Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 48 Records) |
Query Trace: MALL[original query] |
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Arylamine N-acetyltransferase gene polymorphisms: markers for atopic asthma, serum IgE and blood eosinophil counts. Pharmacogenomics 2006 Jul 7 (5): 673-82. Batra Jyotsna, Sharma Surendra K, Ghosh Balar |
Association of TNF haplotypes with asthma, serum IgE levels, and correlation with serum TNF-alpha levels. American journal of respiratory cell and molecular biology 2006 Oct 35 (4): 488-95. Sharma Shilpy, Sharma Amit, Kumar Sarvesh, Sharma Surendra K, Ghosh Balar |
Elevated levels of mannan-binding lectin [corrected] (MBL) and eosinophilia in patients of bronchial asthma with allergic rhinitis and allergic bronchopulmonary aspergillosis associate with a novel intronic polymorphism in MBL. Clinical and experimental immunology 2006 Mar 143 (3): 414-9. Kaur S, Gupta V K, Shah A, Thiel S, Sarma P U, Madan |
Association of inducible nitric oxide synthase with asthma severity, total serum immunoglobulin E and blood eosinophil levels. Thorax 2007 Jan 62 (1): 16-22. Batra J, Pratap Singh T, Mabalirajan U, Sinha A, Prasad R, Ghosh B |
Heterozygotes of NOS3 polymorphisms contribute to reduced nitrogen oxides in high-altitude pulmonary edema. Chest 2006 Nov 130 (5): 1511-9. Ahsan Aarif, Mohd Ghulam, Norboo Tsering, Baig Masroor A, Pasha M A Qad |
Association of a chromosome 1q21 locus in close proximity to a late cornified envelope-like proline-rich 1 (LELP1) gene with total serum IgE levels. Journal of human genetics 2007 52 (4): 378-83. Sharma Mamta, Mehla Kamiya, Batra Jyotsna, Ghosh Balar |
Genetic variants of FOXA2: risk of type 2 diabetes and effect on metabolic traits in North Indians. Journal of human genetics 2008 53 (11-12): 957-65. Tabassum Rubina, Chavali Sreenivas, Dwivedi Om Prakash, Tandon Nikhil, Bharadwaj Dwaipay |
Genetic contribution of chemokine receptor 2 (CCR2) polymorphisms towards increased serum total IgE levels in Indian asthmatics. Genomics 2009 Sep 94 (3): 161-8. Batra Jyotsna, Ghosh Balar |
Association analysis of TNFRSF1B polymorphisms with type 2 diabetes and its related traits in North India. Genomic medicine 2008 Dec 2 (3-4): 93-100. Tabassum Rubina, Chavali Sreenivas, Mahajan Anubha, Ghosh Saurabh, Madhu S V, Tandon Nikhil, Bharadwaj Dwaipay |
Multi-locus interactions of vascular homeostasis genes in essential hypertension: a gender-based study. Clinica chimica acta; international journal of clinical chemistry 2009 Jul 405 (1-2): 87-93. Kumar Rahul, Nejatizadeh Azim, Arif Ehtesham, Akhtar Salman, Gupta Mohit, Tyagi Sanjay, Goyal A K, Jain S K, Qadar Pasha M |
Analysis of flavin-containing monooxygenase 3 genotype data in populations administered the anti-schizophrenia agent olanzapine. Drug metabolism letters 2008 Apr 2 (2): 100-14. Cashman John R, Zhang Jun, Nelson Matthew R, Braun Andre |
Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms. Pharmacogenomics 2009 Feb 10 (2): 277-91. Gupta Meenal, Chauhan Chitra, Bhatnagar Pallav, Gupta Simone, Grover Sandeep, Singh Prashant K, Purushottam Meera, Mukherjee Odity, Jain Sanjeev, Brahmachari Samir K, Kukreti Ritushr |
