IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells (English)
Free access
- New search for: Newman, John H.
- New search for: Shaver, Aaron
- New search for: Sheehan, Jonathan H.
- New search for: Mallal, Simon
- New search for: Stone, John H.
- New search for: Pillai, Shiv
- New search for: Bastarache, Lisa
- New search for: Riebau, Derek
- New search for: Allard‐Chamard, Hugues
- New search for: Stone, William M.
- New search for: Perugino, Cory
- New search for: Pilkinton, Mark
- New search for: Smith, Scott A.
- New search for: McDonnell, Wyatt J.
- New search for: Capra, John A.
- New search for: Meiler, Jens
- New search for: Cogan, Joy
- New search for: Xing, Kelly
- New search for: Mahajan, Vinay S.
- New search for: Mattoo, Hamid
- New search for: Hamid, Rizwan
- New search for: Phillips, John A. III
- New search for: Undiagnosed Disease Network
- New search for: Newman, John H.
- New search for: Shaver, Aaron
- New search for: Sheehan, Jonathan H.
- New search for: Mallal, Simon
- New search for: Stone, John H.
- New search for: Pillai, Shiv
- New search for: Bastarache, Lisa
- New search for: Riebau, Derek
- New search for: Allard‐Chamard, Hugues
- New search for: Stone, William M.
- New search for: Perugino, Cory
- New search for: Pilkinton, Mark
- New search for: Smith, Scott A.
- New search for: McDonnell, Wyatt J.
- New search for: Capra, John A.
- New search for: Meiler, Jens
- New search for: Cogan, Joy
- New search for: Xing, Kelly
- New search for: Mahajan, Vinay S.
- New search for: Mattoo, Hamid
- New search for: Hamid, Rizwan
- New search for: Phillips, John A. III
- New search for: Adams, David R.
- New search for: Aday, Aaron
- New search for: Alejandro, Mercedes E.
- New search for: Allard, Patrick
- New search for: Ashley, Euan A.
- New search for: Azamian, Mahshid S.
- New search for: Bacino, Carlos A.
- New search for: Balasubramanyam, Ashok
- New search for: Barseghyan, Hayk
- New search for: Batzli, Gabriel F.
- New search for: Beggs, Alan H.
- New search for: Behnam, Babak
- New search for: Bellen, Hugo J.
- New search for: Bernstein, Jonathan A.
- New search for: Bican, Anna
- New search for: Bick, David P.
- New search for: Birch, Camille L.
- New search for: Bonner, Devon
- New search for: Boone, Braden E.
- New search for: Bostwick, Bret L.
- New search for: Briere, Lauren C.
- New search for: Brown, Donna M.
- New search for: Brush, Matthew
- New search for: Burke, Elizabeth A.
- New search for: Burrage, Lindsay C.
- New search for: Butte, Manish J.
- New search for: Chen, Shan
- New search for: Clark, Gary D.
- New search for: Coakley, Terra R.
- New search for: Cooper, Cynthia M.
- New search for: Cope, Heidi
- New search for: Craigen, William J.
- New search for: D'Souza, Precilla
- New search for: Davids, Mariska
- New search for: Davidson, Jean M.
- New search for: Dayal, Jyoti G.
- New search for: Dell'Angelica, Esteban C.
- New search for: Dhar, Shweta U.
- New search for: Dipple, Katrina M.
- New search for: Donnell‐Fink, Laurel A.
- New search for: Dorrani, Naghmeh
- New search for: Dorset, Daniel C.
- New search for: Douine, Emilie D.
- New search for: Draper, David D.
- New search for: Dries, Annika M.
- New search for: Eckstein, David J.
- New search for: Emrick, Lisa T.
- New search for: Eng, Christine M.
- New search for: Enns, Gregory M.
- New search for: Eskin, Ascia
- New search for: Esteves, Cecilia
- New search for: Estwick, Tyra
- New search for: Fernandez, Liliana
- New search for: Ferreira, Carlos
- New search for: Fisher, Paul G.
