Publications:

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Expanding the prostate cancer cell line repertoire with ACRJ-PC28, an AR-negative neuroendocrine cell line derived from an African-Caribbean patient.

Cancer Research Communications

Valentine, Henkel H; Aiken, William W; Morrison, Belinda B; Zhao, Ziran Z; Fowle, Holly H; Wasserman, Jason S JS; Thompson, Elon E; Chin, Warren W; Young, Mark M; Clarke, Shannique S; Gibbs, Denise D; Harrison, Sharon S; McLaughlin, Wayne W; Kwok, Tim T; Jin, Fang F; Campbell, Kerry S KS; Horvath, Anelia A; Thompson, Rory R; Lee, Norman H NH; Zhou, Yan Y; Graña, Xavier X; Ragin, Camille C; Badal, Simone S

Publication Date: 2022-11

Variant appearance in text: SELP: V640L; rs6133

PubMed Link: 36643868

Variant Present in the following documents:

• crc-22-0245-s07.xlsx, sheet 1

View BVdb publication page

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Gene variants in pro-coagulant and anti-coagulant genes could be prognostic genetic markers of COVID-19 susceptibility.

Heliyon

Srivastava, Swati S; Kumari, Babita B; Garg, Iti I; Dogra, Vikas V; Ghosh, Nilanjana N; Singh, Yamini Y; Bargotya, Mona M; Bhattar, Sonali S; Gupta, Utkarsh U; Jain, Shruti S; Hussain, Javid J; Varshney, Rajeev R; Ganju, Lilly L

Publication Date: 2022-11

Variant appearance in text: rs6133

PubMed Link: 36387492

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.

Iscience

Bateman, Nicholas W NW; Tarney, Christopher M CM; Abulez, Tamara S TS; Hood, Brian L BL; Conrads, Kelly A KA; Zhou, Ming M; Soltis, Anthony R AR; Teng, Pang-Ning PN; Jackson, Amanda A; Tian, Chunqiao C; Dalgard, Clifton L CL; Wilkerson, Matthew D MD; Kessler, Michael D MD; Goecker, Zachary Z; Loffredo, Jeremy J; Shriver, Craig D CD; Hu, Hai H; Cote, Michele M; Parker, Glendon J GJ; Segars, James J; Al-Hendy, Ayman A; Risinger, John I JI; Phippen, Neil T NT; Casablanca, Yovanni Y; Darcy, Kathleen M KM; Maxwell, G Larry GL; Conrads, Thomas P TP; O'Connor, Timothy D TD

Publication Date: 2022-01-21

Variant appearance in text: SELP: V640L; rs6133

PubMed Link: 35036865

Variant Present in the following documents:

• mmc2.xlsx, sheet 1

View BVdb publication page

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Quantile-Specific Heritability of Inflammatory and Oxidative Stress Biomarkers Linked to Cardiovascular Disease.

Journal Of Inflammation Research

Williams, Paul T PT

Publication Date: 2022

Variant appearance in text: rs6133

PubMed Link: 35023945

Variant Present in the following documents:

• Main text
• jir-15-85.pdf

View BVdb publication page

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Epione application: An integrated web‑toolkit of clinical genomics and personalized medicine in systemic lupus erythematosus.

International Journal Of Molecular Medicine

Papageorgiou, Louis L; Alkenaris, Haris H; Zervou, Maria I MI; Vlachakis, Dimitriοs D; Matalliotakis, Ioannis I; Spandidos, Demetrios A DA; Bertsias, George G; Goulielmos, George N GN; Eliopoulos, Elias E

Publication Date: 2022-01

Variant appearance in text: rs6133

PubMed Link: 34791504

Variant Present in the following documents:

• Main text
• ijmm-49-01-05063.pdf

View BVdb publication page

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Proteogenomics Reveals Perturbed Signaling Networks in Malignant Melanoma Cells Resistant to BRAF Inhibition.

