Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 119 Records) |
Query Trace: ZAK[original query] |
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High Prevalence of Y Chromosome Partial Microdeletions in Overweight Men. Avicenna journal of medical biotechnology 0 7 (3): 97-100. Biabangard Zak Atefeh, Golalipour Masoud, Hadadchi Gholamre |
The CYBA Gene (?)49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease. BioMed research international 2016 2016 1539671. Nowak Tomasz, Niemiec Pawe?, Górczy?ska-Kosiorz Sylwia, Balcerzyk Anna, Iwanicki Tomasz, Krauze Jolanta, Grzeszczak Wladyslaw, Ochalska-Tyka Anna, Iwanicka Joanna, Zak Iwo |
[Desaturases of fatty acids (FADS) and their physiological and clinical implication]. Cas Lek Cesk 2016 155 (2): 15-21. Žák A, Slabý A, Tvrzická E, Jáchymová M, Macášek J, Vecka M, Zeman M, Stanková |
Metabolic dysregulation in first-episode schizophrenia patients with respect to genetic variation in one-carbon metabolism. Psychiatry research 2016 Apr 238 60-7. Misiak B?a?ej, ?aczma?ski ?ukasz, S?oka Natalia Kinga, Szmida El?bieta, Piotrowski Patryk, Loska Olga, ?l?zak Ryszard, Kiejna Andrzej, Frydecka Doro |
Genetic Variation in One-Carbon Metabolism and Changes in Metabolic Parameters in First-Episode Schizophrenia Patients. The international journal of neuropsychopharmacology 2016 Dec . Misiak B?a?ej, ?aczma?ski ?ukasz, S?oka Natalia Kinga, Szmida El?bieta, ?l?zak Ryszard, Piotrowski Patryk, Kiejna Andrzej, Frydecka Doro |
Association of heat shock protein70-2 (HSP70-2) gene polymorphism with obesity. Annals of human biology 2016 Nov 43 (6): 542-546. Mardan-Nik Maryam, Pasdar Alireza, Jamialahmadi Khadijeh, Avan Amir, Mohebati Mohsen, Esmaily Habibollah, Biabangard-Zak Atefeh, Afzal Javan Fahimeh, Rivandi Mahdi, Ferns Gordon A, Ghayour-Mobarhan Maj |
The rs10757278 Polymorphism of the 9p21.3 Locus in Children with Arterial Ischemic Stroke: A Family-Based and Case-Control Study. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2017 Aug . Niemiec Pawel, Balcerzyk Anna, Iwanicki Tomasz, Emich-Widera Ewa, Kopyta Ilona, Nowak Tomasz, Pilarska Ewa, Pienczk-R?c?awowicz Karolina, Kaci?ski Marek, Wendorff Janusz, Gorczynska-Kosiorz Sylwia, Trautsolt Wanda, Grzeszczak W?adys?aw, Zak Iwo |
Adrenergic receptor genotypes influence postoperative outcomes in infants in the Single-Ventricle Reconstruction Trial. The Journal of thoracic and cardiovascular surgery 2017 Jun . Ramroop Ronand, Manase George, Lu Danny, Manase Dorin, Chen Shan, Kim Richard, Lee Teresa, Mahle William T, McHugh Kimberly, Mitchell Mike, Tristani-Firouzi Martin, Wechsler Stephanie B, Wilder Nicole S, Zak Victor, Lafreniere-Roula Myriam, Newburger Jane W, Gaynor J William, Russell Mark W, Mital See |
A pharmacogenetic signature of high response to Copaxone in late-phase clinical-trial cohorts of multiple sclerosis. Genome medicine 2017 May 9 (1): 50. Ross Colin J, Towfic Fadi, Shankar Jyoti, Laifenfeld Daphna, Thoma Mathis, Davis Matthew, Weiner Brian, Kusko Rebecca, Zeskind Ben, Knappertz Volker, Grossman Iris, Hayden Michael |
Non-HLA gene polymorphisms in juvenile idiopathic arthritis: associations with disease outcome. Scandinavian journal of rheumatology 2017 Feb 1-8. Alberdi-Saugstrup M, Enevold C, Zak M, Nielsen S, Nordal E, Berntson L, Fasth A, Rygg M, Müller K, |