- New search for: Fogel, Brent L.
- New search for: Friedman, Noah D.
- New search for: Gahl, William A.
- New search for: Glanton, Emily
- New search for: Godfrey, Rena A.
- New search for: Goldman, Alica M.
- New search for: Goldstein, David B.
- New search for: Gould, Sarah E.
- New search for: Gourdine, Jean‐Philippe F.
- New search for: Groden, Catherine A.
- New search for: Gropman, Andrea L.
- New search for: Haendel, Melissa
- New search for: Hanchard, Neil A.
- New search for: Handley, Lori H.
- New search for: Herzog, Matthew R.
- New search for: High, Francis
- New search for: Holm, Ingrid A.
- New search for: Hom, Jason
- New search for: Howerton, Ellen M.
- New search for: Huang, Yong
- New search for: Jamal, Fariha
- New search for: Jiang, Yong‐hui
- New search for: Johnston, Jean M.
- New search for: Jones, Angela L.
- New search for: Karaviti, Lefkothea
- New search for: Koeller, David M.
- New search for: Kohane, Isaac S.
- New search for: Kohler, Jennefer N.
- New search for: Krasnewich, Donna M.
- New search for: Korrick, Susan
- New search for: Krieg, Elizabeth L.
- New search for: Krier, Joel B.
- New search for: Kyle, Jennifer E.
- New search for: Lalani, Seema R.
- New search for: Christopher Lau, C.
- New search for: Lazar, Jozef
- New search for: LeBlanc, Kimberly
- New search for: Lee, Brendan H.
- New search for: Lee, Hane
- New search for: Levy, Shawn E.
- New search for: Lewis, Richard A.
- New search for: Lincoln, Sharyn A.
- New search for: Loo, Sandra K.
- New search for: Loscalzo, Joseph
- New search for: Maas, Richard L.
- New search for: Macnamara, Ellen F.
- New search for: MacRae, Calum A.
- New search for: Maduro, Valerie V.
- New search for: Majcherska, Marta M.
- New search for: Malicdan, May Christine V.
- New search for: Mamounas, Laura A.
- New search for: Manolio, Teri A.
- New search for: Markello, Thomas C.
- New search for: Marom, Ronit
- New search for: Martin, Martin G.
- New search for: Martínez‐Agosto, Julian A.
- New search for: Marwaha, Shruti
- New search for: May, Thomas
- New search for: McConkie‐Rosell, Allyn
- New search for: McCormack, Colleen E.
- New search for: McCray, Alexa T.
- New search for: Merker, Jason D.
- New search for: Metz, Thomas O.
- New search for: Might, Matthew
- New search for: Moretti, Paolo M.
- New search for: Morimoto, Marie
- New search for: Mulvihill, John J.
- New search for: Murdock, David R.
- New search for: Murphy, Jennifer L.
- New search for: Muzny, Donna M.
- New search for: Nehrebecky, Michele E.
- New search for: Nelson, Stan F.
- New search for: Scott Newberry, J.
- New search for: Nicholas, Sarah K.
- New search for: Novacic, Donna
- New search for: Orange, Jordan S.
- New search for: Orengo, James P.
- New search for: Carl Pallais, J.
- New search for: Palme, Christina G. S.
- New search for: Papp, Jeanette C.
- New search for: Parker, Neil H.
- New search for: Pena, Loren D. M.
- New search for: Posey, Jennifer E.
- New search for: Postlethwait, John H.
- New search for: Potocki, Lorraine
- New search for: Pusey, Barbara N.
- New search for: Reuter, Chloe M.
- New search for: Robertson, Amy K.
- New search for: Rodan, Lance H.
- New search for: Rosenfeld, Jill A.
- New search for: Sampson, Jacinda B.
- New search for: Samson, Susan L.
- New search for: Schoch, Kelly
- New search for: Schroeder, Molly C.
- New search for: Scott, Daryl A.
