Publications:

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Oxidative Stress and Inflammation in B-Cell Lymphomas.

Antioxidants (Basel, Switzerland)

Sousa-Pimenta, Mário M; Estevinho, Maria Manuela MM; Sousa Dias, Miguel M; Martins, Ângelo Â; Estevinho, Letícia M LM

Publication Date: 2023-04-15

Variant appearance in text: NOS2A: Ser608Leu

PubMed Link: 37107311

Variant Present in the following documents:

• Main text
• antioxidants-12-00936.pdf

View BVdb publication page

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Association of nitric oxide synthase gene polymorphism with asthma: A systematic review and meta-analysis.

The Clinical Respiratory Journal

Fan, Zeru Z; Liu, Tao T; Na, Wei W

Publication Date: 2023-04-19

Variant appearance in text: NOS2: Ser608Leu

PubMed Link: 37076778

Variant Present in the following documents:

• Main text
• CRJ-17-516.pdf

View BVdb publication page

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Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications

Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA

Publication Date: 2023-04-03

Variant appearance in text: NOS2: S608L

PubMed Link: 37012232

Variant Present in the following documents:

• 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2

View BVdb publication page

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Molecular Genetics of Abnormal Redox Homeostasis in Type 2 Diabetes Mellitus.

International Journal Of Molecular Sciences

Azarova, Iuliia I; Polonikov, Alexey A; Klyosova, Elena E

Publication Date: 2023-03-01

Variant appearance in text: rs2297518

PubMed Link: 36902173

Variant Present in the following documents:

• Main text
• ijms-24-04738.pdf

View BVdb publication page

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Gene-Folic Acid Interactions and Risk of Conotruncal Heart Defects: Results from the National Birth Defects Prevention Study.

Genes

Webber, Daniel M DM; Li, Ming M; MacLeod, Stewart L SL; Tang, Xinyu X; Levy, Joseph W JW; Karim, Mohammad A MA; Erickson, Stephen W SW; Hobbs, Charlotte A CA; The National Birth Defects Prevention Study,

Publication Date: 2023-01-09

Variant appearance in text: rs2297518

PubMed Link: 36672920

Variant Present in the following documents:

• Main text
• genes-14-00180.pdf

View BVdb publication page

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Genetic polymorphisms and their effects on the severity of silicosis in workers exposed to silica in Brazil.

Jornal Brasileiro De Pneumologia : Publicacao Oficial Da Sociedade Brasileira De Pneumologia E Tisilogia

Castro, Marcos César Santos de MCS; Nani, Angela Santos Ferreira ASF; Salum, Kaio Cezar Rodrigues KCR; Rolando, Jônatas de Mendonça JM; Santos, Júlia Fernandes Barbosa Dos JFBD; Castro, Hermano Albuquerque de HA; Ribeiro, Patrícia Canto PC; Costa, Walter W; Mello, Cícero Brasileiro de CB; Kohlrausch, Fabiana Barzotto FB

Publication Date: 2022

Variant appearance in text: NOS2: Ser608Leu; rs2297518

PubMed Link: 36350953

Variant Present in the following documents:

• Main text
• 1806-3756-jbpneu-48-05-e20220167.pdf

View BVdb publication page

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Eucommia ulmoides Oliver's Multitarget Mechanism for Treatment of Ankylosing Spondylitis: A Study Based on Network Pharmacology and Molecular Docking.

Evidence-Based Complementary And Alternative Medicine : Ecam

Zhang, Hong-Sheng HS; Zhang, Sheng-Nan SN; Guo, Wei-Kun WK; He, Sheng-Hua SH

Publication Date: 2022

Variant appearance in text: rs2297518

PubMed Link: 36267087

Variant Present in the following documents:

• Main text
• ECAM2022-3699146.pdf

View BVdb publication page

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: NOS2: S608L

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2

View BVdb publication page

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: NOS2: S608L; rs2297518

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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Sex-specific association between inflammation and endothelial function relevant gene and vulnerable carotid plaque.

