Pages that link to "Q37478529"

The following pages link to The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel (Q37478529):

Displaying 48 items.

• Glanzmann thrombasthenia (Q21203054) (← links)
• A point mutation in KINDLIN3 ablates activation of three integrin subfamilies in humans (Q24313548) (← links)
• Specificity of G alpha q and G alpha 11 gene expression in platelets and erythrocytes. Expressions of cellular differentiation and species differences (Q24529936) (← links)
• Biased exon/intron distribution of cryptic and de novo 3' splice sites (Q24817064) (← links)
• Inherited platelet disorders: toward DNA-based diagnosis (Q26752148) (← links)
• CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation (Q28118463) (← links)
• Ser-752-->Pro mutation in the cytoplasmic domain of integrin beta 3 subunit and defective activation of platelet integrin alpha IIb beta 3 (glycoprotein IIb-IIIa) in a variant of Glanzmann thrombasthenia (Q28118972) (← links)
• Molecular basis of Glanzmann's Thrombasthenia and current strategies in treatment (Q28216926) (← links)
• Alpha5beta1, alphaVbeta3 and the platelet-associated integrin alphaIIbbeta3 coordinately regulate adhesion and migration of differentiating mouse trophoblast cells (Q28591734) (← 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)
• The GPIIb/IIIa (integrin alphaIIbbeta3) odyssey: a technology-driven saga of a receptor with twists, turns, and even a bend (Q33381441) (← links)
• Glanzmann thrombasthenia: state of the art and future directions (Q33571529) (← links)
• Genetic analysis of integrin function in man: LAD-1 and other syndromes. (Q33998332) (← links)
• Glanzmann thrombasthenia secondary to a Gly273-->Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIb. (Q34119585) (← links)
• Demystified...adhesion molecule deficiencies (Q34158852) (← links)
• The platelet: life on the razor's edge between hemorrhage and thrombosis (Q34175105) (← links)
• Glanzmann thrombasthenia: a review of ITGA2B and ITGB3 defects with emphasis on variants, phenotypic variability, and mouse models (Q34216342) (← links)
• A new variant of Glanzmann's thrombasthenia (Strasbourg I). Platelets with functionally defective glycoprotein IIb-IIIa complexes and a glycoprotein IIIa 214Arg----214Trp mutation (Q34221553) (← links)
• Glanzmann's thrombasthenia: an overview (Q34859954) (← links)
• Platelet gene therapy improves hemostatic function for integrin αIIbβ3-deficient dogs (Q35035160) (← links)
• Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia. (Q35194533) (← links)
• Proteomic approaches to dissect platelet function: Half the story (Q35848791) (← links)
• Translating from the rivers of Babylon to the coronary bloodstream (Q36357988) (← links)
• Hematologically Important Mutations: Glanzmann Thrombasthenia (Q36870012) (← links)
• Neutrophil accumulation on activated, surface-adherent platelets in flow is mediated by interaction of Mac-1 with fibrinogen bound to alphaIIbbeta3 and stimulated by platelet-activating factor (Q37373855) (← links)
• Truncation of the cytoplasmic domain of beta3 in a variant form of Glanzmann thrombasthenia abrogates signaling through the integrin alpha(IIb)beta3 complex (Q37374506) (← links)
• Treatment and outcomes for epistaxis in children with Glanzmann's thrombasthenia (Q37812365) (← links)
• Do cell junction protein mutations cause an airway phenotype in mice or humans? (Q37836200) (← links)
• Are bone defects in rare patients with Glanzmann's thrombasthenia associated withITGB3orITGA2Bmutations? (Q37873940) (← links)
• Understanding the genetic basis of Glanzmann thrombasthenia: implications for treatment (Q38059249) (← links)
• Aberrant 3' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization (Q39113625) (← links)
• A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia (Q40339375) (← links)
• Adhesion molecules in scleroderma: collagen binding integrins (Q40403505) (← links)
• A Val193Met mutation in GPIIIa results in a GPIIb/IIIa receptor with a constitutively high affinity for a small ligand (Q40766649) (← links)
• Integrins and laminins in tissue remodeling (Q41469738) (← links)
• The biologic and clinical spectrum of Glanzmann's Thrombasthenia: implications of integrin αIIbβ3 for its pathogenesis (Q41553346) (← links)
• Severe juvenile vaginal bleeding due to Glanzmann's thrombasthenia: Case report and review of the literature (Q41718142) (← links)
• Lessons Learned from Phagocytic Function Studies in a Large Cohort of Patients with Recurrent Infections (Q43779609) (← links)
• AlphaIIbbeta3 integrin: new allelic variants in Glanzmann thrombasthenia, effects on ITGA2B and ITGB3 mRNA splicing, expression, and structure-function (Q44177708) (← links)
• Two genetic defects in alphaIIb are associated with type I Glanzmann's thrombasthenia in a Great Pyrenees dog: a 14-base insertion in exon 13 and a splicing defect of intron 13. (Q45872916) (← links)
• Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17 (Q47720581) (← links)
• Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in Portugal (Q48034905) (← links)
• Characterization of two new CD18 alleles causing severe leukocyte adhesion deficiency (Q48095907) (← links)
• ITGA2B and ITGB3 gene mutations associated with Glanzmann thrombasthenia (Q48326012) (← links)
• Excessive gingival bleeding in two patients with Glanzmann thrombasthenia. (Q51751582) (← links)
• Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of alphaIIbbeta3 integrin (ITGA2B, ITGB3). (Q51810420) (← links)
• Novel and recurrent mutations of ITGA2B and ITGB3 genes in Korean patients with Glanzmann thrombasthenia. (Q53393838) (← links)
• Isoelectric focusing and immunoblotting of the platelet membrane glycoprotein complex IIb. IIIA following urea solubilization (Q67599484) (← links)