Molecular & Cellular Proteomics : Mcp

Schmitt, Marisa M; Sinnberg, Tobias T; Bratl, Katrin K; Zittlau, Katharina K; Garbe, Claus C; Macek, Boris B; Nalpas, Nicolas C NC

Publication Date: 2021

Variant appearance in text: SELP: V640L; rs6133

PubMed Link: 34673281

Variant Present in the following documents:

• mmc2.xlsx, sheet 11
• mmc2.xlsx, sheet 3

View BVdb publication page

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Proteogenomics Reveals Perturbed Signaling Networks in Malignant Melanoma Cells Resistant to BRAF Inhibition.

Molecular & Cellular Proteomics : Mcp

Schmitt, Marisa M; Sinnberg, Tobias T; Bratl, Katrin K; Zittlau, Katharina K; Garbe, Claus C; Macek, Boris B; Nalpas, Nicolas C NC

Publication Date: 2021-10-19

Variant appearance in text: SELP: V640L; rs6133

PubMed Link: 34673281

Variant Present in the following documents:

• mmc2.xlsx, sheet 3
• mmc2.xlsx, sheet 11

View BVdb publication page

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Role of platelet gene polymorphisms in ischemic pediatric stroke subtypes: a case-control study.

Croatian Medical Journal

Čeri, Andrea A; Leniček Krleža, Jasna J; Coen Herak, Désirée D; Miloš, Marija M; Pavić, Marina M; Barišić, Nina N; Đuranović, Vlasta V; Zadro, Renata R

Publication Date: 2020-02-29

Variant appearance in text: SELP: 1918G>T; rs6133

PubMed Link: 32118374

Variant Present in the following documents:

• Main text

View BVdb publication page

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The Ser290Asn and Thr715Pro Polymorphisms of the SELP Gene Are Associated with A Lower Risk of Developing Acute Coronary Syndrome and Low Soluble P-Selectin Levels in A Mexican Population ‡.

Biomolecules

Herrera-Maya, Gabriel G; Vargas-Alarcón, Gilberto G; Pérez-Méndez, Oscar O; Posadas-Sánchez, Rosalinda R; Masso, Felipe F; Juárez-Cedillo, Teresa T; Escobedo, Galileo G; Vázquez-Montero, Andros A; Fragoso, José Manuel JM

Publication Date: 2020-02-11

Variant appearance in text: rs6133

PubMed Link: 32053880

Variant Present in the following documents:

• Main text
• biomolecules-10-00270.pdf

View BVdb publication page

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YAP1 mediates survival of ALK-rearranged lung cancer cells treated with alectinib via pro-apoptotic protein regulation.

Nature Communications

Tsuji, Takahiro T; Ozasa, Hiroaki H; Aoki, Wataru W; Aburaya, Shunsuke S; Yamamoto Funazo, Tomoko T; Furugaki, Koh K; Yoshimura, Yasushi Y; Yamazoe, Masatoshi M; Ajimizu, Hitomi H; Yasuda, Yuto Y; Nomizo, Takashi T; Yoshida, Hironori H; Sakamori, Yuichi Y; Wake, Hiroaki H; Ueda, Mitsuyoshi M; Kim, Young Hak YH; Hirai, Toyohiro T

Publication Date: 2020-01-03

Variant appearance in text: SELP: V640L

PubMed Link: 31900393

Variant Present in the following documents:

• 41467_2019_13771_MOESM5_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: SELP: V640L; rs6133

PubMed Link: 30894629

Variant Present in the following documents:

• 41598_2019_41277_MOESM4_ESM.xlsx, sheet 13
• 41598_2019_41277_MOESM4_ESM.xlsx, sheet 4
• 41598_2019_41277_MOESM4_ESM.xlsx, sheet 11

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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: SELP: 1918G>T; rs6133

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2
• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3

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: SELP: V640L; rs6133

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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Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma.

Plos One

Marques, Ana Maria AM; Ananina, Galina G; Costa, Vital Paulino VP; de Vasconcellos, José Paulo Cabral JPC; de Melo, Mônica Barbosa MB

Publication Date: 2018

Variant appearance in text: rs6133

PubMed Link: 30444892

Variant Present in the following documents:

• Main text
• pone.0207409.pdf

View BVdb publication page

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Development and validation of a rapid method for genotyping three P-selectin gene polymorphisms based on high resolution melting analysis.

