Publications:

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A case of midbrain germinoma: A literature review for radiographic and clinical features.

Neuro-Oncology Advances

Miyake, Yohei Y; Tateishi, Kensuke K; Oshima, Akito A; Hongo, Takeshi T; Satomi, Kaishi K; Ichimura, Koichi K; Kato, Ayumi A; Iwashita, Hiromichi H; Utsunomiya, Daisuke D; Yamamoto, Tetsuya T

Publication Date: 2023

Variant appearance in text: PLD2: 514C>T; Arg172Cys; rs2286672

PubMed Link: 37215953

Variant Present in the following documents:

• vdad043_suppl_supplementary_tables.xlsx, sheet 1

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: PLD2: R172C

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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Spatial genomic diversity associated with APOBEC mutagenesis in squamous cell carcinoma arising from ovarian teratoma.

Cancer Science

Tamura, Ryo R; Nakaoka, Hirofumi H; Yachida, Nozomi N; Ueda, Haruka H; Ishiguro, Tatsuya T; Motoyama, Teiichi T; Inoue, Ituro I; Enomoto, Takayuki T; Yoshihara, Kosuke K

Publication Date: 2023-02-10

Variant appearance in text: PLD2: 514C>T

PubMed Link: 36762791

Variant Present in the following documents:

• CAS-114-2145-s001.xlsx, sheet 6

View BVdb publication page

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Genome-wide association study for systemic lupus erythematosus in an egyptian population.

Frontiers In Genetics

Elghzaly, Ashraf A AA; Sun, Celi C; Looger, Loren L LL; Hirose, Misa M; Salama, Mohamed M; Khalil, Noha M NM; Behiry, Mervat Essam ME; Hegazy, Mohamed Tharwat MT; Hussein, Mohamed Ahmed MA; Salem, Mohamad Nabil MN; Eltoraby, Ehab E; Tawhid, Ziyad Z; Alwasefy, Mona M; Allam, Walaa W; El-Shiekh, Iman I; Elserafy, Menattallah M; Abdelnaser, Anwar A; Hashish, Sara S; Shebl, Nourhan N; Shahba, Abeer Abdelmonem AA; Elgirby, Amira A; Hassab, Amina A; Refay, Khalida K; El-Touchy, Hanan Mohamed HM; Youssef, Ali A; Shabacy, Fatma F; Hashim, Abdelkader Ahmed AA; Abdelzaher, Asmaa A; Alshebini, Emad E; Fayez, Dalia D; El-Bakry, Samah A SA; Elzohri, Mona H MH; Abdelsalam, Eman Nagiub EN; El-Khamisy, Sherif F SF; Ibrahim, Saleh S; Ragab, Gaafar G; Nath, Swapan K SK

Publication Date: 2022

Variant appearance in text: rs2286672

PubMed Link: 36324510

Variant Present in the following documents:

• Main text
• fgene-13-948505.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: PLD2: R172C; rs2286672

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM7_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM4_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: PLD2: R172C; rs2286672

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
• 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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Neoadjuvant PD-1 Blockade Combined With Chemotherapy Followed by Concurrent Immunoradiotherapy in Locally Advanced Anal Canal Squamous Cell Carcinoma Patients: Antitumor Efficacy, Safety and Biomarker Analysis.

Frontiers In Immunology

Xiao, WeiWei W; Yuan, Yan Y; Wang, SuiHai S; Liao, Zhidong Z; Cai, PeiQiang P; Chen, BaoQing B; Zhang, Rong R; Wang, Fang F; Zeng, ZhiFan Z; Gao, YuanHong Y

Publication Date: 2021

Variant appearance in text: PLD2: R172C

PubMed Link: 35095878

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Association between systemic lupus erythematosus and lung cancer: results from a pool of cohort studies and Mendelian randomization analysis.

Journal Of Thoracic Disease

Peng, Haoxin H; Li, Caichen C; Wu, Xiangrong X; Wen, Yaokai Y; Lin, Jinsheng J; Liang, Hengrui H; Zhong, Ran R; Liu, Jun J; He, Jianxing J; Liang, Wenhua W

Publication Date: 2020-10

Variant appearance in text: rs2286672

PubMed Link: 33209364

Variant Present in the following documents:

• Main text

View BVdb publication page

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Understanding the genetics of systemic lupus erythematosus using Bayesian statistics and gene network analysis.

