Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę ""Burchard, Esteban"" wg kryterium: Autor


Tytuł:
Self-reported racial/ethnic discrimination and bronchodilator response in African American youth with asthma.
Autorzy:
Carlson, Sonia
Borrell, Luisa N.
Eng, Celeste
Nguyen, Myngoc
Thyne, Shannon
LeNoir, Michael A.
Burke-Harris, Nadine
Burchard, Esteban G.
Thakur, Neeta
Pokaż więcej
Temat:
ASTHMA
BRONCHODILATOR agents
TUMOR necrosis factors
SPIROMETRY
REGRESSION analysis
ALBUTEROL
CARCINOGENESIS
Źródło:
PLoS ONE; 6/13/2017, Vol. 12 Issue 6, p1-13, 13p
Czasopismo naukowe
Tytuł:
Racial Differences in Left Atrial Size: Results from the Coronary Artery Risk Development in Young Adults (CARDIA) Study.
Autorzy:
Dewland, Thomas A.
Bibbins-Domingo, Kirsten
Lin, Feng
Vittinghoff, Eric
Foster, Elyse
Ogunyankin, Kofo O.
Lima, Joao A.
Jacobs, David R.
Hu, Donglei
Burchard, Esteban G.
Marcus, Gregory M.
Pokaż więcej
Temat:
ATRIAL fibrillation risk factors
HEART anatomy
CORONARY heart disease risk factors
HEALTH of adults
COMPARATIVE studies
Źródło:
PLoS ONE; 3/17/2016, Vol. 11 Issue 3, p1-11, 11p
Czasopismo naukowe
Tytuł:
PCA-Correlated SNPs for Structure Identification in Worldwide Human Populations.
Autorzy:
Paschou, Peristera
Ziv, Elad
Burchard, Esteban G.
Choudhry, Shweta
Rodriguez-Cintron, William
Mahoney, Michael W.
Drineas, Petros
Pokaż więcej
Temat:
BIOMARKERS
HUMAN population genetics
GENOMES
ALGORITHMS
CHINESE people
JAPANESE people
Źródło:
PLoS Genetics; Sep2007, Vol. 3 Issue 9, p1672-1686, 15p, 3 Charts, 6 Graphs
Terminy geograficzne:
PUERTO Rico
Czasopismo naukowe
Tytuł:
Asthma and its relationship to mitochondrial copy number: Results from the Asthma Translational Genomics Collaborative (ATGC) of the Trans-Omics for Precision Medicine (TOPMed) program.
Autorzy:
Cocco MP; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
White E; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Xiao S; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Hu D; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Mak A; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Sleiman P; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Yang M; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Bobbitt KR; Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan, United States of America.
Gui H; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Levin AM; Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan, United States of America.
Hochstadt S; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Whitehouse K; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Rynkowski D; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Barczak AJ; Lung Biology Center and UCSF CoLabs, University of California San Francisco, San Francisco, California, United States of America.
Abecasis G; Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, United States of America.
Blackwell TW; Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.
Kang HM; Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.
Nickerson DA; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.; Northwest Genomics Center, Seattle, Washington, United States of America.; Brotman Baty Institute, Seattle, Washington, United States of America.
Germer S; New York Genome Center, New York, New York, United States of America.
Ding J; Human Statistical Genetics Unit, Laboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, United States of America.
Lanfear DE; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Gilliland F; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Gauderman WJ; Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
Kumar R; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America.
Erle DJ; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.; Lung Biology Center and UCSF CoLabs, University of California San Francisco, San Francisco, California, United States of America.
Martinez F; Arizona Respiratory Center and Department of Pediatrics, University of Arizona, Tucson, Arizona, United States of America.
Hakonarson H; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Burchard EG; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.; Department of Bioengineering & Therapeutic Sciences, University of California San Francisco, San Francisco, California, United States of America.
Williams LK; Center for Individualized and Genomic Medicine Research (CIGMA), Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, United States of America.
Pokaż więcej
Źródło:
PloS one [PLoS One] 2020 Nov 25; Vol. 15 (11), pp. e0242364. Date of Electronic Publication: 2020 Nov 25 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
DNA Copy Number Variations*
Black or African American/*genetics
Asthma/*genetics
DNA, Mitochondrial/*genetics
Adult ; Asthma/ethnology ; Base Sequence ; Cohort Studies ; DNA, Mitochondrial/blood ; Electron Transport Chain Complex Proteins/genetics ; Female ; Flow Cytometry ; Humans ; Leukocytes/ultrastructure ; Logistic Models ; Male ; Middle Aged ; Proportional Hazards Models ; RNA/genetics ; Sensitivity and Specificity ; Translational Research, Biomedical ; Whole Genome Sequencing ; Young Adult
Czasopismo naukowe
Tytuł:
Towards Equity in Health: Researchers Take Stock.
Autorzy:
Rid A; Department of Global Health & Social Medicine, King's College London, London, United Kingdom.
