| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/HMG/DDW406 |
| P698 | PubMed publication ID | 28062665 |
| P50 | author | Shinji Uemoto | Q91614513 |
| Shintaro Yagi | Q48223820 | ||
| Atsushi Naganuma | Q57451392 | ||
| Kazuaki Chayama | Q87781872 | ||
| Norihiro Kokudo | Q88727177 | ||
| P2093 | author name string | Minoru Nakamura | |
| Yoshihiko Maehara | |||
| Atsushi Tanaka | |||
| Masashi Mizokami | |||
| Osamu Yokosuka | |||
| Tatsuo Kanda | |||
| Kazuhiko Nakao | |||
| Kenichi Harada | |||
| Kiyoshi Migita | |||
| Kaname Yoshizawa | |||
| Michio Yasunami | |||
| Takafumi Ichida | |||
| Masanori Abe | |||
| Yoshiyuki Ueno | |||
| Kaname Kojima | |||
| Masao Nagasaki | |||
| Masahiro Kikuchi | |||
| Shuichi Kaneko | |||
| Yosuke Kawai | |||
| Motoyuki Kohjima | |||
| Tomohiro Tanaka | |||
| Makoto Nakamuta | |||
| Masahiro Ito | |||
| Shotaro Sakisaka | |||
| Atsumasa Komori | |||
| Hiromasa Ohira | |||
| Masataka Seike | |||
| Kazuhide Yamamoto | |||
| Masao Honda | |||
| Shinji Shimoda | |||
| Hitomi Nakamura | |||
| Katsushi Tokunaga | |||
| Hajime Takikawa | |||
| Hiroshi Mano | |||
| Minae Kawashima | |||
| Nao Nishida | |||
| Kazumoto Murata | |||
| Naohiko Masaki | |||
| Hidetaka Shibata | |||
| Hirotoshi Ebinuma | |||
| Masaru Harada | |||
| Masaaki Shimada | |||
| Takashi Himoto | |||
| Hiroto Egawa | |||
| Toyokichi Muro | |||
| Tsutomu Yamashita | |||
| Satoru Joshita | |||
| Takeji Umemura | |||
| Hiroshi Yatsuhashi | |||
| Yoshihiro Aiba | |||
| Hiromi Ishibashi | |||
| Mikio Zeniya | |||
| Satoshi Yamagiwa | |||
| Ken Shirabe | |||
| Kiyoshi Furuta | |||
| Makiko Taniai | |||
| Haruhiro Yamashita | |||
| Akira Mori | |||
| Fujio Makita | |||
| Hideo Nishimura | |||
| Keisuke Ario | |||
| Seigo Abiru | |||
| Shinya Nagaoka | |||
| Yasuhiro Miyake | |||
| Toshiki Nikami | |||
| Etsuko Hashimoto | |||
| Noboru Hirashima | |||
| Yoko Nakamura | |||
| Toshiki Komeda | |||
| Yuki Hitomi | |||
| Kazuhiko Yamauchi | |||
| Nobuyoshi Fukushima | |||
| Hirotaka Kouno | |||
| Hiroshi Kouno | |||
| Eiichi Takesaki | |||
| Hajime Ota | |||
| Kazuhiro Sugi | |||
| Kouki Matsushita | |||
| Michio Senju | |||
| Sumito Tamura | |||
| Tatsuji Komatsu | |||
| Yukio Ohara | |||
| Naohiro Takahashi | |||
| P2860 | cites work | A flexible and accurate genotype imputation method for the next generation of genome-wide association studies | Q21129496 |
| Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants | Q24617796 | ||
| Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis | Q24633290 | ||
| Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants | Q24633806 | ||
| Mapping short DNA sequencing reads and calling variants using mapping quality scores | Q24644612 | ||
| Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies | Q24657654 | ||
| Emerging role of protein kinase C in energy homeostasis: A brief overview | Q27022044 | ||
| Fast gapped-read alignment with Bowtie 2 | Q27860699 | ||
| Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals | Q28607995 | ||
| The Genotype-Tissue Expression (GTEx) project | Q28657968 | ||
| Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis | Q28943317 | ||
| Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population | Q28943429 | ||
| Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis | Q29417041 | ||
| FINEMAP: efficient variable selection using summary data from genome-wide association studies | Q31037165 | ||
| Appropriate data cleaning methods for genome-wide association study | Q31171213 | ||
| Implications of genome-wide association studies in novel therapeutics in primary biliary cirrhosis | Q33579196 | ||
