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TranscriptomicsTranscription profiling of mouse kideney FROM beta catenin deficient animals vs controls AT E12.5
We generated a murine genetic model of beta-catenin deficiency targeted to the ureteric bud cell lineage to study the role of beta-catenin mediated Wnt signaling during ureteric morphogenesis. Experiment Overall Design: A comparison was made between triplicate samples of E12.5 kidneys from either no...
ORGANISM(S): Mus musculus 
2008-04-04 | E-GEOD-9629 | biostudies-arrayexpress
TranscriptomicsExpression Analysis of Macrodactyly
Macrodactyly is a rare family of congenital disorders characterized by the diffuse enlargement of 1 or more digits. To date, no genes or loci have been implicated in the development of macrodactyly. In this study, we performed the first transcriptional profiling of macrodactyly tissue. RNA was isol...
ORGANISM(S): Homo sapiens 
2013-12-31 | E-GEOD-35820 | biostudies-arrayexpress
ProteomicsProtein Turnover Rates in Normal and Hypertrophy Mouse Hearts
This dataset contains the in vivo turnover rate information of ~3,000 proteins from the mouse heart. Data from six common laboratory mouse strains with differential responses to isoproterenol are included
ORGANISM(S): Mus Musculus (ncbitaxon:10090) 
2017-11-08 | MSV000081697 | MassIVE
ProteomicsSTUB1 is an intracellular checkpoint for interferon gamma sensing
Immune checkpoint blockade (ICB) leads to durable and complete tumour regression in some patients but in others gives temporary, partial or no response. Accordingly, significant efforts are underway to identify tumour-intrinsic mechanisms underlying ICB resistance. Results from a published CRISPR sc...
ORGANISM(S): Mus musculus (Mouse) 
2022-08-18 | PXD035392 | Pride
Mouse melanoma cell lines 
ProteomicsProteogenomic Analysis of Medulloblastoma
In order to investigate medulloblastoma biology via its proteome, we undertook a super-SILAC quantitative proteomics survey using 41 clinical tissue samples spanning the 4 genomic subgroups and control cerebellum
ORGANISM(S): Homo sapiens (Human) 
2018-06-10 | PXD008750 | Pride
Medulloblastoma Brain tumor Silac Human Pediatrics 
ProteomicsM.musculus - Heart, NSAF (Lauetal,scidata2016)
abundance based on NSAF, Interaction consistency score: 38.1, Coverage: 31
ORGANISM(S): 10090 
2016-00-00 | 1153777653 | PAXDB
TranscriptomicsThe Clinical impact of Chromosomal microarray on Paediatric care in Hong Kong (CGX-6)
Objective: To evaluate the clinical impact of chromosomal microarray (CMA) on the management of paediatric patients in Hong Kong Methods: We performed NimbleGen 135k oligonucleotide array on 327 children with intellectual disability (ID)/ developmental delay (DD), autism spectrum disorders (ASD), a...
ORGANISM(S): Homo sapiens 
2014-08-31 | E-MTAB-2883 | biostudies-arrayexpress
TranscriptomicsThe Clinical impact of Chromosomal microarray on Paediatric care in Hong Kong (CGX-12)
Objective: To evaluate the clinical impact of chromosomal microarray (CMA) on the management of paediatric patients in Hong Kong Methods: We performed NimbleGen 135k oligonucleotide array on 327 children with intellectual disability (ID)/ developmental delay (DD), autism spectrum disorders (ASD), a...
ORGANISM(S): Homo sapiens 
2014-09-04 | E-MTAB-2884 | biostudies-arrayexpress
TranscriptomicsUse of clinical chromosomal microarray in Chinese patients with autism spectrum disorder - implications of a copy number variation involving dpp10 (CGX-12)
Background: Array-Comparative-Genomic-Hybridization (aCGH) is recommended as first-tier genetic test for children with autism spectrum disorder (ASD). However, result interpretation can be challenging as copy number variants (CNVs) in non-European ASD patients is not well studied. To address this li...
ORGANISM(S): Homo sapiens 
2017-04-07 | E-MTAB-5665 | biostudies-arrayexpress
TranscriptomicsUse of clinical chromosomal microarray in Chinese patients with autism spectrum disorder - implications of a copy number variation involving dpp10 (Perkin Elmer CGX)
Background Array-Comparative-Genomic-Hybridization (aCGH) is recommended as first-tier genetic test for children with autism spectrum disorder (ASD). However, result interpretation can be challenging as copy number variants (CNVs) in non-European ASD patients is not well studied. To address this lit...
ORGANISM(S): Homo sapiens 
2017-04-07 | E-MTAB-5672 | biostudies-arrayexpress
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