Genotype analysis identifies the cause of the "royal disease"
about
Achievements and peculiarities in studies of ancient DNA and DNA from complicated forensic specimensAn interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B.A CpG mutational hotspot in a ONECUT binding site accounts for the prevalent variant of hemophilia B Leyden.Hemophilia A: Dental considerations and management.Delineating the Hemostaseome as an aid to individualize the analysis of the hereditary basis of thrombotic and bleeding disorders.Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP arrayHigh-throughput molecular diagnosis of von Willebrand disease by next generation sequencing methodsBalance between short and long isoforms of cFLIP regulates Fas-mediated apoptosis in vivoTargeting TFPI for hemophilia treatment.Molecular approaches for improved clotting factors for hemophilia.Contrasting selected reproductive challenges of today with those of antiquity--the past is prologue.Historical perspective and future direction of coagulation research.Past, present and future of hemophilia: a narrative review.Haemophilia B: current pharmacotherapy and future directions.Very early onset inflammatory bowel disease associated with aberrant trafficking of IL-10R1 and cure by T cell replete haploidentical bone marrow transplantation.Current management of hemophilia B: recommendations, complications and emerging issues.Haemophilia treatment in 2030.Strict 3' splice site sequence requirements for U2 snRNP recruitment after U2AF binding underlie a genetic defect leading to autoimmune disease.Genes and queens.Gene therapy for hemophilia: the clot thickens.Coagulation Factor IX for Hemophilia B Therapy.Advanced cell-based modeling of the royal disease: characterization of the mutated F9 mRNA.The international factor IX treatment network survey.A Highly Productive CHO Cell Line Secreting Human Blood Clotting Factor IX.
P2860
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P2860
Genotype analysis identifies the cause of the "royal disease"
description
2009 nî lūn-bûn
@nan
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genotype analysis identifies the cause of the "royal disease"
@ast
Genotype analysis identifies the cause of the "royal disease"
@en
Genotype analysis identifies the cause of the "royal disease"
@nl
type
label
Genotype analysis identifies the cause of the "royal disease"
@ast
Genotype analysis identifies the cause of the "royal disease"
@en
Genotype analysis identifies the cause of the "royal disease"
@nl
prefLabel
Genotype analysis identifies the cause of the "royal disease"
@ast
Genotype analysis identifies the cause of the "royal disease"
@en
Genotype analysis identifies the cause of the "royal disease"
@nl
P2093
P356
P1433
P1476
Genotype analysis identifies the cause of the "royal disease"
@en
P2093
Anastasia P Grigorenko
Ellen L W Kittler
Evgeny I Rogaev
Gulnaz Faskhutdinova
Yuri K Moliaka
P2860
P356
10.1126/SCIENCE.1180660
P407
P577
2009-11-06T00:00:00Z