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UnknownDevelopment and evaluation of an extra-curricular programme focussing on high impact career opportunities for medical professionals.
Not available
S-EPMC10124875 | biostudies-literature
UnknownAn experimental test of noncontextuality without unphysical idealizations.
Not available
S-EPMC4909951 | biostudies-literature
UnknownChanges in urinary metabolomic profile during relapsing renal vasculitis.
Not available
S-EPMC5131479 | biostudies-literature
TranscriptomicsSmall molecule inhibitors suppress expression of both type III secretion and amylovoran biosynthesis genes in Erwinia amylovora
Microarray analysis of E. amylovora treated with compounds no. 3 and no. 9 identified a total of 588 significantly differentially expressed genes. Among them, 95 and 78 genes were, respectively, induced and suppressed by both compounds as compared to DMSO control. Majority of T3SS genes in E. amylov...
ORGANISM(S): Erwinia amylovora 
2013-12-24 | E-GEOD-45602 | biostudies-arrayexpress
UnknownZwitterionic Polysulfobetaine Coating and Antiplatelet Liposomes Reduce Fouling in Artificial Lung Circuits.
Not available
S-EPMC10121813 | biostudies-literature
TranscriptomicsComplex Balanced Translocation Disrupting TCF4 and Altering TCF4 Isoform Expression Segregates as Mild Autosomal Dominant Intellectual Disability
Mutations of TCF4, which encodes a basic helix-loop-helix transcription factor, cause Pitt-Hopkins syndrome (PTHS) via multiple genetic mechanisms. TCF4 is a complex locus expressing multiple transcripts by alternative splicing and use of multiple promoters. We report a three-generation family segre...
ORGANISM(S): Homo sapiens 
2016-05-31 | E-GEOD-77742 | biostudies-arrayexpress
UnknownConservation management strategy impacts inbreeding and mutation load in scimitar-horned oryx.
Not available
S-EPMC10160979 | biostudies-literature
UnknownA novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background.
Not available
S-EPMC8883398 | biostudies-literature
UnknownA patient with multisystem dysfunction carries a truncation mutation in human SLC12A2, the gene encoding the Na-K-2Cl cotransporter, NKCC1.
Not available
S-EPMC5111002 | biostudies-literature
TranscriptomicsTranscription profiling of human CD8 T cells in systemic lupus erythematosus (SLE) and vasculitis
Autoimmune diseases are common and debilitating, but their severe manifestations could be reduced if biomarkers were available to allow individual tailoring of the potentially toxic immunosuppressive therapy required for their control. Clinically useful biomarkers have been identified using DNA micr...
ORGANISM(S): Homo sapiens 
2010-06-02 | E-MTAB-157 | biostudies-arrayexpress
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