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Wyświetlanie 1-18 z 18
Tytuł :
Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features.
Autorzy :
Al-Ali AK; Alomran Scientific Chair, King Faisal University, Al-Ahsa, Saudi Arabia.; Department of Clinical Biochemistry, College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, Saudi Arabia.
Alsulaiman A; Alomran Scientific Chair, King Faisal University, Al-Ahsa, Saudi Arabia.; Department of Internal Medicine, King Fahd Hospital, Al-Ahsa, Saudi Arabia.
Alfarhan M; Alomran Scientific Chair, King Faisal University, Al-Ahsa, Saudi Arabia.; Department of Orthopedic Surgery, College of Medicine, King Faisal University, Al-Ahsa, Saudi Arabia.
Safaya S; Alomran Scientific Chair, King Faisal University, Al-Ahsa, Saudi Arabia.
Vatte CB; Department of Clinical Biochemistry, College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, Saudi Arabia.
Albuali WM; Alomran Scientific Chair, King Faisal University, Al-Ahsa, Saudi Arabia.
Qutub HO; Alomran Scientific Chair, King Faisal University, Al-Ahsa, Saudi Arabia.
Alzahrani AJ; Department of Applied Medical Sciences, University of Hafre Al Batin, Saudi Arabia.
Milton JN; Department of Statistics, Boston University School of Public Health, Boston, Massachusetts.
Steinberg MH; Department of Medicine, Center of Excellence in Sickle Cell Disease, Boston University and Boston Medical Center, Boston, Massachusetts.
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Źródło :
American journal of hematology [Am J Hematol] 2021 Apr 01; Vol. 96 (4), pp. E117-E121. Date of Electronic Publication: 2021 Jan 28.
Typ publikacji :
Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Anemia, Sickle Cell/*epidemiology
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Anemia, Sickle Cell/blood ; Anemia, Sickle Cell/genetics ; Child ; Child, Preschool ; Female ; Fetal Hemoglobin/analysis ; Haplotypes/genetics ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Saudi Arabia/epidemiology ; Sickle Cell Trait/epidemiology ; Sickle Cell Trait/genetics ; Tanzania/epidemiology ; Young Adult ; alpha-Globins/genetics ; alpha-Thalassemia/epidemiology ; alpha-Thalassemia/genetics ; beta-Globins/genetics
Raport
Tytuł :
Haemolysis in sickle cell anaemia: effects of polymorphisms in α-globin gene regulatory elements.
Autorzy :
Milton JN; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
Shaikho EM; Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
Steinberg MH; Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
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Źródło :
British journal of haematology [Br J Haematol] 2019 Jul; Vol. 186 (2), pp. 363-364. Date of Electronic Publication: 2019 Mar 10.
Typ publikacji :
Letter; Research Support, N.I.H., Extramural
MeSH Terms :
Anemia, Sickle Cell/*genetics
Hemolysis/*genetics
Polymorphism, Genetic/*genetics
alpha-Globins/*genetics
beta-Thalassemia/*genetics
Anemia, Hemolytic/genetics ; Down-Regulation/genetics ; Hemoglobin, Sickle/genetics ; Humans ; Up-Regulation/genetics
Raport
Tytuł :
Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.
Autorzy :
Chaturvedi S; Division of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Bhatnagar P; McKusick-Nathans Institute of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD.
Bean CJ; Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA.
Steinberg MH; Department of Medicine.; Department of Pediatrics, and.; Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA.
Milton JN; Department of Biostatistics, Boston University School of Public Health, Boston, MA.
Casella JF; Division of Pediatric Hematology, Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, MD; and.
Barron-Casella E; Division of Pediatric Hematology, Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, MD; and.
Arking DE; McKusick-Nathans Institute of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD.
DeBaun MR; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN.
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Źródło :
Blood [Blood] 2017 Aug 03; Vol. 130 (5), pp. 686-688. Date of Electronic Publication: 2017 Jun 05.
Typ publikacji :
Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Epistasis, Genetic*
Genetic Variation*
Polymorphism, Single Nucleotide*
Acute Pain/*etiology
Anemia, Sickle Cell/*complications
Arterial Occlusive Diseases/*etiology
Chromosomes, Human, Pair 4/*genetics
Adolescent ; African Continental Ancestry Group ; Anemia, Sickle Cell/blood ; Anemia, Sickle Cell/genetics ; Child ; Child, Preschool ; Female ; Fetal Hemoglobin/analysis ; Genome-Wide Association Study ; Genotyping Techniques ; Humans ; Male ; Multicenter Studies as Topic ; Prospective Studies
Raport
Tytuł :
Genetic modulation of fetal hemoglobin in hydroxyurea-treated sickle cell anemia.
