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Polymorphisms of the human platelet alloantigens HPA-1, HPA-2, HPA-3, and HPA-4 in ischemic stroke.
- Published in:
- American Journal of Hematology, 2008, v. 83, n. 7, p. 570, doi. 10.1002/ajh.21171
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- Publication type:
- Article
Gene frequencies of human platelet alloantigens in Bahraini Arabs.
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- American Journal of Hematology, 2007, v. 82, n. 3, p. 242, doi. 10.1002/ajh.20769
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- Publication type:
- Article
Distinct association of factor V‐Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon.
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- American Journal of Hematology, 2006, v. 81, n. 8, p. 641, doi. 10.1002/ajh.20582
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- Publication type:
- Article
Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages.
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- American Journal of Hematology, 2005, v. 80, n. 1, p. 12, doi. 10.1002/ajh.20419
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- Publication type:
- Article
Factor V G1691A (Leiden) and prothrombin G20210A single‐nucleotide polymorphisms in type 2 diabetes mellitus.
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- American Journal of Hematology, 2005, v. 80, n. 1, p. 84, doi. 10.1002/ajh.20406
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- Publication type:
- Article
Reduction in coagulation factor VII plasma levels by R353Q but not the -323P0/10 promoter polymorphism in healthy Tunisians.
- Published in:
- American Journal of Hematology, 2005, v. 79, n. 1, p. 11, doi. 10.1002/ajh.20328
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- Publication type:
- Article
Factor V‐Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia.
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- American Journal of Hematology, 2004, v. 76, n. 3, p. 307, doi. 10.1002/ajh.20087
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- Publication type:
- Article
Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population.
- Published in:
- American Journal of Hematology, 2004, v. 76, n. 1, p. 85, doi. 10.1002/ajh.20047
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- Publication type:
- Article
Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.
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- American Journal of Hematology, 2002, v. 71, n. 4, p. 300, doi. 10.1002/ajh.10223
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- Publication type:
- Article
Prevalence and distribution of the prothrombin G20210A mutation.
- Published in:
- American Journal of Hematology, 2002, v. 71, n. 3, p. 235, doi. 10.1002/ajh.10218
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- Publication type:
- Article
Clinical and mechanistic differences between FK506 (tacrolimus) and cyclosporin A.
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- Nephrology Dialysis Transplantation, 2000, v. 15, n. 12, p. 1916, doi. 10.1093/ndt/15.12.1916
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- Publication type:
- Article
Authors' reply re: Genetic variation in the progesterone receptor gene and susceptibility to recurrent pregnancy loss: a case-control study.
- Published in:
- 2018
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- Publication type:
- letter
The genetic heterogeneity of Arab populations as inferred from HLA genes.
- Published in:
- PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0192269
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- Publication type:
- Article
Genetic diversity of human papillomavirus (HPV) as specified by the detection method, gender, and year of sampling: a retrospective cross-sectional study.
- Published in:
- Archives of Gynecology & Obstetrics, 2023, v. 307, n. 5, p. 1469, doi. 10.1007/s00404-022-06907-4
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- Publication type:
- Article
Apolipoprotein E Polymorphism in a Healthy Lebanese Population.
- Published in:
- Medical Principles & Practice, 1999, v. 8, n. 2, p. 105, doi. 10.1159/000026078
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- Publication type:
- Article
Relationship between VEGFA polymorphisms and serum VEGF protein levels and recurrent spontaneous miscarriage.
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- 2013
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- Publication type:
- Journal Article
Relationship between VEGFA polymorphisms and serum VEGF protein levels and recurrent spontaneous miscarriage.
- Published in:
- Human Reproduction, 2013, v. 28, n. 10, p. 2628, doi. 10.1093/humrep/det308
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- Publication type:
- Article
Maternal HLA class II alleles and haplotypes associated with altered risk of recurrent pregnancy loss: A case‐control study.
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- American Journal of Reproductive Immunology, 2024, v. 91, n. 2, p. 1, doi. 10.1111/aji.13817
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- Publication type:
- Article
Relation of resistin gene variants to resistin plasma levels and altered susceptibility to polycystic ovary syndrome: A case control study.
- Published in:
- American Journal of Reproductive Immunology, 2023, v. 90, n. 1, p. 1, doi. 10.1111/aji.13731
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- Publication type:
- Article
Evaluation of the angiogenic factors sFlt‐1, PlGF, and the sFlt‐1/PlGF ratio in preeclampsia and associated features.