Prevalence of Genetic Disorders and GLUT1 Deficiency in a Ketogenic Diet Clinic. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2017 Nov 1-4. Hewson Stacy, Brunga Ledia, Ojeda Matilde Fernandez, Imhof Elizabeth, Patel Jaina, Zak Maria, Donner Elizabeth J, Kobayashi Jeff, Salomons Gajja S, Mercimek-Andrews Saad |
Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer. Molecular carcinogenesis 2017 Oct . Feng Yun, Wang Yanru, Liu Hongliang, Liu Zhensheng, Mills Coleman, Owzar Kouros, Xie Jichun, Han Younghun, Qian David C, Hung Rj Rayjean J, Brhane Yonathan, McLaughlin John, Brennan Paul, Bickeböller Heike, Rosenberger Albert, Houlston Richard S, Caporaso Neil, Landi Maria Teresa, Brüske Irene, Risch Angela, Ye Yuanqing, Wu Xifeng, Christiani David C, Amos Christopher I, Wei Qing |
IDH1 and IDH2 mutations in patients with acute myeloid leukemia: Suitable targets for minimal residual disease monitoring? Clinical biochemistry 2018 9 61 34-39. Petrova Lucie, Vrbacky Filip, Lanska Miriam, Zavrelova Alzbeta, Zak Pavel, Hrochova Kateri |
Assessment of the FTO gene polymorphisms in male patients with metabolic syndrome. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2018 Aug . ?l?zak Ryszard, Leszczy?ski Przemys?aw, Warzecha Magdalena, ?aczma?ski ?ukasz, Misiak B?a? |
The significance of enzyme and transporter polymorphisms for imatinib plasma levels and achieving an optimal response in chronic myeloid leukemia patients. Archives of medical science : AMS 2018 Oct 14 (6): 1416-1423. Belohlavkova Petra, Vrbacky Filip, Voglova Jaroslava, Racil Zdenek, Zackova Daniela, Hrochova Katerina, Malakova Jana, Mayer Jiri, Zak Pav |
Analysis of selected promoter polymorphisms and haplotypes of the CYBA gene encoding the p22phox, subunit of NADPH oxidases, in patients with coronary artery disease. Free radical research 2018 Oct 1-201. Nowak Tomasz, Niemiec Pawe?, Iwanicki Tomasz, Balcerzyk Anna, Krauze Jolanta, Ochalska-Tyka Anna, Zak Iwo |
Chromosomal Abnormalities and Prognosis in NPM1-Mutated Acute Myeloid Leukemia: A Pooled Analysis of Individual Patient Data From Nine International Cohorts. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2019 8 37 (29): 2632-2642. Angenendt Linus, Röllig Christoph, Montesinos Pau, Martínez-Cuadrón David, Barragan Eva, García Raimundo, Botella Carmen, Martínez Pilar, Ravandi Farhad, Kadia Tapan, Kantarjian Hagop M, Cortes Jorge, Juliusson Gunnar, Lazarevic Vladimir, Höglund Martin, Lehmann Sören, Recher Christian, Pigneux Arnaud, Bertoli Sarah, Dumas Pierre-Yves, Dombret Hervé, Preudhomme Claude, Micol Jean-Baptiste, Terré Christine, Rá?il Zden?k, Novák Jan, Žák Pavel, Wei Andrew H, Tiong Ing S, Wall Meaghan, Estey Elihu, Shaw Carole, Exeler Rita, Wagenführ Lisa, Stölzel Friedrich, Thiede Christian, Stelljes Matthias, Lenz Georg, Mikesch Jan-Henrik, Serve Hubert, Ehninger Gerhard, Berdel Wolfgang E, Kramer Michael, Krug Utz, Schliemann Christo |
Prognostic significance of mutation profile at diagnosis and mutation persistence during disease remission in adult acute myeloid leukaemia patients. British journal of haematology 2019 4 186 (2): 300-310. Folta Adam, Culen Martin, Jeziskova Ivana, Herudkova Zdenka, Tom Nikola, Hlubinkova Tereza, Janeckova Veronika, Durinikova Anna, Vydra Jan, Semerad Lukas, Dvorakova Dana, Remesova Hana, Cerovska Ela, Cetkovsky Petr, Jindra Pavel, Szotkowski Tomas, Zak Pavel, Mayer Jiri, Racil Zden |
Associations of Serum Uric Acid with Endogenous Cholesterol Synthesis Indices in Men with High Cardiometabolic Risk. Metabolic syndrome and related disorders 2020 3 18 (4): 212-218. Vecka Marek, Žák Aleš, Tvrzická Eva, Dušejovská Magdalena, Sta?ková Barbora, Zeman Mirosl |
