2000
DOI: 10.1016/s0003-9969(99)00105-3
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Expression of myogenic regulatory factors during the development of mouse tongue striated muscle

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Cited by 64 publications
(70 citation statements)
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“…Total RNA extraction, treatment with deoxyribonuclease I, and reverse transcription were performed as previously described Yamane et al, 2000). Briefly, total RNA was isolated from individual soleus muscles according to the manufacturer's specifications (Trizol, Life Technologies, Gaithersburg, MD).…”
Section: Quantitative Rt-pcrmentioning
confidence: 99%
“…Total RNA extraction, treatment with deoxyribonuclease I, and reverse transcription were performed as previously described Yamane et al, 2000). Briefly, total RNA was isolated from individual soleus muscles according to the manufacturer's specifications (Trizol, Life Technologies, Gaithersburg, MD).…”
Section: Quantitative Rt-pcrmentioning
confidence: 99%
“…Desmin, Mck, and Tnnc are three marker genes for identifying the states of myofiber development. Yamane et al (2000) detected the developmental expression profiles of these three maker genes in the tongue and limb muscle tissues in mice and compared the developmental differences of the two muscle tissues (Yamane et al 2000). In our research, the developmental expression profiles of these three maker genes have been detected in the in vitro cultured duck myoblasts at different stages.…”
Section: Discussionmentioning
confidence: 75%
“…Among them, Desmin will be highly expressed when myoblasts reentering into the cell cycle, Mck will be highly expressed when the multinucleotide myotubes begin differentiating and Tnnc will be expressed during myofiber formation and maturation (Yamane et al 2000). However, the developmental states of in vitro cultured myoblasts are usually distinguished by their external characteristics, which will hardly give an exact result.…”
Section: Introductionmentioning
confidence: 99%
“…Total RNA extraction, treatment with DNase I and reverse transcription were performed as described previously (27). SYBR Green real-time PCR was performed using the Thermal Cycler Dice Real Time System (Takara Bio Inc.) with the following cycling parameters: denaturation at 95ºC for 10 min, followed by 40 cycles of denaturation 95ºC for 15 s, and annealing and extension at 55ºC for 15 s. The quantities of target mRNAs were normalized by the quantity of murine glyceraldehyde-3-phosphate dehydrogenase (Gapdh) mRNA.…”
Section: Analysis Of the Target Sequences For Mir-29smentioning
confidence: 99%