Clinical And Experimental Pediatrics

Nam, Seoung Wan SW; Lee, Kwang Seob KS; Yang, Jae Won JW; Ko, Younhee Y; Eisenhut, Michael M; Lee, Keum Hwa KH; Shin, Jae Il JI; Kronbichler, Andreas A

Publication Date: 2021-05

Variant appearance in text: rs2286672

PubMed Link: 32683804

Variant Present in the following documents:

• Main text
• cep-2020-00633.pdf

View BVdb publication page

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Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis

Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q

Publication Date: 2020-09

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

View BVdb publication page

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: PLD2: 514C>T; R172C; rs2286672

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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Mammalian phospholipase D: Function, and therapeutics.

Progress In Lipid Research

McDermott, M I MI; Wang, Y Y; Wakelam, M J O MJO; Bankaitis, V A VA

Publication Date: 2020-04

Variant appearance in text: PLD2: R172C

PubMed Link: 31830503

Variant Present in the following documents:

• Main text

View BVdb publication page

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The molecular landscape of ETMR at diagnosis and relapse.

Nature

Lambo, Sander S; Gröbner, Susanne N SN; Rausch, Tobias T; Waszak, Sebastian M SM; Schmidt, Christin C; Gorthi, Aparna A; Romero, July Carolina JC; Mauermann, Monika M; Brabetz, Sebastian S; Krausert, Sonja S; Buchhalter, Ivo I; Koster, Jan J; Zwijnenburg, Danny A DA; Sill, Martin M; Hübner, Jens-Martin JM; Mack, Norman N; Schwalm, Benjamin B; Ryzhova, Marina M; Hovestadt, Volker V; Papillon-Cavanagh, Simon S; Chan, Jennifer A JA; Landgraf, Pablo P; Ho, Ben B; Milde, Till T; Witt, Olaf O; Ecker, Jonas J; Sahm, Felix F; Sumerauer, David D; Ellison, David W DW; Orr, Brent A BA; Darabi, Anna A; Haberler, Christine C; Figarella-Branger, Dominique D; Wesseling, Pieter P; Schittenhelm, Jens J; Remke, Marc M; Taylor, Michael D MD; Gil-da-Costa, Maria J MJ; Łastowska, Maria M; Grajkowska, Wiesława W; Hasselblatt, Martin M; Hauser, Peter P; Pietsch, Torsten T; Uro-Coste, Emmanuelle E; Bourdeaut, Franck F; Masliah-Planchon, Julien J; Rigau, Valérie V; Alexandrescu, Sanda S; Wolf, Stephan S; Li, Xiao-Nan XN; Schüller, Ulrich U; Snuderl, Matija M; Karajannis, Matthias A MA; Giangaspero, Felice F; Jabado, Nada N; von Deimling, Andreas A; Jones, David T W DTW; Korbel, Jan O JO; von Hoff, Katja K; Lichter, Peter P; Huang, Annie A; Bishop, Alexander J R AJR; Pfister, Stefan M SM; Korshunov, Andrey A; Kool, Marcel M

Publication Date: 2019-12

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 31802000

Variant Present in the following documents:

• NIHMS1541318-supplement-Supplementary_Table_5.xlsx, sheet 1

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: PLD2: R172C; rs2286672

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1

View BVdb publication page

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A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.

Scientific Reports

Stringer, Brett W BW; Day, Bryan W BW; D'Souza, Rochelle C J RCJ; Jamieson, Paul R PR; Ensbey, Kathleen S KS; Bruce, Zara C ZC; Lim, Yi Chieh YC; Goasdoué, Kate K; Offenhäuser, Carolin C; Akgül, Seçkin S; Allan, Suzanne S; Robertson, Thomas T; Lucas, Peter P; Tollesson, Gert G; Campbell, Scott S; Winter, Craig C; Do, Hongdo H; Dobrovic, Alexander A; Inglis, Po-Ling PL; Jeffree, Rosalind L RL; Johns, Terrance G TG; Boyd, Andrew W AW

Publication Date: 2019-03-20

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 30894629

Variant Present in the following documents:

• 41598_2019_41277_MOESM4_ESM.xlsx, sheet 5
• 41598_2019_41277_MOESM4_ESM.xlsx, sheet 13

View BVdb publication page

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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease

Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D

Publication Date: 2019-02-27

Variant appearance in text: rs2286672

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2

View BVdb publication page

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Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports

Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS

Publication Date: 2018-12-04

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 30514953

Variant Present in the following documents:

• 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: PLD2: 514C>T; Arg172Cys; rs2286672

PubMed Link: 30319441

Variant Present in the following documents:

• Table_6.xlsx, sheet 1
• Table_5.xlsx, sheet 1
• Table_7.xlsx, sheet 1

View BVdb publication page

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Profiling RNA-Seq at multiple resolutions markedly increases the number of causal eQTLs in autoimmune disease.