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- American Journal of Reproductive Immunology, 2023, v. 90, n. 1, p. 1, doi. 10.1111/aji.13715
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- Publication type:
- Article
Human forkhead box protein 3 gene variants associated with altered susceptibility to idiopathic recurrent pregnancy loss: A retrospective case‐control study.
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- American Journal of Reproductive Immunology, 2022, v. 88, n. 2, p. 1, doi. 10.1111/aji.13551
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- Publication type:
- Article
Maternal HLA‐DR, HLA‐DQ, and HLA‐DP loci are linked with altered risk of recurrent pregnancy loss in Lebanese women: A case‐control study.
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- American Journal of Reproductive Immunology, 2019, v. 82, n. 4, p. N.PAG, doi. 10.1111/aji.13173
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- Publication type:
- Article
Levels of CD40L and other inflammatory biomarkers in obese and non-obese women with polycystic ovary syndrome.
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- American Journal of Reproductive Immunology, 2016, v. 76, n. 4, p. 285, doi. 10.1111/aji.12549
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- Publication type:
- Article
The effects of sildenafil citrate on intrauterine growth restriction: a systematic review and meta-analysis.
- Published in:
- BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05747-7
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- Publication type:
- Article
The prevalence of factor V R506Q mutation-Leiden among apparently healthy Lebanese.
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- American Journal of Hematology, 2000, v. 65, n. 1, p. 45, doi. 10.1002/1096-8652(200009)65:1<45::AID-AJH8>3.0.CO;2-V
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- Publication type:
- Article
Analysis of the Origin of Emiratis as Inferred from a Family Study Based on HLA-A , -C , -B , - DRB1 , and -DQB1 Genes.
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- Genes, 2023, v. 14, n. 6, p. 1159, doi. 10.3390/genes14061159
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- Publication type:
- Article
Utility of Circulating Cell-Free DNA in Assessing Microsatellite Instability and Loss of Heterozygosity in Breast Cancer Using Human Identification Approach.
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- Genes, 2022, v. 13, n. 4, p. 590, doi. 10.3390/genes13040590
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- Publication type:
- Article
Estimates of the incidence, prevalence, and factors associated with common sexually transmitted infections among Lebanese women.
- Published in:
- PLoS ONE, 2024, v. 19, n. 4, p. 1, doi. 10.1371/journal.pone.0301231
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- Publication type:
- Article
HLA allele and haplotype frequencies in Kazakhstani Russians and their relationship with other populations.
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- HLA: Immune Response Genetics, 2023, v. 101, n. 3, p. 249, doi. 10.1111/tan.14937
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- Publication type:
- Article
Origin of the Ukrainian minority of Kazakhstan as inferred from HLA‐A, ‐B, ‐C, ‐DRB1, and ‐DQB1 alleles and haplotypes distribution.
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- HLA: Immune Response Genetics, 2021, v. 98, n. 6, p. 525, doi. 10.1111/tan.14377
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- Publication type:
- Article
Distribution of HLA Class I and Class II alleles and haplotypes in German and Uzbek minorities in Kazakhstan, and relationship to other populations.
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- HLA: Immune Response Genetics, 2020, v. 96, n. 5, p. 615, doi. 10.1111/tan.14057
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- Publication type:
- Article
Contrasting association of Leptin receptor polymorphisms and haplotypes with polycystic ovary syndrome in Bahraini and Tunisian women: a case-control study.
- Published in:
- Bioscience Reports, 2021, v. 41, n. 1, p. 1, doi. 10.1042/BSR20202726
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- Publication type:
- Article
IKZF1 genetic variants rs4132601 and rs11978267 and acute lymphoblastic leukemia risk in Tunisian children: a case-control study.
- Published in:
- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0900-1
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- Publication type:
- Article
Detection of genetic mutations in patients with breast cancer from Saudi Arabia using Ion AmpliSeq™ Cancer Hotspot Panel v.2.0.
- Published in:
- Biomedical Reports, 2022, v. 16, n. 4, p. N.PAG, doi. 10.3892/br.2022.1509
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- Publication type:
- Article
The relation of vascular endothelial growth factor ( VEGF) gene polymorphisms on VEGF levels and the risk of vasoocclusive crisis in sickle cell disease.