Frontiers In Physiology

Li, Jie J; Zhang, Ping P; Yi, Xingyang X; Luo, Hua H; Yu, Ming M; Chen, Hong H; Wang, Chun C

Publication Date: 2022

Variant appearance in text: rs2297518

PubMed Link: 36060677

Variant Present in the following documents:

• Main text
• fphys-13-977578.pdf

View BVdb publication page

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Outcomes of Genetic Testing-Based Cardiac Rehabilitation Program in Patients with Acute Myocardial Infarction after Percutaneous Coronary Intervention.

Cardiology Research And Practice

Yu, Xing X; Fan, Yuxuan Y; Sun, Xiaopeng X; Wang, Xiaojing X; Guo, Qi Q; Fan, Zhiqing Z

Publication Date: 2022

Variant appearance in text: rs2297518

PubMed Link: 36032316

Variant Present in the following documents:

• 9742071.f1.xlsx, sheet 1
• CRP2022-9742071.pdf

View BVdb publication page

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Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.

Npj Parkinson'S Disease

Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD

Publication Date: 2022-06-29

Variant appearance in text: NOS2: S608L; rs2297518

PubMed Link: 35768426

Variant Present in the following documents:

• 41531_2022_346_MOESM2_ESM.xlsx, sheet 1
• 41531_2022_346_MOESM4_ESM.xlsx, sheet 1

View BVdb publication page

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Variation of genes encoding nitric oxide synthases and antioxidant enzymes as potential risks of multiple sclerosis development: a preliminary study.

Scientific Reports

Wigner, Paulina P; Dziedzic, Angela A; Synowiec, Ewelina E; Miller, Elzbieta E; Bijak, Michal M; Saluk-Bijak, Joanna J

Publication Date: 2022-06-22

Variant appearance in text: NOS2: Ser608Leu; rs2297518

PubMed Link: 35732787

Variant Present in the following documents:

• Main text
• 41598_2022_Article_14795.pdf

View BVdb publication page

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Gasotransmitters in the tumor microenvironment: Impacts on cancer chemotherapy (Review).

Molecular Medicine Reports

Salihi, Abbas A; Al-Naqshabandi, Mohammed A MA; Khudhur, Zhikal Omar ZO; Housein, Zjwan Z; Hama, Harmand A HA; Abdullah, Ramyar M RM; Hussen, Bashdar Mahmud BM; Alkasalias, Twana T

Publication Date: 2022-07

Variant appearance in text: NOS2: Ser608Leu

PubMed Link: 35616143

Variant Present in the following documents:

• mmr-26-01-12749.pdf

View BVdb publication page

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Single-nucleotide polymorphisms as important risk factors of diabetes among Middle East population.

Human Genomics

Akhlaghipour, Iman I; Bina, Amir Reza AR; Mogharrabi, Mohammad Reza MR; Fanoodi, Ali A; Ebrahimian, Amir Reza AR; Khojasteh Kaffash, Soroush S; Babazadeh Baghan, Atefeh A; Khorashadizadeh, Mohammad Erfan ME; Taghehchian, Negin N; Moghbeli, Meysam M

Publication Date: 2022-04-02

Variant appearance in text: rs2297518

PubMed Link: 35366956

Variant Present in the following documents:

• Main text

View BVdb publication page

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Congenital Zika Syndrome: Genetic Avenues for Diagnosis and Therapy, Possible Management and Long-Term Outcomes.

Journal Of Clinical Medicine

Gullo, Giuseppe G; Scaglione, Marco M; Cucinella, Gaspare G; Riva, Arianna A; Coldebella, Davide D; Cavaliere, Anna Franca AF; Signore, Fabrizio F; Buzzaccarini, Giovanni G; Spagnol, Giulia G; Laganà, Antonio Simone AS; Noventa, Marco M; Zaami, Simona S

Publication Date: 2022-03-01

Variant appearance in text: rs2297518

PubMed Link: 35268441

Variant Present in the following documents:

• Main text
• jcm-11-01351.pdf

View BVdb publication page

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Preeclampsia, Natural History, Genes, and miRNAs Associated with the Syndrome.

Journal Of Pregnancy

Parada-Niño, Laura L; Castillo-León, Luisa Fernanda LF; Morel, Adrien A

Publication Date: 2022

Variant appearance in text: rs2297518

PubMed Link: 35198246

Variant Present in the following documents:

• JP2022-3851225.pdf

View BVdb publication page

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Nitric Oxide Synthase 2 Promoter Polymorphism Is a Risk Factor for Allergic Asthma in Children.

