Citation: | Gurumurthy Channabasavaiah B., Saunders Thomas L., Ohtsuka Masato. Designing and generating a mouse model: frequently asked questions[J]. The Journal of Biomedical Research, 2021, 35(2): 76-90. DOI: 10.7555/JBR.35.20200197 |
[1] |
Palmiter RD, Brinster RL. Transgenic mice[J]. Cell, 1985, 41(2): 343–345. doi: 10.1016/s0092-8674(85)80004-0
|
[2] |
Saunders TL. The history of transgenesis[M]//Larson MA. Transgenic Mouse: Transgenic Mouse. New York: Humana, 2020: 1–26, doi: 10.1007/978-1-4939-9837-1_1.
|
[3] |
Brinster RL, Braun RE, Lo D, et al. Targeted correction of a major histocompatibility class II E alpha gene by DNA microinjected into mouse eggs[J]. Proc Natl Acad Sci U S A, 1989, 86(18): 7087–7091. doi: 10.1073/pnas.86.18.7087
|
[4] |
Cain-Hom C, Splinter E, van Min M, et al. Efficient mapping of transgene integration sites and local structural changes in Cre transgenic mice using targeted locus amplification[J]. Nucleic Acids Res, 2017, 45(8): e62. doi: 10.1093/nar/gkw1329
|
[5] |
Chiang C, Jacobsen JC, Ernst C, et al. Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration[J]. Nat Genet, 2012, 44(4): 390–397. doi: 10.1038/ng.2202
|
[6] |
Dubose AJ, Lichtenstein ST, Narisu N, et al. Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene[J]. Nucleic Acids Res, 2013, 41(6): e70. doi: 10.1093/nar/gks1463
|
[7] |
Goodwin LO, Splinter E, Davis TL, et al. Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis[J]. Genome Res, 2019, 29(3): 494–505. doi: 10.1101/gr.233866.117
|
[8] |
Meisler MH. Insertional mutation of 'classical' and novel genes in transgenic mice[J]. Trends Genet, 1992, 8(10): 341–344. doi: 10.1016/0168-9525(92)90278-C
|
[9] |
Clark AJ, Bissinger P, Bullock DW, et al. Chromosomal position effects and the modulation of transgene expression[J]. Reprod Fertil Dev, 1994, 6(5): 589–598. doi: 10.1071/RD9940589
|
[10] |
Gödecke N, Zha LS, Spencer S, et al. Controlled re-activation of epigenetically silenced Tet promoter-driven transgene expression by targeted demethylation[J]. Nucleic Acids Res, 2017, 45(16): e147. doi: 10.1093/nar/gkx601
|
[11] |
Lin TP. Microinjection of mouse eggs[J]. Science, 1966, 151(3708): 333–337. doi: 10.1126/science.151.3708.333
|
[12] |
Wilson IB, Bolton E, Cuttler RH. Preimplantation differentiation in the mouse egg as revealed by microinjection of vital markers[J]. J Embryol Exp Morphol, 1972, 27(2): 467–469. https://dev.biologists.org/content/27/2/467.long
|
[13] |
Gordon JW, Scangos GA, Plotkin DJ, et al. Genetic transformation of mouse embryos by microinjection of purified DNA[J]. Proc Natl Acad Sci U S A, 1980, 77(12): 7380–7384. doi: 10.1073/pnas.77.12.7380
|
[14] |
Ohtsuka M, Ogiwara S, Miura H, et al. Pronuclear injection-based mouse targeted transgenesis for reproducible and highly efficient transgene expression[J]. Nucleic Acids Res, 2010, 38(22): e198. doi: 10.1093/nar/gkq860
|
[15] |
Ohtsuka M, Miura H, Mochida K, et al. One-step generation of multiple transgenic mouse lines using an improved Pronuclear Injection-based Targeted Transgenesis (i-PITT)[J]. BMC Genomics, 2015, 16(1): 274. doi: 10.1186/s12864-015-1432-5
|
[16] |
Tasic B, Hippenmeyer S, Wang C, et al. Site-specific integrase-mediated transgenesis in mice via pronuclear injection[J]. Proc Natl Acad Sci U S A, 2011, 108(19): 7902–7907. doi: 10.1073/pnas.1019507108
|
[17] |
Capecchi MR. Gene targeting in mice: functional analysis of the mammalian genome for the twenty-first century[J]. Nat Rev Genet, 2005, 6(6): 507–512. doi: 10.1038/nrg1619
|
[18] |
Sauer B, Henderson N. Site-specific DNA recombination in mammalian cells by the Cre recombinase of bacteriophage P1[J]. Proc Natl Acad Sci U S A, 1988, 85(14): 5166–5170. doi: 10.1073/pnas.85.14.5166
|
[19] |
Skarnes WC, Rosen B, West AP, et al. A conditional knockout resource for the genome-wide study of mouse gene function[J]. Nature, 2011, 474(7351): 337–342. doi: 10.1038/nature10163
|
[20] |
White JK, Gerdin AK, Karp NA, et al. Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes[J]. Cell, 2013, 154(2): 452–464. doi: 10.1016/j.cell.2013.06.022
|
[21] |
Meier ID, Bernreuther C, Tilling T, et al. Short DNA sequences inserted for gene targeting can accidentally interfere with off-target gene expression[J]. FASEB J, 2010, 24(6): 1714–1724. doi: 10.1096/fj.09-140749
|
[22] |
Bult CJ, Blake JA, Smith CL, et al. Mouse Genome Database (MGD) 2019[J]. Nucleic Acids Res, 2019, 47(D1): D801–D806. doi: 10.1093/nar/gky1056
|
[23] |
Gurumurthy CB, Joshi PS, Kurz SG, et al. Validation of simple sequence length polymorphism regions of commonly used mouse strains for marker assisted speed congenics screening[J]. Int J Genomics, 2015, 2015: 735845. doi: 10.1155/2015/735845
|
[24] |
Song AJ, Palmiter RD. Detecting and avoiding problems when using the Cre–lox system[J]. Trends Genet, 2018, 34(5): 333–340. doi: 10.1016/j.tig.2017.12.008
|
[25] |
Madisen L, Zwingman TA, Sunkin SM, et al. A robust and high-throughput Cre reporting and characterization system for the whole mouse brain[J]. Nat Neurosci, 2010, 13(1): 133–140. doi: 10.1038/nn.2467
|
[26] |
Fernández-Chacón M, Casquero-García V, Luo W, et al. iSuRe-Cre is a genetic tool to reliably induce and report Cre-dependent genetic modifications[J]. Nat Commun, 2019, 10(1): 2262. doi: 10.1038/s41467-019-10239-4
|
[27] |
Soriano P. Generalized lacZ expression with the ROSA26 Cre reporter strain[J]. Nat Genet, 1999, 21(1): 70–71. doi: 10.1038/5007
|
[28] |
Niwa H, Yamamura K, Miyazaki J. Efficient selection for high-expression transfectants with a novel eukaryotic vector[J]. Gene, 1991, 108(2): 193–199. doi: 10.1016/0378-1119(91)90434-d
|
[29] |
Sakai N. Principles for the use of in vivo transgene techniques: overview and an introductory practical guide for the selection of tetracycline-controlled transgenic mice[M]//Shiozawa S. Arthritis Research: Methods and Protocols. New York: Humana Press, 2014: 33–40, doi: 10.1007/978-1-4939-0404-4_4.
|
[30] |
Chen XY, Zaro JL, Shen WC. Fusion protein linkers: property, design and functionality[J]. Adv Drug Deliv Rev, 2013, 65(10): 1357–1369. doi: 10.1016/j.addr.2012.09.039
|
[31] |
Ryan MD, King AMQ, Thomas GP. Cleavage of foot-and-mouth disease virus polyprotein is mediated by residues located within a 19 amino acid sequence[J]. J Gen Virol, 1991, 72(11): 2727–2732. doi: 10.1099/0022-1317-72-11-2727
|
[32] |
Kim JH, Lee SR, Li LH, et al. High cleavage efficiency of a 2A peptide derived from porcine teschovirus-1 in human cell lines, zebrafish and mice[J]. PLoS One, 2011, 6(4): e18556. doi: 10.1371/journal.pone.0018556
|
[33] |
Hosur V, Low BE, Li D, et al. Genes adapt to outsmart gene-targeting strategies in mutant mouse strains by skipping exons to reinitiate transcription and translation[J]. Genome Biol, 2020, 21(1): 168. doi: 10.1186/s13059-020-02086-0
|
[34] |
El-Brolosy MA, Kontarakis Z, Rossi A, et al. Genetic compensation triggered by mutant mRNA degradation[J]. Nature, 2019, 568(7751): 193–197. doi: 10.1038/s41586-019-1064-z
|
[35] |
