Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: ITGA2B[original query] |
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An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees. Journal of thrombosis and haemostasis : JTH 2006 1 4 (1): 137-47. Kunicki T J, Baronciani L, Canciani M T, Gianniello F, Head S R, Mondala T S, Salomon D R, Federici A |
Molecular defects in ITGA2B and ITGB3 genes in patients with Glanzmann thrombasthenia. Journal of thrombosis and haemostasis : JTH 2009 Nov 7 (11): 1878-85. Kannan M, Ahmad F, Yadav B K, Kumar R, Choudhry V P, Saxena |
Lack of association between aspirin responsiveness and seven candidate gene haplotypes in patients with symptomatic vascular disease. Thrombosis and haemostasis 2009 Jan 101 (1): 123-33. Kunicki Thomas J, Williams Shirley A, Nugent Diane J, Harrison Paul, Segal Helen C, Syed Anila, Rothwell Peter |
Human platelet antigen allele frequencies and new mutations on platelet glycoprotein genes in the Chinese Han population. Transfusion medicine (Oxford, England) 2011 Oct 21 (5): 330-7. Xu X, Liu Y, Ying Y, Tao S, Hong X, Zhu F, Lv H, Yan |
Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012 Jun 27 (6): 2328-37. Bertinetto Francesca Eleonora, Calafell Francesc, Roggero Stefano, Chidichimo Rossella, Garino Elena, Marcuccio Cristina, Coppo Rosanna, Scolari Francesco, Frascá Giovanni Maria, Savoldi Silvana, Schena Francesco Paolo, Amoroso Antonio, |
Prevalence of the HPA-18w to -21w alleles in the Chinese Han population. International journal of immunogenetics 2012 Aug . Liu Y, Hong X, Xu X, Ying Y, He J, Zhu F, Lv H, Yan L |
The association of four common polymorphisms from four candidate genes (COX-1, COX-2, ITGA2B, ITGA2) with aspirin insensitivity: a meta-analysis. PloS one 2013 8 (11): e78093. Weng Zhiyuan, Li Xiaobo, Li Yuqiong, Lin Jinxiu, Peng Feng, Niu Wenqu |
Noninvasive fetal genotyping of human platelet antigen-1a using targeted massively parallel sequencing. Transfusion 2015 Jun 55 (6 Pt 2): 1538-44. Wienzek-Lischka Sandra, Krautwurst Annika, Fröhner Vanessa, Hackstein Holger, Gattenlöhner Stefan, Bräuninger Andreas, Axt-Fliedner Roland, Degenhardt Jan, Deisting Christina, Santoso Sentot, Sachs Ulrich J, Bein Greg |
Identification of ITGA2B and ITGB3 Single-Nucleotide Polymorphisms and Their Influences on the Platelet Function. BioMed research international 2016 2016 5675084. Xiang Qian, Ji Shun-Dong, Zhang Zhuo, Zhao Xia, Cui Yi-M |
[Diagnostic analysis of glanzmann thrombasthenia caused by two novel ITGA2B gene mutations]. Zhonghua er ke za zhi = Chinese journal of pediatrics 2017 9 55 (9): 708-709. Sun A X, Yi X L, Mao |
Prognostic value of integrin variants and expression in post-operative patients with HBV-related hepatocellular carcinoma. Oncotarget 2017 Sep 8 (44): 76816-76831. Shang Liming, Ye Xinping, Zhu Guangzhi, Su Hao, Su Zhixiong, Chen Bin, Xiao Kaiyin, Li Lequn, Peng Minhao, Peng T |
ITGA2B and ITGB3 gene mutations associated with Glanzmann thrombasthenia. Platelets 2017 11 29 (1): 98-101. Nurden Alan T, Pillois Xavi |
Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients. NPJ genomic medicine 2019 2 4 4. Owaidah Tarek, Saleh Mahasen, Baz Batoul, Abdulaziz Basma, Alzahrani Hazza, Tarawah Ahmed, Almusa Abdulrahman, AlNounou Randa, AbaAlkhail Hala, Al-Numair Nouf, Altahan Rahaf, Abouelhoda Mohammed, Alamoudi Thamer, Monies Dorota, Jabaan Amjad, Al Tassan Na |
Prevalence of the Mutations Responsible for Glanzmann Thrombasthenia in Horses in Brazil. Animals : an open access journal from MDPI 2019 11 9 (11): . Leite Raíssa O, Ferreira Júlia F, Araújo César E T, Delfiol Diego J Z, Takahira Regina K, Borges Alexandre S, Oliveira-Filho Jose |
Association of autosomal-recessive-type distal renal tubular acidosis and Glanzmann thrombasthenia as a consequence of runs of homozygosity. Clinical case reports 2022 7 10 (7): e6070. Aso Keiko, Soutome Takehiko, Satoh Mari, Aoki Takako, Ogura Hiromi, Yamamoto Toshiyuki, Kanno Hitoshi, Takahashi Hiroyu |
Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease. Genes 2022 6 13 (6): . Naveed Muhammad Asif, Abid Aiysha, Ali Nadir, Hassan Yaqoob, Amar Ali, Javed Aymen, Qamar Khansa, Mustafa Ghulam, Raza Ali, Saleem Umera, Hussain Shabbir, Shakoor Madiha, Khaliq Shagufta, Mohsin Shahi |
Association of polymorphisms in genes encoding prothrombotic and cardiovascular risk factors with disease severity in COVID-19 patients: A pilot study. Journal of medical virology 2022 4 94 (8): 3669-3675. Lapi? Ivana, Radi? Antolic Margareta, Horvat Ivana, Premuži? Vedran, Pali? Jozefina, Rogi? Dunja, Zadro Rena |
Simultaneous genotyping for human platelet antigen systems and HLA-A and HLA-B loci by targeted next-generation sequencing. Frontiers in immunology 2022 10 13 945994. Wang Jielin, You Xuan, He Yanmin, Hong Xiaozhen, He Ji, Tao Sudan, Zhu Fami |
Whole-exome and targeted gene sequencing of large-cell lung carcinoma reveals recurrent mutations in the PI3K pathway. British journal of cancer 2023 5 . Jun-Hong Guo, Yu-Shui Ma, Jie-Wei Lin, Geng-Xi Jiang, Juan He, Hai-Min Lu, Wei Wu, Xun Diao, Qi-Yu Fan, Chun-Yan Wu, Ji-Bin Liu, Da Fu, Li-Kun H |
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