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Aspartyl proteinase genes from apicomplexan parasites: evidence for evolution of the gene structure
TRENDS IN PARASITOLOGY
Biased distribution of inverted and direct Alus in the human genome: Implications for insertion, exclusion, and genome stability
GENOME RESEARCH
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome
HUMAN MUTATION
Characterization of CD44 splicing patterns in normal keratinocytes, dysplastic and squamous carcinoma cell lines
INTERNATIONAL JOURNAL OF ONCOLOGY
A genomic clone for a chitinase gene from the silkworm, Bombyx mori: structural organization identifies functional motifs
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
B-cell neoplasia associated gene with multiple splicing (BCMS): the candidate B-CLL gene on 13q14 comprises more than 560 kb covering all critical regions
HUMAN MOLECULAR GENETICS
Thirteen UDPglucuronosyltransferase genes are encoded at the human UGT1 gene complex locus
PHARMACOGENETICS
The multiple untranslated first exons system of the human estrogen receptor beta (ER beta) gene
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
Mutations in c-kit gene exons 9 and 13 in gastrointestinal stromal tumors among Japanese
JAPANESE JOURNAL OF CANCER RESEARCH
Colour bar coding on combed DNA revealed large gene rearrangements of BRCA1 gene
M S-MEDECINE SCIENCES
Missense mutations of the fibrillin-1 gene in two Chinese patients with severe Marfan syndrome
CHINESE MEDICAL JOURNAL
Splice-site mutations and atherosclerosis: mechanisms and prediction models
ZEITSCHRIFT FUR KARDIOLOGIE
Transcriptional and translational mechanisms of cytochrome b(5) reductase isoenzyme generation in humans
BIOCHEMICAL JOURNAL
Diagnostic application of CD44 variant expression in pancreatic juice for detection of pancreatic neoplasm
ANTICANCER RESEARCH
Reference point logistic regression and the identification of DNA functional sites
JOURNAL OF CLASSIFICATION
An algorithm to predict 3 ' intron splice sites in Plasmodium falciparum genomic sequences
MOLECULAR AND BIOCHEMICAL PARASITOLOGY
Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis
AMERICAN JOURNAL OF MEDICAL GENETICS
Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP
AMERICAN JOURNAL OF MEDICAL GENETICS
Vertebrate tropomyosin: distribution, properties and function
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
Influence of the small leader exons 2 and 3 on human immunodeficiency virus type 1 gene expression
VIROLOGY
Nutritional regulation of IGF-I expression during brain development in mice
PEDIATRIC RESEARCH
Variation in sequence and RNA editing within core domains of mitochondrialgroup II introns among plants
MOLECULAR AND GENERAL GENETICS
Adenoviral gene transfer restores lysyl hydroxylase activity in type VI Ehlers-Danlos syndrome
JOURNAL OF INVESTIGATIVE DERMATOLOGY
A novel orthotopic implantation model of human esophageal carcinoma in nude rats: CD44H mediates cancer cell invasion in vitro and in vivo
INTERNATIONAL JOURNAL OF CANCER
Hyaluronidase can modulate expression of CD44
EXPERIMENTAL CELL RESEARCH
Constitutive intracellular expression and activation-induced cell surface up-regulation of CD44v3 in human T lymphocytes
EUROPEAN JOURNAL OF IMMUNOLOGY
Chromatin structure of the bovine Cyp19 promoter 1.1 - DNaseI hypersensitive sites and DNA hypomethylation correlate with placental expression
EUROPEAN JOURNAL OF BIOCHEMISTRY
Expression of the rabbit cytochrome P450 aromatase encoding gene uses alternative tissue-specific promoters
EUROPEAN JOURNAL OF BIOCHEMISTRY
Genetic mechanisms involved in the periodicity of flight
CARYOLOGIA
Analysis of the tissue factor pathway inhibitor gene and antigen levels inrelation to venous thrombosis
BRITISH JOURNAL OF HAEMATOLOGY
Genomic structure of the gene encoding human 3-hydroxy-3-methyl-glutaryl coenzyme A reductase: comparison of exon/intron organization of sterol-sensing domains among four related genes
JOURNAL OF HUMAN GENETICS
Novel mutations of the FANCG gene causing alternative splicing in JapaneseFanconi anemia
JOURNAL OF HUMAN GENETICS
Molecular cloning and characterization of two novel genes on chromosome 8p21.3
JOURNAL OF HUMAN GENETICS