Medicina (Kaunas, Lithuania)

Nowakowska, Joanna J; Sobkowiak, Paulina P; Bręborowicz, Anna A; Mrówczyńska, Magdalena M; Wojsyk-Banaszak, Irena I; Szczepankiewicz, Aleksandra A

Publication Date: 2021-12-08

Variant appearance in text: rs2297518

PubMed Link: 34946286

Variant Present in the following documents:

• Main text
• medicina-57-01341.pdf

View BVdb publication page

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Nitric Oxide Synthase 2 Promoter Polymorphism Is a Risk Factor for Allergic Asthma in Children.

Medicina (Kaunas, Lithuania)

Nowakowska, Joanna J; Sobkowiak, Paulina P; Bręborowicz, Anna A; Mrówczyńska, Magdalena M; Wojsyk-Banaszak, Irena I; Szczepankiewicz, Aleksandra A

Publication Date: 2021-12-08

Variant appearance in text: rs2297518

PubMed Link: 34946286

Variant Present in the following documents:

• Main text
• medicina-57-01341.pdf

View BVdb publication page

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Genome-Wide Landscape of North-Eastern European Populations: A View from Lithuania.

Genes

Urnikyte, Alina A; Molyte, Alma A; Kučinskas, Vaidutis V

Publication Date: 2021-10-28

Variant appearance in text: rs2297518

PubMed Link: 34828336

Variant Present in the following documents:

• Main text
• genes-12-01730.pdf

View BVdb publication page

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An Overview of NO Signaling Pathways in Aging.

Molecules (Basel, Switzerland)

Pourbagher-Shahri, Ali Mohammad AM; Farkhondeh, Tahereh T; Talebi, Marjan M; Kopustinskiene, Dalia M DM; Samarghandian, Saeed S; Bernatoniene, Jurga J

Publication Date: 2021-07-27

Variant appearance in text: rs2297518

PubMed Link: 34361685

Variant Present in the following documents:

• Main text
• molecules-26-04533.pdf

View BVdb publication page

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The Role of Single Nucleotide Variants of NOS1, NOS2, and NOS3 Genes in the Development of the Phenotype of Migraine and Arterial Hypertension.

Brain Sciences

Moskaleva, Polina V PV; Shnayder, Natalya A NA; Petrova, Marina M MM; Kaskaeva, Daria S DS; Gavrilyuk, Oksana A OA; Radostev, Sergey V SV; Garganeeva, Natalia P NP; Sharavii, Victoria B VB; Vaiman, Elena E EE; Nasyrova, Regina F RF

Publication Date: 2021-06-07

Variant appearance in text: rs2297518

PubMed Link: 34200123

Variant Present in the following documents:

• Main text
• brainsci-11-00753.pdf

View BVdb publication page

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Association of NOS2A gene polymorphisms with susceptibility to bovine tuberculosis in Chinese Holstein cattle.

Plos One

Chai, Jun J; Wang, Qinglu Q; Qin, Bo B; Wang, Shengkui S; Wang, Youtao Y; Shahid, Muhammad M; Liu, Kai K; Zhang, Yifang Y; Qu, Weijie W

Publication Date: 2021

Variant appearance in text: rs2297518

PubMed Link: 34138949

Variant Present in the following documents:

• Main text
• pone.0253339.pdf

View BVdb publication page

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Medication-related osteonecrosis of the jaw (MRONJ) and eNOS Polymorphisms in multiple myeloma patients: a single center experience.

Bmc Oral Health

Taş Ozyurtseven, Betul B; Serin, Istemi I; Nursal, Ayse Feyda AF; Pehlivan, Sacide S; Pehlivan, Mustafa M

Publication Date: 2021-05-18

Variant appearance in text: rs2297518

PubMed Link: 34006261

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Susceptibility to Drug Teratogenicity: A Systematic Literature Review.