Autorzy :
Aleluia MM; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
Santiago RP; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
da Guarda CC; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
Fonseca TC; Centro de Referência a Doença Falciforme de Itabuna, Itabuna, Bahia, Brasil.
Neves FI; Centro de Referência a Doença Falciforme de Itabuna, Itabuna, Bahia, Brasil.
Quinto RS; Centro de Referência a Doença Falciforme de Itabuna, Itabuna, Bahia, Brasil.
Figueiredo CV; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
Yahouédéhou SC; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
Oliveira RM; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
Ferreira JR; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
Cerqueira BA; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.; Universidade Estadual da Bahia (UNEB), Salvador, Bahia, Brasil.
Barbosa CG; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
Milton JN; Boston University School of Public Health, Boston, Massachusetts, USA.
Steinberg MH; Boston University School of Medicine, Boston, Massachusetts, USA.
de Souza Gonçalves M; Laboratório de Hematologia e Genética Computacional, Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Bahia, Brasil.; Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brasil.
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Źródło :
American journal of hematology [Am J Hematol] 2017 May; Vol. 92 (5), pp. E70-E72. Date of Electronic Publication: 2017 Mar 10.
Typ publikacji :
Letter
MeSH Terms :
Anemia, Sickle Cell*/blood
Anemia, Sickle Cell*/drug therapy
Anemia, Sickle Cell*/genetics
Fetal Hemoglobin*/genetics
Fetal Hemoglobin*/metabolism
Chromosomes, Human, Pair 11/*genetics
Chromosomes, Human, Pair 2/*genetics
Hydroxyurea/*administration & dosage
Adolescent ; Adult ; Child ; Child, Preschool ; Female ; Genome-Wide Association Study ; Humans ; Male
Opinia redakcyjna
Tytuł :
Ear biometrics for patient identification in global health: a cross-sectional study to test the feasibility of a simplified algorithm.
Autorzy :
Ragan EJ; Department of Global Health, Boston University School of Public Health, Boston, MA, USA.; Center for Global Health and Development, Boston University School of Public Health, Boston, MA, USA.
Johnson C; Department of Global Health, Boston University School of Public Health, Boston, MA, USA.
Milton JN; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
Gill CJ; Department of Global Health, Boston University School of Public Health, Boston, MA, USA. .; Center for Global Health and Development, Boston University School of Public Health, Boston, MA, USA. .
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Źródło :
BMC research notes [BMC Res Notes] 2016 Nov 02; Vol. 9 (1), pp. 484. Date of Electronic Publication: 2016 Nov 02.
Typ publikacji :
Journal Article
MeSH Terms :
Algorithms*
Biometric Identification/*methods
Ear/*anatomy & histology
Patient Identification Systems/*methods
Adult ; African Continental Ancestry Group ; Aged ; Cross-Sectional Studies ; Developing Countries ; European Continental Ancestry Group ; Global Health ; Humans ; Middle Aged ; Principal Component Analysis
Czasopismo naukowe
Tytuł :
Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.
Autorzy :
Vathipadiekal V; Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Alsultan A; Sickle Cell Disease Research Center and Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Baltrusaitis K; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Farrell JJ; Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Al-Rubaish AM; Department of Internal Medicine, College of Medicine, University of Dammam, Dammam, Kingdom of Saudi Arabia.
Al-Muhanna F; Department of Internal Medicine, College of Medicine, University of Dammam, Dammam, Kingdom of Saudi Arabia.
Naserullah Z; Alomran Scientific Chair for Hematological Diseases, King Faisal University, King Faisal University, King Fahd Hospital, Hafof, Al-Ahsa, Kingdom of Saudi Arabia.; Department of Pediatrics, Maternity & Child Hospital, Dammam, Kingdom of Saudi Arabia.
Suliman A; Alomran Scientific Chair, King Faisal University, King Fahd Hospital, Hafof, Al-Ahsa, Kingdom of Saudi Arabia.
Patra PK; Department of Biochemistry, Pt. J.N.M. Medical College, Raipur, Chhattisgarh, India.
Milton JN; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Farrer LA; Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Chui DH; Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Al-Ali AK; Center for Research & Medical Consultation, University of Dammam, Dammam, Saudi Arabia.
Sebastiani P; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Steinberg MH; Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.
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Źródło :
American journal of hematology [Am J Hematol] 2016 Jun; Vol. 91 (6), pp. E308-11. Date of Electronic Publication: 2016 Apr 28.
Typ publikacji :
Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Anemia, Sickle Cell/*genetics
Arabs/*genetics
Fetal Hemoglobin/*genetics
gamma-Globins/*genetics
Adolescent ; Adult ; Anemia, Sickle Cell/blood ; Genome-Wide Association Study ; Haplotypes ; Homozygote ; Humans ; Polymorphism, Single Nucleotide ; Young Adult
Raport
Tytuł :
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.
Autorzy :
Sebastiani P; Department of Biostatistics, Boston University School of Public Health, Boston, MA, United States. Electronic address: .
Farrell JJ; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Alsultan A; Sickle Cell Disease Research Center and Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Wang S; Department of Biostatistics, Boston University School of Public Health, Boston, MA, United States.
Edward HL; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Shappell H; Department of Biostatistics, Boston University School of Public Health, Boston, MA, United States.
Bae H; College of Public Health and Human Sciences, Oregon State University, Corvallis, OR, United States.
Milton JN; Department of Biostatistics, Boston University School of Public Health, Boston, MA, United States.
Baldwin CT; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Al-Rubaish AM; Department of Internal Medicine, College of Medicine, University of Dammam, Dammam, Saudi Arabia.
Naserullah Z; Department of Pediatrics, Maternity & Child Hospital, Dammam, Saudi Arabia.
Al-Muhanna F; Department of Internal Medicine, College of Medicine, University of Dammam, Dammam, Saudi Arabia.
Alsuliman A; Department of Hematology, King Fahd Hospital, Hafof, Al-Ahsa, Saudi Arabia.
Patra PK; Deptartment of Biochemistry, Pt. J.N.M. Medical College, Raipur, Chattisgarh, India.
Farrer LA; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Ngo D; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Vathipadiekal V; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Chui DH; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Al-Ali AK; Prince Mohammed Center for Research & Consultation Studies, University of Dammam, Dammam, Saudi Arabia.
Steinberg MH; Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
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Źródło :
Blood cells, molecules & diseases [Blood Cells Mol Dis] 2015 Mar; Vol. 54 (3), pp. 224-30. Date of Electronic Publication: 2015 Jan 30.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Polymorphism, Single Nucleotide*
Anemia, Sickle Cell/*genetics
Carrier Proteins/*genetics
Fetal Hemoglobin/*genetics
Nuclear Proteins/*genetics
Adolescent ; Adult ; African Americans/genetics ; Arabs/genetics ; Asian Continental Ancestry Group/genetics ; Child ; Female ; Genotype ; Haplotypes ; Humans ; Male ; Middle Aged ; Repressor Proteins ; Young Adult
Czasopismo naukowe
Tytuł :
Evaluation of an ensemble of genetic models for prediction of a quantitative trait.
Autorzy :
Milton JN; Department of Biostatistics, School of Public Health, Boston University Boston, MA, USA.
Steinberg MH; Department of Medicine, School of Medicine, Boston University Boston, MA, USA.
Sebastiani P; Department of Biostatistics, School of Public Health, Boston University Boston, MA, USA.
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Źródło :
Frontiers in genetics [Front Genet] 2015 Jan 13; Vol. 5, pp. 474. Date of Electronic Publication: 2015 Jan 13 (Print Publication: 2014).
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Rare genetic variant analysis on blood pressure in related samples.
Autorzy :
Chen H; Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston, MA 02118, USA.
Choi SH; Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston, MA 02118, USA.
Hong J; Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston, MA 02118, USA.
Lu C; Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston, MA 02118, USA.
Milton JN; Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston, MA 02118, USA.
Allard C; Département de Mathématiques, Université de Sherbrooke, 2500 Boulevard de l'Université, Sherbrooke, QC J1K 2R1, Canada.
Lacey SM; Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston, MA 02118, USA.
Lin H; Department of Medicine, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA.
Dupuis J; Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston, MA 02118, USA.
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Źródło :
BMC proceedings [BMC Proc] 2014 Jun 17; Vol. 8 (Suppl 1), pp. S35. Date of Electronic Publication: 2014 Jun 17 (Print Publication: 2014).
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models.
Autorzy :
Milton JN; Department of Biostatistics, Boston University School of Public Health, Boston, MA.
Gordeuk VR
Taylor JG 6th
Gladwin MT
Steinberg MH
Sebastiani P
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Źródło :
Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2014 Apr; Vol. 7 (2), pp. 110-5. Date of Electronic Publication: 2014 Mar 01.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Anemia, Sickle Cell/*genetics
Fetal Hemoglobin/*genetics
Adolescent ; Anemia, Sickle Cell/diagnosis ; Anemia, Sickle Cell/metabolism ; Child ; Child, Preschool ; Cohort Studies ; Female ; Fetal Hemoglobin/metabolism ; Genetic Variation ; Humans ; Male ; Middle Aged ; Models, Genetic ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł :
Genetic modulation of HbF in Brazilians with HbSC disease and sickle cell anemia.
