Zebra F Refill Ballpoint Pen for F-301, F-701, Expandz & Spiral. Pack of 12 Black

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Zebra F Refill Ballpoint Pen for F-301, F-701, Expandz & Spiral. Pack of 12 Black

Zebra F Refill Ballpoint Pen for F-301, F-701, Expandz & Spiral. Pack of 12 Black

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Steiner AB, Kim T, Cabot V, Hudspeth AJ (April 2014). "Dynamic gene expression by putative hair-cell progenitors during regeneration in the zebrafish lateral line". Proceedings of the National Academy of Sciences of the United States of America. 111 (14): E1393–E1401. Bibcode: 2014PNAS..111E1393S. doi: 10.1073/pnas.1318692111. PMC 3986164. PMID 24706895. a b Head JR, Gacioch L, Pennisi M, Meyers JR (July 2013). "Activation of canonical Wnt/β-catenin signaling stimulates proliferation in neuromasts in the zebrafish posterior lateral line". Developmental Dynamics. 242 (7): 832–846. doi: 10.1002/dvdy.23973. PMID 23606225.

An SDK reference manual describing the programming functions that control operations and deliver data for Zebra card printers. Cho SJ, Park E, Baker A, Reid AY (2020-09-10). "Age Bias in Zebrafish Models of Epilepsy: What Can We Learn From Old Fish?". Frontiers in Cell and Developmental Biology. 8: 573303. doi: 10.3389/fcell.2020.573303. PMC 7511771. PMID 33015065. In Memory of George Streisinger, "Founding Father" of Zebrafish Developmental and Genetic Research". University of Oregon. Archived from the original on September 29, 2015 . Retrieved September 23, 2015. Meijer AH, van der Vaart M, Spaink HP (January 2014). "Real-time imaging and genetic dissection of host-microbe interactions in zebrafish". Cellular Microbiology. 16 (1): 39–49. doi: 10.1111/cmi.12236. PMID 24188444.Zebrafish have been used as model organisms for bone metabolism, tissue turnover, and resorbing activity. These processes are largely evolutionary conserved. They have been used to study osteogenesis (bone formation), evaluating differentiation, matrix deposition activity, and cross-talk of skeletal cells, to create and isolate mutants modeling human bone diseases, and test new chemical compounds for the ability to revert bone defects. [138] [139] The larvae can be used to follow new ( de novo) osteoblast formation during bone development. They start mineralising bone elements as early as 4 days post fertilisation. Recently, adult zebrafish are being used to study complex age related bone diseases such as osteoporosis and osteogenesis imperfecta. [140] The (elasmoid) scales of zebrafish function as a protective external layer and are little bony plates made by osteoblasts. These exoskeletal structures are formed by bone matrix depositing osteoblasts and are remodeled by osteoclasts. The scales also act as the main calcium storage of the fish. They can be cultured ex-vivo (kept alive outside of the organism) in a multi-well plate, which allows manipulation with drugs and even screening for new drugs that could change bone metabolism (between osteoblasts and osteoclasts). [140] [141] [142] Diabetes [ edit ] Zebrafish are omnivorous, primarily eating zooplankton, phytoplankton, insects and insect larvae, although they can eat a variety of other foods, such as worms and small crustaceans, if their preferred food sources are not readily available. [16] Teske, Christopher. "An Evolving Role for Notch Signaling in Heart Regeneration of the Zebrafish Danio rerio". Researchgate.com . Retrieved 4 October 2022.

Rederstorff M, Castets P, Arbogast S, Lainé J, Vassilopoulos S, Beuvin M, etal. (2011). "Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy". PLOS ONE. 6 (8): e23094. Bibcode: 2011PLoSO...623094R. doi: 10.1371/journal.pone.0023094. PMC 3152547. PMID 21858002.The zebrafish is a derived member of the genus Brachydanio, of the family Cyprinidae. It has a sister-group relationship with Danio aesculapii. [4] Zebrafish are also closely related to the genus Devario, as demonstrated by a phylogenetic tree of close species. [5] Distribution [ edit ] Range [ edit ] Zebrafish has been extensively used as a model organism to study vertebrate innate immunity. The innate immune system is capable of phagocytic activity by 28 to 30 h postfertilization (hpf) [114] while adaptive immunity is not functionally mature until at least 4 weeks postfertilization. [115] Infectious diseases [ edit ]



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