Serum levels of selected cytokines and soluble adhesion molecules in acute myeloid leukemia: Soluble receptor for interleukin-2 predicts overall survival. Cytokine 2020 Jan 128 155005. Kupsa Tomas, Vanek Jan, Zak Pavel, Jebavy Ladislav, Horacek Jan |
Polymorphisms rs2167444 and rs508384 in the SCD1 Gene Are Linked with High ApoB-48 Levels and Adverse Profile of Cardiometabolic Risk Factors. Folia biologica 2019 65 (4): 159-169. Stanková B, Macášek J, Zeman M, Vecka M, Tvrzická E, Jáchymová M, Slabý A, Žák |
The Phenotypic Spectrum of Tuberous Sclerosis Complex: A Canadian Cohort. Child neurology open 2021 5 8 2329048X211012817. Alsowat Daad, Whitney Robyn, Hewson Stacy, Jain Puneet, Chan Valerie, Kabir Nadia, Amburgey Kimberly, Noone Damien, Lemaire Mathieu, McCoy Blathnaid, Zak Mar |
Altered Indices of Fatty Acid Elongases ELOVL6, ELOVL5, and ELOVL2 Activities in Patients with Impaired Fasting Glycemia. Metabolic syndrome and related disorders 2021 5 19 (7): 386-392. Macášek Jaroslav, Zeman Miroslav, Žák Aleš, Sta?ková Barbora, Vecka Mar |
A Matched Case-Control Study of Noncholesterol Sterols and Fatty Acids in Chronic Hemodialysis Patients. Metabolites 2021 Nov 11 (11): . Vecka Marek, Dušejovská Magdalena, Sta?ková Barbora, Rychlík Ivan, Žák Al |
Influence of Genetic Polymorphisms on Clinical Outcomes of Glatiramer Acetate in Multiple Sclerosis Patients. Journal of personalized medicine 2021 Oct 11 (10): . Zarzuelo-Romero María José, Pérez-Ramírez Cristina, Cura Yasmín, Carrasco-Campos María Isabel, Marangoni-Iglecias Luciana María, Ramírez-Tortosa María Carmen, Jiménez-Morales Alber |
Comparison of myeloid neoplasms with nonclassic 3q26.2/MECOM versus classic inv(3)/t(3;3) rearrangements reveals diverse clinicopathologic features, genetic profiles, and molecular mechanisms of MECOM activation. Genes, chromosomes & cancer 2021 10 61 (2): 71-80. Gao Juehua, Gurbuxani Sandeep, Zak Taylor, Kocherginsky Masha, Ji Peng, Wehbe Firas, Chen Qing, Chen Yi-Hua, Lu Xinyan, Jennings Lawrence, Frankfurt Olga, Altman Jessica, Sukhanova Madi |
Single and multiple point NRAS mutations in acute myeloid leukemia: a study of 327 well molecularly characterized patients. Leukemia & lymphoma 2022 9 63 (13): 3237-3240. Durinikova Anna, Folta Adam, Pardy Filip, Svaton Jan, Drncova Marie, Weinbergerova Barbora, Cetkovsky Petr, Racil Zdenek, Jindra Pavel, Szotkowski Tomas, Zak Pavel, Mayer Jiri, Jeziskova Iva |
FADS Polymorphisms Affect the Clinical and Biochemical Phenotypes of Metabolic Syndrome. Metabolites 2022 6 12 (6): . Žák Aleš, Jáchymová Marie, Burda Michal, Sta?ková Barbora, Zeman Miroslav, Slabý Adolf, Vecka Marek, Šeda Ond? |
Paraoxonase 1 rs662 polymorphism, its related variables, and COVID-19 intensity: Considering gender and post-COVID complications. Experimental biology and medicine (Maywood, N.J.) 2022 10 15353702221128563. Ghoreshi Zohreh-Al-Sadat, Abbasi-Jorjandi Mojtaba, Asadikaram Gholamreza, Sharif-Zak Mohsen, Seyedi Fatemeh, Khaksari Haddad Mohammad, Zangouey Mohammadre |
PTPN22 intron polymorphism rs1310182 (c.2054-852T>C) is associated with type 1 diabetes mellitus in patients of Armenian descent. PloS one 2023 6 18 (6): e0286743. Robert Žak, Lusine Navasardyan, Ján Hunák, Ji?ina Martin?, Petr Henebe |
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- Page last updated:Apr 29, 2024
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