Johansson MA; Division of Vector-Borne Diseases, Centers for Disease Control and Prevention, San Juan, Puerto Rico.; Center for Communicable Disease Dynamics, T.H. Chan School of Public Health, Boston, Massachusetts, United States of America.
Leung G; Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Valantine H; Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.; Laboratory of Genome Transplantation, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Burchard EG; Department of Bioengineering & Therapeutic Sciences, University of California San Francisco, San Francisco, California, United States of America.; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Oh SS; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Zimmerman C; Department of Global Health and Development, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Pokaż więcej
Corporate Authors:
PLOS Medicine Editors
Źródło:
PLoS medicine [PLoS Med] 2016 Nov 29; Vol. 13 (11), pp. e1002186. Date of Electronic Publication: 2016 Nov 29 (Print Publication: 2016).
Typ publikacji:
Editorial
MeSH Terms:
Health Equity*/trends
Social Justice*/trends
Humans
Opinia redakcyjna
Tytuł:
Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma.
Autorzy:
Campbell CD; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Mohajeri K; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Malig M; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Hormozdiari F; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Nelson B; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Du G; Department of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Patterson KM; Department of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Eng C; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Torgerson DG; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Hu D; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Herman C; Department of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Chong JX; Department of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Ko A; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
O'Roak BJ; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Krumm N; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Vives L; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Lee C; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Roth LA; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Rodriguez-Cintron W; Veterans Caribbean Health Care System, San Juan, Puerto Rico, United States of America.
Rodriguez-Santana J; Centro de Neumología Pediátrica, San Juan, Puerto Rico, United States of America.
Brigino-Buenaventura E; Department of Allergy & Immunology, Kaiser Permanente-Vallejo Medical Center, Vallejo, California, United States of America.
Davis A; Children's Hospital and Research Center Oakland, Oakland, California, United States of America.
Meade K; Children's Hospital and Research Center Oakland, Oakland, California, United States of America.
LeNoir MA; Bay Area Pediatrics, Oakland, California, United States of America.
Thyne S; San Francisco General Hospital, San Francisco, California, and the Department of Pediatrics, University of California San Francisco, San Francisco, California, United States of America.
Jackson DJ; Department of Pediatrics, University of Wisconsin, Madison, Wisconsin, United States of America.
Gern JE; Department of Pediatrics, University of Wisconsin, Madison, Wisconsin, United States of America.
Lemanske RF Jr; Department of Pediatrics, University of Wisconsin, Madison, Wisconsin, United States of America; Department of Medicine, University of Wisconsin, Madison, Wisconsin, United States of America.
Shendure J; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Abney M; Department of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Burchard EG; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America; Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, United States of America.
Ober C; Department of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.
Eichler EE; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America; Howard Hughes Medical Institute, Seattle, Washington, United States of America.
Pokaż więcej
Źródło:
PloS one [PLoS One] 2014 Aug 12; Vol. 9 (8), pp. e104396. Date of Electronic Publication: 2014 Aug 12 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Founder Effect*
Genetic Predisposition to Disease*
Genome, Human*
Genome-Wide Association Study*
Asthma/*genetics
Alleles ; Chromosome Mapping ; Comparative Genomic Hybridization ; DNA Copy Number Variations ; Endosomal Sorting Complexes Required for Transport/genetics ; Female ; Gene Frequency ; Genetic Variation ; High-Throughput Nucleotide Sequencing ; Humans ; Introns ; Male ; Nedd4 Ubiquitin Protein Ligases ; Polymorphism, Single Nucleotide ; Population Groups/genetics ; Sequence Deletion ; Ubiquitin-Protein Ligases/genetics
Czasopismo naukowe
Tytuł:
Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene.
Autorzy:
Himes BE; Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, United States of America. />Sheppard K
Berndt A
Leme AS
Myers RA
Gignoux CR
Levin AM
Gauderman WJ
Yang JJ
Mathias RA
Romieu I
Torgerson DG
Roth LA
Huntsman S
Eng C
Klanderman B
Ziniti J
Senter-Sylvia J
Szefler SJ
Lemanske RF Jr
Zeiger RS
Strunk RC
Martinez FD
Boushey H
Chinchilli VM
Israel E
Mauger D
Koppelman GH
Postma DS
Nieuwenhuis MA
Vonk JM
Lima JJ
Irvin CG
Peters SP
Kubo M
Tamari M
Nakamura Y
Litonjua AA
Tantisira KG
Raby BA
Bleecker ER
Meyers DA
London SJ
Barnes KC
Gilliland FD
Williams LK
Burchard EG
Nicolae DL
Ober C
DeMeo DL
Silverman EK
Paigen B
Churchill G
Shapiro SD
Weiss ST
Pokaż więcej
Źródło:
PloS one [PLoS One] 2013; Vol. 8 (2), pp. e56179. Date of Electronic Publication: 2013 Feb 14.
Typ publikacji:
Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Asthma/*genetics
Kv Channel-Interacting Proteins/*genetics
Animals ; Base Sequence ; Female ; Genome-Wide Association Study ; Genotype ; Humans ; Male ; Mice ; Phenotype
Czasopismo naukowe

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies