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Quoted phrase not found in phrase index: "Type 2 muscle fiber predominance"
Page 1
Spatial fiber type distribution in normal human muscle Histochemical and tensiomyographical evaluation.
Dahmane R, Djordjevic S, Simunic B, Valencic V. Dahmane R, et al. J Biomech. 2005 Dec;38(12):2451-9. doi: 10.1016/j.jbiomech.2004.10.020. J Biomech. 2005. PMID: 16214493 Clinical Trial.
The aim of this study was to determine the extent to which the relative occurrence of different fiber types and subtypes varies within human limb muscles in function to depth and to predict fiber type proportions with a non-invasive TMG method. The distribution of differen …
The aim of this study was to determine the extent to which the relative occurrence of different fiber types and subtypes varies within human …
Traumatic musculotendinous injuries of the knee: diagnosis with MR imaging.
Bencardino JT, Rosenberg ZS, Brown RR, Hassankhani A, Lustrin ES, Beltran J. Bencardino JT, et al. Radiographics. 2000 Oct;20 Spec No:S103-20. doi: 10.1148/radiographics.20.suppl_1.g00oc16s103. Radiographics. 2000. PMID: 11046166 Review.
Three discrete categories of acute injuries to the musculotendinous unit can be defined: muscle contusion, myotendinous strain, and tendon avulsion. Among the quadriceps muscles, the rectus femoris is the most susceptible to injury at the myotendinous junction due to its s …
Three discrete categories of acute injuries to the musculotendinous unit can be defined: muscle contusion, myotendinous strain, and t …
Changes in skeletal muscle morphology and biochemistry after cardiac transplantation.
Bussières LM, Pflugfelder PW, Taylor AW, Noble EG, Kostuk WJ. Bussières LM, et al. Am J Cardiol. 1997 Mar 1;79(5):630-4. doi: 10.1016/s0002-9149(96)00829-6. Am J Cardiol. 1997. PMID: 9068522
Fiber type analysis revealed a predominance of type II fibers before cardiac transplantation (66 +/- 10%); the ratio did not change after transplantation. ...Peak oxygen uptake also increased significantly after cardiac transplantation (19.5 +/- 8.1 ml/kg/min at 12 …
Fiber type analysis revealed a predominance of type II fibers before cardiac transplantation (66 +/- 10%); the ratio did not c …
Congenital myopathy with uniform type 1 fiber predominance and type 2 fiber hypoplasia: report of one case.
Huang ML, Tsai CH, Lee CC. Huang ML, et al. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1998 Jan-Feb;39(1):62-4. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1998. PMID: 9553297
Growth retardation with body weight and length below the third percentile, and head girth below the tenth percentile, were noted on admission. Generalized hypotonia, mild proximal muscle weakness and diminished tendon reflex were also noted. A biopsy from the left quadrice …
Growth retardation with body weight and length below the third percentile, and head girth below the tenth percentile, were noted on admissio …
Clinical and histologic changes in the follow-up of a congenital myopathy.
Camacho A, Villarejo A, Simón R, Mateos F, Cabello A. Camacho A, et al. Pediatr Neurol. 2005 Aug;33(2):139-41. doi: 10.1016/j.pediatrneurol.2005.02.012. Pediatr Neurol. 2005. PMID: 16087062
A 19-year-old woman was born with congenital hypotonia, generalized weakness, and dysmorphic features. A muscle biopsy performed at age 18 months found that type I fibers were smaller and more numerous than type II fibers, and she was diagnosed with congenita …
A 19-year-old woman was born with congenital hypotonia, generalized weakness, and dysmorphic features. A muscle biopsy performed at a …
Targeted disruption of the ATP2A1 gene encoding the sarco(endo)plasmic reticulum Ca2+ ATPase isoform 1 (SERCA1) impairs diaphragm function and is lethal in neonatal mice.
Pan Y, Zvaritch E, Tupling AR, Rice WJ, de Leon S, Rudnicki M, McKerlie C, Banwell BL, MacLennan DH. Pan Y, et al. J Biol Chem. 2003 Apr 11;278(15):13367-75. doi: 10.1074/jbc.M213228200. Epub 2003 Jan 28. J Biol Chem. 2003. PMID: 12556521 Free article.
Mutations in the ATP2A1 gene, encoding isoform 1 of the sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA1), are one cause of Brody disease, characterized in humans by exercise-induced contraction of fast twitch (type II) skeletal muscle fibers. In an …
Mutations in the ATP2A1 gene, encoding isoform 1 of the sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA1), are one cause of Brody disease, …