- New search for: Sharma, Prashant
- New search for: Shashi, Vandana
- New search for: Silverman, Edwin K.
- New search for: Sinsheimer, Janet S.
- New search for: Smith, Kevin S.
- New search for: Spillmann, Rebecca C.
- New search for: Stoler, Joan M.
- New search for: Stong, Nicholas
- New search for: Sullivan, Jennifer A.
- New search for: Sweetser, David A.
- New search for: Tan, Queenie K.‐G.
- New search for: Tifft, Cynthia J.
- New search for: Toro, Camilo
- New search for: Tran, Alyssa A.
- New search for: Urv, Tiina K.
- New search for: Valivullah, Zaheer M.
- New search for: Vilain, Eric
- New search for: Vogel, Tiphanie P.
- New search for: Waggott, Daryl M.
- New search for: Wahl, Colleen E.
- New search for: Walley, Nicole M.
- New search for: Walsh, Chris A.
- New search for: Walker, Melissa
- New search for: Wan, Jijun
- New search for: Wangler, Michael F.
- New search for: Ward, Patricia A.
- New search for: Waters, Katrina M.
- New search for: Webb‐Robertson, Bobbie‐Jo M.
- New search for: Westerfield, Monte
- New search for: Wheeler, Matthew T.
- New search for: Wise, Anastasia L.
- New search for: Wolfe, Lynne A.
- New search for: Worthey, Elizabeth A.
- New search for: Yamamoto, Shinya
- New search for: Yang, Yaping
- New search for: Yoon, Amanda J.
- New search for: Yu, Guoyun
- New search for: Zastrow, Diane B.
- New search for: Zhao, Chunli
- New search for: Zheng, Allison
- New search for: Undiagnosed Disease Network
In:
Molecular Genetics & Genomic Medicine
;
7
, 6
;
2019
-
ISSN:
- Article (Journal) / Electronic Resource
-
Title:IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells
-
Contributors:Newman, John H. ( author ) / Shaver, Aaron ( author ) / Sheehan, Jonathan H. ( author ) / Mallal, Simon ( author ) / Stone, John H. ( author ) / Pillai, Shiv ( author ) / Bastarache, Lisa ( author ) / Riebau, Derek ( author ) / Allard‐Chamard, Hugues ( author ) / Stone, William M. ( author )
-
Published in:
-
Publisher:
-
Publication date:2019-06-01
-
Size:8 pages
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Keywords:
-
Source:
Table of contents – Volume 7, Issue 6
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
-
Associations of intercellular adhesion molecule‐1 rs5498 polymorphism with ischemic stroke: A meta‐analysisGao, Hua / Zhang, Xinhua et al. | 2019
-
Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencingYu, Dongyi / Zhang, Kai / Han, Meiyan / Pan, Wei / Chen, Ying / Wang, Yunfeng / Jiao, Hongyan / Duan, Ling / Zhu, Qiying / Song, Xiaojie et al. | 2019
-
Novel heterozygous BPIFC variant in a Chinese pedigree with hereditary trichilemmal cystsFu, Xian‐Guo / Huang, Zhao / Zhou, Su‐Juan / Yang, Jing / Peng, Yun‐Juan / Cao, Luo‐Yuan / Guo, Hua / Wu, Guang‐Hui / Lin, Ying‐Hua / Huang, Bao‐Ying et al. | 2019
-
Identifying gene mutations of Chinese patients with polycystic kidney disease through targeted next‐generation sequencing technologyWang, Tao / Li, Qinggang / Shang, Shunlai / Geng, Guangrui / Xie, Yuansheng / Cai, Guangyan / Chen, Xiangmei et al. | 2019
-
Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate geneLundin, Johanna / Markljung, Ellen / Baranowska Körberg, Izabella / Hofmeister, Wolfgang / Cao, Jia / Nilsson, Daniel / Holmdahl, Gundela / Barker, Gillian / Anderberg, Magnus / Vukojević, Vladana et al. | 2019
-
Estimation of CYP3A4*1B single nucleotide polymorphism in patients with recurrent Major Depressive DisorderŚwiechowski, Rafał / Jeleń, Agnieszka / Mirowski, Marek / Talarowska, Monika / Gałecki, Piotr / Pietrzak, Jacek / Wodziński, Damian / Balcerczak, Ewa et al. | 2019
-
miR‐584‐5p regulates hepatocellular carcinoma cell migration and invasion through targeting KCNE2Wei, Huamei / Wang, Jianchu / Xu, Zuoming / Lu, Yuan / Wu, Xianjian / Zhuo, Chenyi / Tan, Chuan / Tang, Qianli / Pu, Jian et al. | 2019
-
Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern ChinaZhang, Jie / Yang, Yang / Li, Peng / Yan, Yuanlong / Lv, Tao / Zhao, Tingting / Zeng, Xiaohong / Li, Dongmei / Zhou, Xiaoyan / Chen, Hong et al. | 2019
-
A case of combined 21‐hydroxylase deficiency and CHARGE syndrome featuring micropenis and cryptorchidismUmino, Satoko / Kitamura, Miyuki / Katoh‐Fukui, Yuko / Fukami, Maki / Usui, Takeshi / Yatsuga, Shuichi / Koga, Yasutoshi et al. | 2019
-
Co‐occurrence of ATXN3 and ATXN2repeat expansions in Chinese ataxia patients with slow saccadesWu, Chao / Cai, Qiong / You, Huajing / Zhou, Xiangxue / Chen, Dingbang / Mo, Guiling / Li, Xunhua et al. | 2019
-
Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4Cappuccio, Gerarda / Brunetti‐Pierri, Raffaella / Torella, Annalaura / Pinelli, Michele / Castello, Raffaele / Casari, Giorgio / Nigro, Vincenzo / Banfi, Sandro / Simonelli, Francesca / Brunetti‐Pierri, Nicola et al. | 2019
-
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, MéxicoGarcía‐de Teresa, Benilde / Frias, Sara / Molina, Bertha / Villarreal, María Teresa / Rodriguez, Alfredo / Carnevale, Alessandra / López‐Hernández, Gerardo / Vollbrechtshausen, Lilia / Olaya‐Vargas, Alberto / Torres, Leda et al. | 2019
-
Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy‐associated genes among children undergoing exome sequencing reflect healthy population variationHeadrick, Andrew T. / Rosenfeld, Jill A. / Yang, Yaping / Tunuguntla, Hari / Allen, Hugh D. / Penny, Daniel J. / Kim, Jeffrey J. / Landstrom, Andrew P. et al. | 2019
-
Effects of RHD gene polymorphisms on distinguishing weak D or DEL from RhD− in blood donation in a Chinese populationShi, Jie / Luo, Ying et al. | 2019
-
Diverse phenotypes in children with PAX2‐related disorderDeng, Haiyue / Zhang, Yanqin / Xiao, Huijie / Yao, Yong / Liu, Xiaoyu / Su, Baige / Zhang, Hongwen / Xu, Ke / Wang, Suxia / Wang, Fang et al. | 2019
-
Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype‐phenotype correlation analyses of TP63‐related disordersZheng, Jinglei / Liu, Haochen / Zhan, Yuan / Liu, Yang / Wong, Sing‐Wai / Cai, Tao / Feng, Hailan / Han, Dong et al. | 2019
-
The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association ConsortiumUgai, Tomotaka / Milne, Roger L. / Ito, Hidemi / Aronson, Kristan J. / Bolla, Manjeet K. / Chan, Tsun / Chan, Ching W. / Choi, Ji‐Yeob / Conroy, Don M. / Dennis, Joe et al. | 2019