Journal Of Clinical Laboratory Analysis

Ceri, Andrea A; Pavic, Marina M; Horvat, Ivana I; Radic Antolic, Margareta M; Zadro, Renata R

Publication Date: 2019-03

Variant appearance in text: SELP: 1918G>T; Val640Leu; rs6133

PubMed Link: 30350887

Variant Present in the following documents:

• Main text

View BVdb publication page

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Polymorphisms in the selectin gene cluster are associated with fertility and survival time in a population of Holstein Friesian cows.

Plos One

Chen, Xing X; Zhang, Shujun S; Cheng, Zhangrui Z; Cooke, Jessica S JS; Werling, Dirk D; Wathes, D Claire DC; Pollott, Geoffrey E GE

Publication Date: 2017

Variant appearance in text: SELP: Val640Leu; rs6133

PubMed Link: 28419109

Variant Present in the following documents:

• Main text
• pone.0175555.pdf

View BVdb publication page

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Polymorphisms of Platelet Glycoprotein Receptors and Cell Adhesion Molecules in Fetuses with Fetal Growth Restriction and Their Mothers As Detected with Pyrosequencing.

In Vivo (Athens, Greece)

Simou, Maria M; Kouskouni, Evaggelia E; Vitoratos, Nikolaos N; Economou, Emmanuel E; Creatsas, George G

Publication Date: 2017

Variant appearance in text: SELP: Val640Leu

PubMed Link: 28358707

Variant Present in the following documents:

• Main text

View BVdb publication page

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Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.

The Journal Of Pathology

Maguire, Sarah L SL; Peck, Barrie B; Wai, Patty T PT; Campbell, James J; Barker, Holly H; Gulati, Aditi A; Daley, Frances F; Vyse, Simon S; Huang, Paul P; Lord, Christopher J CJ; Farnie, Gillian G; Brennan, Keith K; Natrajan, Rachael R

Publication Date: 2016-11

Variant appearance in text: SELP: V640L; rs6133

PubMed Link: 27512948

Variant Present in the following documents:

• PATH-240-315-s015.xlsx, sheet 1

View BVdb publication page

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Clonal relationships between lobular carcinoma in situ and other breast malignancies.

Breast Cancer Research : Bcr

Begg, Colin B CB; Ostrovnaya, Irina I; Carniello, Jose V Scarpa JV; Sakr, Rita A RA; Giri, Dilip D; Towers, Russell R; Schizas, Michail M; De Brot, Marina M; Andrade, Victor P VP; Mauguen, Audrey A; Seshan, Venkatraman E VE; King, Tari A TA

Publication Date: 2016-06-23

Variant appearance in text: SELP: V640L

PubMed Link: 27334989

Variant Present in the following documents:

• 13058_2016_727_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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ABO blood group associations with markers of endothelial dysfunction in the Multi-Ethnic Study of Atherosclerosis.

Atherosclerosis

Larson, Nicholas B NB; Bell, Elizabeth J EJ; Decker, Paul A PA; Pike, Mindy M; Wassel, Christina L CL; Tsai, Michael Y MY; Pankow, James S JS; Tang, Weihong W; Hanson, Naomi Q NQ; Alexander, Kristine K; Zakai, Neil A NA; Cushman, Mary M; Bielinski, Suzette J SJ

Publication Date: 2016-08

Variant appearance in text: rs6133

PubMed Link: 27298014

Variant Present in the following documents:

• Main text

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: rs6133

PubMed Link: 26659599

Variant Present in the following documents:

• pone.0144692.s002.xlsx, sheet 1

View BVdb publication page

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An Inflammatory Polymorphisms Risk Scoring System for the Differentiation of Ischemic Stroke Subtypes.

Mediators Of Inflammation

Muiño, Elena E; Krupinski, Jurek J; Carrera, Caty C; Gallego-Fabrega, Cristina C; Montaner, Joan J; Fernández-Cadenas, Israel I

Publication Date: 2015

Variant appearance in text: rs6133

PubMed Link: 26355258

Variant Present in the following documents:

• Main text
• MI2015-569714.pdf

View BVdb publication page

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P-selectin Plasma Levels and Genetic Variant Associated With Diabetic Retinopathy in African Americans.

