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1Academic Journal
المؤلفون: Simona Viglio, Nicoletta Zoppi, Antonella Sangalli, Angelo Gallanti, Sergio Barlati, Monica Mottes, Marina Colombi, Maurizia Valli
المصدر: The Scientific World Journal, Vol 8, Pp 956-958 (2008)
مصطلحات موضوعية: Technology, Medicine, Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1537-744X
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2Academic Journal
المؤلفون: Chiara Stefani, Antonella Sangalli, Elena Locatelli, Tania Federico, Giovanni Malerba, Maria Grazia Romanelli, Gustavo Adolfo Argañaraz, Bosco Christiano Maciel Da Silva, Alberto Jose Duarte Da Silva, Jorge Casseb, Enrique Roberto Argañaraz, Alessandra Ruggiero, Donato Zipeto
المصدر: International Journal of Molecular Sciences; Volume 23; Issue 23; Pages: 14852
مصطلحات موضوعية: AIDS progression, HLA-C stability, HIV-1 infection control, ASPCR, MHC class I
جغرافية الموضوع: agris
وصف الملف: application/pdf
Relation: Molecular Immunology; https://dx.doi.org/10.3390/ijms232314852
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3
المؤلفون: Maria Grazia Romanelli, Marcella Neri, Lorenzo Verriello, Francesca Gualandi, Paola Tonin, Katarzyna Pruszczyk, Elia Pancheri, Valeria Guglielmi, Rafał Płoski, Tomasz Stoklosa, Marcin M Machnicki, Antonella Sangalli, Joanna Kosińska, Gaetano Vattemi, Małgorzata Rydzanicz, Giuliano Tomelleri
المصدر: Neurological Sciences
مصطلحات موضوعية: 0301 basic medicine, Candidate gene, TTN, LMNA, Dermatology, Biology, medicine.disease_cause, 03 medical and health sciences, Myofibrillar myopathies, Protein Aggregates, 0302 clinical medicine, Exome Sequencing, medicine, RYR1, Missense mutation, Humans, Gene, Exome sequencing, Genetics, Mutation, Protein aggregate myopathies, General Medicine, Phenotype, Psychiatry and Mental health, 030104 developmental biology, Whole-exome sequencing, Original Article, Female, Neurology (clinical), 030217 neurology & neurosurgery, Myopathies, Structural, Congenital
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4Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk
المؤلفون: Antonella Sangalli, Albino Poli, Monica Rodolfo, Francesca Belpinati, Laura Ceccuzzi, Macarena Gomez-Lira, Melissa Dal Toè, Giovanni Malerba, Elisabetta Vergani, Alberto Turco
المصدر: Experimental dermatologyREFERENCES. 29(10)
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Skin Neoplasms, Population, functional SNP, Single-nucleotide polymorphism, macromolecular substances, Dermatology, Biology, Biochemistry, Polymorphism, Single Nucleotide, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Cell Line, Tumor, Genotype, medicine, HaCaT Cells, Humans, Enhancer of Zeste Homolog 2 Protein, Genetic Predisposition to Disease, Allele, education, Promoter Regions, Genetic, Molecular Biology, Melanoma, Alleles, Aged, education.field_of_study, EZH2, Haplotype, DNA polymorphisms, Middle Aged, medicine.disease, predisposition, 030104 developmental biology, HEK293 Cells, Gene Expression Regulation, Haplotypes, Case-Control Studies, Cancer research, Female, transient transfection, Skin cancer
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5
المؤلفون: Donato Zipeto, A. Dal Molin, Maria Grazia Romanelli, Giovanni Malerba, Pamela Lorenzi, Stefania Fochi, Antonella Sangalli
المصدر: The International Journal of Biochemistry & Cell Biology. 106:74-83