- Published in:
- European Journal of Haematology, 2012, v. 89, n. 5, p. 403, doi. 10.1111/ejh.12003
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- Publication type:
- Article
Human platelet alloantigens (HPA) 1, HPA2, HPA3, HPA4, and HPA5 polymorphisms in sickle cell anemia patients with vaso-occlusive crisis.
- Published in:
- European Journal of Haematology, 2009, v. 83, n. 6, p. 579, doi. 10.1111/j.1600-0609.2009.01339.x
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- Publication type:
- Article
Sex Matching Plays a Role in Outcome of Kidney Transplant.
- Published in:
- Experimental & Clinical Transplantation, 2012, v. 10, n. 5, p. 466, doi. 10.6002/ect.2011.0205
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- Publication type:
- Article
Differential Association of FTO Gene variants and Haplotypes with the Susceptibility to Polycystic Ovary Syndrome According To Obesity in Women with PCOS.
- Published in:
- Reproductive Sciences, 2023, v. 30, n. 7, p. 2166, doi. 10.1007/s43032-022-01149-w
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- Publication type:
- Article
Contribution of ADIPOQ Variants to the Genetic Susceptibility of Recurrent Pregnancy Loss.
- Published in:
- Reproductive Sciences, 2021, v. 28, n. 1, p. 263, doi. 10.1007/s43032-020-00274-8
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- Publication type:
- Article
Protein Z Variants Associated With Protein Z Plasma Levels and With Risk of Idiopathic Recurrent Miscarriage.
- Published in:
- Reproductive Sciences, 2013, v. 20, n. 9, p. 1062, doi. 10.1177/1933719112473659
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- Publication type:
- Article
Impact of VEGFA −583C > T polymorphism on serum VEGF levels and the susceptibility to acute chest syndrome in pediatric patients with sickle cell disease.
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- Pediatric Blood & Cancer, 2014, v. 61, n. 12, p. 2310, doi. 10.1002/pbc.25158
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- Publication type:
- Article
Impact of VEGFA 583C>T Polymorphism on Serum VEGF Levels and the Susceptibility to Acute Chest Syndrome in Pediatric Patients With Sickle Cell Disease.
- Published in:
- Pediatric Blood & Cancer, 2014, v. 61, p. 2310, doi. 10.1002/pbc.25158
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- Publication type:
- Article
Contribution of Selective HLA-DRB1/DQB1 Alleles and Haplotypes to the Genetic Susceptibility of Type 1 Diabetes among Lebanese and Bahraini Arabs.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 9, p. 5104, doi. 10.1210/jc.2005-1166
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- Publication type:
- Article
Association of common IL-10 promoter gene variants with the susceptibility to head and neck cancer in Tunisia.
- Published in:
- Turkish Journal of Medical Sciences, 2019, v. 49, n. 1, p. 123, doi. 10.3906/sag-1805-21
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- Publication type:
- Article
Interleukin-10–592C/A, –819C/T and –1082A/G promoter variants affect the susceptibility to nephropathy in Tunisian type 2 diabetes (T2DM) patients.
- Published in:
- Clinical Endocrinology, 2009, v. 70, n. 3, p. 401, doi. 10.1111/j.1365-2265.2008.03337.x
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- Publication type:
- Article
Endothelial nitric oxide synthase Glu298Asp, 4b/a, and T-786C polymorphisms in type 2 diabetic retinopathy.
- Published in:
- Clinical Endocrinology, 2008, v. 68, n. 4, p. 542, doi. 10.1111/j.1365-2265.2007.03089.x
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- Publication type:
- Article
Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining study.
- Published in:
- BMC Medical Genomics, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s12920-020-00730-z
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- Publication type:
- Article
Identification of specific angiotensin-converting enzyme variants and haplotypes that confer risk and protection against type 2 diabetic nephropathy.
- Published in:
- Diabetes/Metabolism Research & Reviews, 2009, v. 25, n. 8, p. 717, doi. 10.1002/dmrr.1006
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- Publication type:
- Article
Predictive value of interleukin-10 promoter genotypes and haplotypes in determining the susceptibility to nephropathy in type 2 diabetes patients.
- Published in:
- Diabetes/Metabolism Research & Reviews, 2009, v. 25, n. 1, p. 57, doi. 10.1002/dmrr.892
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- Publication type:
- Article
Analysis of VEGFA Variants and Changes in VEGF Levels Underscores the Contribution of VEGF to Polycystic Ovary Syndrome.
- Published in:
- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0165636
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- Publication type:
- Article