-
Mutations in the mitochondrial tryptophanyl‐tRNA synthetase cause growth retardation and progressive leukoencephalopathyMaffezzini, Camilla / Laine, Isabelle / Dallabona, Cristina / Clemente, Paula / Calvo‐Garrido, Javier / Wibom, Rolf / Naess, Karin / Barbaro, Michela / Falk, Anna / Donnini, Claudia et al. | 2019
-
Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3: Beyond crouzon syndrome and acanthosis nigricansRymer, Karen / Shiang, Rita / Hsiung, Anting / Pandya, Arti / Bigdeli, Tim / Webb, Bradley T. / Rhodes, Jennifer et al. | 2019
-
Long noncoding RNA NEAT1 regulates the development of osteosarcoma through sponging miR‐34a‐5p to mediate HOXA13 expression as a competitive endogenous RNAJi, Shaolin / Wang, Shunsheng / Zhao, Xiaodan / Lv, Li et al. | 2019
-
The association of nucleotide‐binding oligomerization domain 2 gene polymorphisms with the risk of asthma in the Chinese Han populationCai, Xulong / Xu, Qiaolan / Zhou, Chenrong / Zhou, Li / Dai, Weihua / Ji, Guanchi et al. | 2019
-
Association of PTPN22 polymorphism and its correlation with Graves' disease susceptibility in Polish adult population—A preliminary studyWawrusiewicz‐Kurylonek, Natalia / Koper‐Lenkiewicz, Olga Martyna / Gościk, Joanna / Myśliwiec, Janusz / Pawłowski, Przemysław / Krętowski, Adam Jacek et al. | 2019
-
Two de novo GJA1 mutation in two sporadic patients with erythrokeratodermia variabilis et progressivaLi, Changxing / Liang, Jingyao / Chen, Pingjiao / Zeng, Kang / Xue, Rujun / Tian, Xin / Liang, Liuping / Wang, Qi / Shi, Minglan / Zhang, Xibao et al. | 2019
-
A risk assessment model of acute liver allograft rejection by genetic polymorphism of CD276Yu, Xiaobo / Wei, Bajin / Su, Rong / Yao, Jia / Feng, Xiaowen / Jiang, Guoping / Xie, Haiyang / Wu, Jian / Xu, Xiao / Zhang, Min et al. | 2019
-
Novel mutations of COL4A3, COL4A4, and COL4A5genes in Chinese patients with Alport Syndrome using next generation sequence techniqueZhao, Xuechao / Chen, Chen / Wei, Yanfu / Zhao, Ganye / Liu, Lina / Wang, Conghui / Zhang, Junjun / Kong, Xiangdong et al. | 2019
-
CCDN1 rs603965 polymorphism may serve as a genetic biomarker of brain tumor: A meta‐analysis of 5,769 subjectsLan, Jiarong / Li, Min / Wang, Haifeng et al. | 2019
-
Prioritization and comprehensive analysis of genes related to major depressive disorderLiu, Yi / Fan, Pengfei / Zhang, Shiyuan / Wang, Yidan / Liu, Dan et al. | 2019
-
Genotype–phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21‐hydroxylase deficiencyXu, Chao / Jia, Wenyu / Cheng, Xiangdeng / Ying, Hui / Chen, Jing / Xu, Jin / Guan, Qingbo / Zhou, Xinli / Zheng, Dongmei / Li, Guimei et al. | 2019
-
Comprehensive analysis of serum tumor markers and BRCA1/2 germline mutations in Chinese ovarian cancer patientsDeng, Hongyu / Chen, Ming / Guo, Xinwu / Heng, Jianfu / Xu, Xunxun / Peng, Limin / Jiang, Hui / Li, Guoli / Day, Julia X. / Li, Jinliang et al. | 2019
-
Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice‐site and Charcot‐Marie‐Tooth phenotype with early onset symptomsCassini, Thomas A. / Duncan, Laura / Rives, Lynette C. / Newman, John H. / Phillips, John A. / Koziura, Mary E. / Brault, Jennifer / Hamid, Rizwan / Cogan, Joy / Undiagnosed Diseases Network et al. | 2019
