Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes. (Q35100466)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25705109%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

title

Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes (English)

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1 March 2020

7

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1 March 2020

author name string

Merlin G Butler

1

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1 March 2020

Kun Wang

2

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1 March 2020

Jan D Marshall

3

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1 March 2020

Jürgen K Naggert

4

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1 March 2020

Jasmine A Rethmeyer

5

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1 March 2020

Sumedha S Gunewardena

6

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1 March 2020

publication date

1 January 2015

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Advances in genomics and genetics

1 March 2020

published in

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volume

2015

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1 March 2020

issue

5

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1 March 2020

page(s)

53-75

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Creative Commons Attribution-NonCommercial 3.0 Unported

1 March 2020

copyright license

start time

1 January 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome

9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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MicroRNAs modulate hematopoietic lineage differentiation

9 July 2018

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9 July 2018

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Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons

9 July 2018

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A microRNA array reveals extensive regulation of microRNAs during brain development

9 July 2018

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9 July 2018

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Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

9 July 2018

1 reference

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Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome

9 July 2018

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Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

9 July 2018

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Human Nop5/Nop58 is a component common to the box C/D small nucleolar ribonucleoproteins

9 July 2018

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Guiding ribose methylation of rRNA

9 July 2018

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Eukaryotic ribosomal RNA: the recent excitement in the nucleotide modification problem

9 July 2018

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Intron-encoded, antisense small nucleolar RNAs: the characterization of nine novel species points to their direct role as guides for the 2'-O-ribose methylation of rRNAs

9 July 2018

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9 July 2018

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9 July 2018

1 reference

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Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients

9 July 2018

1 reference

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9 July 2018

1 reference

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Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

9 July 2018

1 reference

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Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

9 July 2018

1 reference

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Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

9 July 2018

1 reference

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Prader-Willi syndrome: current understanding of cause and diagnosis

9 July 2018

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Argonaute regulation: two roads to the same destination.

9 July 2018

1 reference

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ChIP-Chip Identifies SEC23A, CFDP1, and NSD1 as TFII-I Target Genes in Human Neural Crest Progenitor Cells

27 September 2018

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The RanBP2/RanGAP1*SUMO1/Ubc9 complex is a multisubunit SUMO E3 ligase.

27 September 2018

1 reference

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27 September 2018

Prader-Willi syndrome

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Navajo microvillous inclusion disease is due to a mutation in MYO5B.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

27 September 2018

Prader-Willi syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

Dual role for argonautes in microRNA processing and posttranscriptional regulation of microRNA expression.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndrome

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

Retinoblastoma Protein (pRB) Was Significantly Phosphorylated through a Ras-to-MAPK Pathway in Mutant K-ras Stably Transfected Human Adrenocortical Cells

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4334166

A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25705109

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular basis of Williams-Beuren syndrome: TFII-I regulated targets involved in craniofacial development

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25705109

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2147/AGG.S74598

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25705109%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25705109%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

PubMed publication ID

25705109

1 reference