Frontiers In Genetics

Gomes, Julia do Amaral JDA; Olstad, Emilie Willoch EW; Kowalski, Thayne Woycinck TW; Gervin, Kristina K; Vianna, Fernanda Sales Luiz FSL; Schüler-Faccini, Lavínia L; Nordeng, Hedvig Marie Egeland HME

Publication Date: 2021

Variant appearance in text: rs2297518

PubMed Link: 33981330

Variant Present in the following documents:

• Main text

View BVdb publication page

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Antioxidants-Related Superoxide Dismutase (SOD), Catalase (CAT), Glutathione Peroxidase (GPX), Glutathione-S-Transferase (GST), and Nitric Oxide Synthase (NOS) Gene Variants Analysis in an Obese Population: A Preliminary Case-Control Study.

Antioxidants (Basel, Switzerland)

Gusti, Amani M T AMT; Qusti, Safaa Y SY; Alshammari, Eida M EM; Toraih, Eman A EA; Fawzy, Manal S MS

Publication Date: 2021-04-13

Variant appearance in text: NOS2: S608L; rs2297518

PubMed Link: 33924357

Variant Present in the following documents:

• Main text

View BVdb publication page

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The Role of Single-Nucleotide Variants of NOS1, NOS2, and NOS3 Genes in the Comorbidity of Arterial Hypertension and Tension-Type Headache.

Molecules (Basel, Switzerland)

Shnayder, Natalia A NA; Petrova, Marina M MM; Moskaleva, Polina V PV; Shesternya, Pavel A PA; Pozhilenkova, Elena A EA; Nasyrova, Regina F RF

Publication Date: 2021-03-12

Variant appearance in text: rs2297518

PubMed Link: 33809023

Variant Present in the following documents:

• Main text

View BVdb publication page

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Single-Nucleotide Polymorphisms in Oxidative Stress-Related Genes and the Risk of a Stroke in a Polish Population-A Preliminary Study.

Brain Sciences

Synowiec, Ewelina E; Wigner, Paulina P; Cichon, Natalia N; Watala, Cezary C; Czarny, Piotr P; Saluk-Bijak, Joanna J; Miller, Elzbieta E; Sliwinski, Tomasz T; Zielinska-Nowak, Ewa E; Bijak, Michal M

Publication Date: 2021-03-19

Variant appearance in text: NOS2: 1823C>T; Ser608Leu; rs2297518

PubMed Link: 33808851

Variant Present in the following documents:

• Main text

View BVdb publication page

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Glutathione S-Transferase (GSTT1 rs17856199) and Nitric Oxide Synthase (NOS2 rs2297518) Genotype Combination as Potential Oxidative Stress-Related Molecular Markers for Type 2 Diabetes Mellitus.

Diabetes, Metabolic Syndrome And Obesity : Targets And Therapy

Gusti, Amani M T AMT; Qusti, Safaa Y SY; Bahijri, Suhad M SM; Toraih, Eman A EA; Bokhari, Samia S; Attallah, Sami M SM; Alzahrani, Abdulwahab A; Alshehri, Wafaa M A WMA; Alotaibi, Hawazin H; Fawzy, Manal S MS

Publication Date: 2021

Variant appearance in text: NOS2: S608L; rs2297518

PubMed Link: 33790606

Variant Present in the following documents:

• Main text
• dmso-14-1385.pdf

View BVdb publication page

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Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.

Plos One

Sebate, Boiketlo B; Cuttler, Katelyn K; Cloete, Ruben R; Britz, Marcell M; Christoffels, Alan A; Williams, Monique M; Carr, Jonathan J; Bardien, Soraya S

Publication Date: 2021

Variant appearance in text: NOS2: 1823C>T; S608L; rs2297518

PubMed Link: 33770142

Variant Present in the following documents:

• pone.0249324.s003.xlsx, sheet 1

View BVdb publication page

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Association between Genetic Variants in NOS2 and TNF Genes with Congenital Zika Syndrome and Severe Microcephaly.

Viruses

Gomes, Julia A JA; Sgarioni, Eduarda E; Boquett, Juliano A JA; Terças-Trettel, Ana Cláudia P ACP; da Silva, Juliana H JH; Ribeiro, Bethânia F R BFR; Galera, Marcial F MF; de Oliveira, Thalita M TM; Carvalho de Andrade, Maria Denise F MDF; Carvalho, Isabella F IF; Schüler-Faccini, Lavínia L; Vianna, Fernanda S L FSL

Publication Date: 2021-02-20

Variant appearance in text: rs2297518

PubMed Link: 33672623

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variation in the immune system and malaria susceptibility in infants: a nested case-control study in Nanoro, Burkina Faso.