Plos Genetics

Odhams, Christopher A CA; Cunninghame Graham, Deborah S DS; Vyse, Timothy J TJ

Publication Date: 2017-10

Variant appearance in text: rs2286672

PubMed Link: 29059182

Variant Present in the following documents:

• Main text
• pgen.1007071.pdf

View BVdb publication page

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Phospholipase D2 loss results in increased blood pressure via inhibition of the endothelial nitric oxide synthase pathway.

Scientific Reports

Nelson, Rochelle K RK; Ya-Ping, Jiang J; Gadbery, John J; Abedeen, Danya D; Sampson, Nicole N; Lin, Richard Z RZ; Frohman, Michael A MA

Publication Date: 2017-08-22

Variant appearance in text: PLD2: R172C

PubMed Link: 28831159

Variant Present in the following documents:

• Main text
• 41598_2017_Article_9852.pdf

View BVdb publication page

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs2286672

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Evaluation of 10 SLE susceptibility loci in Asian populations, which were initially identified in European populations.

Scientific Reports

Zhang, Yue-Miao YM; Zhou, Xu-Jie XJ; Nath, Swapan K SK; Sun, Celi C; Zhao, Ming-Hui MH; Zhang, Hong H

Publication Date: 2017-01-27

Variant appearance in text: rs2286672

PubMed Link: 28128292

Variant Present in the following documents:

• Main text

View BVdb publication page

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Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus.

Human Molecular Genetics

Odhams, Christopher A CA; Cortini, Andrea A; Chen, Lingyan L; Roberts, Amy L AL; Viñuela, Ana A; Buil, Alfonso A; Small, Kerrin S KS; Dermitzakis, Emmanouil T ET; Morris, David L DL; Vyse, Timothy J TJ; Cunninghame Graham, Deborah S DS

Publication Date: 2017-03-01

Variant appearance in text: rs2286672

PubMed Link: 28062664

Variant Present in the following documents:

• Main text

View BVdb publication page

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Chromatin landscapes and genetic risk in systemic lupus.

Arthritis Research & Therapy

Hui-Yuen, Joyce S JS; Zhu, Lisha L; Wong, Lai Ping LP; Jiang, Kaiyu K; Chen, Yanmin Y; Liu, Tao T; Jarvis, James N JN

Publication Date: 2016-12-01

Variant appearance in text: rs2286672

PubMed Link: 27906046

Variant Present in the following documents:

• Main text

View BVdb publication page

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Recapitulation of Candidate Systemic Lupus Erythematosus-Associated Variants in Koreans.

Genomics & Informatics

Kwon, Ki-Sung KS; Cho, Hye-Young HY; Chung, Yeun-Jun YJ

Publication Date: 2016-09

Variant appearance in text: rs2286672

PubMed Link: 27729837

Variant Present in the following documents:

• Main text
• gni-14-85.pdf

View BVdb publication page

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Several Critical Cell Types, Tissues, and Pathways Are Implicated in Genome-Wide Association Studies for Systemic Lupus Erythematosus.

G3 (Bethesda, Md.)

Liu, Lu L; Yin, Xianyong X; Wen, Leilei L; Yang, Chao C; Sheng, Yujun Y; Lin, Yan Y; Zhu, Zhengwei Z; Shen, Changbing C; Shi, Yinjuan Y; Zheng, Yajie Y; Yang, Sen S; Zhang, Xuejun X; Cui, Yong Y

Publication Date: 2016-06-01

Variant appearance in text: rs2286672

PubMed Link: 27172182

Variant Present in the following documents:

• supp_g3.116.027326_TableS1.pdf

View BVdb publication page

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Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One

Holehouse, Alex S AS; Naegle, Kristen M KM

Publication Date: 2015

Variant appearance in text: rs2286672

PubMed Link: 26659599

Variant Present in the following documents:

• pone.0144692.s002.xlsx, sheet 1

View BVdb publication page

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Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.

