Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("GREGG, R. G")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 34

  • Page / 2

Export

Selection :

  • and

Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31COFFEEN, C. M; MCKENNA, C. E; FU, Y.-H et al.Human molecular genetics (Print). 2000, Vol 9, Num 5, pp 787-793, issn 0964-6906Article

Newborn screening for cystic fibrosis in Wisconsin: Comparison of biochemical and molecular methodsGREGG, R. G; SIMANTEL, A; SPLAINGARD, M et al.Pediatrics (Evanston). 1997, Vol 99, Num 6, pp 819-824, issn 0031-4005Article

Localization of a non-specific X-linked mental retardation gene, MRX23, to Xq23-q24GREGG, R. G; PALMER, C; KIRKPATRICK, S et al.Human molecular genetics (Print). 1996, Vol 5, Num 3, pp 411-414, issn 0964-6906Article

Assignment of the human gene for the β subunit of the voltage-dependent calcium channel (CACNLB1) to chromosome 17 using somatic cell hybrids and linkage mappingGREGG, R. G; POWERS, P. A; HOGAN, K et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 1, pp 185-187, issn 0888-7543Article

Dinucleotide repeat polymorphism at the RYR1 locus (19q13.1)COUCH, F. J; HOGAN, K; MCCARTHY, T. V et al.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5094Article

Structure and alternative splicing of the gene encoding the human β1 subunit of voltage dependent calcium channelsHOGAN, K; GREGG, R. G; POWERS, P. A et al.Neuroscience letters. 1999, Vol 277, Num 2, pp 111-114, issn 0304-3940Article

Morphological and physiological consequences of the selective elimination of rod photoreceptors in transgenic miceMCCALL, M. A; GREGG, R. G; MERRIMAN, K et al.Experimental eye research. 1996, Vol 63, Num 1, pp 35-49, issn 0014-4835Article

The structure of the gene encoding the human skeletal muscle α1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3)HOGAN, K; GREGG, R. G; POWERS, P. A et al.Genomics (San Diego, Calif.). 1996, Vol 31, Num 3, pp 392-394, issn 0888-7543Article

Dinucleotide repeat polymorphism at the D17S518 locusCOUCH, F. J; MCCARTHY, T. V; GREGG, R. G et al.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5093Article

Hepatic cholesterol synthesis and hydroxymethylglutaryl CoA reductase activity after injection of methylazoxymethanol acetateGREGG, R. G; WILCE, P. A.Cancer biochemistry biophysics. 1987, Vol 9, Num 3, pp 281-287, issn 0305-7232Article

Cardiac troponin I gene knockout : A mouse model of myocardial troponin I deficiencyXUPEI HUANG; YEQING PI; LEE, K. J et al.Circulation research. 1999, Vol 84, Num 1, pp 1-8, issn 0009-7330Article

A calcium channel mutation causing hypokalemic periodic paralysisJURKAT-ROTT, K; LEHMANN-HORN, F; FONTAINE, B et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1415-1419, issn 0964-6906Article

Assignment of the human gene for the α1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32GREGG, R. G; COUCH, F; HOGAN, K et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 1, pp 107-112, issn 0888-7543Article

Targetted correction of a mutant HPRT gene in mouse embryonic stem cellsDOETSCHMAN, T; GREGG, R. G; MAEDA, N et al.Nature (London). 1987, Vol 330, Num 6148, pp 576-578, issn 0028-0836Article

Efficient transformation and frequent single-site, single-copy insertion of DNA can be obtained in mouse erythroleukemia cells transformed by electroporationBOGGS, S. S; GREGG, R. G; BORENSTEIN, N et al.Experimental hematology. 1986, Vol 14, Num 10, pp 988-994, issn 0301-472XArticle

Application of DNA analysis in a population-screening program for neonatal diagnosis of cystic fibrosis (CF) : comparison of screening protocolsGREGG, R. G; WILFOND, B. S; FARRELL, P. M et al.American journal of human genetics. 1993, Vol 52, Num 3, pp 616-626, issn 0002-9297Article

G to A polymorphism in the CACNLG geneOLCKERS, A; JEDLICKA, A. E; POWERS, P. A et al.Human molecular genetics (Print). 1993, Vol 2, Num 12, issn 0964-6906, p. 2198Article

A cysteine-for-arginine substitution (R614C) in the human skeletal muscle calcium release channel cosegregates with malignant hyperthermiaHOGAN, K; COUCH, F; POWERS, P. A et al.Anesthesia and analgesia. 1992, Vol 75, Num 3, pp 441-448, issn 0003-2999Article

Assignment of the human gene for the α1 subunit of the cardiac DHP-sensitive Ca2+ channel (CCHL1A1) to chromosome 12p12-pterPOWERS, P. A; GREGG, R. G; LALLEY, P. A et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 3, pp 835-839, issn 0888-7543, 5 p.Article

Dinucleotide repeat polymorphism at the D8S161 locusCOUCH, F. J; MCCARTHY, T. V; GREGG, R. G et al.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5093Article

Regulated expression of genes inserted at the human chromosomal β-globin locus by homologous recombinationNANDI, A. K; ROGINSKI, R. S; GREGG, R. G et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 11, pp 3845-3849, issn 0027-8424Article

A naturally occurring mouse model of X-linked congenital stationary night blindnessPARDUE, M. T; MCCALL, M. A; LAVAIL, M. M et al.Investigative ophthalmology & visual science. 1998, Vol 39, Num 12, pp 2443-2449, issn 0146-0404Article

Localization of the gene encoding the α2/δ subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21-q22 by somatic cell hybrid analysisPOWERS, P. A; SCHERER, S. W; LAP-CHEE TSUI et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 1, pp 192-193, issn 0888-7543Article

Molecular characterization of the gene encoding the γ subunit of the human skeletal muscle 1,4-dihydropyridine-sensitive Ca2+ channel (CACNLG), cDNA sequence, gene structure, and chromosomal locationPOWERS, P. A; SHUYING LIU; HOGAN, K et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 13, pp 9275-9279, issn 0021-9258Article

Refined genetic localization for central core diseaseMULLEY, J. C; KOZMAN, H. M; HAAN, E. A et al.American journal of human genetics. 1993, Vol 52, Num 2, pp 398-405, issn 0002-9297Article

  • Page / 2