BACE1 gene promoter single-nucleotide polymorphisms in Alzheimer's disease. Journal of molecular neuroscience : MN 2010 Sep 42 (1): 127-33. Zhou Weihui, Cai Fang, Li Yu, Yang George S, O'Connor Kathleen D, Holt Robert A, Song Weiho |
Absence of a general association between ABCB1 genetic variants and response to antiepileptic drugs in epilepsy patients. Biochimie 2010 Sep 92 (9): 1207-12. Grover Sandeep, Bala Kiran, Sharma Sangeeta, Gourie-Devi M, Baghel Ruchi, Kaur Harpreet, Gupta Meenal, Talwar Puneet, Kukreti Ritushr |
Obesity-dependent association of TNF-LTA locus with type 2 diabetes in North Indians. Journal of molecular medicine (Berlin, Germany) 2010 May 88 (5): 515-22. Mahajan Anubha, Tabassum Rubina, Chavali Sreenivas, Dwivedi Om Prakash, Chauhan Ganesh, Tandon Nikhil, Bharadwaj Dwaipay |
Combinatorial effect of TIMP-1 and a1AT gene polymorphisms on development of chronic obstructive pulmonary disease. Clinical biochemistry 2011 Sep 44 (13): 1067-73. Kumar Manish, Bhadoria D P, Dutta Koushik, Singh Seema, Gupta Jyotsana, Kumar Ram, Chhillar Anil K, Yadav Vibha, Singh Bharat, Sharma G |
Depressive rumination and the C957T polymorphism of the DRD2 gene. Cognitive, affective & behavioral neuroscience 2012 Dec 12 (4): 741-7. Whitmer Anson J, Gotlib Ian |
The a(1)AT and TIMP-1 Gene Polymorphism in the Development of Asthma. Comparative and functional genomics 2012 2012 968267. Kumar Manish, Bhadoria D P, Dutta Koushik, Kumar F Mitesh, Singh Bharat, Singh Seema, Chhillar Anil K, Behera D, Sharma G |
Association of adiponectin gene functional polymorphisms (-11377C/G and +45T/G) with nonalcoholic fatty liver disease. Gene 2012 Mar 496 (1): 63-7. Gupta Abhishak Chandra, Misra Richa, Sakhuja Puja, Singh Yogendra, Basir Seemi Farhat, Sarin Shiv Kum |
Traffic, asthma and genetics: combining international birth cohort data to examine genetics as a mediator of traffic-related air pollution's impact on childhood asthma. European journal of epidemiology 2013 Jul 28 (7): 597-606. MacIntyre Elaina A, Carlsten Christopher, MacNutt Meaghan, Fuertes Elaine, Melén Eric, Tiesler Carla M T, Gehring Ulrike, Krämer Ursula, Klümper Claudia, Kerkhof Marjan, Chan-Yeung Moira, Kozyrskyj Anita L, Berdel Dietrich, Bauer Carl Peter, Herbarth Olf, Bauer Mario, Schaaf Beate, Koletzko Sibylle, Pershagen Goran, Brunekreef Bert, Heinrich Joachim, Brauer Micha |
Airway mucus obstruction triggers macrophage activation and matrix metalloproteinase 12-dependent emphysema. American journal of respiratory cell and molecular biology 2014 Nov 51 (5): 709-20. Trojanek Joanna B, Cobos-Correa Amanda, Diemer Stefanie, Kormann Michael, Schubert Susanne C, Zhou-Suckow Zhe, Agrawal Raman, Duerr Julia, Wagner Claudius J, Schatterny Jolanthe, Hirtz Stephanie, Sommerburg Olaf, Hartl Dominik, Schultz Carsten, Mall Marcus |
Antisense oligonucleotide eluforsen improves CFTR function in F508del cystic fibrosis. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2018 11 18 (4): 536-542. Sermet-Gaudelus Isabelle, Clancy John P, Nichols David P, Nick Jerry A, De Boeck Kris, Solomon George M, Mall Marcus A, Bolognese James, Bouisset Florilene, den Hollander Wilhelmina, Paquette-Lamontagne Nicolas, Tomkinson Nigel, Henig Noreen, Elborn J Stuart, Rowe Steven |
