, P. D; CARLOCK, L. R.Journal of neuroscience research. 1993, Vol 36, Num 5, pp 588-595, issn 0360-4012Article

Molecular approach to analyzing the human 5p delection syndrome, Cri du chatCARLOCK, L. R; WASMUTH, J. J.Somatic cell and molecular genetics. 1985, Vol 11, Num 3, pp 267-276, issn 0740-7750Article

Timing the excitotoxic induction of heat shock protein 70 transcriptionWALKER, P. D; CARLOCK, L. R.Neuroreport (Oxford). 1993, Vol 4, Num 6, pp 699-702, issn 0959-4965Article

Genetic counterselective procedure to isolate interspecific cell hybrids containing single human chromosome: construction of cell hybrids and recombinant DNA libraries specific for human chromosomes 3 and 4CARLOCK, L. R; SMITH, D; WASMUTH, J. J et al.Somatic cell and molecular genetics. 1986, Vol 12, Num 2, pp 163-174, issn 0740-7750Article

Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase lociMURRAY, J. C; SHIANG, R; CARLOCK, L. R et al.Human genetics. 1987, Vol 76, Num 3, pp 274-277, issn 0340-6717Article

An anonymous genomic clone that defects a frequent RFLP adajacent to the D4S10 (G8) marker and Huntington's diseaseCARLOCK, L. R; VO, T. D; DEHAVEN, C. R et al.Nucleic acids research. 1987, Vol 15, Num 1, issn 0305-1048, 377Article

Deletion mapping of human chromosome 5 using chromosome-specific DNA probesCARLOCK, L. R; SKARECKY, D; DANA, S. L et al.American journal of human genetics. 1985, Vol 37, Num 5, pp 839-852, issn 0002-9297Article

Preprotachykinin and preproenkephalin mRNA expression within striatal subregions in response to altered serotonin transmissionWALKER, P. D; CAPODILUPO, J. G; WOLF, W. A et al.Brain research. 1996, Vol 732, Num 1-2, pp 25-35, issn 0006-8993Article

The identification of a functional nuclear localization signal in the Huntington disease proteinBESSERT, D. A; GUTRIDGE, K. L; DUNBAR, J. C et al.Molecular brain research. 1995, Vol 33, Num 1, pp 165-173, issn 0169-328XArticle

cDNA cloning and chromosomal localization (4q11-13) of a gene for statherin, a regulator of calcium in salivaSABATINI, L. M; CARLOCK, L. R; JOHNSON, G. W et al.American journal of human genetics. 1987, Vol 41, Num 6, pp 1048-1060, issn 0002-9297Article

Progress towards cloning the cystic fibrosis geneTSUI, L.-C; ROMMENS, J. M; BURNS, J et al.Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 1988, Vol 319, Num 1194, pp 263-273, issn 0080-4622Conference Paper

A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease geneWASMUTH, J. J; CARLOCK, L. R; SMITH, B et al.American journal of human genetics. 1986, Vol 39, Num 3, pp 397-403, issn 0002-9297Article

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