Pages that link to "Q22009978"
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The following pages link to Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1 (Q22009978):
Displaying 50 items.
- Protein O-mannosyltransferase 1 (Q21120465) (← links)
- Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity (Q24303491) (← links)
- PIG-V involved in transferring the second mannose in glycosylphosphatidylinositol (Q24337024) (← links)
- Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome (Q24561808) (← links)
- The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy (Q26827638) (← links)
- Mammalian O-mannosylation: unsolved questions of structure/function (Q26860991) (← links)
- O-Mannosylation and human disease (Q27014986) (← links)
- A Conserved Acidic Motif Is Crucial for Enzymatic Activity of Protein O-Mannosyltransferases (Q27931927) (← links)
- Members of the evolutionarily conserved PMT family of protein O-mannosyltransferases form distinct protein complexes among themselves (Q27932724) (← links)
- LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy (Q28512184) (← links)
- Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality (Q28512333) (← links)
- Expression of the murine Pomt1 gene in both the developing brain and adult muscle tissues and its relationship with clinical aspects of Walker-Warburg syndrome (Q28584992) (← links)
- Glycosylation defects: a new mechanism for muscular dystrophy? (Q28587952) (← links)
- Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy. (Q30446533) (← links)
- Functional conservation of subfamilies of putative UDP-N-acetylgalactosamine:polypeptide N-acetylgalactosaminyltransferases in Drosophila, Caenorhabditis elegans, and mammals. One subfamily composed of l(2)35Aa is essential in Drosophila (Q31046911) (← links)
- Malformations of cortical development: genetic mechanisms and diagnostic approach (Q31162335) (← links)
- Characterization of the PMT gene family in Cryptococcus neoformans (Q33487159) (← links)
- Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy-dystroglycanopathy C1. (Q33844672) (← links)
- Comparative Analysis of Protein Glycosylation Pathways in Humans and the Fungal Pathogen Candida albicans (Q33930289) (← links)
- Protein glycosylation: nature, distribution, enzymatic formation, and disease implications of glycopeptide bonds (Q34131204) (← links)
- Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation (Q34198632) (← links)
- Characterization of pancreatic ERj3p, a homolog of yeast DnaJ-like protein Scj1p. (Q34326851) (← links)
- O-glycosylation (Q34500194) (← links)
- Physical and functional association of human protein O-mannosyltransferases 1 and 2. (Q34525616) (← links)
- Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families (Q34578450) (← links)
- The twisted gene encodes Drosophila protein O-mannosyltransferase 2 and genetically interacts with the rotated abdomen gene encoding Drosophila protein O-mannosyltransferase 1. (Q34587283) (← links)
- Protein O-mannosylation: conserved from bacteria to humans (Q34980261) (← links)
- Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function. (Q35056189) (← links)
- Protein glycosylation in disease: new insights into the congenital muscular dystrophies (Q35111636) (← links)
- Protein Glycosylation inAspergillus fumigatusIs Essential for Cell Wall Synthesis and Serves as a Promising Model of Multicellular Eukaryotic Development (Q35250951) (← links)
- Hansenula polymorpha Pmt4p Plays Critical Roles in O-Mannosylation of Surface Membrane Proteins and Participates in Heteromeric Complex Formation (Q35680745) (← links)
- Membrane association is a determinant for substrate recognition by PMT4 protein O-mannosyltransferases (Q35808740) (← links)
- The role of defective glycosylation in congenital muscular dystrophy (Q35824015) (← links)
- Structure, function and pathology of O-mannosyl glycans (Q35910278) (← links)
- O-Mannosyltransferase 1 in Aspergillus fumigatus (AfPmt1p) is crucial for cell wall integrity and conidium morphology, especially at an elevated temperature (Q36313753) (← links)
- The o-mannosylation pathway: glycosyltransferases and proteins implicated in congenital muscular dystrophy (Q36666131) (← links)
- Defect in glycosylation that causes muscular dystrophy (Q36667103) (← links)
- Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypes (Q37723603) (← links)
- Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDG. (Q38043952) (← links)
- Glycobiology of α-dystroglycan and muscular dystrophy (Q38266217) (← links)
- The twisted abdomen phenotype of Drosophila POMT1 and POMT2 mutants coincides with their heterophilic protein O-mannosyltransferase activity (Q38338552) (← links)
- Morphogenesis, adhesive properties, and antifungal resistance depend on the Pmt6 protein mannosyltransferase in the fungal pathogen candida albicans (Q39499662) (← links)
- POMT2, a key enzyme in Walker-Warburg syndrome: somatic sPOMT2, but not testis-specific tPOMT2, is crucial for mannosyltransferase activity in vivo (Q39980665) (← links)
- Aberrant processing of the WSC family and Mid2p cell surface sensors results in cell death of Saccharomyces cerevisiae O-mannosylation mutants. (Q40376802) (← links)
- O-mannosylation precedes and potentially controls the N-glycosylation of a yeast cell wall glycoprotein. (Q40773041) (← links)
- POMT1 is Essential for Protein O-Mannosylation in Mammals (Q42917956) (← links)
- NMR studies of mannitol-terminating oligosaccharides derived by reductive alkaline hydrolysis from brain glycoproteins (Q43634571) (← links)
- cDNA encoding protein O-mannosyltransferase from the filamentous fungus Trichoderma reesei; functional equivalence to Saccharomyces cerevisiae PMT2. (Q44396584) (← links)
- Synaptic defects in a Drosophila model of congenital muscular dystrophy. (Q46667133) (← links)
- LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. (Q47375901) (← links)