American Journal Of Ophthalmology

Penman, Alan A; Hoadley, Suzanne S; Wilson, James G JG; Taylor, Herman A HA; Chen, Ching J CJ; Sobrin, Lucia L

Publication Date: 2015-06

Variant appearance in text: rs6133

PubMed Link: 25794792

Variant Present in the following documents:

• Main text

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: rs6133

PubMed Link: 25773295

Variant Present in the following documents:

• srep09124-s3.xls, sheet 1

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: SELP: V640L; rs6133

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

View BVdb publication page

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The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.

Nucleic Acids Research

Tang, Xiaojia X; Baheti, Saurabh S; Shameer, Khader K; Thompson, Kevin J KJ; Wills, Quin Q; Niu, Nifang N; Holcomb, Ilona N IN; Boutet, Stephane C SC; Ramakrishnan, Ramesh R; Kachergus, Jennifer M JM; Kocher, Jean-Pierre A JP; Weinshilboum, Richard M RM; Wang, Liewei L; Thompson, E Aubrey EA; Kalari, Krishna R KR

Publication Date: 2014-12-16

Variant appearance in text: SELP: V640L; rs6133

PubMed Link: 25352556

Variant Present in the following documents:

• supp_gku1005_nar-01266-met-n-2014-File012.xlsx, sheet 5
• supp_gku1005_nar-01266-met-n-2014-File012.xlsx, sheet 24

View BVdb publication page

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P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans.

Frontiers In Genetics

Kochunov, P P; Glahn, D C DC; Hong, L E LE; Lancaster, J J; Curran, J E JE; Johnson, M P MP; Winkler, A M AM; Holcomb, H H HH; Kent, J W JW; Mitchell, B B; Kochunov, V V; Olvera, R L RL; Cole, S A SA; Dyer, T D TD; Moses, E K EK; Goring, H H; Almasy, L L; Duggirala, R R; Blangero, J J

Publication Date: 2012

Variant appearance in text: rs6133

PubMed Link: 22558002

Variant Present in the following documents:

• fgene-03-00065.pdf

View BVdb publication page

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An evolutionary history of the selectin gene cluster in humans.

Heredity

Fumagalli, M M; Fracassetti, M M; Cagliani, R R; Forni, D D; Pozzoli, U U; Comi, G P GP; Marini, F F; Bresolin, N N; Clerici, M M; Sironi, M M

Publication Date: 2012-08

Variant appearance in text: SELP: Val640Leu; rs6133

PubMed Link: 22549518

Variant Present in the following documents:

• Main text

View BVdb publication page

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Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

Investigative Ophthalmology & Visual Science

Sobrin, Lucia L; Green, Todd T; Sim, Xueling X; Jensen, Richard A RA; Tai, E Shyong ES; Tay, Wan Ting WT; Wang, Jie Jin JJ; Mitchell, Paul P; Sandholm, Niina N; Liu, Yiyuan Y; Hietala, Kustaa K; Iyengar, Sudha K SK; , ; Brooks, Matthew M; Buraczynska, Monika M; Van Zuydam, Natalie N; Smith, Albert V AV; Gudnason, Vilmundur V; Doney, Alex S F AS; Morris, Andrew D AD; Leese, Graham P GP; Palmer, Colin N A CN; , ; Swaroop, Anand A; Taylor, Herman A HA; Wilson, James G JG; Penman, Alan A; Chen, Ching J CJ; Groop, Per-Henrik PH; Saw, Seang-Mei SM; Aung, Tin T; Klein, Barbara E BE; Rotter, Jerome I JI; Siscovick, David S DS; Cotch, Mary Frances MF; Klein, Ronald R; Daly, Mark J MJ; Wong, Tien Y TY

Publication Date: 2011-09-29

Variant appearance in text: rs6133

PubMed Link: 21873659

Variant Present in the following documents:

• Main text

View BVdb publication page

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Evaluation of variants in the selectin genes in age-related macular degeneration.

