المؤلفون: BRUNETTI PIERRI, NICOLA, Grange DK, Zhishuo O, Peiffer DA, Peacock SKG, Cooper ML, Eng PA, Lalani SR, Chinault AC, Gunderson KL, Craigen WJ, Cheung S.W.

المساهمون: BRUNETTI PIERRI, Nicola, Grange, Dk, Zhishuo, O, Peiffer, Da, Peacock, Skg, Cooper, Ml, Eng, Pa, Lalani, Sr, Chinault, Ac, Gunderson, Kl, Craigen, Wj, Cheung, S. W.

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3730::a80f1ed2ad51c798e370623f7026f168
http://hdl.handle.net/11588/363088

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المؤلفون: Lai LA; Department of Pathology,University of Washington, Seattle, WA, USA., Kostadinov R, Barrett MT, Peiffer DA, Pokholok D, Odze R, Sanchez CA, Maley CC, Reid BJ, Gunderson KL, Rabinovitch PS

المصدر: Molecular cancer research : MCR [Mol Cancer Res] 2010 Aug; Vol. 8 (8), pp. 1084-94. Date of Electronic Publication: 2010 Jul 20.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Association for Cancer Research Country of Publication: United States NLM ID: 101150042 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-3125 (Electronic) Linking ISSN: 15417786 NLM ISO Abbreviation: Mol Cancer Res Subsets: MEDLINE

مواضيع طبية MeSH: Genomic Instability* , Loss of Heterozygosity*, Adenocarcinoma/*genetics , Barrett Esophagus/*genetics , Chromosome Fragile Sites/*genetics , Esophageal Neoplasms/*genetics , Neoplasm Proteins/*genetics, Adenocarcinoma/pathology ; Barrett Esophagus/pathology ; Chromosome Fragility ; Chromosomes, Human, Pair 17/genetics ; Chromosomes, Human, Pair 9/genetics ; Comparative Genomic Hybridization ; Esophageal Neoplasms/pathology ; Gene Dosage ; Gene Expression Profiling ; Humans ; In Situ Hybridization, Fluorescence ; Oligonucleotide Array Sequence Analysis ; Polymorphism, Single Nucleotide ; RNA, Messenger/genetics ; Reverse Transcriptase Polymerase Chain Reaction

المؤلفون: Yatsenko SA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA., Kruer MC, Bader PI, Corzo D, Schuette J, Keegan CE, Nowakowska B, Peacock S, Cai WW, Peiffer DA, Gunderson KL, Ou Z, Chinault AC, Cheung SW

المصدر: Clinical genetics [Clin Genet] 2009 Jul; Vol. 76 (1), pp. 54-62. Date of Electronic Publication: 2009 Jun 22.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Deletion*, Chromosomes, Human, Pair 10/*genetics, Adult ; Child ; Child, Preschool ; Female ; Humans ; Infant, Newborn ; Karyotyping ; Male ; Syndrome

المؤلفون: Bi W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA., Sapir T, Shchelochkov OA, Zhang F, Withers MA, Hunter JV, Levy T, Shinder V, Peiffer DA, Gunderson KL, Nezarati MM, Shotts VA, Amato SS, Savage SK, Harris DJ, Day-Salvatore DL, Horner M, Lu XY, Sahoo T, Yanagawa Y, Beaudet AL, Cheung SW, Martinez S, Lupski JR, Reiner O

المصدر: Nature genetics [Nat Genet] 2009 Feb; Vol. 41 (2), pp. 168-77. Date of Electronic Publication: 2009 Jan 11.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

مواضيع طبية MeSH: Gene Expression Regulation, Developmental*/physiology, 1-Alkyl-2-acetylglycerophosphocholine Esterase/*genetics , 1-Alkyl-2-acetylglycerophosphocholine Esterase/*physiology , Brain/*embryology , Microtubule-Associated Proteins/*genetics , Microtubule-Associated Proteins/*physiology, 1-Alkyl-2-acetylglycerophosphocholine Esterase/metabolism ; Adolescent ; Animals ; Base Sequence ; Brain/growth & development ; Child ; Child, Preschool ; Chromosome Aberrations ; Chromosomes, Human, Pair 17 ; Classical Lissencephalies and Subcortical Band Heterotopias/genetics ; Embryo, Mammalian ; Female ; Gene Duplication ; Humans ; Male ; Mice ; Mice, Transgenic ; Microtubule-Associated Proteins/metabolism ; Molecular Sequence Data ; Pedigree ; Up-Regulation/physiology

المؤلفون: Peiffer DA; Illumina, Inc., San Diego, CA, USA., Gunderson KL

المصدر: Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2009; Vol. 529, pp. 51-61.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Humana Press Country of Publication: United States NLM ID: 9214969 Publication Model: Print Cited Medium: Print ISSN: 1064-3745 (Print) Linking ISSN: 10643745 NLM ISO Abbreviation: Methods Mol Biol Subsets: MEDLINE

مواضيع طبية MeSH: Genome-Wide Association Study*, Genome, Human/*genetics , Oligonucleotide Array Sequence Analysis/*methods , Polymorphism, Single Nucleotide/*genetics, Gene Dosage ; Genotype ; Humans

المؤلفون: Li X; Divisions of Human Biology and Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA. xili@fhcrc.org, Galipeau PC, Sanchez CA, Blount PL, Maley CC, Arnaudo J, Peiffer DA, Pokholok D, Gunderson KL, Reid BJ

المصدر: Cancer prevention research (Philadelphia, Pa.) [Cancer Prev Res (Phila)] 2008 Nov; Vol. 1 (6), pp. 413-23.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Association for Cancer Research Country of Publication: United States NLM ID: 101479409 Publication Model: Print Cited Medium: Internet ISSN: 1940-6215 (Electronic) Linking ISSN: 19406215 NLM ISO Abbreviation: Cancer Prev Res (Phila) Subsets: MEDLINE

مواضيع طبية MeSH: Aneuploidy* , Gene Dosage* , Loss of Heterozygosity*, Barrett Esophagus/*genetics , Barrett Esophagus/*pathology , Genome-Wide Association Study/*methods, Adenocarcinoma/genetics ; Adenocarcinoma/pathology ; Aged ; Chromosome Aberrations ; Chromosomes, Human, Pair 17 ; Chromosomes, Human, Pair 9 ; Cross-Sectional Studies ; Disease Progression ; Esophageal Neoplasms/genetics ; Esophageal Neoplasms/pathology ; Female ; Genome, Human ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide