A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. - Wikidata - awgldk - TriplyDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

http://www.wikidata.org/entity/Q34256214

about

Genomic approaches to identifying targets for treating β hemoglobinopathies Genetics of human metabolism: an update The genetics of complex cholestatic disorders Genetic determinants of haemolysis in sickle cell anaemia.Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene Combined effects of smoking and bilirubin levels on the risk of lung cancer in Korea: the severance cohort study Genetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liver NRMT1 knockout mice exhibit phenotypes associated with impaired DNA repair and premature aging.Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.Genetic modifiers of sickle cell disease Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction.Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognostication.Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.Applications of high-throughput DNA sequencing to benign hematology The search for genetic modifiers of disease severity in the β-hemoglobinopathies.Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.Emerging point-of-care technologies for sickle cell disease screening and monitoring.UGT1A1 (TA)n genotype is not the major risk factor of cholelithiasis in sickle cell disease children.Multiple Testing in the Context of Gene Discovery in Sickle Cell Disease Using Genome-Wide Association Studies.UGT1A1 gene linkage analysis: application of polymorphic markers rs4148326/rs4124874 in the Iranian population.Comment on "Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia".Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease.Is there a role for pharmacogenetics in the treatment of sickle cell disease?Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?

P2860

Q26799214-00CCEB82-0FA6-4B66-B304-20FFADB655B0 Q26992154-4538D99D-6DE2-42FE-B34B-3B103A9C89E5 Q26992279-7216D799-67BA-4727-A1BA-3837C12FD102 Q29417116-D7E7C623-F213-440E-A617-E7FB07EA4351 Q30448607-4FF2949A-3002-4912-A6F7-7C59FE37E557 Q34011326-0669D234-3D42-448E-B58E-4C4DD2A6527C Q34211851-DF1912F8-A9A7-4D73-8C90-C11E3F5DF3BF Q34470316-5BDA0FD3-7011-465B-B709-4B003BC7726E Q35565624-72C8ED68-5594-4D9A-ADC3-2677AC1C475A Q36035471-858DD9FD-29C9-4344-87E7-73379F86B788 Q36193715-5FC6FD43-54E0-42C9-8C0D-2F21A9301E17 Q36224628-C0960C3A-0325-4876-85EC-F3A56316388C Q36913577-4E91E560-6B9C-4456-9EBD-E3E7E0E5ADDA Q37026772-FCFA6E79-8B25-473E-B626-15D7F6950EA6 Q37334703-14931F55-DD31-4B33-A2EA-26A83BF5ABB8 Q38048766-7972FEB4-DA02-4482-B52D-D6621A0E3547 Q38758451-CDC1E568-59FC-4CA4-995F-A9EDE8904E23 Q38804432-73642D04-5FFA-4C11-A72A-DD46C33AC302 Q40422332-4187FBEE-644C-4F98-8A2A-A48BE2A83514 Q41232448-1E7EFCBC-974E-445D-9B98-856B7140D8CA Q43122090-9B44F9C3-4466-46FF-A427-0D66349204AB Q43133996-D59C630F-37AE-44AE-8593-1343C783C89A Q50061134-F89CE1ED-44D7-4513-8126-763B50DD999C Q52785790-33D73674-C493-4E29-80F1-1140FC9EAADA Q54117269-868D7757-09B5-4EDB-95FE-32040D22B14E

P2860

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

http://www.wikidata.org/entity/Q34256214

description

2012 nî lūn-bûn

@nan

2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

A genome-wide association stud ...... is risk in sickle cell anemia.

@ast

A genome-wide association stud ...... is risk in sickle cell anemia.

@en

A genome-wide association stud ...... is risk in sickle cell anemia.

@nl

type

label

A genome-wide association stud ...... is risk in sickle cell anemia.

@ast

A genome-wide association stud ...... is risk in sickle cell anemia.

@en

A genome-wide association stud ...... is risk in sickle cell anemia.

@nl

prefLabel

A genome-wide association stud ...... is risk in sickle cell anemia.

@ast

A genome-wide association stud ...... is risk in sickle cell anemia.

@en

A genome-wide association stud ...... is risk in sickle cell anemia.

