Pages that link to "Q69530327"
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The following pages link to Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization (Q69530327):
Displaying 33 items.
- Chromosomal localisation of the mouse and human peripherin genes (Q24292956) (← links)
- CDNA cloning of p112, the largest regulatory subunit of the human 26s proteasome, and functional analysis of its yeast homologue, sen3p (Q24308679) (← links)
- Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene (Q24314922) (← links)
- Cloning, mapping and expression of PEBP2 alpha C, a third gene encoding the mammalian Runt domain (Q24319877) (← links)
- Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans (Q24323096) (← links)
- AAV9-mediated gene transfer of desmin ameliorates cardiomyopathy in desmin-deficient mice. (Q27323272) (← links)
- Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin (Q33157399) (← links)
- Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11. (Q33763900) (← links)
- Characterization of three different transgenic mouse lines that carry human poliovirus receptor gene--influence of the transgene expression on pathogenesis. (Q34316914) (← links)
- Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics (Q34735154) (← links)
- Two desmin gene mutations associated with myofibrillar myopathies in Polish families (Q34776342) (← links)
- Desmin splice variants causing cardiac and skeletal myopathy (Q35433637) (← links)
- Familial desminopathy: myopathy with accumulation of desmin-type intermediate filaments (Q36976715) (← links)
- Tragedy in a heartbeat: malfunctioning desmin causes skeletal and cardiac muscle disease (Q37241396) (← links)
- Intermediate filament diseases: desminopathy. (Q37419742) (← links)
- Application of fluorescence in situ hybridization in genome analysis of the mouse (Q40541328) (← links)
- Structural and functional analysis of a new desmin variant causing desmin-related myopathy (Q40773437) (← links)
- Fusion and amplification of two originally non-syntenic chromosomal regions in a mammary carcinoma cell line (Q41616468) (← links)
- Mouse chromosome 1. (Q44036292) (← links)
- The host resistance locus Bcg is tightly linked to a group of cytoskeleton-associated protein genes that include villin and desmin (Q44172905) (← links)
- Myotubular myopathy: arrest of morphogenesis of myofibres associated with persistence of fetal vimentin and desmin. Four cases compared with fetal and neonatal muscle. (Q46101159) (← links)
- Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation (Q47843308) (← links)
- TGF-alpha, EGF, and their cognate EGF receptor are co-expressed with desmin during embryonic, fetal, and neonatal myogenesis in mouse tongue development (Q48649336) (← links)
- Desmin - Protein Surplus Myopathies, 96th European Neuromuscular Centre (ENMC)-sponsored International Workshop held 14-16 September 2001, Naarden, The Netherlands. (Q53311250) (← links)
- Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach (Q54177537) (← links)
- Localization of PMP-22 gene (candidate gene for the Charcot-Marie-Tooth disease 1a) to band 17p11.2 by direct r-banding fluoreschenceIn situ hybridization (Q67479716) (← links)
- Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by nonisotopic in situ hybridization (Q68583871) (← links)
- R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1) (Q68624541) (← links)
- Assignment of the mouse desmin gene to chromosome 1 band C3 (Q68852948) (← links)
- Molecular and cytogenetic analysis of chromosomal arms 2q and 13q in alveolar rhabdomyosarcoma (Q70228509) (← links)
- Desmin myopathy: a multisystem disorder involving skeletal, cardiac, and smooth muscle (Q72054052) (← links)
- Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy (Q73741071) (← links)
- Desmin myopathy involving cardiac, skeletal, and vascular smooth muscle: report of a case with immunoelectron microscopy (Q77124971) (← links)