Sequencing of ACVR1/ALK2 in patient derived DIPG cell lines
Report outlining how genomic DNA was extracted from patient derived diffuse intrinsic pontine glioma cell lines*, PCR was used to amplify commonly mutated exons of ACVR1, and the regions Sanger sequenced.
Brown, Elizabeth, Bullock, Alex
openaire +1 more source
Multi-Cancer Computational Analysis Reveals Metastasis-Associated Variant of Desmoplastic Reaction Involving INHBA and THBS2 [PDF]
Despite extensive research, the details of the metastasis-associated biological mechanisms are largely unknown. Here, we analyze data from multiple cancers using a novel computational method identifying sets of genes whose coordinated overexpression ...
Dimitris Anastassiou +3 more
core +1 more source
Purification Of Acvr1 Alone And Tgfbr1 (Alk5) Complexed With Fkbp12
Purifications of ALK2 and ALK5 (the latter in complex with FKBP12) and crystal ...
Adamson, Roslin +3 more
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The HIF-1α and mTOR Pathways Amplify Heterotopic Ossification
Fibrodysplasia ossificans progressiva (FOP; MIM# 135100) is an ultra-rare congenital disorder caused by gain-of-function point mutations in the Activin receptor A type I (ACVR1, also known as ALK2) gene.
Haitao Wang +2 more
doaj +1 more source
The Mütter Museum of the College of Physicians of Philadelphia: An introduction to its history and resources for the teaching of human developmental biology [PDF]
Grunwald, Gerald B.
core +4 more sources
Histone Variant H3.3: A versatile H3 variant in health and in disease [PDF]
core +1 more source
ACVR mutation [NM_001105.4:c.774G>T (p.Arg258Ser)] in pediatric fibrodysplasia ossificans progressiva complicated by scoliosis: a case report. [PDF]
Yang F, Liu M, Pei S, Huang J, Wang H.
europepmc +1 more source
Effects of miR-128-3p on Renal Inflammation in a Rat Periodontitis Model. [PDF]
Nurhamim M +7 more
europepmc +1 more source