Malaria Journal

Natama, Hamatandi Magloire HM; Rovira-Vallbona, Eduard E; Krit, Meryam M; Guetens, Pieter P; Sorgho, Hermann H; Somé, M Athanase MA; Traoré-Coulibaly, Maminata M; Valéa, Innocent I; Mens, Petra F PF; Schallig, Henk D F H HDFH; Berkvens, Dirk D; Kestens, Luc L; Tinto, Halidou H; Rosanas-Urgell, Anna A

Publication Date: 2021-02-16

Variant appearance in text: rs2297518

PubMed Link: 33593344

Variant Present in the following documents:

• Main text
• 12936_2021_Article_3628.pdf

View BVdb publication page

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Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss.

Bmc Medical Genomics

Yang, Guangxian G; Yin, Yi Y; Tan, Zhiping Z; Liu, Jian J; Deng, Xicheng X; Yang, Yifeng Y

Publication Date: 2021-01-21

Variant appearance in text: rs2297518

PubMed Link: 33478437

Variant Present in the following documents:

• 12920_2021_871_MOESM2_ESM.xls, sheet 1

View BVdb publication page

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Analysis of NOS Gene Polymorphisms in Relation to Cluster Headache and Predisposing Factors in Sweden.

Brain Sciences

Ran, Caroline C; Michalska, Julia M JM; Fourier, Carmen C; Sjöstrand, Christina C; Waldenlind, Elisabet E; Steinberg, Anna A; Belin, Andrea C AC

Publication Date: 2020-12-31

Variant appearance in text: rs2297518

PubMed Link: 33396232

Variant Present in the following documents:

• Main text

View BVdb publication page

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Polygenic Risk Score for Early Prediction of Sepsis Risk in the Polytrauma Screening Cohort.

Frontiers In Genetics

Lu, Hongxiang H; Wen, Dalin D; Sun, Jianhui J; Du, Juan J; Qiao, Liang L; Zhang, Huacai H; Zeng, Ling L; Zhang, Lianyang L; Jiang, Jianxin J; Zhang, Anqiang A

Publication Date: 2020

Variant appearance in text: rs2297518

PubMed Link: 33281864

Variant Present in the following documents:

• Main text
• fgene-11-545564.pdf

View BVdb publication page

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Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.

European Journal Of Human Genetics : Ejhg

Publication Date: 2020-12

Variant appearance in text: rs2297518

PubMed Link: 33262486

Variant Present in the following documents:

• Main text

View BVdb publication page

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Cancer neoantigen prioritization through sensitive and reliable proteogenomics analysis.

Nature Communications

Wen, Bo B; Li, Kai K; Zhang, Yun Y; Zhang, Bing B

Publication Date: 2020-04-09

Variant appearance in text: NOS2: S608L

PubMed Link: 32273506

Variant Present in the following documents:

• 41467_2020_15456_MOESM6_ESM.xlsx, sheet 1

View BVdb publication page

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Nitrosative Stress Biomarkers in the Non-Stimulated and Stimulated Saliva, as well as Gingival Crevicular Fluid of Patients with Periodontitis: Review and Clinical Study.

Antioxidants (Basel, Switzerland)

Toczewska, Joanna J; Konopka, Tomasz T; Zalewska, Anna A; Maciejczyk, Mateusz M

Publication Date: 2020-03-21

Variant appearance in text: rs2297518

PubMed Link: 32245286

Variant Present in the following documents:

• Main text

View BVdb publication page

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Epistasis of polymorphisms related to the articular cartilage extracellular matrix in knee osteoarthritis: Analysis-based multifactor dimensionality reduction.

Genetics And Molecular Biology

Fernández-Torres, Javier J; Martínez-Nava, Gabriela Angélica GA; Zamudio-Cuevas, Yessica Y; Lozada, Carlos C; Garrido-Rodríguez, Daniela D; Martínez-Flores, Karina K

Publication Date: 2020

Variant appearance in text: rs2297518

PubMed Link: 32240281

Variant Present in the following documents:

• Main text
• 1415-4757-GMB-43-2-e20180349.pdf

View BVdb publication page

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Genetic Factors of Nitric Oxide's System in Psychoneurologic Disorders.