-
IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cellsNewman, John H. / Shaver, Aaron / Sheehan, Jonathan H. / Mallal, Simon / Stone, John H. / Pillai, Shiv / Bastarache, Lisa / Riebau, Derek / Allard‐Chamard, Hugues / Stone, William M. et al. | 2019
-
Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literatureScelsa, Barbara / Gasperini, Serena / Righini, Andrea / Iascone, Maria / Brazzoduro, Valeria G. / Veggiotti, Pierangelo et al. | 2019
-
Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancerWang, Xiaozhen / Liu, Haimeng / Maimaitiaili, Amina / Zhao, Gang / Li, Sijie / Lv, Zheng / Wu, Di / Shi, Aiping / Guan, Xin / Jia, Hongyao et al. | 2019
-
Identification of novel mutations in preaxial polydactyly patients through whole‐exome sequencingWang, Tao / Xuan, Zhaopeng / Dou, Yichen / Liu, Yang / Fu, Yanyan / Ren, Jingyan / Lu, Laijin et al. | 2019
-
The Enamel Phenotype in Homozygous Fam83h Truncation MiceWang, Shih‐Kai / Hu, Yuanyuan / Smith, Charles E. / Yang, Jie / Zeng, Chunhua / Kim, Jung‐Wook / Hu, Jan C‐C. / Simmer, James P. et al. | 2019
-
Genetics and genomic medicine in Sri LankaSirisena, Nirmala D. / Dissanayake, Vajira H. W. et al. | 2019
-
Genetic analysis in the bariatric clinic; impact of a PTEN gene mutationCooiman, Mellody I. / Kleinendorst, Lotte / van der Zwaag, Bert / Janssen, Ignace M. C. / Berends, Frits J. / van Haelst, Mieke M. et al. | 2019
-
A rapid and accurate methylation‐sensitive high‐resolution melting analysis assay for the diagnosis of Prader Willi and Angelman patientsRibeiro Ferreira, Igor / Darleans dos Santos Cunha, Wilton / Henrique Ferreira Gomes, Leonardo / Azevedo Cintra, Hiago / Lopes Cabral Guimarães Fonseca, Letícia / Ferreira Bastos, Elenice / Clinton Llerena, Juan Jr. / Farias Meira de Vasconcelos, Zilton / da Cunha Guida, Letícia et al. | 2019
-
Concurrent manifestation of oligodontia and thrombocytopenia caused by a contiguous gene deletion in 12p13.2: A three‐generation clinical reportRoss, Jamila / Fennis, Willem / de Leeuw, Nicole / Cune, Marco / Willemze, Annemieke / Rosenberg, Antoine / Ploos van Amstel, Hans‐Kristian / Créton, Marijn / van den Boogaard, Marie‐José et al. | 2019
-
Myeloid malignancies‐related somatic mutations in aging individualsCoutinho, Diego F. / Zalcberg, Ilana R. / Monte‐Mór, Bárbara C. R. et al. | 2019
-
Clinical utility in infants with suspected monogenic conditions through next‐generation sequencingHong, Sha / Wang, Li / Zhao, Dongying / Zhang, Yonghong / Chen, Yan / Tan, Jintong / Liang, Lili / Zhu, Tianwen et al. | 2019
-
Cognition in adults with Williams syndrome—A 20‐year follow‐up studySauna‐aho, Oili / Bjelogrlic‐Laakso, Nina / Sirén, Auli / Kangasmäki, Virpi / Arvio, Maria et al. | 2019
-
Severe presentation and complex brain malformations in an individual carrying a CCND2 variantCappuccio, Gerarda / Ugga, Lorenzo / Parrini, Elena / D’Amico, Alessandra / Brunetti‐Pierri, Nicola et al. | 2019
-