Bmc Medical Genetics

Mullins, Robert F RF; Skeie, Jessica M JM; Folk, James C JC; Solivan-Timpe, Frances M FM; Oetting, Thomas A TA; Huang, Jian J; Wang, Kai K; Stone, Edwin M EM; Fingert, John H JH

Publication Date: 2011-04-26

Variant appearance in text: SELP: Val640Leu; rs6133

PubMed Link: 21521525

Variant Present in the following documents:

• Main text
• 1471-2350-12-58.pdf

View BVdb publication page

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Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years.

American Journal Of Obstetrics And Gynecology

Clark, Erin A S EA; Mele, Lisa L; Wapner, Ronald J RJ; Spong, Catherine Y CY; Sorokin, Yoram Y; Peaceman, Alan A; Iams, Jay D JD; Leveno, Kenneth J KJ; Harper, Margaret M; Caritis, Steve N SN; Miodovnik, Menachem M; Mercer, Brian M BM; Thorp, John M JM; Ramin, Susan M SM; Carpenter, Marshall M; Rouse, Dwight J DJ; ,

Publication Date: 2010-07

Variant appearance in text: SELP: val640leu; rs6133

PubMed Link: 20417488

Variant Present in the following documents:

• Main text

View BVdb publication page

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A candidate gene association study of 77 polymorphisms in migraine.

The Journal Of Pain

Schürks, Markus M; Kurth, Tobias T; Buring, Julie E JE; Zee, Robert Y L RY

Publication Date: 2009-07

Variant appearance in text: rs6133

PubMed Link: 19559392

Variant Present in the following documents:

• Main text

View BVdb publication page

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Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.

Genes And Immunity

Morris, D L DL; Graham, R R RR; Erwig, L-P LP; Gaffney, P M PM; Moser, K L KL; Behrens, T W TW; Vyse, T J TJ; Graham, D S Cunninghame DS

Publication Date: 2009-07

Variant appearance in text: rs6133

PubMed Link: 19404301

Variant Present in the following documents:

• Main text

View BVdb publication page

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SELP and SELPLG genetic variation is associated with cell surface measures of SELP and SELPLG: the Atherosclerosis Risk in Communities Carotid MRI Study.

Clinical Chemistry

Volcik, Kelly A KA; Catellier, Diane D; Folsom, Aaron R AR; Matijevic, Nena N; Wasserman, Bruce B; Boerwinkle, Eric E

Publication Date: 2009-06

Variant appearance in text: rs6133

PubMed Link: 19395438

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.

Journal Of Hypertension

Conen, David D; Cheng, Suzanne S; Steiner, Lori L LL; Buring, Julie E JE; Ridker, Paul M PM; Zee, Robert Y L RY

Publication Date: 2009-03

Variant appearance in text: rs6133

PubMed Link: 19330901

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.

Clinica Chimica Acta; International Journal Of Clinical Chemistry

Zee, Robert Y L RY; Bubes, Vadim V; Shrivastava, Sanjay S; Ridker, Paul M PM; Glynn, Robert J RJ

Publication Date: 2009-04

Variant appearance in text: rs6133

PubMed Link: 19263529

Variant Present in the following documents:

• Main text

View BVdb publication page

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A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.

Stroke

Wang, Xingyu X; Cheng, Suzanne S; Brophy, Victoria H VH; Erlich, Henry A HA; Mannhalter, Christine C; Berger, Klaus K; Lalouschek, Wolfgang W; Browner, Warren S WS; Shi, Yu Y; Ringelstein, E Bernd EB; Kessler, Christof C; Luedemann, Jan J; Lindpaintner, Klaus K; Liu, Lisheng L; Ridker, Paul M PM; Zee, Robert Y L RY; Cook, Nancy R NR; ,

Publication Date: 2009-03

Variant appearance in text: rs6133

PubMed Link: 19131662

Variant Present in the following documents:

• Main text

View BVdb publication page

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Soluble P-selectin, SELP polymorphisms, and atherosclerotic risk in European-American and African-African young adults: the Coronary Artery Risk Development in Young Adults (CARDIA) Study.

