about
Mechanisms underlying structural variant formation in genomic disordersCopy number variants in candidate genes are genetic modifiers of Hirschsprung diseaseIntegrated analysis of copy number variation and genome-wide expression profiling in colorectal cancer tissuesIdentification of structural variation in mouse genomes.Relating CNVs to transcriptome data at fine resolution: assessment of the effect of variant size, type, and overlap with functional regions.Transcriptomic analysis of genetically defined autism candidate genes reveals common mechanisms of actionRNA-Seq and human complex diseases: recent accomplishments and future perspectives.The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile.Phenotypic impact of genomic structural variation: insights from and for human disease.Identification of both copy number variation-type and constant-type core elements in a large segmental duplication region of the mouse genome.Genomic and transcriptomic differences in community acquired methicillin resistant Staphylococcus aureus USA300 and USA400 strains.Deciphering the pathogenic consequences of chromosomal aberrations in human genetic disease.Structural variation-associated expression changes are paralleled by chromatin architecture modifications.A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 PathologyMediation of Drosophila autosomal dosage effects and compensation by network interactions.Diversity and regulatory impact of copy number variation in the primate Macaca fascicularisGene expression analysis of matched ovarian primary tumors and peritoneal metastasisGenomic Profiling Reveals Unique Molecular Alterations in Hepatoblastomas and Adjacent Hepatocellular Carcinomas in B6C3F1 Mice.Copy number variations and cognitive phenotypes in unselected populationsClinical and Genetic Heterogeneity of the 15q13.3 Microdeletion SyndromeIdentifying anti-cancer drug response related genes using an integrative analysis of transcriptomic and genomic variations with cell line-based drug perturbationsIn silico QTL mapping of maternal nurturing ability with the mouse diversity panel.Duplication of chicken defensin7 gene generated by gene conversion and homologous recombination.An investigation of the role of gene copy number variations in sorafenib sensitivity in metastatic hepatocellular carcinoma patients.Principle considerations for the use of transcriptomics in doping research.The synapse in schizophrenia.The impact of chromosomal rearrangements on regulation of gene expression.Adaptive potential of genomic structural variation in human and mammalian evolution.Construction and phenotypic analysis of mice carrying a duplication of the major histocompatibility class I (MHC-I) locus.Deciphering the Correlation between Breast Tumor Samples and Cell Lines by Integrating Copy Number Changes and Gene Expression Profiles.An Integrative Breakage Model of genome architecture, reshuffling and evolution
P2860
Q26765934-21E451E9-68B3-4699-9D5A-AEAEB7BBCA29Q31021758-BFCC64E0-F7D8-4D99-92E5-86FDFC66B571Q31155184-9B8B758A-5B4E-4F8C-BDFA-6C1C65720969Q33836160-7E765F66-666F-4DD8-B133-560A37BD5912Q34001429-9F064BAE-1399-4CBF-A95B-F28B89CF09C3Q34249424-16E1D4E5-6BFF-4286-BA3E-E1993D2F0B56Q34284546-B0A7FD31-3F70-450D-9513-65914BE833F3Q34285719-3029050A-96C9-4083-A9C1-7DBF5309EE0AQ34323221-82517F25-0BC1-4082-A843-7DC740EF0DDEQ34802529-1C64094E-5BE0-440E-A6DF-4EB8D5AE17F6Q34984553-77B2523B-9AC4-48EC-8BA4-47CA98D5B018Q34987350-9B8C5361-B8CE-45E3-9229-CA90C882018BQ35050556-622C8706-531D-476D-AE49-9C310409649CQ36060885-5DE18E5E-E78D-4976-8E9A-3C116BC3D37AQ36245261-2E06064C-C743-41B3-BC47-50B0F8208E15Q36275980-B9DD587E-EF5D-4C56-8319-648B21541A19Q36335072-B61E5676-B0C9-4805-B9EC-92BF3B2E2CB5Q36348318-B79A9774-A558-44E8-8AEB-0827E036BB57Q36384798-80C8E1E6-A5AC-4B61-B437-1D5B2442C5A7Q36635250-962D99FC-BD6E-4378-B360-47AF4B275179Q36962620-AF53785B-4D3C-4596-953F-36F444D3CCE9Q37175776-9140D0A8-AEE1-4F78-870F-68CEF374C923Q37473730-8DC7990C-59F6-4153-A780-5EBCB2612EFCQ37738067-8D0E1670-5AE0-4018-8018-8BDFC6473792Q37949929-64CA0143-EAC8-4D5B-A17D-01EF353D7F7AQ38203024-032B7422-44AF-4B01-B836-0EB68BFC2120Q38218372-803782E6-A1FB-4D73-B59C-A745F6AE6094Q38499991-F24CE2CE-498C-4C2E-BC93-CCA035DB809EQ39294873-233DF766-D897-46D1-B0F4-DB018D9910F0Q42428131-B85F66ED-5D5A-4DF7-9D58-818B83233EE8Q59208664-51D660DB-9091-4545-8250-629804C98F5B
P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Copy number variation modifies expression time courses
@ast
Copy number variation modifies expression time courses
@en
Copy number variation modifies expression time courses
@nl
type
label
Copy number variation modifies expression time courses
@ast
Copy number variation modifies expression time courses
@en
Copy number variation modifies expression time courses
@nl
prefLabel
Copy number variation modifies expression time courses
@ast
Copy number variation modifies expression time courses
@en
Copy number variation modifies expression time courses
@nl
P2093
P2860
P356
P1433
P1476
Copy number variation modifies expression time courses
@en
P2093
Charlotte N Henrichsen
Emilie Aït Yahya-Graison
Evelyne Chaignat
Frédéric Schütz
Jacqueline Chrast
Sylvain Pradervand
P2860
P304
P356
10.1101/GR.112748.110
P577
2010-11-17T00:00:00Z