PMS2 germline mutation c.943C>T (p.Arg315*)‐induced Lynch syndrome‐associated ovarian cancerGuo, Xiaoqing / Wu, Weimin / Gao, Hao / Li, Xiaofeng / He, Qizhi / Zhu, Yong / Liu, Na et al. | 2019
-
The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancyRudolf, Gorazd / Lovrečić, Luca / Tul, Nataša / Teran, Nataša / Peterlin, Borut et al. | 2019
-
Association of OPG gene polymorphisms with the risk of knee osteoarthritis among Chinese peopleQi, Yuxin / An, Feimeng / Wang, Jiaqi / Liu, Yuan / Gao, Hongyan / Ge, Zhe / Jiang, Enze / Cai, Donggao / Shi, Jianping / Wang, Jianzhong et al. | 2019
-
Reduction of expression of IL‐18, IL‐1β genes in the articular joint by sumac fruit extract (Rhus coriaria L.)Momeni, Amin / Maghsoodi, Hossein / Rezapour, Sadegh / Shiravand, Mostafa / Mardani, Mahnaz et al. | 2019
-
Comparison of gene mutation spectrum of thalassemia in different regions of China and Southeast AsiaYang, Zhuo / Cui, Quexuan / Zhou, Wenzhe / Qiu, Ling / Han, Bing et al. | 2019
-
Transcriptome analysis identifies metallothionein as biomarkers to predict recurrence in hepatocellular cacinomaWang, Sufang / Gribskov, Michael et al. | 2019
-
A familial case of pseudohypoaldosteronism type II (PHA2) with a novel mutation (D564N) in the acidic motif in WNK4Sakoh, Takashi / Sekine, Akinari / Mori, Takayasu / Mizuno, Hiroki / Kawada, Masahiro / Hiramatsu, Rikako / Hasegawa, Eiko / Hayami, Noriko / Yamanouchi, Masayuki / Suwabe, Tatsuya et al. | 2019
-
Lnc‐GIHCG promotes cell proliferation and migration in gastric cancer through miR‐ 1281 adsorptionLiu, Guozheng / Jiang, Zaipeng / Qiao, Mingliang / Wang, Fengyong et al. | 2019
-
Issue Information| 2019
-
The identification of a RNA splice variant in TULP1 in two siblings with early‐onset photoreceptor dystrophyVerbakel, Sanne K. / Fadaie, Zeinab / Klevering, B. Jeroen / van Genderen, Maria M. / Feenstra, Ilse / Cremers, Frans P. M. / Hoyng, Carel B. / Roosing, Susanne et al. | 2019
-
BRPF1‐associated intellectual disability, ptosis, and facial dysmorphism in a multiplex familyPode‐Shakked, Naomi / Barel, Ortal / Pode‐Shakked, Ben / Eliyahu, Aviva / Singer, Amihood / Nayshool, Omri / Kol, Nitzan / Raas‐Rothschild, Annick / Pras, Elon / Shohat, Mordechai et al. | 2019
-
Association between polymorphisms of MIR17HGand risk of colorectal cancer in the Chinese Han populationChen, Peng / Bai, Yuwei / Li, Yaru / Yuan, Yuemin / Cheng, Yimin / Pang, Jianjian / Zhu, Hongli / Chen, Chao et al. | 2019
-
Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing lossLi, Xinlei / Tan, Bo / Wang, Xiaoqian / Xu, Xiaofei / Wang, Cuicui / Zhong, Mingjun / Zhao, Qiuling / Bao, Zhongwei / Peng, Weihua / Zhang, Lei et al. | 2019
-
Maternal genetic markers for risk of celiac disease and their potential association with neural tube defects in offspringHoang, Thanh T. / Lei, Yunping / Mitchell, Laura E. / Sharma, Shreela V. / Swartz, Michael D. / Waller, D. Kim / Finnell, Richard H. / Benjamin, Renata H. / Browne, Marilyn L. / Canfield, Mark A. et al. | 2019
-
CoverZheng, Jinglei / Liu, Haochen / Zhan, Yuan / Liu, Yang / Wong, Sing‐Wai / Cai, Tao / Feng, Hailan / Han, Dong et al. | 2019