The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer.
about
A genome-wide study of cytogenetic changes in colorectal cancer using SNP microarrays: opportunities for future personalized treatmentLoss of Heterozygosity Drives Adaptation in Hybrid YeastGenome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment.Insulin and insulin-like growth factor 1 receptors are required for normal expression of imprinted genes.Germline DNA copy number aberrations identified as potential prognostic factors for breast cancer recurrence.Immunodeficiency and autoimmune enterocolopathy linked to NFAT5 haploinsufficiencyValidation of gene expression biomarker analysis for biopsy-based clinical trials in Crohn's diseaseAn integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.Patterns of somatic uniparental disomy identify novel tumor suppressor genes in colorectal cancer.Role of ART in imprinting disordersGermline large genomic alterations on 7q in patients with multiple primary cancers.The role of high-throughput technologies in clinical cancer genomics.Different characteristics identified by single nucleotide polymorphism array analysis in leukemia suggest the need for different application strategies depending on disease category.Genome-wide acquired uniparental disomy as well as chromosomal gains and losses in an uterine epithelioid leiomyoma.Pediatric T-cell acute lymphoblastic leukemia.Allelic imbalance at an 8q24 oncogenic SNP is involved in activating MYC in human colorectal cancer.The prevalence of chromosomal aberrations associated with myelodysplastic syndromes in China.Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge.Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families.A novel regulatory defect in the branched-chain α-keto acid dehydrogenase complex due to a mutation in the PPM1K gene causes a mild variant phenotype of maple syrup urine disease.Mutant allele specific imbalance in oncogenes with copy number alterations: Occurrence, mechanisms, and potential clinical implications.Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.Paternal uniparental disomy with segmental loss of heterozygosity of chromosome 11 are hallmark characteristics of syndromic and sporadic embryonal rhabdomyosarcoma.A high resolution genomic portrait of bladder cancer: correlation between genomic aberrations and the DNA damage response.Positive Caricature Transcriptomic Effects Associated with Broad Genomic Aberrations in Colorectal Cancer
P2860
Q28480975-3E4D35D3-BD19-491E-9FFC-123328DF8114Q33757192-2EA8A4F1-256D-4DF9-9C20-2D7A08425170Q34396556-016E5F37-E739-4F95-A08C-00AEAC60466DQ34407440-9A00653D-DCD8-4AC1-88A8-E14849ADA33AQ34558816-DB3F59ED-8352-47F9-9967-F27A726EA619Q35164201-82F1B18B-9230-4E78-91D6-BF7ABC3351DBQ35498214-583D22F4-D460-40E5-9449-58E740B5B513Q35974493-A5C935DA-54CB-49C8-B87D-C0FC4838EC6BQ36139202-03DDE2EC-E2FC-4F68-B85B-3D29BD07D91BQ37338436-9472A74F-9FD5-4FDD-9F32-EE36D9FFF305Q37615396-6CAB73A6-934C-4645-8384-C01608F18289Q38088010-6E1B30B0-C34D-45F7-BCDB-315DAFEADE2AQ38321218-DA0DBE14-604B-4D24-B4C3-141C2BBEE574Q38903539-78000483-6D3A-4F7B-B93A-3FC3774A72F8Q38956273-3F7618E8-63E9-4859-A402-4F5B520BE4D2Q39037289-4CB9CEFA-66AE-4D20-B064-18345CD59CD1Q40735858-3D8778AD-C9BD-4EBA-A43E-BC74950C77FAQ42377406-B251B630-69A4-45B0-8E06-2298F30FAE52Q42426333-7CDE2C7E-F315-472C-8D75-DDBC79F011E6Q44238023-648B513E-27E6-430F-B003-72603ADE811BQ47164988-4F7C7CD6-F776-4BEE-9331-1D3A5C78AB6FQ50531355-5664417B-40D0-42FB-9908-2FB49D0E8F2AQ52679444-66E3E260-37FA-43AE-B874-A8556C2BEB0BQ52850947-E78B9EF7-3A0F-42EE-A64C-62F34F40ED8BQ54487776-A3A2DDF8-EA07-4C57-9F6B-324E1D08A0E2Q57031949-8FA5DCCD-679D-478A-9BB7-FACD95CCF861
P2860
The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The consequences of uniparenta ...... human development and cancer.
@en
The consequences of uniparenta ...... human development and cancer.
@nl
type
label
The consequences of uniparenta ...... human development and cancer.
@en
The consequences of uniparenta ...... human development and cancer.
@nl
prefLabel
The consequences of uniparenta ...... human development and cancer.
@en
The consequences of uniparenta ...... human development and cancer.
@nl
P2860
P356
P1433
P1476
The consequences of uniparenta ...... human development and cancer.
@en
P2093
David Monk
Pablo Lapunzina
P2860
P304
P356
10.1042/BC20110013
P577
2011-07-01T00:00:00Z