Nature Genetics

Bentham, James J; Morris, David L DL; Graham, Deborah S Cunninghame DSC; Pinder, Christopher L CL; Tombleson, Philip P; Behrens, Timothy W TW; Martín, Javier J; Fairfax, Benjamin P BP; Knight, Julian C JC; Chen, Lingyan L; Replogle, Joseph J; Syvänen, Ann-Christine AC; Rönnblom, Lars L; Graham, Robert R RR; Wither, Joan E JE; Rioux, John D JD; Alarcón-Riquelme, Marta E ME; Vyse, Timothy J TJ

Publication Date: 2015-12

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 26502338

Variant Present in the following documents:

• Main text
• emss-65418.pdf

View BVdb publication page

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GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics

Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J

Publication Date: 2015-07-25

Variant appearance in text: PLD2: R172C

PubMed Link: 26206375

Variant Present in the following documents:

• 12859_2015_673_MOESM1_ESM.xls, sheet 1

View BVdb publication page

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Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

Scientific Reports

Steinberg, Karyn Meltz KM; Yu, Bing B; Koboldt, Daniel C DC; Mardis, Elaine R ER; Pamphlett, Roger R

Publication Date: 2015-03-16

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 25773295

Variant Present in the following documents:

• srep09124-s3.xls, sheet 1

View BVdb publication page

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The phospholipase D superfamily as therapeutic targets.

Trends In Pharmacological Sciences

Frohman, Michael A MA

Publication Date: 2015-03

Variant appearance in text: PLD2: R172C

PubMed Link: 25661257

Variant Present in the following documents:

• Main text

View BVdb publication page

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Two sites of action for PLD2 inhibitors: The enzyme catalytic center and an allosteric, phosphoinositide biding pocket.

Biochimica Et Biophysica Acta

Ganesan, Ramya R; Mahankali, Madhu M; Alter, Gerald G; Gomez-Cambronero, Julian J

Publication Date: 2015-03

Variant appearance in text: PLD2: R172C

PubMed Link: 25532944

Variant Present in the following documents:

• Main text

View BVdb publication page

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Whole-genome sequencing of the world's oldest people.

Plos One

Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK

Publication Date: 2014

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

View BVdb publication page

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Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.

Plos One

Patiño, Liliana Catherine LC; Battu, Rajani R; Ortega-Recalde, Oscar O; Nallathambi, Jeyabalan J; Anandula, Venkata Ramana VR; Renukaradhya, Umashankar U; Laissue, Paul P

Publication Date: 2014

Variant appearance in text: PLD2: R172C

PubMed Link: 25333361

Variant Present in the following documents:

• pone.0109576.s001.xls, sheet 3
• pone.0109576.s003.xls, sheet 3
• pone.0109576.s002.xls, sheet 3

View BVdb publication page

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Mechanism of enzymatic reaction and protein-protein interactions of PLD from a 3D structural model.

Cellular Signalling

Mahankali, Madhu M; Alter, Gerald G; Gomez-Cambronero, Julian J

Publication Date: 2015-01

Variant appearance in text: PLD2: R172C

PubMed Link: 25308783

Variant Present in the following documents:

• Main text

View BVdb publication page

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Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio

Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M

Publication Date: 2014

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 24490137

Variant Present in the following documents:

• mmc5.xlsx, sheet 2
• mmc5.xlsx, sheet 3

View BVdb publication page

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Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.

Cancer Science

Nasuno, Tomomitsu T; Mimaki, Sachiyo S; Okamoto, Makito M; Esumi, Hiroyasu H; Tsuchihara, Katsuya K

Publication Date: 2014-02

Variant appearance in text: PLD2: R172C; rs2286672

PubMed Link: 24219164

Variant Present in the following documents:

• cas0105-0202-SD3.xlsx, sheet 1

View BVdb publication page

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Identification of the catalytic site of phospholipase D2 (PLD2) newly described guanine nucleotide exchange factor activity.

The Journal Of Biological Chemistry

Mahankali, Madhu M; Henkels, Karen M KM; Alter, Gerald G; Gomez-Cambronero, Julian J

Publication Date: 2012-11-30

Variant appearance in text: PLD2: R172C

PubMed Link: 23035122

Variant Present in the following documents:

• Main text

View BVdb publication page

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Increased cell growth due to a new lipase-GEF (Phospholipase D2) fastly acting on Ras.

Cellular Signalling

Henkels, Karen M KM; Mahankali, Madhu M; Gomez-Cambronero, Julian J

Publication Date: 2013-01

Variant appearance in text: PLD2: R172C

PubMed Link: 22960035

Variant Present in the following documents:

• Main text

View BVdb publication page

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