Pages that link to "Q36275014"
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The following pages link to Growth and muscle defects in mice lacking adult myosin heavy chain genes (Q36275014):
Displaying 34 items.
- Comparative sequence analysis of the complete human sarcomeric myosin heavy chain family: implications for functional diversity (Q22010189) (← links)
- Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved (Q24672975) (← links)
- Muscle cell and motor protein function in patients with a IIa myosin missense mutation (Glu-706 to Lys) (Q24674205) (← links)
- Transcription enhancer factor 1 binds multiple muscle MEF2 and A/T-rich elements during fast-to-slow skeletal muscle fiber type transitions (Q24681195) (← links)
- Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene (Q24684848) (← links)
- Abundant expression of myosin heavy-chain IIB RNA in a subset of human masseter muscle fibres (Q28349439) (← links)
- Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb (Q28513616) (← links)
- Gene mutations and genomic rearrangements in the mouse as a result of transposon mobilization from chromosomal concatemers (Q33258825) (← links)
- Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations (Q33620883) (← links)
- Functional diversity among a family of human skeletal muscle myosin motors (Q33667075) (← links)
- Hybrid skeletal muscle fibres: a rare or common phenomenon? (Q34319693) (← links)
- A novel intronic single nucleotide polymorphism in the myosin heavy polypeptide 4 gene is responsible for the mini-muscle phenotype characterized by major reduction in hind-limb muscle mass in mice (Q34372647) (← links)
- Changes in αB-crystallin, tubulin, and MHC isoforms by hindlimb unloading show different expression patterns in various hindlimb muscles (Q34563387) (← links)
- How to make rapid eye movements "rapid": the role of growth factors for muscle contractile properties (Q34666810) (← links)
- Molecular and cellular mechanisms involved in the generation of fiber diversity during myogenesis (Q34670818) (← links)
- Puralpha and Purbeta collaborate with Sp3 to negatively regulate beta-myosin heavy chain gene expression during skeletal muscle inactivity (Q35641874) (← links)
- Fine mapping of "mini-muscle," a recessive mutation causing reduced hindlimb muscle mass in mice (Q37324197) (← links)
- Are biological sensors modulated by their structural scaffolds? The role of the structural muscle proteins alpha-actinin-2 and alpha-actinin-3 as modulators of biological sensors (Q37761966) (← links)
- Myosinopathies: pathology and mechanisms (Q38037315) (← links)
- Nuclear protein binding at the beta-myosin heavy chain A/T-rich element is enriched following increased skeletal muscle activity (Q38319503) (← links)
- Fast/Glycolytic muscle fiber growth reduces fat mass and improves metabolic parameters in obese mice (Q39280475) (← links)
- MiR-23a inhibits myogenic differentiation through down regulation of fast myosin heavy chain isoforms (Q39318263) (← links)
- Diversity in transcriptional start site selection and alternative splicing affects the 5'-UTR of mouse striated muscle myosin transcripts. (Q40259328) (← links)
- What makes us human: revisiting an age-old question in the genomic era. (Q40265359) (← links)
- Cancer cachexia is regulated by selective targeting of skeletal muscle gene products (Q40529830) (← links)
- Different pathways regulate expression of the skeletal myosin heavy chain genes. (Q40781174) (← links)
- Developmental MYH3 Myopathy Associated with Expression of Mutant Protein and Reduced Expression Levels of Embryonic MyHC. (Q42007395) (← links)
- Skeletal muscle adaptations in response to voluntary wheel running in myosin heavy chain null mice (Q43823879) (← links)
- Knockout of human muscle genes revealed by large scale whole-exome studies (Q49919753) (← links)
- Mutation of the IIB myosin heavy chain gene results in muscle fiber loss and compensatory hypertrophy. (Q52141003) (← links)
- Human skeletal myosin heavy chain genes are tightly linked in the order embryonic-IIa-IId/x-ILb-perinatal-extraocular (Q73079696) (← links)
- Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb (Q89746492) (← links)
- Myosin heavy chain-embryonic regulates skeletal muscle differentiation during mammalian development (Q89864890) (← links)
- Sarcopenia: Aging-Related Loss of Muscle Mass and Function (Q93067806) (← links)