(Q37546986)

20 August 2017

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title

Application of serial analysis of gene expression to the study of human genetic disease (English)

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20 August 2017

Martin P Horan

1

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20 August 2017

publication date

10 July 2009

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20 August 2017

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20 August 2017

volume

126

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20 August 2017

issue

5

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20 August 2017

page(s)

605-614

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-009-0719-5

20 August 2017

exact match

0 references

cites work

Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophy

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-009-0719-5

Silent brain infarcts in 755 consecutive patients with a first-ever supratentorial ischemic stroke. Relationship with index-stroke subtype, vascular risk factors, and mortality

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-009-0719-5

Gene expression profiles in human cardiac cells subjected to hypoxia or expressing a hybrid form of HIF-1 alpha

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-009-0719-5

Comprehensive serial analysis of gene expression of the cervical transcriptome

21 January 2018

1 reference

12 December 2020

PARK10 candidate RNF11 is expressed by vulnerable neurons and localizes to Lewy bodies in Parkinson disease brain

1 reference

12 December 2020

Family history of stroke in patients with transient ischemic attack in relation to hypertension and other intermediate phenotypes

1 reference

12 December 2020

Activation of PPARgamma coactivator-1 through transcription factor docking

1 reference

12 December 2020

Using the transcriptome to annotate the genome

1 reference

12 December 2020

Serial analysis of gene expression identifies connective tissue growth factor expression as a prognostic biomarker in gallbladder cancer

1 reference

12 December 2020

SAGE application in the study of diabetes

1 reference

12 December 2020

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

1 reference

12 December 2020

Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease

1 reference

12 December 2020

Impact of mitochondrial reactive oxygen species and apoptosis signal-regulating kinase 1 on insulin signaling

1 reference

12 December 2020

Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease

1 reference

12 December 2020

Serial analysis of gene expression reveals differential expression between endometriosis and normal endometrium. Possible roles for AXL and SHC1 in the pathogenesis of endometriosis

1 reference

12 December 2020

Next-generation DNA sequencing methods

1 reference

12 December 2020

Global up-regulation of chromosome 21 gene expression in the developing down syndrome brain

1 reference

12 December 2020

Angiographic distribution of lower extremity atherosclerosis in patients with and without diabetes

1 reference

12 December 2020

Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease

1 reference

12 December 2020

Identification of dysregulated genes in lymphocytes from children with Down syndrome.

1 reference

12 December 2020

Complete genomic screen in Parkinson disease: evidence for multiple genes.

1 reference

12 December 2020

Sampling the Arabidopsis transcriptome with massively parallel pyrosequencing

1 reference

12 December 2020

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

1 reference

12 December 2020

SuperSAGE: a modern platform for genome-wide quantitative transcript profiling

1 reference

12 December 2020

Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke

1 reference

12 December 2020

Peripheral cytokines profile in Parkinson's disease.

1 reference

12 December 2020

Comparison between the gene expression profile of human Müller cells and two spontaneous Müller cell lines

1 reference

12 December 2020

Requirement of a novel gene, Xin, in cardiac morphogenesis

1 reference

12 December 2020

Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1

1 reference

12 December 2020

Gene expression profiles in acute myeloid leukemia with common translocations using SAGE.

1 reference

12 December 2020

Age at onset in two common neurodegenerative diseases is genetically controlled

1 reference

12 December 2020

Serial analysis of gene expression in adrenocortical hyperplasia caused by a germline PRKAR1A mutation

1 reference

12 December 2020

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

12 December 2020

Quantitative gene expression profiling of mouse brain regions reveals differential transcripts conserved in human and affected in disease models

1 reference

12 December 2020

Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approach.

1 reference

12 December 2020

Biosynthesis of major platelet proteins in human blood platelets.

1 reference

12 December 2020

Heritability of ischemic stroke in relation to age, vascular risk factors, and subtypes of incident stroke in population-based studies

1 reference

12 December 2020

Use of serial analysis of gene expression to generate kidney expression libraries

1 reference

12 December 2020

PGC-1 promotes insulin resistance in liver through PPAR-alpha-dependent induction of TRB-3.

1 reference

12 December 2020

Gene expression profiling by massively parallel sequencing.

1 reference

12 December 2020

Combined cDNA array comparative genomic hybridization and serial analysis of gene expression analysis of breast tumor progression

1 reference

12 December 2020

Protocols to establish genotype-phenotype correlations in Down syndrome

1 reference

12 December 2020

Comparative analysis of proteome and transcriptome in human hepatocellular carcinoma using 2D-DIGE and SAGE

1 reference

12 December 2020

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

1 reference

12 December 2020

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

1 reference

12 December 2020

Scaling of gene expression data allowing the comparison of different gene expression platforms

1 reference

12 December 2020

PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

1 reference

12 December 2020

Serial analysis of gene expression as a tool to assess the human thyroid expression profile and to identify novel thyroidal genes

1 reference

12 December 2020

Transcript profiling of human platelets using microarray and serial analysis of gene expression

1 reference

12 December 2020

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

1 reference

12 December 2020

Neuronal pathway from the liver modulates energy expenditure and systemic insulin sensitivity

1 reference

12 December 2020

Insulin signalling and the regulation of glucose and lipid metabolism

1 reference

12 December 2020

High-resolution analysis of the 5'-end transcriptome using a next generation DNA sequencer

1 reference

12 December 2020

Increased progenitor cell proliferation and astrogenesis in the partial progressive 6-hydroxydopamine model of Parkinson's disease.

