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1دورية أكاديمية
المؤلفون: Sutherland, H. F., Pick, E., Francis, F., Lehrach, H., Frischauf, A. -M.
المصدر: Mammalian Genome: Incorporating Mouse Genome. July 1995 6(7):449-453
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2دورية أكاديمية
المؤلفون: Obermayr, F., Sutherland, H. F., Kraus, B., Frischauf, A. -M.
المصدر: Mammalian Genome: Incorporating Mouse Genome. February 1995 6(2):149-150
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المؤلفون: Sutherland, H. F., Wadey, R., Mckie, J. M., Taylor, C., Atif, U., Johnstone, K. A., Halford, S., Kim, U. -J, Goodship, J., Antonio Baldini, Scambler, P. J.
المساهمون: H. F., Sutherland, R., Wadey, J. M., Mckie, C., Taylor, U., Atif, K. A., Johnstone, S., Halford, U. J., Kim, J., Goodship, Baldini, Antonio, P. J., Scambler
المصدر: Scopus-Elsevier
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8c0c211a37fdccaf38ac5c96388ca607
http://hdl.handle.net/11588/462664 -
4دورية
المؤلفون: McKie, J M, Wadey, R B, Sutherland, H F, Taylor, C L, Scambler, P J
المصدر: Genome Research; August 1998, Vol. 8 Issue: 8 p834-841, 8p
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5دورية
المؤلفون: Sutherland, H. F., Lovell-Badge, R. H., Jackson, I. J.
المصدر: Gene; 1993, Vol. 131 Issue: 2 p265-265, 1p
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6دورية أكاديمية
المؤلفون: Lindsay EA; Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA., Vitelli F, Su H, Morishima M, Huynh T, Pramparo T, Jurecic V, Ogunrinu G, Sutherland HF, Scambler PJ, Bradley A, Baldini A
المصدر: Nature [Nature] 2001 Mar 01; Vol. 410 (6824), pp. 97-101.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium: Print ISSN: 0028-0836 (Print) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE
مواضيع طبية MeSH: Aorta, Thoracic/*pathology , DiGeorge Syndrome/*pathology , T-Box Domain Proteins/*genetics, Animals ; Aorta, Thoracic/embryology ; Cell Line ; DiGeorge Syndrome/embryology ; Gene Deletion ; Gene Targeting ; Haplotypes ; Humans ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Molecular Sequence Data ; Mutagenesis ; T-Box Domain Proteins/physiology
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7دورية أكاديمية
المؤلفون: Kimber WL; Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Hsieh P, Hirotsune S, Yuva-Paylor L, Sutherland HF, Chen A, Ruiz-Lozano P, Hoogstraten-Miller SL, Chien KR, Paylor R, Scambler PJ, Wynshaw-Boris A
المصدر: Human molecular genetics [Hum Mol Genet] 1999 Nov; Vol. 8 (12), pp. 2229-37.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Print ISSN: 0964-6906 (Print) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
مواضيع طبية MeSH: Chromosome Deletion* , Chromosomes, Human, Pair 22*, DiGeorge Syndrome/*genetics, Animals ; Base Sequence ; DNA Primers ; Heterozygote ; Humans ; Male ; Mice
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8دورية أكاديمية
المؤلفون: Sutherland HF; Molecular Medicine Unit, Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, United Kingdom., Kim UJ, Scambler PJ
المصدر: Genomics [Genomics] 1998 Aug 15; Vol. 52 (1), pp. 37-43.
نوع المنشور: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 8800135 Publication Model: Print Cited Medium: Print ISSN: 0888-7543 (Print) Linking ISSN: 08887543 NLM ISO Abbreviation: Genomics Subsets: MEDLINE
مواضيع طبية MeSH: Cell Cycle Proteins* , Chromosome Mapping*/methods, DiGeorge Syndrome/*genetics, Animals ; Bacteriophage P1/genetics ; Chromosomes, Artificial, Yeast/chemistry ; Chromosomes, Artificial, Yeast/genetics ; Chromosomes, Bacterial/genetics ; Chromosomes, Human, Pair 22/genetics ; Cloning, Molecular ; Histone Chaperones ; Humans ; Mice ; Mice, Inbred Strains ; Nuclear Proteins/genetics ; Sequence Analysis, DNA ; Transcription Factors/genetics
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9دورية أكاديمية
المؤلفون: McKie JM; Molecular Medicine Unit, Institute of Child Health, London, UK., Sutherland HF, Harvey E, Kim UJ, Scambler PJ
المصدر: Human genetics [Hum Genet] 1997 Nov; Vol. 101 (1), pp. 6-12.
نوع المنشور: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print Cited Medium: Print ISSN: 0340-6717 (Print) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
مواضيع طبية MeSH: Drosophila Proteins* , Microfilament Proteins*, Cell Cycle Proteins/*genetics , Chromosomes, Human, Pair 22/*genetics , DiGeorge Syndrome/*genetics, Adult ; Amino Acid Sequence ; Animals ; Base Sequence ; Chromosome Mapping ; DNA Primers/genetics ; DNA, Complementary/genetics ; Female ; GTP Phosphohydrolases/genetics ; Gene Expression ; Genes, Insect ; Humans ; In Situ Hybridization, Fluorescence ; Insect Proteins/genetics ; Mice ; Molecular Sequence Data ; Pregnancy ; Septins ; Sequence Homology, Amino Acid ; Tissue Distribution
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10دورية أكاديمية
المؤلفون: Sutherland HF; Molecular Medicine Unit, Institute of Child Health, London., Wadey R, McKie JM, Taylor C, Atif U, Johnstone KA, Halford S, Kim UJ, Goodship J, Baldini A, Scambler PJ
المصدر: American journal of human genetics [Am J Hum Genet] 1996 Jul; Vol. 59 (1), pp. 23-31.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
مواضيع طبية MeSH: Translocation, Genetic*, DiGeorge Syndrome/*genetics , RNA/*genetics, Animals ; Base Sequence ; Chromosome Deletion ; Chromosome Mapping ; Chromosomes, Human, Pair 22/genetics ; DNA Primers/genetics ; DNA, Complementary/genetics ; Exons ; Humans ; Introns ; Mice ; Molecular Sequence Data ; Transcription, Genetic