Smabf1
Webb1 maj 1991 · SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1 (OMIM - 616866) Similar Articles . To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation. WebbImmunofluorescent analysis of ASC1 in HeLa cells. Samples were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100, blocked with 10% serum (45 min at 25°C) incubated with ASC1 polyclonal antibody (Product # PA5-101174) using a dilution of 1:200 (1 hr, 37°C), and followed by goat anti-rabbit IgG Alexa Fluor 594 at a dilution of …
Smabf1
Did you know?
WebbOsztályozás. Az érintett izmok típusa alapján a gerinc izomsorvadásai a következőkre oszthatók: Proximális gerincizom -sorvadások, azaz olyan állapotok, amelyek elsősorban a proximális izmokat érintik ;; A gerinc disztális izomsorvadásai (amelyek jelentősen átfedik a disztális örökletes motoros neuronopathiákkal), ahol elsősorban a distalis izmokat érintik . WebbSPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1; Functional Complementation Data Functional complementation data is computed by FlyBase using a combination of the orthology data obtained from DIOPT and OrthoDB and the allele-level genetic interaction data curated from the literature. Interactions ...
WebbSMABF1 (atrophy, muscular, spinal, with congenital bone fractures, type 1 (SMABF-1)) HGMD: TRIP4: GeneCards: TRIP4: GeneTests: TRIP4: Orphanet: TRIP4: Active transcripts. Legend Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. WebbTRIP4 has 3,710 functional associations with biological entities spanning 8 categories (molecular profile, organism, chemical, functional term, phrase or reference, disease, …
WebbRare diseases are not rare. About 30 million people in the U.S. are affected by a rare disease. As you and your caregivers adjust to a rare disease diagnosis, it is normal to be … WebbContact Creative Biolabs to Customize trip4 Antibody, which reacts with Zebrafish (Danio rerio). This product is a mouse antibody against trip4. It can be used for trip4 detection in Western Blot, Enzyme-Linked Immunosorbent Assay.
Webb(220870-PE) ASC-1 (Activating Signal cointegrator 1, ASC1, Thyroid Receptor-interacting Protein 4, TR-interacting Protein 4, TRIP-4, TRIP4) (PE) - US Biological - CiteAb
WebbSpinal muscular atrophy (SMA) is characterized by muscle weakness and atrophy resulting from progressive degeneration and irreversible loss of the anterior horn cells in the … how to say alexia in japaneseWebbOMIM®: 57 Spinal muscular atrophy with congenital bone fractures is an autosomal recessive severe neuromuscular disorder characterized by onset of severe hypotonia … how to say alexis in frenchWebb9 aug. 2016 · In 5 patients from 3 unrelated families with spinal muscular atrophy with congenital bone fractures-1 (SMABF1; 616866), Knierim et al. (2016) identified … how to say alex in espanolWebbMutations in this gene are associated with spinal muscular atrophy with congenital bone fractures-1 (SMABF1). [provided by RefSeq, Apr 2016] TRIP4 (thyroid hormone receptor interactor 4) - Rat Genome Database northfield post officeWebbSMABF1: Name: atrophy, muscular, spinal, with congenital bone fractures, type 1 (SMABF-1) OMIM ID: 616866: Human Phenotype Ontology Project (HPO) HPO: Inheritance: … how to say alexis in germanWebbSMABF1; zinc finger, C2HC5-type; ZC2HC5; TRIP-4; thyroid receptor-interacting protein 4; MDCDC; HsT17391; ASC-1; ASC1; activating signal cointegrator 1; TR-interacting protein 4. Protein Names Activating signal cointegrator 1, Thyroid receptor-interacting protein 4, … how to say alfie in frenchWebbthyroid hormone receptor interactor 4 , ASC-1 , ASC1 , HsT17391 , MDCDC , SMABF1 , ZC2HC5 Cellular Localization Nucleus,Cytoplasm, cytosol Background This gene ... how to say alfie in japanese