Enzymatic amplification of platelet-specific messenger RNA using the polymerase chain reaction.
about
Gene expression analysis of human red blood cellsMolecular cloning, primary structure, and expression of the human platelet/erythroleukemia cell 12-lipoxygenaseMaple syrup urine disease. Complete defect of the E1 beta subunit of the branched chain alpha-ketoacid dehydrogenase complex due to a deletion of an 11-bp repeat sequence which encodes a mitochondrial targeting leader peptide in a family with the diMolecular cloning of platelet factor XI, an alternative splicing product of the plasma factor XI geneSpecificity of G alpha q and G alpha 11 gene expression in platelets and erythrocytes. Expressions of cellular differentiation and species differencesPlatelet genomics and proteomics in human health and disease.A single nucleotide change in the prolidase gene in fibroblasts from two patients with polypeptide positive prolidase deficiency. Expression of the mutant enzyme in NIH 3T3 cellsSequences of complementary DNAs that encode the NA1 and NA2 forms of Fc receptor III on human neutrophilsHuman monoamine oxidase A gene determines levels of enzyme activityMolecular biology for platelet alloantigen typing.The GPIIb/IIIa (integrin alphaIIbbeta3) odyssey: a technology-driven saga of a receptor with twists, turns, and even a bend.Human platelet-specific alloantigens: update.Transactivation of interleukin 2 and its receptor induces immune activation in human T-cell lymphotropic virus type I-associated myelopathy: pathogenic implications and a rationale for immunotherapy.Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure.The human platelet alloantigens Br(a) and Brb are associated with a single amino acid polymorphism on glycoprotein Ia (integrin subunit alpha 2)Diagnostic evaluation of the MRP-8/14 for the emergency assessment of chest painThe intrinsic complement regulator decay-accelerating factor modulates the biological response to vascular injuryGlanzmann thrombasthenia resulting from a single amino acid substitution between the second and third calcium-binding domains of GPIIb. Role of the GPIIb amino terminus in integrin subunit associationThe human proteinase-activated receptor-3 (PAR-3) gene. Identification within a Par gene cluster and characterization in vascular endothelial cells and platelets.Protein synthesis by platelets: historical and new perspectives.The human platelet alloantigens, PlA1 and PlA2, are associated with a leucine33/proline33 amino acid polymorphism in membrane glycoprotein IIIa, and are distinguishable by DNA typing.Historical perspective and future directions in platelet research.A uniquely high level of recombination at the HLA-B locus.An amino acid polymorphism within the RGD binding domain of platelet membrane glycoprotein IIIa is responsible for the formation of the Pena/Penb alloantigen systemmTOR-dependent synthesis of Bcl-3 controls the retraction of fibrin clots by activated human platelets.Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival.Proteomic approaches to dissect platelet function: Half the story.Integrin-dependent control of translation: engagement of integrin alphaIIbbeta3 regulates synthesis of proteins in activated human platelets.Signal-dependent protein synthesis by activated platelets: new pathways to altered phenotype and function.Genetic dissection of platelet function in health and disease using systems biology."Message in the platelet"--more than just vestigial mRNA!Identification of a point mutation in type IIB von Willebrand disease illustrating the regulation of von Willebrand factor affinity for the platelet membrane glycoprotein Ib-IX receptor.The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in IsraelCloning and expression of the delayed-rectifier IsK channel from neonatal rat heart and diethylstilbestrol-primed rat uterusPlatelet biology and receptor pathways.Platelet p24/CD9, a member of the tetraspanin family of proteins.Illegitimate transcription: its use for studying genetic abnormalities in lymphoblastoid cells from patients with Glanzmann thrombasthenia.Alzheimer's presenilin 1 gene expression in platelets and megakaryocytes. Identification of a novel splice variant.Maple syrup urine disease: clinical and biochemical significance of gene analysis.
P2860
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P2860
Enzymatic amplification of platelet-specific messenger RNA using the polymerase chain reaction.
description
1988 nî lūn-bûn
@nan
1988 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Enzymatic amplification of pla ...... the polymerase chain reaction.
@ast
Enzymatic amplification of pla ...... the polymerase chain reaction.
@en
Enzymatic amplification of pla ...... the polymerase chain reaction.
@nl
type
label
Enzymatic amplification of pla ...... the polymerase chain reaction.
@ast
Enzymatic amplification of pla ...... the polymerase chain reaction.
@en
Enzymatic amplification of pla ...... the polymerase chain reaction.
@nl
prefLabel
Enzymatic amplification of pla ...... the polymerase chain reaction.
@ast
Enzymatic amplification of pla ...... the polymerase chain reaction.
@en
Enzymatic amplification of pla ...... the polymerase chain reaction.
@nl
P2093
P2860
P356
P1476
Enzymatic amplification of pla ...... the polymerase chain reaction.
@en
P2093
P2860
P304
P356
10.1172/JCI113656
P407
P577
1988-08-01T00:00:00Z