Bendriem RM, Singh S, Aleem AA, et al. Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex[J]. eLife, 2019, 8: e49376. doi: 10.7554/eLife.49376
|
[36] |
Popp MW, Maquat LE. Leveraging rules of nonsense-mediated Mrna decay for genome engineering and personalized medicine[J]. Cell, 2016, 165(6): 1319–1322. doi: 10.1016/j.cell.2016.05.053
|
[37] |
Lyu Q, Dhagia V, Han Y, et al. CRISPR-Cas9-mediated epitope tagging provides accurate and versatile assessment of myocardin-brief report[J]. Arterioscler Thromb Vasc Biol, 2018, 38(9): 2184–2190. doi: 10.1161/ATVBAHA.118.311171
|
[38] |
Choi M, Lu YW, Zhao JJ, et al. Transcriptional control of a novel long noncoding RNA Mymsl in smooth muscle cells by a single Cis-element and its initial functional characterization in vessels[J]. J Mol Cell Cardiol, 2020, 138: 147–157. doi: 10.1016/j.yjmcc.2019.11.148
|
[39] |
Miano JM, Long XC. The short and long of noncoding sequences in the control of vascular cell phenotypes[J]. Cell Mol Life Sci, 2015, 72(18): 3457–3488. doi: 10.1007/s00018-015-1936-9
|
[40] |
Miano JM, Long XC, Lyu Q. CRISPR links to long noncoding RNA function in mice: a practical approach[J]. Vascul Pharmacol, 2019, 114: 1–12. doi: 10.1016/j.vph.2019.02.004
|
[41] |
Isakova A, Fehlmann T, Keller A, et al. A mouse tissue atlas of small noncoding RNA[J]. Proc Natl Acad Sci U S A, 2020, 117(41): 25634–25645. doi: 10.1073/pnas.2002277117
|
[42] |
Ratnere I, Dubchak I. Obtaining comparative genomic data with the VISTA family of computational tools[J]. Curr Protoc Bioinformatics, 2009, 26(1): 10.6.1–10.6.17. doi: 10.1002/0471250953.bi1006s26
|
[43] |
Economides AN, Frendewey D, Yang P, et al. Conditionals by inversion provide a universal method for the generation of conditional alleles[J]. Proc Natl Acad Sci U S A, 2013, 110(34): E3179–E3188. doi: 10.1073/pnas.1217812110
|
[44] |
Guzzardo PM, Rashkova C, Dos Santos RL, et al. A small cassette enables conditional gene inactivation by CRISPR/Cas9[J]. Sci Rep, 2017, 7(1): 16770. doi: 10.1038/s41598-017-16931-z
|
[45] |
Xie F, Zhou XY, Lin TT, et al. Production of gene-edited pigs harboring orthologous human mutations via double cutting by CRISPR/Cas9 with long single-stranded DNAs as homology-directed repair templates by zygote injection[J]. Transgenic Res, 2020, 29(5-6): 587–598. doi: 10.1007/s11248-020-00218-7
|
[46] |
Nakamura Y, Gojobori T, Ikemura T. Codon usage tabulated from international DNA sequence databases: status for the year 2000[J]. Nucleic Acids Res, 2000, 28(1): 292. doi: 10.1093/nar/28.1.292
|
[47] |
Quadros RM, Miura H, Harms DW, et al. Easi-CRISPR: a robust method for one-step generation of mice carrying conditional and insertion alleles using long ssDNA donors and CRISPR ribonucleoproteins[J]. Genome Biol, 2017, 18(1): 92. doi: 10.1186/s13059-017-1220-4
|
[48] |
Miura H, Quadros RM, Gurumurthy CB, et al. Easi-CRISPR for creating knock-in and conditional knockout mouse models using long ssDNA donors[J]. Nat Protoc, 2018, 13(1): 195–215. doi: 10.1038/nprot.2017.153
|
[49] |
Chu VT, Weber T, Graf R, et al. Efficient generation of Rosa26 knock-in mice using CRISPR/Cas9 in C57BL/6 zygotes[J]. BMC Biotechnol, 2016, 16: 4. doi: 10.1186/s12896-016-0234-4
|
[50] |
Gu B, Posfai E, Rossant J. Efficient generation of targeted large insertions by microinjection into two-cell-stage mouse embryos[J]. Nat Biotechnol, 2018, 36(7): 632–637. doi: 10.1038/nbt.4166
|
[51] |
Abe T, Inoue KI, Furuta Y, et al. Pronuclear microinjection during s-phase increases the efficiency of CRISPR-Cas9-assisted knockin of large DNA donors in mouse zygotes[J]. Cell Rep, 2020, 31(7): 107653. doi: 10.1016/j.celrep.2020.107653
