| scholarly article | Q13442814 |
| P50 | author | Sara E. Mole | Q42563205 |
| Bonnie Ann Wallace | Q41770829 | ||
| P2093 | author name string | R M Gardiner | |
| P B Munroe | |||
| H M Mitchison | |||
| R W Janes | |||
| P2860 | cites work | Yeast genes and human disease | Q48066231 |
| Basic local alignment search tool | Q25938991 | ||
| A simple method for displaying the hydropathic character of a protein | Q26778481 | ||
| Multiple sequence alignment with hierarchical clustering | Q27860956 | ||
| The ENZYME data bank | Q28239413 | ||
| A knowledge base for predicting protein localization sites in eukaryotic cells | Q29618927 | ||
| The SWISS-PROT protein sequence data bank: current status | Q33463176 | ||
| Identifying nonpolar transbilayer helices in amino acid sequences of membrane proteins | Q34181973 | ||
| PROSITE: recent developments | Q34870115 | ||
| Neuronal ceroid-lipofuscinoses in childhood | Q39649997 | ||
| Waterlogged Molecules | Q40164690 | ||
| Batten disease and mitochondrial pathways of proteolysis | Q41115539 | ||
| The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase | Q41197592 | ||
| Prediction of O-glycosylation of mammalian proteins: specificity patterns of UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase | Q42091424 | ||
| P433 | issue | 1-2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 75-77 | |
| P577 | publication date | 1996-12-01 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | A model for Batten disease protein CLN3: functional implications from homology and mutations | |
| P478 | volume | 399 |
| Q45094647 | A dileucine motif and a cluster of acidic amino acids in the second cytoplasmic domain of the batten disease-related CLN3 protein are required for efficient lysosomal targeting |
| Q24298716 | A galactosylceramide binding domain is involved in trafficking of CLN3 from Golgi to rafts via recycling endosomes |
| Q34386791 | Advances in the genetics of progressive myoclonus epilepsy |
| Q34238658 | Biochemistry of neuronal ceroid lipofuscinoses |
| Q24310339 | Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease |
| Q55043107 | C-terminal prenylation of the CLN3 membrane glycoprotein is required for efficient endosomal sorting to lysosomes. |
| Q22254722 | CLN3 protein regulates lysosomal pH and alters intracellular processing of Alzheimer's amyloid-beta protein precursor and cathepsin D in human cells |
| Q34238646 | Cellular pathology and pathogenic aspects of neuronal ceroid lipofuscinoses |
| Q41981224 | Characteristics of 29 novel atypical solute carriers of major facilitator superfamily type: evolutionary conservation, predicted structure and neuronal co-expression. |
| Q34427575 | Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses |
| Q24315800 | Defective endoplasmic reticulum-resident membrane protein CLN6 affects lysosomal degradation of endocytosed arylsulfatase A |
| Q27318704 | FRET-assisted determination of CLN3 membrane topology |
| Q34068976 | Hemichannels in neurodegenerative diseases: is there a link to pathology? |
| Q24802601 | Identification of genes involved in ceramide-dependent neuronal apoptosis using cDNA arrays |
| Q22009144 | Intracellular trafficking of the JNCL protein CLN3 |
| Q33948573 | Lysosomal transport disorders |
| Q24300266 | Membrane topology of CLN3, the protein underlying Batten disease |
| Q33710784 | Molecular genetics of the neuronal ceroid lipofuscinoses |
| Q24633059 | Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse |
| Q34238591 | Neuronal ceroid lipofuscinoses: classification and diagnosis |
| Q34238638 | Outlook for future treatment |
| Q33639100 | Paul Dyken Lecture of the Southern Pediatric Neurology Society. Inherited neurodegenerative disease: the evolution of our thinking |
| Q41010705 | Specific alterations in levels of mannose 6-phosphorylated glycoproteins in different neuronal ceroid lipofuscinoses |
| Q24678552 | Spectrum of mutations in the Batten disease gene, CLN3 |
| Q22009145 | Studies of membrane association of CLN3 protein |
| Q90377163 | The CLN3 gene and protein: What we know |
| Q77421409 | The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses |
| Q34302797 | The genetic spectrum of human neuronal ceroid-lipofuscinoses |
| Q35681065 | The intracellular location and function of proteins of neuronal ceroid lipofuscinoses |
| Q31148303 | The transmembrane topology of Batten disease protein CLN3 determined by consensus computational prediction constrained by experimental data |
| Q40648630 | Two motifs target Batten disease protein CLN3 to lysosomes in transfected nonneuronal and neuronal cells |
| Q39598497 | btn1 affects endocytosis, polarization of sterol-rich membrane domains and polarized growth in Schizosaccharomyces pombe |
Search more.