@nl

P1433

Q34256214-AA3B0104-8380-4D3A-905D-83B9CB567D34

P1476

Q34256214-898AE82B-D6B2-4475-AB5E-E4C8625F75BB

P2093

Q34256214-035B8164-6176-4326-8911-1C68A606D0FF

Q34256214-03FAFC3F-00B7-4D98-9FE0-B8DBA76CA389

Q34256214-19966912-4DB2-403D-849B-2A3EB295FBCD

Q34256214-1E92109A-249A-46FD-A5D8-CC8BF87C5D0C

Q34256214-23647154-516C-4C97-8503-403442DB6695

Q34256214-3A2C7FE7-0460-485D-BA7F-14B5C763886A

Q34256214-7D719105-D93E-4516-885E-912B8FBD003E

Q34256214-8E2AF8CF-F927-4CB4-8A59-E4B7AC353607

Q34256214-A1B888F3-73E6-460E-8F4F-86AF495A8FD0

Q34256214-B066762D-2056-4A4C-92DB-29B52970EEB6

P2860

Q34256214-0F6E3881-6DF2-45D8-B184-EB1578500241

Q34256214-142E1C3D-B368-4352-B1A6-73F32A6B9F80

Q34256214-208CFDE0-F591-4AC2-A5ED-F1141C1AB7DF

Q34256214-252F3F44-ADC5-4A7A-9FDE-2CFF04D8D0F4

Q34256214-2532F09C-D6F2-4A1E-B871-186170F0B5B6

Q34256214-26DA07B7-D08C-46BE-A01B-365D8CB34A33

Q34256214-33592B33-B628-40A5-8AFD-137FB5EFBD77

Q34256214-340A8728-0080-4766-AB4E-89003CB6CE0C

Q34256214-3A56E706-848F-4677-A471-F71D3A9D65F3

Q34256214-3ADE943D-96B3-4A87-A33F-8751A6162B29

P304

Q34256214-87968905-43A2-48F8-ACCC-E04F3FC111AD

P31

Q34256214-9B65C664-65D7-419A-B950-C1B9CBC40E4D

P356

Q34256214-559AFB30-F1EB-4AD7-B52D-DD0C214E813F

P407

Q34256214-F01F74C9-E219-4441-9AD0-D17DA4D2B5C5

P433

Q34256214-67A3F2A6-F07E-48B1-B6D1-59729CE81D9F

P478

Q34256214-813BB7E6-4404-4D8D-9D02-831734EE0C11

P50

Q34256214-0A035BC4-9A71-48AE-BC2F-A879221090F9

Q34256214-1AB05724-B8E4-422E-8406-9762668449DA

Q34256214-37B35A2D-FC3E-48B9-93C6-40B4325060A9

Q34256214-46E7DD21-45D2-449C-9405-2F745C985EB3

Q34256214-4C45401E-52CD-4FC6-AD20-0879EB924E95

Q34256214-58F4F544-3B8B-41A6-ABFC-D33D7E766855

Q34256214-D72DD5D9-70F6-45FB-B82F-1D4A2F7F3C50

P577

Q34256214-7D1A11A2-C210-4275-8EA7-9299C2C3DFD4

P5875

Q34256214-32B484B0-7552-475A-8CD4-80435C042BCA

P698

Q34256214-0B3BC2E7-E7E2-428C-A9B4-20A34847BF91

P921

Q34256214-0B909EA8-C0A3-45E8-B52D-79C5EB62E268

Q34256214-C070719C-A00A-4690-A5C0-BC2D8B8279C0

Q34256214-FAC897D4-9C27-47FB-A0AC-0627C484577B

P932

Q34256214-A8EF6636-E9E2-4838-AB23-22E1BB269B17

P356

JOURNAL.PONE.0034741

P1433

P1476

A genome-wide association stud ...... is risk in sickle cell anemia.

@en

P2093

Christopher J Bean

http://www.w3.org/2001/XMLSchema#string

Dan E Arking

http://www.w3.org/2001/XMLSchema#string

Emily Barron-Casella

http://www.w3.org/2001/XMLSchema#string

Jacqueline N Milton

http://www.w3.org/2001/XMLSchema#string

James F Casella

http://www.w3.org/2001/XMLSchema#string

Karen Soldano

http://www.w3.org/2001/XMLSchema#string

Marilyn J Telen

http://www.w3.org/2001/XMLSchema#string

Melanie E Garrett

http://www.w3.org/2001/XMLSchema#string

Michael R DeBaun

http://www.w3.org/2001/XMLSchema#string

Nadia Solovieff

http://www.w3.org/2001/XMLSchema#string

P2860

Genome-wide association with select biomarker traits in the Framingham Heart Study

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia

Genome-wide association meta-analysis for total serum bilirubin levels

Principal components analysis corrects for stratification in genome-wide association studies

Expression of the UDP-glucuronosyltransferase 1A locus in human colon. Identification and characterization of the novel extrahepatic UGT1A8

The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.

Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain

ProbABEL package for genome-wide association analysis of imputed data.

Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene.

P304

e34741

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0034741

http://www.w3.org/2001/XMLSchema#string

P407

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

7

http://www.w3.org/2001/XMLSchema#string

P50

Allison Ashley-Koch

Clinton Baldwin

Martin H Steinberg

Daniel A Dworkis

Elizabeth S Klings

Paola Sebastiani

P577

2012-04-27T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

224899324

http://www.w3.org/2001/XMLSchema#string

P698

22558097

http://www.w3.org/2001/XMLSchema#string

P921

genome-wide association study

sickle-cell disease

P932

3338756

http://www.w3.org/2001/XMLSchema#string