Biblio

2018
Jones JMcAndrew, DePaul M, Gregory CR, Lang BT, Xie H, Zhu M, Rutten M, Mays R, Busch S, Pati S, et al. Multipotent adult progenitor cells, but not TIMP3, increase tissue sparing and reduce urological complications following spinal cord injury. J Neurotrauma. 2018.
James DA, Ng J, Wei J, Vandemeulebroecke M. Multistate modeling and simulation of patient trajectories after allogeneic hematopoietic stem cell transplantation to inform drug development. Biom J. 2018.
Fujiwara H, Tsutsui K, Morita R. Multi-tasking epidermal stem cells: Beyond epidermal maintenance. Dev Growth Differ. 2018.
Dorsey TB, Kim D, Grath A, James D, Dai G. Multivalent biomaterial platform to control the distinct arterial venous differentiation of pluripotent stem cells. Biomaterials. 2018;185:1-12.
Inaba S, Hinohara A, Tachibana M, Tsujikawa K, Fukada S-I. Muscle regeneration is disrupted by cancer cachexia without loss of muscle stem cell potential. PLoS One. 2018;13(10):e0205467.
Verma M, Asakura Y, Murakonda BSai Rohit, Pengo T, Latroche C, Chazaud B, McLoon LK, Asakura A. Muscle Satellite Cell Cross-Talk with a Vascular Niche Maintains Quiescence via VEGF and Notch Signaling. Cell Stem Cell. 2018;23(4):530-543.e9.
Wang S, Zhang B, Addicks GC, Zhang H, Menzies KJ, Zhang H. Muscle Stem Cell Immunostaining. Curr Protoc Mouse Biol. 2018:e47.
Wosczyna MN, Rando TA. A Muscle Stem Cell Support Group: Coordinated Cellular Responses in Muscle Regeneration. Dev Cell. 2018;46(2):135-143.
Musavi L, Brandacher G, Höke A, Darrach H, Lee WPAndrew, Kumar A, Lopez J. Muscle-derived stem cells: important players in peripheral nerve repair. Expert Opin Ther Targets. 2018.
Tsai P-F, Dell'Orso S, Rodriguez J, Vivanco KO, Ko K-D, Jiang K, Juan AH, Sarshad AA, Vian L, Tran M, et al. A Muscle-Specific Enhancer RNA Mediates Cohesin Recruitment and Regulates Transcription In trans. Mol Cell. 2018;71(1):129-141.e8.
Cutler AA, Olwin BB. Muscling in on the Awesome Proliferative Power of the Terrible Teratoma. Cell Stem Cell. 2018;23(1):1-2.
Zhou T, Chen C, Xu C, Zhou H, Gao B, Su D, Liao Z, Li Y, Yang S, Su P. Mutant MAPK7-Induced Idiopathic Scoliosis is Linked to Impaired Osteogenesis. Cell Physiol Biochem. 2018;48(3):880-890.
Brunetti L, Gundry MC, Sorcini D, Guzman AG, Huang Y-H, Ramabadran R, Gionfriddo I, Mezzasoma F, Milano F, Nabet B, et al. Mutant NPM1 Maintains the Leukemic State through HOX Expression. Cancer Cell. 2018;34(3):499-512.e9.
Duncavage EJ, Jacoby MA, Chang GSu, Miller CA, Edwin N, Shao J, Elliott K, Robinson J, Abel H, Fulton RS, et al. Mutation Clearance after Transplantation for Myelodysplastic Syndrome. N Engl J Med. 2018;379(11):1028-1041.
Ross J, Kuzin A, Brody T, Odenwald WF. Mutational analysis of a Drosophila neuroblast enhancer governing nubbin expression during CNS development. Genesis. 2018.
Konjikusic MJ, Yeetong P, Boswell CW, Lee C, Roberson EC, Ittiwut R, Suphapeetiporn K, Ciruna B, Gurnett CA, Wallingford JB, et al. Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development. PLoS Genet. 2018;14(11):e1007817.
Vahidnezhad H, Youssefian L, Saeidian AHossein, Touati A, Pajouhanfar S, Baghdadi T, Shadmehri AAhmadi, Giunta C, Kraenzlin M, Syx D, et al. Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency. Matrix Biol. 2018.
Gallot YS, Straughn AR, Bohnert KR, Xiong G, Hindi SM, Kumar A. MyD88 is required for satellite cell-mediated myofiber regeneration in dystrophin-deficient mdx mice. Hum Mol Genet. 2018.
Galaverna F, Ruggeri A, Locatelli F. Myelodysplastic syndromes in children. Curr Opin Oncol. 2018.
Bapat A, Keita N, Martelly W, Kang P, Seet C, Jacobsen JR, Stoilov P, Hu C, Crooks GM, Sharma S. Myeloid disease mutations of splicing factor SRSF2 cause G2-M arrest and skewed differentiation of human hematopoietic stem and progenitor cells. Stem Cells. 2018.
Belluschi S, Calderbank EF, Ciaurro V, Pijuan-Sala B, Santoro A, Mende N, Diamanti E, Sham KYen Chi, Wang X, W Y Lau W, et al. Myelo-lymphoid lineage restriction occurs in the human haematopoietic stem cell compartment before lymphoid-primed multipotent progenitors. Nat Commun. 2018;9(1):4100.
Zaninetti C, De Rocco D, Giangregorio T, Bozzi V, Demeter J, Leoni P, Noris P, Ryhänen S, Barozzi S, Pecci A, et al. MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder. Hamostaseologie. 2018.
Wu J, Matthias N, Lo J, Ortiz-Vitali JL, Shieh AW, Wang SH, Darabi R. A Myogenic Double-Reporter Human Pluripotent Stem Cell Line Allows Prospective Isolation of Skeletal Muscle Progenitors. Cell Rep. 2018;25(7):1966-1981.e4.
Neph A, Onishi K, Wang JH-C. Myths and Facts of In-Office Regenerative Procedures for Tendinopathy: Literature Review. Am J Phys Med Rehabil. 2018.
Lee S-G, Mikhalchenko AE, Yim SHee, Gladyshev VN. A naked mole rat iPSC line expressing drug-inducible mouse pluripotency factors developed from embryonic fibroblasts. Stem Cell Res. 2018;31:197-200.

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