|
[52] |
Yoshimi K, Oka Y, Miyasaka Y, et al. Combi-CRISPR: combination of NHEJ and HDR provides efficient and precise plasmid-based knock-ins in mice and rats[J]. Hum Genet, 2021, 140(2): 277–287. doi: 10.1007/s00439-020-02198-4
|
[53] |
Hashimoto M, Takemoto T. Electroporation enables the efficient mRNA delivery into the mouse zygotes and facilitates CRISPR/Cas9-based genome editing[J]. Sci Rep, 2015, 5: 11315. doi: 10.1038/srep11315
|
[54] |
Qin WN, Dion SL, Kutny PM, et al. Efficient CRISPR/Cas9-mediated genome editing in mice by zygote electroporation of nuclease[J]. Genetics, 2015, 200(2): 423–430. doi: 10.1534/genetics.115.176594
|
[55] |
Wang WB, Kutny PM, Byers SL, et al. Delivery of Cas9 protein into mouse zygotes through a series of electroporation dramatically increases the efficiency of model creation[J]. J Genet Genomics, 2016, 43(5): 319–327. doi: 10.1016/j.jgg.2016.02.004
|
[56] |
Chen SA, Lee B, Lee AYF, et al. Highly efficient mouse genome editing by CRISPR ribonucleoprotein electroporation of zygotes[J]. J Biol Chem, 2016, 291(28): 14457–14467. doi: 10.1074/jbc.M116.733154
|
[57] |
Tröder SE, Ebert LK, Butt L, et al. An optimized electroporation approach for efficient CRISPR/Cas9 genome editing in murine zygotes[J]. PLoS One, 2018, 13(5): e0196891. doi: 10.1371/journal.pone.0196891
|
[58] |
Takahashi G, Gurumurthy CB, Wada K, et al. GONAD: genome-editing via Oviductal nucleic acids delivery system: a novel microinjection independent genome engineering method in mice[J]. Sci Rep, 2015, 5: 11406. doi: 10.1038/srep11406
|
[59] |
Gurumurthy CB, Takahashi G, Wada K, et al. GONAD: a novel CRISPR/Cas9 genome editing method that does not require ex vivo handling of embryos[J]. Curr Protoc Hum Genet, 2016, 88(1): 15.8.1–15.8.12. doi: 10.1002/0471142905.hg1508s88
|
[60] |
Ohtsuka M, Sato M, Miura H, et al. i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases[J]. Genome Biol, 2018, 19(1): 25. doi: 10.1186/s13059-018-1400-x
|
[61] |
Gurumurthy CB, Sato M, Nakamura A, et al. Creation of CRISPR-based germline-genome-engineered mice without ex vivo handling of zygotes by i-GONAD[J]. Nat Protoc, 2019, 14(8): 2452–2482. doi: 10.1038/s41596-019-0187-x
|
[62] |
Shen B, Zhang J, Wu HY, et al. Generation of gene-modified mice via Cas9/RNA-mediated gene targeting[J]. Cell Res, 2013, 23(5): 720–723. doi: 10.1038/cr.2013.46
|
[63] |
Yen ST, Zhang M, Deng JM, et al. Somatic mosaicism and allele complexity induced by CRISPR/Cas9 RNA injections in mouse zygotes[J]. Dev Biol, 2014, 393(1): 3–9. doi: 10.1016/j.ydbio.2014.06.017
|
[64] |
Wu Y, Zhang J, Peng BY, et al. Generating viable mice with heritable embryonically lethal mutations using the CRISPR-Cas9 system in two-cell embryos[J]. Nat Commun, 2019, 10(1): 2883. doi: 10.1038/s41467-019-10748-2
|
[65] |
Quadros RM, Harms DW, Ohtsuka M, et al. Insertion of sequences at the original provirus integration site of mouse ROSA26 locus using the CRISPR/Cas9 system[J]. FEBS Open Bio, 2015, 5(1): 191–197. doi: 10.1016/j.fob.2015.03.003
|
[66] |
Mianné J, Codner GF, Caulder A, et al. Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control[J]. Methods, 2017, 121-122: 68–76. doi: 10.1016/j.ymeth.2017.03.016
|
[67] |
Parker-Thornburg J. Breeding strategies for genetically modified mice[M]//Larson MA. Transgenic Mouse: Methods and Protocols. New York: Humana, 2020: 163–169, doi: 10.1007/978-1-4939-9837-1_14.
