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UnknownTelehealth Support for Dementia Caregivers During the COVID-19 Pandemic: Lessons Learned From the NYU Family Support Program.
Not available
S-EPMC9424119 | biostudies-literature
TranscriptomicsX chromosome cDNA microarray screen of lymphoblasts from males with XLMR
The goal of this study is to identify genes that show altered transcript levels in lymphoblasts from male patients with XLMR as candidate genes that are responsible for XLMR. Keywords: disease state Using a custom X chromosome cDNA microarray, we studied X chromosome gene expression in lymphoblasts ...
ORGANISM(S): Homo sapiens 
2010-06-11 | E-GEOD-7470 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of Mycobacterium avium subspecies paratuberculosis Types I, II and III genomes by pan-genome microarray analysis
Data is also available from http://bugs.sgul.ac.uk/E-BUGS-69
ORGANISM(S): Mycobacterium avium 
2009-01-16 | E-BUGS-69 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of Arabidopsis iae1 and iae2 phenotypes
The mutants iae1 and iae2 have been mapped to two distinct loci on chromosome 2. With the aid of the GetCID service, we believe iae1 has been localised to a relatively small region (~100kb); while mapping has restricted iae2 to a small interval (~50kb) with a very limited number of candidate genes....
ORGANISM(S): Arabidopsis thaliana 
2008-06-14 | E-GEOD-6175 | biostudies-arrayexpress
ProteomicsInteractome analysis of FAM50A via affinity purification coupled to mass spectrometry
FAM50A missense variants are present in Armfield XLID syndrome patients. Zebrafish lacking fam50a display related phenotypes and show dysregulation of the transcriptome, increased spliceosome mRNAs and a preponderance of 3’ alternative splicing events, suggesting a role for Fam50a in the spliceosome...
ORGANISM(S): Homo sapiens (Human) 
2020-05-08 | PXD017642 | Pride
Protein interactions Streptavidin affinity purification Fam50a Nanolc-ms/ms 
UnknownGene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome.
Not available
S-EPMC6487024 | biostudies-literature
UnknownAn X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity.
Not available
S-EPMC3459470 | biostudies-literature
UnknownRenpenning syndrome maps to Xp11.
Not available
S-EPMC1377092 | biostudies-literature
UnknownKey apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects.
Not available
S-EPMC5838979 | biostudies-literature
UnknownA recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
Not available
S-EPMC2365467 | biostudies-literature
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