| Structural basis of protein kinase C isoform function | Q33973406 | ||
| Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis | Q34087671 | ||
| Protein kinase C beta (PKC beta): normal functions and diseases | Q34989333 | ||
| Biological interpretation of genome-wide association studies using predicted gene functions | Q35571093 | ||
| LD Score regression distinguishes confounding from polygenicity in genome-wide association studies | Q35831121 | ||
| Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes. | Q35990216 | ||
| International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways | Q36087896 | ||
| Heterozygous mis-sense mutations in Prkcb as a critical determinant of anti-polysaccharide antibody formation | Q36912619 | ||
| Protein Kinase Cβ Is Required for Lupus Development in Sle Mice | Q37146459 | ||
| Pathway-based analysis of primary biliary cirrhosis genome-wide association studies | Q37191674 | ||
| A polymorphism in the protein kinase C gene PRKCB is associated with α2-adrenoceptor-mediated vasoconstriction | Q37551273 | ||
| Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population | Q41615335 | ||
| Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women | Q43186907 | ||
| Novel modulating effects of PKC family genes on the relationship between serum vitamin D and relapse in multiple sclerosis. | Q43805147 | ||
| Primary biliary cirrhosis in monozygotic and dizygotic twins: genetics, epigenetics, and environment | Q46795010 | ||
| Follow-up study identifies two novel susceptibility loci PRKCB and 8p11.21 for systemic lupus erythematosus | Q54628341 | ||
| Genetic variants of the protein kinase C-beta 1 gene and development of end-stage renal disease in patients with type 2 diabetes. | Q54654030 | ||
| Primary biliary cirrhosis | Q56428273 | ||
| P433 | issue | 3 | |
| P921 | main subject | ascending cholangitis | Q603644 |
| genome-wide association study | Q1098876 | ||
| susceptibility locus | Q62091149 | ||
| P304 | page(s) | 650-659 | |
| P577 | publication date | 2017-01-05 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population | |
| P478 | volume | 26 |
| Q47827554 | Genetics and epigenetics in the pathogenesis of primary biliary cholangitis. |
| Q92259854 | Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis |
| Q54936233 | Genome-wide haplotype association analysis of primary biliary cholangitis risk in Japanese. |
| Q33767342 | Identification of the functional variant driving ORMDL3 and GSDMB expression in human chromosome 17q12-21 in primary biliary cholangitis |
| Q94503843 | Integrated GWAS and mRNA Microarray Analysis Identified IFNG and CD40L as the Central Upstream Regulators in Primary Biliary Cholangitis |
| Q55049196 | NELFCD and CTSZ loci are associated with jaundice-stage progression in primary biliary cholangitis in the Japanese population. |
| Q90351565 | NFKB1 and MANBA Confer Disease Susceptibility to Primary Biliary Cholangitis via Independent Putative Primary Functional Variants |
| Q60909951 | POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33 |
| Q94512665 | Population-Specific Genetic and Expression Differentiation in Europeans |
| Q41328248 | Principal contribution of HLA-DQ alleles, DQB1*06:04 and DQB1*03:01, to disease resistance against primary biliary cholangitis in a Japanese population. |
| Q55009231 | Serum Autotaxin Is a Useful Disease Progression Marker in Patients with Primary Biliary Cholangitis. |
| Q47109078 | Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases |
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