International Journal Of Molecular Sciences

Nasyrova, Regina F RF; Moskaleva, Polina V PV; Vaiman, Elena E EE; Shnayder, Natalya A NA; Blatt, Nataliya L NL; Rizvanov, Albert A AA

Publication Date: 2020-02-26

Variant appearance in text: NOS2: 1823C>T; rs2297518

PubMed Link: 32111088

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of candidate gene polymorphisms with diabetic retinopathy in Chinese patients with type 2 diabetes.

International Journal Of Ophthalmology

Fan, Wen-Ying WY; Gu, Hong H; Yang, Xiu-Fen XF; She, Chong-Yang CY; Liu, Xi-Pu XP; Liu, Ning-Pu NP

Publication Date: 2020

Variant appearance in text: rs2297518

PubMed Link: 32090041

Variant Present in the following documents:

• Main text

View BVdb publication page

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Meta-analysis and field synopsis of genetic variants associated with the risk and severity of acute pancreatitis.

Bjs Open

van den Berg, F F FF; Kempeneers, M A MA; van Santvoort, H C HC; Zwinderman, A H AH; Issa, Y Y; Boermeester, M A MA

Publication Date: 2020-02

Variant appearance in text: rs2297518

PubMed Link: 32011822

Variant Present in the following documents:

• BJS5-4-3-s002.xlsx, sheet 2

View BVdb publication page

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Inflammation and Endothelial Function Relevant Genetic Polymorphisms and Carotid Plaque in Chinese Population.

Journal Of Atherosclerosis And Thrombosis

Yi, Xingyang X; Zhu, Ling L; Sui, Guo G; Li, Jie J; Luo, Hua H; Yu, Ming M; Wang, Chun C; Chen, Xiaorong X; Wei, Wei W; Bao, Shaozhi S

Publication Date: 2020-09-01

Variant appearance in text: rs2297518

PubMed Link: 31956237

Variant Present in the following documents:

• Main text
• jat-27-978.pdf

View BVdb publication page

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External Replication of Urinary Bladder Cancer Prognostic Polymorphisms in the UK Biobank.

Frontiers In Oncology

Lipunova, Nadezda N; Wesselius, Anke A; Cheng, Kar K KK; van Schooten, Frederik J FJ; Cazier, Jean-Baptiste JB; Bryan, Richard T RT; Zeegers, Maurice P MP

Publication Date: 2019

Variant appearance in text: rs2297518

PubMed Link: 31681611

Variant Present in the following documents:

• Main text

View BVdb publication page

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Ankylosing spondylitis: etiology, pathogenesis, and treatments.

Bone Research

Zhu, Wei W; He, Xuxia X; Cheng, Kaiyuan K; Zhang, Linjie L; Chen, Di D; Wang, Xiao X; Qiu, Guixing G; Cao, Xu X; Weng, Xisheng X

Publication Date: 2019

Variant appearance in text: rs2297518

PubMed Link: 31666997

Variant Present in the following documents:

• Main text
• 41413_2019_Article_57.pdf

View BVdb publication page

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Mechanism and role of nitric oxide signaling in periodontitis.

Experimental And Therapeutic Medicine

Wang, Yan Y; Huang, Xiangdao X; He, Fuming F

Publication Date: 2019-11

Variant appearance in text: rs2297518

PubMed Link: 31641379

Variant Present in the following documents:

• Main text

View BVdb publication page

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: NOS2: S608L; rs2297518

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1

View BVdb publication page

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Exome Sequencing Reveals Immune Genes as Susceptibility Modifiers in Individuals with α1-Antitrypsin Deficiency.

Scientific Reports

Rigobello, Chiara C; Baraldo, Simonetta S; Tinè, Mariaenrica M; Ferrarotti, Ilaria I; Corsico, Angelo Guido AG; Bazzan, Erica E; Turato, Graziella G; Balestro, Elisabetta E; Biondini, Davide D; Valle, Giorgio G; Saetta, Marina M; Cosio, Manuel G MG

Publication Date: 2019-09-11

Variant appearance in text: rs2297518

PubMed Link: 31511551

Variant Present in the following documents:

• Main text

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