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Unknown
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Transcriptomics
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Homo sapiens
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biostudies-arrayexpress
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Illumina HiSeq 2500
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2009
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Profiling of Primary and Mature miRNA Expression in Atherosclerosis-Associated Cell Types.
Not available
S-EPMC8216629
|
biostudies-literature
Cite
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology.
Not available
S-EPMC4988259
|
biostudies-literature
Cite
Two new Neuratelia Rondani (Diptera, Mycetophilidae) species from Western Palaearctic: a case of limited congruence between morphology and DNA sequence data.
Not available
S-EPMC4410159
|
biostudies-literature
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The human WBSCR22 protein is involved in the biogenesis of the 40S ribosomal subunits in mammalian cells.
Not available
S-EPMC3781059
|
biostudies-literature
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The Stability of Ribosome Biogenesis Factor WBSCR22 Is Regulated by Interaction with TRMT112 via Ubiquitin-Proteasome Pathway.
Not available
S-EPMC4516353
|
biostudies-literature
Cite
The Common Partner of Several Methyltransferases TRMT112 Regulates the Expression of N6AMT1 Isoforms in Mammalian Cells.
Not available
S-EPMC6769652
|
biostudies-literature
Cite
Hyperphenylalaninaemias in Estonia: Genotype-Phenotype Correlation and Comparative Overview of the Patient Cohort Before and After Nation-Wide Neonatal Screening.
Not available
S-EPMC6122019
|
biostudies-literature
Cite
An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature.
Not available
S-EPMC4974439
|
biostudies-literature
Cite
The Prevalence of PMM2-CDG in Estonia Based on Population Carrier Frequencies and Diagnosed Patients.
Not available
S-EPMC5953896
|
biostudies-literature
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The evaluation of phenylalanine levels in Estonian phenylketonuria patients during eight years by electronic laboratory records.
Not available
S-EPMC6434493
|
biostudies-literature
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