The sequence and analysis of duplication-rich human chromosome 16
about
DNA sequence and analysis of human chromosome 18DNA sequence and analysis of human chromosome 8Individualization of treatments with drugs metabolized by CES1: combining genetics and metabolomics.Further delineation of a rare recessive encephalomyopathy linked to mutations in GFER thanks to data sharing of whole exome sequencing data.Chromosomal evolution of the PKD1 gene family in primates.A computational method for prediction of matrix proteins in endogenous retroviruses.Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.Regional regulation of transcription in the bovine genome.Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16.A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease riskMolecular diagnostics for autosomal dominant polycystic kidney diseaseEvidence for widespread reticulate evolution within human dupliconsIdentification of polymorphic inversions from genotypes.Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.Phenotypic manifestations of copy number variation in chromosome 16p13.11.ECHO: a reference-free short-read error correction algorithm.Validation and genotyping of multiple human polymorphic inversions mediated by inverted repeats reveals a high degree of recurrence.Recurrent duplication-driven transposition of DNA during hominoid evolution.Familial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrierHuman inversions and their functional consequencesEvolutionary change--patterns and processes.Genetic contribution and associated pathophysiology in end-stage renal diseaseUsing population admixture to help complete maps of the human genome.Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.A common 16p11.2 inversion underlies the joint susceptibility to asthma and obesity.InvFEST, a database integrating information of polymorphic inversions in the human genome.Quantitation of human metallothionein isoforms: a family of small, highly conserved, cysteine-rich proteins.Something silent this way forms: the functional organization of the repressive nuclear compartment.Copy number variants: a new molecular frontier in clinical psychiatry.Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes.Clinical utility gene card for: 16p13.11 microdeletion syndromeGenotype-based gene signature of glioma risk.Xenobiotic/medium chain fatty acid: CoA ligase - a critical review on its role in fatty acid metabolism and the detoxification of benzoic acid and aspirin.Detailed analysis of inversions predicted between two human genomes: errors, real polymorphisms, and their origin and population distribution.Molecular diagnosis of autosomal dominant polycystic kidney disease.Tandem repeats modify the structure of human genes hosted in segmental duplications.Ancient duplicated conserved noncoding elements in vertebrates: a genomic and functional analysis.Human SULT1A1 gene: copy number differences and functional implications.Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review.Mutations of N-Methyl-D-Aspartate Receptor Subunits in Epilepsy.
P2860
Q28273560-2095BE74-A120-4EBA-8DD0-CE1D9A64D6E2Q28292530-2634C45B-F897-4C34-AAC4-0AFFD3E14367Q30373969-EC543035-0FEF-4FDB-817B-A801E0C53B6CQ31159196-39CB97F4-1F89-4AF7-BE5E-B16F6382C4A4Q33372432-A9E49ABD-9F93-4788-A5D6-A13A8A4D8E0EQ33637668-B8E3E3AF-24D4-4F30-A022-ADFE1A275D60Q33741872-B9B4F4B4-6BE2-40F4-AE6E-1B642688CD58Q33932915-9592C653-A7B2-46BE-8372-6F4F60973992Q33942582-1595CBE1-3829-4BBF-8164-56007084400CQ34091599-CE59C65F-0B81-45C8-8D0F-4D345652A906Q34100184-2D763753-5D9A-4F4E-A565-97E5C0F226B5Q34106726-1EAB41E3-3E5A-4155-B6CB-34B30F0B2FF2Q34155398-A154506B-95CC-4629-B28D-74ECAE7F78BDQ34700227-671C5522-22B2-46C7-9B90-135A4804376CQ34705135-B2B28F46-D1FC-408E-87A0-1C53555032B5Q35085300-2137EBCB-59E2-46AA-AACE-B861005BF0DEQ35126612-8836C727-BC5F-4D77-964F-977ECB2A40BFQ35214947-AD0DFB93-F998-4F05-8766-6A5FE261B361Q35379284-3C3A345B-0255-400E-8677-D7A0E2D7CCB7Q36077972-3C1F806D-F639-465A-9A8E-4DB00BF40C2AQ36338119-8196168C-3DDC-43DE-9C33-0E9CA3BEB374Q36925161-6A972BD7-641D-40E8-89B5-C9285F30068EQ36932681-4A0816E8-95FC-4698-B487-78D4EB96063AQ37135729-F3313E90-A32B-4D13-9452-06EF5DFE31CFQ37634115-F6804496-ABD7-492E-B9B0-61166BD5FE21Q37662023-371765B4-5B09-4C8C-B4A2-A1CB77411126Q37687411-E91AC625-C3DD-4F5A-95EF-20CADB895F0FQ37723762-A799FBBA-757D-40C0-8264-65488DBB35A2Q37831223-FF7622EF-306D-4A54-B526-BB6340E36514Q38576674-8203BBA0-A769-4117-A254-02B2AED46334Q38839935-92855151-CD4F-49C2-832F-CEF086BBF523Q38878860-320BA24F-3D13-4F64-B8AE-520CD0E63D5AQ38879491-B8B99CF9-6470-4F10-874B-FBC3D8BA154DQ39063310-36CD5CF1-CE22-4D06-82E6-44D0F7FC8F6AQ39445724-7F89492D-5102-4109-BEFB-7095CC8D87B9Q41848828-D0080BEA-C89E-4235-9261-5B50AAB6EF33Q42274741-58FFED74-C10B-477A-8304-8833AC48A814Q46307374-8CF6ECF5-466F-47E9-AB1F-31B1DA082B73Q47102023-71B5D512-B1F8-4764-8E08-21152C191566Q47619589-1B49A1D0-5166-47F1-81D5-EE70EC320F8E
P2860
The sequence and analysis of duplication-rich human chromosome 16
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
The sequence and analysis of duplication-rich human chromosome 16
@ast
The sequence and analysis of duplication-rich human chromosome 16
@en
The sequence and analysis of duplication-rich human chromosome 16
@en-gb
The sequence and analysis of duplication-rich human chromosome 16
@nl
type
label
The sequence and analysis of duplication-rich human chromosome 16
@ast
The sequence and analysis of duplication-rich human chromosome 16
@en
The sequence and analysis of duplication-rich human chromosome 16
@en-gb
The sequence and analysis of duplication-rich human chromosome 16
@nl
prefLabel
The sequence and analysis of duplication-rich human chromosome 16
@ast
The sequence and analysis of duplication-rich human chromosome 16
@en
The sequence and analysis of duplication-rich human chromosome 16
@en-gb
The sequence and analysis of duplication-rich human chromosome 16
@nl
P2093
P2860
P50
P921
P356
P1433
P1476
The sequence and analysis of duplication-rich human chromosome 16
@en
P2093
A Christine Munk
Albert L Williams
Alex Rodriguez
Andrea Aerts
Anna Ustaszewska
Arthur Kobayashi
Astrid Terry
Beverly Parson-Quintana
Carl E Hildebrand
Chenier Caoile
P2860
P2888
P304
P356
10.1038/NATURE03187
P407
P50
P577
2004-12-23T00:00:00Z
P5875
P6179
1036253344