VX-659-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles. The New England journal of medicine 2018 10 379 (17): 1599-1611. Davies Jane C, Moskowitz Samuel M, Brown Cynthia, Horsley Alexander, Mall Marcus A, McKone Edward F, Plant Barry J, Prais Dario, Ramsey Bonnie W, Taylor-Cousar Jennifer L, Tullis Elizabeth, Uluer Ahmet, McKee Charlotte M, Robertson Sarah, Shilling Rebecca A, Simard Christopher, Van Goor Fredrick, Waltz David, Xuan Fengjuan, Young Tim, Rowe Steven M, |
Fatigue and depression predict health-related quality of life in patients with pediatric-onset multiple sclerosis. Multiple sclerosis and related disorders 2019 9 36 101368. Storm Van's Gravesande Karin, Blaschek Astrid, Calabrese Pasquale, Rostásy Kevin, Huppke Peter, Kessler J Josef, Kalbe Elke, Mall Volker, |
Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease. BMC research notes 2019 Nov 12 (1): 759. Eltermaa Mall, Jakobson Maili, Utt Meeme, Kõks Sulev, Mägi Reedik, Starkopf Jo |
CRISPRi-mediated functional analysis of lung disease-associated loci at non-coding regions. NAR genomics and bioinformatics 2020 6 2 (2): lqaa036. Stuart William D, Guo Minzhe, Fink-Baldauf Iris M, Coleman Alan M, Clancy John P, Mall Marcus A, Lim Foong-Yen, Brewington John J, Maeda Yuta |
Oncogenic states dictate the prognostic and predictive connotations of intratumoral immune response. Journal for immunotherapy of cancer 2020 5 8 (1): . Roelands Jessica, Hendrickx Wouter, Zoppoli Gabriele, Mall Raghvendra, Saad Mohamad, Halliwill Kyle, Curigliano Giuseppe, Rinchai Darawan, Decock Julie, Delogu Lucia G, Turan Tolga, Samayoa Josue, Chouchane Lotfi, Ballestrero Alberto, Wang Ena, Finetti Pascal, Bertucci Francois, Miller Lance D, Galon Jerome, Marincola Francesco M, Kuppen Peter J K, Ceccarelli Michele, Bedognetti Davi |
De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy. Genetics in medicine : official journal of the American College of Medical Genetics 2020 5 22 (8): 1413-1417. Singh Sakshi, Gupta Aditi, Zech Michael, Sigafoos Ashley N, Clark Karl J, Dincer Yasemin, Wagner Matias, Humberson Jennifer B, Green Sarah, van Gassen Koen, Brandt Tracy, Schnur Rhonda E, Millan Francisca, Si Yue, Mall Volker, Winkelmann Juliane, Gavrilova Ralitza H, Klee Eric W, Engleman Kendra, Safina Nicole P, Slaugh Rachel, Bryant Emily M, Tan Wen-Hann, Granadillo Jorge, Misra Sunita N, Schaefer G Bradley, Towner Shelley, Brilstra Eva H, Koeleman Bobby P |
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study. European journal of public health 2022 2 32 (3): 422-428. Sanin Veronika, Schmieder Raphael, Ates Sara, Schlieben Lea Dewi, Wiehler Jens, Sun Ruoyu, Decker Manuela, Sander Michaela, Holdenrieder Stefan, Kohlmayer Florian, Friedmann Anna, Mall Volker, Feiler Therese, Dreßler Arne, Strom Tim M, Prokisch Holger, Meitinger Thomas, von Scheidt Moritz, Koenig Wolfgang, Leipold Georg, Schunkert Heribert, |
Two rare copy number variants involving loss of NPHP1, MALL, and MTLN genes contribute to nephronophthisis-induced nephropathy progression in a family: A case report. Nigerian journal of clinical practice 2023 5 26 (4): 524-527. C H Liu, L J Li, M Tian, G H Cao, S F Zhang, J T |
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- Page last updated:Apr 22, 2024
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