|
[68] |
Boroviak K, Fu BY, Yang FT, et al. Revealing hidden complexities of genomic rearrangements generated with Cas9[J]. Sci Rep, 2017, 7(1): 12867. doi: 10.1038/s41598-017-12740-6
|
[69] |
Kosicki M, Tomberg K, Bradley A. Repair of double-strand breaks induced by CRISPR-Cas9 leads to large deletions and complex rearrangements[J]. Nat Biotechnol, 2018, 36(8): 765–771. doi: 10.1038/nbt.4192
|
[70] |
Iyer V, Shen B, Zhang WS, et al. Off-target mutations are rare in Cas9-modified mice[J]. Nat Methods, 2015, 12(6): 479. doi: 10.1038/nmeth.3408
|
[71] |
Anderson KR, Haeussler M, Watanabe C, et al. CRISPR off-target analysis in genetically engineered rats and mice[J]. Nat Methods, 2018, 15(7): 512–514. doi: 10.1038/s41592-018-0011-5
|
[72] |
Doench JG, Fusi N, Sullender M, et al. Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9[J]. Nat Biotechnol, 2016, 34(2): 184–191. doi: 10.1038/nbt.3437
|
[73] |
Vakulskas CA, Dever DP, Rettig GR, et al. A high-fidelity Cas9 mutant delivered as a ribonucleoprotein complex enables efficient gene editing in human hematopoietic stem and progenitor cells[J]. Nat Med, 2018, 24(8): 1216–1224. doi: 10.1038/s41591-018-0137-0
|
[74] |
McBeath E, Parker-Thornburg J, Fujii Y, et al. Rapid evaluation of CRISPR guides and donors for engineering mice[J]. Genes, 2020, 11(6): 628. doi: 10.3390/genes11060628
|
[75] |
Muzumdar MD, Tasic B, Miyamichi K, et al. A global double-fluorescent Cre reporter mouse[J]. Genes, 2007, 45(9): 593–605. doi: 10.1002/dvg.20335
|
[76] |
Madisen L, Garner AR, Shimaoka D, et al. Transgenic mice for intersectional targeting of neural sensors and effectors with high specificity and performance[J]. Neuron, 2015, 85(5): 942–958. doi: 10.1016/j.neuron.2015.02.022
|
[77] |
Daigle TL, Madisen L, Hage TA, et al. A suite of transgenic driver and reporter mouse lines with enhanced brain-cell-type targeting and functionality[J]. Cell, 2018, 174(2): 465–480. doi: 10.1016/j.cell.2018.06.035
|
[78] |
Gurumurthy CB, Quadros RM, Richardson GP, et al. Genetically modified mouse models to help fight COVID-19[J]. Nat Protoc, 2020, 15(12): 3777–3787. doi: 10.1038/s41596-020-00403-2
|
[79] |
Müller U. Ten years of gene targeting: targeted mouse mutants, from vector design to phenotype analysis[J]. Mech Dev, 1999, 82(1-2): 3–21. doi: 10.1016/s0925-4773(99)00021-0
|
[80] |
Palmiter RD, Brinster RL. Germ-line transformation of mice[J]. Annu Rev Genet, 1986, 20: 465–499. doi: 10.1146/annurev.ge.20.120186.002341
|
[81] |
Xu WH. Microinjection and micromanipulation: a historical perspective[M]//Liu CY, Du YB. Microinjection: Methods and Protocols. New York: Humana Press, 2019: 1–16, doi: 10.1007/978-1-4939-8831-0_1.
|
[82] |
Anastassiadis K, Glaser S, Kranz A, et al. A practical summary of site-specific recombination, conditional mutagenesis, and tamoxifen induction of CreERT2[J]. Methods Enzymol, 2010, 477: 109–123. doi: 10.1016/S0076-6879(10)77007-5
|
[83] |
Nagy A. Cre recombinase: the universal reagent for genome tailoring[J]. Genesis, 2000, 26(2): 99–109. doi: 10.1002/(SICI)1526-968X(200002)26:2<99::AID-GENE1>3.0.CO;2-B
|
[84] |
Gurumurthy CB, Lloyd KCK. Generating mouse models for biomedical research: technological advances[J]. Dis Model Mech, 2019, 12(1): dmm029462. doi: 10.1242/dmm.029462
|
[85] |
Miano JM, Zhu QM, Lowenstein CJ. A CRISPR path to engineering new genetic mouse models for cardiovascular research[J]. Arterioscler Thromb Vasc Biol, 2016, 36(6): 1058–1075. doi: 10.1161/ATVBAHA.116.304790
|
[86] |
Doetschman T, Gregg RG, Maeda N, et al. Targetted correction of a mutant HPRT gene in mouse embryonic stem cells[J]. Nature, 1987, 330(6148): 576–578. doi: 10.1038/330576a0
|
[87] |
Thomas KR, Capecchi MR. Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells[J]. Cell, 1987, 51(3): 503–512. doi: 10.1016/0092-8674(87)90646-5
|
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