Autorzy :
Barbosa CG; Faculdade de Farmácia, Universidade Federal da Bahia, Salvador-BA, Brasil.
Aleluia AC
Pacheco AP
Paz SS
Zanette AM
Lyra IM
Steinberg MH
Milton JN
Goncalves MS
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Źródło :
American journal of hematology [Am J Hematol] 2013 Oct; Vol. 88 (10), pp. 923-4. Date of Electronic Publication: 2013 Sep 03.
Typ publikacji :
Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Polymorphism, Single Nucleotide*
Anemia, Sickle Cell/*genetics
Fetal Hemoglobin/*genetics
Hemoglobin SC Disease/*genetics
Brazil ; Chromosomes, Human/genetics ; Female ; Haplotypes/genetics ; Humans ; Male
Raport
Tytuł :
Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.
Autorzy :
Bhatnagar P; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Barron-Casella E
Bean CJ
Milton JN
Baldwin CT
Steinberg MH
Debaun M
Casella JF
Arking DE
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Źródło :
PloS one [PLoS One] 2013 Sep 13; Vol. 8 (9), pp. e74193. Date of Electronic Publication: 2013 Sep 13 (Print Publication: 2013).
Typ publikacji :
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural
MeSH Terms :
Blood Pressure*
Genetic Predisposition to Disease*
Polymorphism, Single Nucleotide*
Anemia, Sickle Cell/*genetics
Cerebral Infarction/*genetics
Hypertension/*genetics
Adolescent ; African Americans ; Anemia, Sickle Cell/complications ; Anemia, Sickle Cell/ethnology ; Anemia, Sickle Cell/physiopathology ; Cerebral Infarction/ethnology ; Cerebral Infarction/etiology ; Cerebral Infarction/physiopathology ; Child ; Female ; Genetic Loci ; Genome-Wide Association Study ; Humans ; Hypertension/complications ; Hypertension/ethnology ; Hypertension/physiopathology ; Male ; Phenotype ; Risk Factors
Czasopismo naukowe
Tytuł :
Genetic determinants of haemolysis in sickle cell anaemia.
Autorzy :
Milton JN; Biostatistics, Boston University School of Medicine, 72 E. Concord St., Boston, MA 02118, USA.
Rooks H
Drasar E
McCabe EL
Baldwin CT
Melista E
Gordeuk VR
Nouraie M
Kato GR
Minniti C
Taylor J
Campbell A
Luchtman-Jones L
Rana S
Castro O
Zhang Y
Thein SL
Sebastiani P
Gladwin MT
Steinberg MH
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Corporate Authors :
Walk-PHAAST Investigators
Źródło :
British journal of haematology [Br J Haematol] 2013 Apr; Vol. 161 (2), pp. 270-8. Date of Electronic Publication: 2013 Feb 14.
Typ publikacji :
Clinical Trial; Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Alleles*
Genetic Loci*
Polymorphism, Single Nucleotide*
Response Elements*
Anemia, Sickle Cell/*genetics
Hemolysis/*genetics
Nuclear Proteins/*genetics
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Anemia, Sickle Cell/metabolism ; Child ; Cohort Studies ; Female ; GTPase-Activating Proteins ; Glycated Hemoglobin A/genetics ; Glycated Hemoglobin A/metabolism ; Hemoglobins, Abnormal/genetics ; Hemoglobins, Abnormal/metabolism ; Humans ; Introns/genetics ; Linkage Disequilibrium ; Male ; Middle Aged ; Nuclear Proteins/metabolism
Czasopismo naukowe
Tytuł :
Whole genome sequences of a male and female supercentenarian, ages greater than 114 years.
Autorzy :
Sebastiani P; Department of Biostatistics, Boston University School of Public Health Boston, MA, USA.
Riva A
Montano M
Pham P
Torkamani A
Scherba E
Benson G
Milton JN
Baldwin CT
Andersen S
Schork NJ
Steinberg MH
Perls TT
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Źródło :
Frontiers in genetics [Front Genet] 2012 Jan 03; Vol. 2, pp. 90. Date of Electronic Publication: 2012 Jan 03 (Print Publication: 2011).
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Autorzy :
Milton JN; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, United States of America.