Reduced expression of CD44 variant 9 is related to lymph node metastasis and poor survival in squamous cell carcinoma of tongue
ORAL ONCOLOGY
Prediction of genetic structure in eukaryotic DNA using reference point logistic regression and sequence alignment
BIOINFORMATICS
Gene identification using exon amplification on human chromosome 18q21: implications for bipolar disorder
MOLECULAR PSYCHIATRY
Elevated serum soluble CD44 level in sarcoidosis
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
CD44 expression in the developing and growing rat intervertebral disc
DEVELOPMENTAL DYNAMICS
X-linked Alport syndrome: Natural history in 195 families and genotype-phenotype correlations in males
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Decreased CD44H expression in early-stage tongue carcinoma associates withlate nodal metastases following interstitial brachytherapy
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
Cis-acting elements regulating the placenta-specific promoter of the bovine Cyp19 gene
JOURNAL OF MOLECULAR ENDOCRINOLOGY
Revised genomic structure of the human MAGP1 gene and identification of alternate transcripts in human and mouse tissues
MATRIX BIOLOGY
Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activityand causes Ehlers-Danlos syndrome type VI
MATRIX BIOLOGY
Complete exon-intron organization of the gene for human lysyl hydroxylase 3 (LH3)
MATRIX BIOLOGY
Expression of the aromatase-encoding gene in cattle and sheep
REPRODUCTION IN DOMESTIC ANIMALS
Mutational analysis of COL4A5 gene in Korean Alport syndrome
PEDIATRIC NEPHROLOGY
Molecular organization, structural features, and ligand binding characteristics of CD44, a highly variable cell surface glycoprotein with multiple functions
PROTEINS-STRUCTURE FUNCTION AND GENETICS
Cloning, genomic organization and chromosomal localization of the gene encoding the murine sodium-dependent, purine-selective, concentrative nucleoside transporter (CNT2)
GENE
Physical activity and antidepressant treatment potentiate the expression of specific brain-derived neurotrophic factor transcripts in the rat hippocampus
NEUROSCIENCE
Involvement of Sp1 in the transcriptional regulation of the rat insulin-like growth factor-1 gene
MOLECULAR AND CELLULAR ENDOCRINOLOGY
Expression of CD44 variants in lung cancer and its relationship to hyaluronan binding
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH
Isolation of the bovine CYP19 promoter 1.2 and identification of genetic variants
ANIMAL GENETICS
Correlations in DNA sequences across the three domains of life
PHYSICA D
Actin and the smooth muscle regulatory proteins: a structural perspective
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
E-cadherin and CD44 expression in cervical intraepithelial neoplasia: Comparison between HIV-positive and HIV-negative women and correlation with HPVstatus
GYNECOLOGIC ONCOLOGY
Somatic mosaicism associated with a mild Alport syndrome phenotype
JOURNAL OF MEDICAL GENETICS
Ig light chain receptor editing in anergic B cells
JOURNAL OF IMMUNOLOGY
Distinct expression of splice variants of neuronal nitric oxide synthase in the human gastrointestinal tract
GASTROENTEROLOGY
Identification of three novel mutations in the insulin receptor gene in type A insulin resistant patients
CLINICAL GENETICS
Isolation of two novel genes, DSCR5 and DSCR6, from Down syndrome criticalregion on human chromosome 21q22.2
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Genomic sequence, splicing, and gene annotation
AMERICAN JOURNAL OF HUMAN GENETICS
Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels
AMERICAN JOURNAL OF HUMAN GENETICS
Neurodegenerative disease with a mutation at codon 279 (N279 K) in exon 10of the protein Tau gene
BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
Donor site competition is involved in the regulation of alternative splicing of the rat beta-tropomyosin pre-mRNA
RNA-A PUBLICATION OF THE RNA SOCIETY
A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 gene
MOLECULAR GENETICS AND METABOLISM
Prenatal exclusion of Ehlers-Danlos Syndrome type VI by mutational analysis
PROCEEDINGS OF THE ASSOCIATION OF AMERICAN PHYSICIANS
RNAs in the sera of Persian Gulf War veterans have segments homologous to chromosome 22q11.2
