170 results on '"Peretz H"'
Search Results
2. Point mutations regarded as missense mutations cause splicing defects in the factor XI gene
3. The cultural lens
4. The type I mutation causing factor XI deficiency in Ashkenazi Jews is a founder mutation of recent Eastern European origin: PA 3.14–3
5. Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients
6. Triggered C-reactive protein (CRP) concentrations and the CRP gene −717A>G polymorphism in acute stroke or transient ischemic attack
7. A 13-bp deletion in αIIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia
8. Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population
9. Time dependent protection of amifostine from renal and hematopoietic cisplatin induced toxicity
10. A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency
11. C01/060 THE INCIDENCE OF HCV GENOTYPES IN ISRAEL
12. The Human Platelet αIIb Gene Is Not Closely Linked to Its Integrin Partner β3
13. Molecular biology techniques in the diagnosis of monogenic diseases
14. HVEGF165 increases survival of transplanted hepatocytes within portal radicles: suggested mechanism for early cell engraftment
15. Value of IT Services
16. Visualization of the ultrastructural interface of cells with the outer and inner-surface of coral skeletons
17. Erratum: Aragonite crystalline matrix as an instructive microenvironment for neural development.Journal of Tissue Engineering and Regenerative Medicine2008; 2: 463-471.
18. Aragonite crystalline matrix as an instructive microenvironment for neural development
19. Interconnected Network of Ganglion-Like Neural Cell Spheres Formed on Hydrozoan Skeleton
20. Aragonite Crystalline Biomatrices Support Astrocytic Tissue Formationin Vitroandin Vivo
21. Aragonite Crystalline Biomatrices Support Astrocytic Tissue Formation in Vitro and in Vivo
22. Mo-P6:440 Association of common CRP gene polymorphisms with carotid atherosclerosis
23. O94 Feasibility of warfarin therapy in carriers of allelic variants of CYP2C9
24. The Human Platelet IIb Gene Is Not Closely Linked to Its Integrin Partner β3
25. Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene
26. One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews [see comments]
27. Factor VIII gene rearrangement in hemophilia A carrier detection: a word of caution [letter]
28. Screening for Down syndrome in the second trimester of pregnancy
29. Molecular biology techniques in the diagnosis of monogenic diseases
30. Detection of the Glanzmann's Thrombasthenia Mutations in Arab and Iraqi-Jewish Patients by Polymerase Chain Reaction and Restriction Analysis of Blood or Urine Samples
31. Type I mutation in the F11gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews
32. Long-term cerebral effects of small doses of X-irradiation in childhood as manifested in adult visual evoked responses.
33. A 13-bp deletion in αIIbgene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia
34. Cytokine network in nonresponding chronic hepatitis C patients with genotype 1: role of triple therapy with interferon alpha, ribavirin, and ursodeoxycholate
35. The Human Platelet ?IIb Gene Is Not Closely Linked to Its Integrin Partner ß3
36. Pheochromocytoma due to unilateral adrenal medullary hyperplasia
37. Detection of Hemophilia a Carriers by Repeated Factor VIII Activity/Antigen Determinations
38. Enzyme analysis of amniotic fluid for prenatal diagnosis of cystic fibrosis in high-risk pregnancies.
39. SYNOVIAL AND SERUM LEVELS OF METHOTREXATE DURING METHOTREXATE THERAPY OF RHEUMATOID ARTHRITIS
40. Lack of phosphatase activity in the "ultra fast" isoenzyme band.
41. A SHORT STUDY OF THE COMPLICATIONS OF CATARACT EXTRACTION IN EGYPT WITH SOME PRACTICAL SUGGESTIONS
42. Melatonin and mental capacities in newborn infants.
43. Erratum: Aragonite crystalline matrix as an instructive microenvironment for neural development. Journal of Tissue Engineering and Regenerative Medicine 2008; 2: 463-471.
44. Detection of Hemophilia a Carriers by Repeated Factor VIII Activity/Antigen Determinations
45. O94 Feasibility of warfarin therapy in carriers of allelic variants of CYP2C9
46. Interprofessional online course for telehealth delivery of pediatric developmental services.
47. Service Climate and Nurses' Collaboration with Families of Older Patients in the Care Process during Hospitalization.
48. Factors Predicting Older Patients' Family Involvement by Nursing Staff in Hospitals: The View of Hospital Nurses in Israel.
49. Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects.
50. Adjustment to Higher Education: A Comparison of Students With and Without Disabilities.
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