Pages that link to "Q12403602"
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The following pages link to Uri Seligsohn (Q12403602):
Displaying 50 items.
- ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families (Q28139538) (← links)
- The human platelet alphaIIb gene is not closely linked to its integrin partner beta3 (Q28143952) (← links)
- Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex (Q28201444) (← links)
- Identification and functional analysis of two novel mutations in the multidrug resistance protein 2 gene in Israeli patients with Dubin-Johnson syndrome (Q28209501) (← links)
- Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism (Q28211016) (← links)
- The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans (Q28344711) (← links)
- Glanzmann thrombasthenia: a model disease which paved the way to powerful therapeutic agents (Q29030850) (← links)
- An αIIb mutation in patients with Glanzmann thrombasthenia located in the N‐terminus of blade 1 of the β‐propeller (Asn2Asp) disrupts a calcium binding site in blade 6 (Q30395492) (← links)
- Discerning the ancestry of European Americans in genetic association studies (Q33315561) (← links)
- Clinical and genetic aspects of Glanzmann's thrombasthenia in Israel: report of 22 cases (Q33344939) (← links)
- ADAMTS-13 regulates platelet adhesion under flow. A new method for differentiation between inherited and acquired thrombotic thrombocytopenic purpura. (Q33372189) (← links)
- Trp207Gly in platelet glycoprotein Ibalpha is a novel mutation that disrupts the connection between the leucine-rich repeat domain and the disulfide loop structure and causes Bernard-Soulier syndrome (Q33373167) (← links)
- False-positive tests for heparin-induced thrombocytopenia in patients with antiphospholipid syndrome and systemic lupus erythematosus (Q33383739) (← links)
- Persistent neonatal thrombocytopenia can be caused by IgA antiplatelet antibodies in breast milk of immune thrombocytopenic mothers (Q33423643) (← links)
- Thrombasthenia in Iraqi Jews. (Q33466562) (← links)
- The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies (Q33610047) (← links)
- Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency (Q33934481) (← links)
- Dubin-Johnson syndrome in Israel. I. Clinical, laboratory, and genetic aspects of 101 cases (Q34053915) (← links)
- Characterization of seven novel mutations causing factor XI deficiency (Q34714901) (← links)
- Inhibitors to Factor XI in patients with severe Factor XI deficiency (Q36374056) (← links)
- Rare bleeding disorders (Q36473094) (← links)
- Genotype-phenotype correlation in combined deficiency of factor V and factor VIII. (Q36713533) (← links)
- Activation of human factor VII in plasma and in purified systems: roles of activated factor IX, kallikrein, and activated factor XII (Q37042626) (← links)
- Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping (Q37363234) (← links)
- The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel (Q37478529) (← links)
- Factor XI deficiency in humans (Q37561466) (← links)
- A unique interaction between alphaIIb and beta3 in the head region is essential for outside-in signaling-related functions of alphaIIbbeta3 integrin (Q38345507) (← links)
- Thromboembolic events in patients with severe inherited fibrinogen deficiency (Q38681844) (← links)
- The role of protein disulfide isomerase in the post-ligation phase of β3 integrin-dependent cell adhesion (Q38823834) (← links)
- Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndrome (Q38895475) (← links)
- Natural and artificial mutations in αIIb integrin lead to a structural deformation of a calcium-binding site (Q38957041) (← links)
- Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation (Q39012904) (← links)
- The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin (Q39192187) (← links)
- Age estimates of ancestral mutations causing factor VII deficiency and Dubin-Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrations (Q39266576) (← links)
- Unique disulfide bonds in epidermal growth factor (EGF) domains of β3 affect structure and function of αIIbβ3 and αvβ3 integrins in different manner (Q39401120) (← links)
- A mutation in the β3 cytoplasmic tail causes variant Glanzmann thrombasthenia by abrogating transition of αIIb β3 to an active state (Q39434031) (← links)
- A mutation in LMAN1 (ERGIC-53) causing combined factor V and factor VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia (Q39443697) (← links)
- Dubin-Johnson syndrome in Israel. II. Association with factor-VII deficiency (Q39444889) (← links)
- Repeat infusion of recombinant tissue-type plasminogen activator in patients with acute myocardial infarction and early recurrent myocardial ischemia (Q39514798) (← links)
- A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene. (Q39633085) (← links)
- Specific cysteines in beta3 are involved in disulfide bond exchange-dependent and -independent activation of alphaIIbbeta3. (Q39985185) (← links)
- A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia (Q40339375) (← links)
- Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients (Q40509506) (← links)
- Glanzmann thrombasthenia: new insights from an historical perspective. (Q40577006) (← links)
- Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus (Q40667595) (← links)
- Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene (Q40744627) (← links)
- Platelet fibrinogen and vitronectin in Glanzmann thrombasthenia: evidence consistent with specific roles for glycoprotein IIb/IIIA and alpha v beta 3 integrins in platelet protein trafficking (Q41141289) (← links)
- Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene (Q41380736) (← links)
- Activated factor VII: presence in factor IX concentrates and persistence in the circulation after infusion (Q41545752) (← links)
- Clinical utility gene card for: Glanzmann thrombasthenia (Q42007238) (← links)