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
Genomic organization of a voltage-gated Na+ channel in a hydrozoan jellyfish: Insights into the evolution of voltage-gated Na+ channel genes
RECEPTORS & CHANNELS
Detection of mutations in COL4A5 in patients with Alport syndrome
HUMAN MUTATION
Detailed transcript map of a 810-kb region at 11p14 involving identification of 10 novel human 3 ' exons
EUROPEAN JOURNAL OF HUMAN GENETICS
CD44 cleavage induced by a membrane-associated metalloprotease plays a critical role in tumor cell migration
ONCOGENE
CD44 splice variants in draining lymph nodes precede allograft rejection of endocrine cells
JOURNAL OF MOLECULAR MEDICINE-JMM
Localization of matrix metalloproteinase 9 to the cell surface provides a mechanism for CD44-mediated tumor invasion
GENES & DEVELOPMENT
Allelic variation in the intron 2 and 3 of the MICA gene
JOURNAL OF BIOLOGICAL REGULATORS AND HOMEOSTATIC AGENTS
Molecular cloning of the human Nurr1 gene: characterization of the human gene and cDNAs
GENE
Protein-coding regions prediction combining similarity searches and conservative evolutionary properties of protein-coding sequences
GENE
Altered expression of CD45 isoforms in differentiation of acute myeloid leukemia
AMERICAN JOURNAL OF HEMATOLOGY
A long open reading frame in the mitochondrial LSU rRNA group-I intron of Cryphonectria parasitica encodes a putative S5 ribosomal protein fused to amaturase
CURRENT GENETICS
Irreducible complexity and the problem of biochemical emergence
BIOLOGY & PHILOSOPHY
Genomic organisation of rainbow trout, Oncorhynchus mykiss TGF-beta
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
A multi-agent system simulating human splice site recognition
COMPUTERS & CHEMISTRY
Cosmid-based exon trapping
CDNA PREPARATION AND CHARACTERIZATION
A SOD1 gene mutation in a patient with slowly progressing familial ALS
NEUROLOGY
Down-regulation of CD44 standard and variant isoforms during the development and progression of uterine cervical tumours
JOURNAL OF PATHOLOGY
Cutting edge: An inducible sialidase regulates the hyaluronic acid bindingability of CD44-bearing human monocytes
JOURNAL OF IMMUNOLOGY
Characterization of the heparan sulfate and chondroitin sulfate assembly sites in CD44
JOURNAL OF BIOLOGICAL CHEMISTRY
Generation of artificial proteoglycans containing glycosaminoglycan-modified CD44 - Demonstration of the interaction between RANTES and chondroitin sulfate
JOURNAL OF BIOLOGICAL CHEMISTRY
Distribution of microsomal glutathione transferase 1 in mammalian tissues - A predominant alternate first exon in human tissues
EUROPEAN JOURNAL OF BIOCHEMISTRY
Growth hormone-mediated regulation of insulin-like growth factor I promoter activity in C6 glioma cells
ENDOCRINOLOGY
Identification of core sequences involved in metabolism-dependent nuclear protein binding to the rat insulin-like growth factor I gene
ENDOCRINOLOGY
Three novel mutations in the COL4A5 gene in Mexican Alport syndrome patients
CLINICAL GENETICS
Heparan sulfate composition of alternatively spliced CD44 fusion proteins
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Structural variability of CD44v molecules and reliability of immunodetection of CD44 isoforms using mAbs specific for CD44 variant exon products
AMERICAN JOURNAL OF PATHOLOGY
Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: Distinct effects on biochemical and clinical phenotypes
AMERICAN JOURNAL OF HUMAN GENETICS
NITRIC-OXIDE SYNTHASE-1 MESSENGER-RNA - TISSUE-SPECIFIC VARIANTS FROMRAT WITH ALTERNATIVE FIRST EXONS
Biological chemistry
IMMUNOLOCALIZATION OF AROMATASE IN HUMAN MINOR SALIVARY-GLANDS OF THELOWER LIP WITH PRIMARY SJOGRENS-SYNDROME
Pathology international
POSITIONALLY CLONED GENE FOR A NOVEL GLOMERULAR PROTEIN - NEPHRIN - IS MUTATED IN CONGENITAL NEPHROTIC SYNDROME
MOLECULAR CELL
POLYMORPHISMS IN FELINE TUMOR-SUPPRESSOR GENE P53 - MUTATIONS IN AN OSTEOSARCOMA AND A MAMMARY-CARCINOMA
Veterinary journal
THE MOUSE FORMIN (FMN) GENE - ABUNDANT CIRCULAR RNA TRANSCRIPTS AND GENE-TARGETED DELETION ANALYSIS
Molecular medicine (Cambridge, Mass.)
FINDING INTRON EXON SPLICE JUNCTIONS USING INFO, INTERRUPTION FINDER AND ORGANIZER/
Journal of computational biology