Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q
about
Finishing the euchromatic sequence of the human genomeIdentification of a cytokine-induced antiapoptotic molecule anamorsin essential for definitive hematopoiesisThe sequence and analysis of duplication-rich human chromosome 16Complex genomic rearrangements lead to novel primate gene functionCloning of a type I cytokine receptor most related to the IL-2 receptor beta chainGGAs: a family of ADP ribosylation factor-binding proteins related to adaptors and associated with the Golgi complexNovel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP)Phylogenomic approaches to common problems encountered in the analysis of low copy repeats: the sulfotransferase 1A gene family exampleGenomic organization of the 5' end of human beta-ENaC and preliminary characterization of its promoterDivergent origins and concerted expansion of two segmental duplications on chromosome 16Schwannomin inhibits tumorigenesis through direct interaction with the eukaryotic initiation factor subunit c (eIF3c)The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genomeIdentification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney diseaseEstimation of synteny conservation and genome compaction between pufferfish (Fugu) and humanThe wild boar (Sus scrofa) lymphocyte function-associated antigen-1 (CD11a/CD18) receptor: cDNA sequencing, structure analysis and comparison with homologuesChromosomal evolution of the PKD1 gene family in primates.Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.Pooled genomic indexing of rhesus macaque.Genetic mechanisms and signaling pathways in autosomal dominant polycystic kidney disease.Mutation analysis of the entire PKD1 gene: genetic and diagnostic implicationsPositive selection of a gene family during the emergence of humans and African apes.Molecular diagnostics for autosomal dominant polycystic kidney diseaseLinkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.Identification of gene mutations in autosomal dominant polycystic kidney disease through targeted resequencing.Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families.Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.Familial juvenile hyperuricemic nephropathy: localization of the gene on chromosome 16p11.2-and evidence for genetic heterogeneityMutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver DiseasePhenotypic manifestations of copy number variation in chromosome 16p13.11.Recurrent duplication-driven transposition of DNA during hominoid evolution.Familial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrierGenome-wide detection and analysis of recent segmental duplications within mammalian organisms.ABCC6 Mutation in Patients with Angioid StreaksRecurrent 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.Characterization of large rearrangements in autosomal dominant polycystic kidney disease and the PKD1/TSC2 contiguous gene syndrome.Translational control gone awry: a new mechanism of tumorigenesis and novel targets of cancer treatments.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.Effect of siRNA-mediated knockdown of eIF3c gene on survival of colon cancer cells.Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms.
P2860
Q22122488-A43F21D9-DBBC-4CE0-81A8-B315251E89B7Q24309295-7A50F96E-7D2D-42DA-82DE-5C6CB4FBE512Q24329232-054F8E20-E435-4463-A639-2765DC24697AQ24556569-F3410E9E-9075-4527-BDA4-31B596764733Q24673607-245FEB91-363B-490B-AF8F-E1FEB88AD667Q24685976-AF4B03A6-E796-410F-9BBF-1E03D49F265FQ24799068-A3BEA3D0-0FA2-4B2B-8D16-490406831C57Q24804582-7E0624F7-C5F0-4E1A-8CA7-F73481024D64Q28212938-1C01C659-73A9-4B35-B530-33FDF9C29E90Q28214407-7428A5E6-2AAF-49C4-9289-062BEFBD98F3Q28298948-F6EDC4A7-79B6-45FB-B498-F1DC89BEA97EQ28776452-CD4CAD62-662D-475D-9050-10B7D2CFDBC5Q30410875-BF31F848-395D-4259-9D50-6D4CB4E0D425Q30649558-AC70AD05-C8AD-413F-8DE1-4CCCDD0950E3Q33302692-C8AB405A-1065-473D-9FC0-CD567DA6A857Q33372432-9C12E762-1578-4F6F-BE42-F42B33D476DDQ33741872-255D4662-32D9-4EF4-A70C-FD2B1853637EQ33763087-66B83D46-63DE-4BDD-84A4-3F5F2FC272C6Q33780853-64051FCB-217D-4325-A991-40D7C995488FQ33872509-5F39AF9E-03F1-4C0F-A11E-5A505EA28E02Q34043790-D0FC8641-392D-4E05-80EB-36133449DC77Q34093749-F863C8BF-4D39-4CAB-9AF9-B5AEE27F6633Q34100184-C43BF0DD-7DB2-4ACF-9433-E3757388C1BBQ34113338-88323345-18BE-4799-A28C-FC116F666DFEQ34181261-7BE1960C-BFB5-4B5E-AA4F-09CD2930EC77Q34350444-4E8EA114-C6A5-4920-9ABC-86886C16435FQ34353007-6B2ADCC7-739A-4F12-A693-FE849A97C36EQ34390610-03D10DF9-74E5-430B-A8E4-33C6D35E0651Q34529587-816FAF8D-AB84-4183-BD92-836E0F16C3B3Q34705135-C3EBE6DD-BE26-4437-96ED-0F46337D12A3Q35214947-1C6294BA-6059-4BAA-B7E6-C255533D7D37Q35379284-CFCA38E7-8C5E-4111-AC03-CE7AE1F85F28Q35875132-5276D18F-CEB1-4381-B3D2-C8BF72624A81Q36735098-354FA4BB-A7B1-486B-B018-712594900FE1Q37135729-3CAD703D-F4F9-427C-965E-B8804B03E09BQ37374452-9EC059E0-8501-4F15-8058-A3A06D10C928Q37801949-7B08905E-5EB1-4679-9239-2085ED7E8E93Q38879491-AE13B4DD-AA7D-4FBE-803B-617A48E4AEE9Q39144259-19B3AEC7-A07A-4A34-A853-89EAFC0ABC1EQ39753491-8137E5E3-4558-4FC3-908D-09D2E9A9888C
P2860
Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Genome duplications and other ...... m human chromosome 16p and 16q
@ast
Genome duplications and other ...... m human chromosome 16p and 16q
@en
Genome duplications and other ...... m human chromosome 16p and 16q
@nl
type
label
Genome duplications and other ...... m human chromosome 16p and 16q
@ast
Genome duplications and other ...... m human chromosome 16p and 16q
@en
Genome duplications and other ...... m human chromosome 16p and 16q
@nl
prefLabel
Genome duplications and other ...... m human chromosome 16p and 16q
@ast
Genome duplications and other ...... m human chromosome 16p and 16q
@en
Genome duplications and other ...... m human chromosome 16p and 16q
@nl
P2093
P356
P1433
P1476
Genome duplications and other ...... m human chromosome 16p and 16q
@en
P2093
B J Loftus
E E Eichler
J Fuhrmann
M Barnstead
M L Crosby
P C Harris
P304
P356
10.1006/GENO.1999.5927
P407
P577
1999-09-15T00:00:00Z