1 reference

12 December 2020

An expression profile of human pancreatic islet mRNAs by Serial Analysis of Gene Expression (SAGE).

1 reference

12 December 2020

Serial analysis of gene expression

1 reference

12 December 2020

A novel gene (Cmya3) induced in the heart by angiotensin II-dependent but not salt-dependent hypertension in mice.

1 reference

12 December 2020

Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra

1 reference

12 December 2020

Insulin and glucose play a role in foam cell formation and function

1 reference

12 December 2020

Sequencing Medicago truncatula expressed sequenced tags using 454 Life Sciences technology

1 reference

12 December 2020

Genes involved in oxidative phosphorylation are coordinately upregulated with fasting hyperglycaemia in livers of patients with type 2 diabetes.

1 reference

12 December 2020

Seven placental transcripts characterize HELLP-syndrome

1 reference

12 December 2020

Lipopolysaccharide regulated protein expression is only partly impaired in monocytes from patients with type I diabetes

1 reference

12 December 2020

Serial analysis of gene expression to assess the endothelial cell response to an atherogenic stimulus

1 reference

12 December 2020

Reactive oxygen species have a causal role in multiple forms of insulin resistance

1 reference

12 December 2020

The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men

1 reference

12 December 2020

PPARGC1A variation associated with DNA damage, diabetes, and cardiovascular diseases: the Boston Puerto Rican Health Study.

1 reference

12 December 2020

Genetic variations related to hypertension: a review.

1 reference

12 December 2020

Direct comparison of GeneChip and SAGE on the quantitative accuracy in transcript profiling analysis

1 reference

12 December 2020

Defining the human macula transcriptome and candidate retinal disease genes using EyeSAGE.

1 reference

12 December 2020

Gain-of-function R225Q mutation in AMP-activated protein kinase gamma3 subunit increases mitochondrial biogenesis in glycolytic skeletal muscle

1 reference

12 December 2020

Association of UCP2 and UCP3 polymorphisms with heart rate variability in Japanese men

1 reference

12 December 2020

Identification of DEIN, a novel gene with high expression levels in stage IVS neuroblastoma

1 reference

12 December 2020

Global gene expression in a type 2 Gaucher disease brain

1 reference

12 December 2020

Comprehensive gene expression profile of a normal human liver

1 reference

12 December 2020

Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF).

1 reference

12 December 2020

A quantitative and validated SAGE transcriptome reference for adult mouse heart

1 reference

12 December 2020

Xin repeats define a novel actin-binding motif.

1 reference

12 December 2020

The 5'-AMP-activated protein kinase gamma3 isoform has a key role in carbohydrate and lipid metabolism in glycolytic skeletal muscle

1 reference

12 December 2020

Mutations in NR4A2 associated with familial Parkinson disease

1 reference

12 December 2020

SAGE identification of differentiation responsive genes in P19 embryonic cells induced to form cardiomyocytes in vitro.

1 reference

12 December 2020

Transcription analysis in the MeLiM swine model identifies RACK1 as a potential marker of malignancy for human melanocytic proliferation

1 reference

12 December 2020

Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1

1 reference

12 December 2020

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

12 December 2020

CREB regulates hepatic gluconeogenesis through the coactivator PGC-1

1 reference

12 December 2020

Gene expression profile of human Down syndrome leukocytes

1 reference

12 December 2020

Combining serial analysis of gene expression and array technologies to identify genes differentially expressed in breast cancer

1 reference

12 December 2020

Enzymatic amplification of platelet-specific messenger RNA using the polymerase chain reaction

1 reference

12 December 2020

Atherosclerotic plaque macrophage transcriptional regulators are expressed in blood and modulated by tristetraprolin

1 reference

12 December 2020

Mitochondrial dysfunction and type 2 diabetes

1 reference

12 December 2020

A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease

1 reference

12 December 2020

Loss of insulin signaling in hepatocytes leads to severe insulin resistance and progressive hepatic dysfunction

1 reference

12 December 2020

10.1007/S00439-009-0719-5

Identifiers

DOI

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release_n2jo3pflgnbudbulxefl6fhizm

20 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/n2jo3pflgnbudbulxefl6fhizm

24 November 2022

mapped directly with Wikidata item

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