Arteriosclerosis, Thrombosis, And Vascular Biology

Reiner, Alexander P AP; Carlson, Christopher S CS; Thyagarajan, Bharat B; Rieder, Mark J MJ; Polak, Joseph F JF; Siscovick, David S DS; Nickerson, Deborah A DA; Jacobs, David R DR; Gross, Myron D MD

Publication Date: 2008-08

Variant appearance in text: rs6133

PubMed Link: 18535285

Variant Present in the following documents:

• Main text

View BVdb publication page

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Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study.

Atherosclerosis

Volcik, Kelly A KA; Ballantyne, Christie M CM; Coresh, Josef J; Folsom, Aaron R AR; Boerwinkle, Eric E

Publication Date: 2007-11

Variant appearance in text: rs6133

PubMed Link: 17420019

Variant Present in the following documents:

• Main text

View BVdb publication page

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Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.

Circulation

Podgoreanu, M V MV; White, W D WD; Morris, R W RW; Mathew, J P JP; Stafford-Smith, M M; Welsby, I J IJ; Grocott, H P HP; Milano, C A CA; Newman, M F MF; Schwinn, D A DA; ,

Publication Date: 2006-07-04

Variant appearance in text: rs6133

PubMed Link: 16820586

Variant Present in the following documents:

• Main text

View BVdb publication page

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A comprehensive candidate gene study on bronchial asthma and juvenile idiopathic arthritis.

Disease Markers

Schubert, K K; von Bonnsdorf, H H; Burke, M M; Ahlert, I I; Braun, S S; Berner, R R; Deichmann, K A KA; Heinzmann, A A

Publication Date: 2006

Variant appearance in text: rs6133

PubMed Link: 16788246

Variant Present in the following documents:

• DM22-03-373620.pdf

View BVdb publication page

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Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans.

Genes And Immunity

Brassat, D D; Motsinger, A A AA; Caillier, S J SJ; Erlich, H A HA; Walker, K K; Steiner, L L LL; Cree, B A C BA; Barcellos, L F LF; Pericak-Vance, M A MA; Schmidt, S S; Gregory, S S; Hauser, S L SL; Haines, J L JL; Oksenberg, J R JR; Ritchie, M D MD

Publication Date: 2006-06

Variant appearance in text: rs6133

PubMed Link: 16625214

Variant Present in the following documents:

• Main text

View BVdb publication page

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Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations.

American Journal Of Respiratory And Critical Care Medicine

Weiss, Lauren A LA; Lester, Lucille A LA; Gern, James E JE; Wolf, Raoul L RL; Parry, Rodney R; Lemanske, Robert F RF; Solway, Julian J; Ober, Carole C

Publication Date: 2005-07-01

Variant appearance in text: SELP: Val640Leu

PubMed Link: 15817799

Variant Present in the following documents:

• Main text

View BVdb publication page

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Gene-environment interaction effects on the development of immune responses in the 1st year of life.

American Journal Of Human Genetics

Hoffjan, Sabine S; Nicolae, Dan D; Ostrovnaya, Irina I; Roberg, Kathy K; Evans, Michael M; Mirel, Daniel B DB; Steiner, Lori L; Walker, Karen K; Shult, Peter P; Gangnon, Ronald E RE; Gern, James E JE; Martinez, Fernando D FD; Lemanske, Robert F RF; Ober, Carole C

Publication Date: 2005-04

Variant appearance in text: SELP: V640L; rs6133

PubMed Link: 15726497

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association studies for asthma and atopic diseases: a comprehensive review of the literature.

Respiratory Research

Hoffjan, Sabine S; Nicolae, Dan D; Ober, Carole C

Publication Date: 2003

Variant appearance in text: SELP: Val640Leu

PubMed Link: 14748924

Variant Present in the following documents:

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Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus.

American Journal Of Human Genetics

Bourgain, Catherine C; Hoffjan, Sabine S; Nicolae, Raluca R; Newman, Dina D; Steiner, Lori L; Walker, Karen K; Reynolds, Rebecca R; Ober, Carole C; McPeek, Mary Sara MS

Publication Date: 2003-09

Variant appearance in text: SELP: Val640Leu

PubMed Link: 12929084

Variant Present in the following documents:

• Main text

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