Sebastiani P
Solovieff N
Hartley SW
Bhatnagar P
Arking DE
Dworkis DA
Casella JF
Barron-Casella E
Bean CJ
Hooper WC
DeBaun MR
Garrett ME
Soldano K
Telen MJ
Ashley-Koch A
Gladwin MT
Baldwin CT
Steinberg MH
Klings ES
Pokaż więcej
Źródło :
PloS one [PLoS One] 2012; Vol. 7 (4), pp. e34741. Date of Electronic Publication: 2012 Apr 27.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
African Americans/*genetics
Anemia, Sickle Cell/*complications
Anemia, Sickle Cell/*genetics
Bilirubin/*blood
Cholelithiasis/*blood
Cholelithiasis/*etiology
Glucuronosyltransferase/*genetics
Anemia, Sickle Cell/blood ; Bilirubin/genetics ; Cohort Studies ; Genome-Wide Association Study ; Genotype ; Humans ; Inheritance Patterns/genetics ; Isoenzymes/genetics ; Polymorphism, Single Nucleotide/genetics ; Principal Component Analysis ; Risk Factors
Czasopismo naukowe
Tytuł :
Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1.
Autorzy :
Dworkis DA; Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Klings ES
Solovieff N
Li G
Milton JN
Hartley SW
Melista E
Parente J
Sebastiani P
Steinberg MH
Baldwin CT
Pokaż więcej
Źródło :
American journal of hematology [Am J Hematol] 2011 Feb; Vol. 86 (2), pp. 220-3.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Anemia, Sickle Cell/*blood
Anemia, Sickle Cell/*physiopathology
Receptors, Tumor Necrosis Factor, Type I/*blood
Vascular Cell Adhesion Molecule-1/*blood
Adult ; Anemia, Sickle Cell/genetics ; Biomarkers/blood ; Female ; Genome-Wide Association Study ; Guanine Nucleotide Exchange Factors/genetics ; Humans ; Introns ; Male ; Polymorphism, Single Nucleotide ; Promoter Regions, Genetic ; Severity of Illness Index ; United States ; Vascular Cell Adhesion Molecule-1/genetics
Czasopismo naukowe
Tytuł :
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
Autorzy :
Solovieff N; Department of Biostatistics, Boston University School of Public Health, MA, USA.
Milton JN
Hartley SW
Sherva R
Sebastiani P
Dworkis DA
Klings ES
Farrer LA
Garrett ME
Ashley-Koch A
Telen MJ
Fucharoen S
Ha SY
Li CK
Chui DH
Baldwin CT
Steinberg MH
Pokaż więcej
Źródło :
Blood [Blood] 2010 Mar 04; Vol. 115 (9), pp. 1815-22. Date of Electronic Publication: 2009 Dec 16.
Typ publikacji :
Journal Article; Multicenter Study; Research Support, N.I.H., Extramural
MeSH Terms :
Multigene Family*
Polymorphism, Single Nucleotide*
Anemia, Sickle Cell/*blood
Anemia, Sickle Cell/*genetics
Fetal Hemoglobin/*genetics
Fetal Hemoglobin/*metabolism
Receptors, Odorant/*genetics
Adolescent ; Adult ; African Americans/genetics ; Carrier Proteins/genetics ; Child ; Child, Preschool ; Chromosomes, Human, Pair 11/genetics ; Chromosomes, Human, X/genetics ; Female ; Genome-Wide Association Study ; Hemoglobin E/genetics ; Hong Kong ; Humans ; Male ; Nuclear Proteins/genetics ; Regulatory Sequences, Nucleic Acid ; Repressor Proteins ; Thailand ; Young Adult ; beta-Thalassemia/genetics
Czasopismo naukowe
Tytuł :
Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study.
Autorzy :
Sebastiani P; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA. />Solovieff N
Hartley SW
Milton JN
Riva A
Dworkis DA
Melista E
Klings ES
Garrett ME
Telen MJ
Ashley-Koch A
Baldwin CT
Steinberg MH
Pokaż więcej
Źródło :
American journal of hematology [Am J Hematol] 2010 Jan; Vol. 85 (1), pp. 29-35.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Phenotype*
Polymorphism, Single Nucleotide*
Anemia, Sickle Cell/*complications
Anemia, Sickle Cell/*genetics
Adolescent ; Adult ; Anemia, Sickle Cell/physiopathology ; Child ; Complement C8/genetics ; Computational Biology ; Genome-Wide Association Study ; Humans ; MAP Kinase Kinase Kinases/genetics ; Middle Aged ; Potassium Channels, Tandem Pore Domain/genetics ; Severity of Illness Index ; Tankyrases/genetics ; Young Adult
Czasopismo naukowe
    Wyświetlanie 1-18 z 18

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