مصطلحات موضوعية: RRM, 0301 basic medicine, Formins, RNA-binding protein, PTBP1, Biology, Biochemistry, Heterogeneous-Nuclear Ribonucleoproteins, 03 medical and health sciences, Exon, 0302 clinical medicine, Idiopathic dilated cardiomyopathy, Humans, Protein Isoforms, Gene, Actin, RBM20, Microfilament Proteins, Alternative splicing, FHOD3, alternative splicing, sarcomere, RNA-Binding Proteins, Cell Biology, Cell biology, Alternative Splicing, 030104 developmental biology, 030220 oncology & carcinogenesis, RNA splicing, HeLa Cells, Polypyrimidine Tract-Binding Protein
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6
المؤلفون: Albino Poli, Macarena Gomez Lira, Monica Rodolfo, Giovanni Malerba, Morena Nicolis, Mario Santinami, Silvia Ferronato, Antonella Sangalli, Elisa Orlandi, Andrea Maurichi
مصطلحات موضوعية: Male, 0301 basic medicine, Cancer Research, melanoma, miR-146a, ribonuclease L, polymorphisms rs2910164, polymorphisms rs486907, Skin Neoplasms, Dermatology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Sex Factors, Endoribonucleases, medicine, Humans, Genetic Predisposition to Disease, Gene, Genetics, biology, Melanoma, Middle Aged, medicine.disease, Sex specific, Melanoma skin cancer, MicroRNAs, 030104 developmental biology, Snp snp interaction, Oncology, biology.protein, Female, Ribonuclease L
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7
المؤلفون: M. Bellizzi, F. Soli, Antonella Sangalli, M. Buganza, Monica Margoni, E. Cecchini
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Member 1, ATP Binding Cassette Transporter, Disease, Biology, medicine.disease_cause, peroxisome disorders, Asymptomatic, ATP Binding Cassette Transporter, Subfamily D, Member 1, 03 medical and health sciences, 0302 clinical medicine, Physiology (medical), Peroxisomal disorder, medicine, Humans, X-linked adrenoleukodystrophy, Adrenoleukodystrophy, Child, Gene, Aged, Genetics, Mutation, Peroxisome disorders, Very long chain fatty acids, Female, Pedigree, General Medicine, Membrane transport, medicine.disease, very long chain fatty acids, Phenotype, Subfamily D, 030104 developmental biology, Neurology, Surgery, Neurology (clinical), medicine.symptom, 030217 neurology & neurosurgery
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8
المؤلفون: S. Mirandola, Mauro Zamboni, Maurizio Rossini, Antonella Sangalli, Monica Mottes, Silvano Adami, Vania Braga, Giovanni Malerba, Davide Gatti
المصدر: Calcified Tissue International. 70:457-462
مصطلحات موضوعية: Male, Bone density, Endocrinology, Diabetes and Metabolism, Osteoporosis, Calcitriol receptor, Bone remodeling, Endocrinology, Sex hormone-binding globulin, Bone Density, Sex Hormone-Binding Globulin, Receptors, 80 and over, Medicine, Testosterone, genetics, Orthopedics and Sports Medicine, Aged, 80 and over, Bone mineral, Lumbar Vertebrae, Estradiol, biology, Femur Neck, COLIA1, Middle Aged, FokI, Italy, male osteoporosis, Bone Remodeling, Adult, Calcitonin, musculoskeletal diseases, medicine.medical_specialty, Sp1 Transcription Factor, sex hormones, Collagen Type I, Calcitriol, Genetic, Internal medicine, Humans, Polymorphism, Aged, Polymorphism, Genetic, business.industry, Free androgen index, Receptors, Calcitonin, Alkaline Phosphatase, medicine.disease, Radiography, biology.protein, Receptors, Calcitriol, CTR, business, Biomarkers
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9
المؤلفون: Paola Perego, Giovanni Malerba, Monica Rodolfo, Mario Santinami, Alberto Turco, Andrea Maurichi, Antonella Sangalli, Macarena Gomez-Lira, Silvia Ferronato
المصدر: Experimental dermatology. 23(10)
مصطلحات موضوعية: Adult, Male, Skin Neoplasms, malignant melanoma, Gene Expression, Dermatology, Biology, medicine.disease_cause, Biochemistry, Polymorphism, Single Nucleotide, Gene expression, medicine, Humans, expression analysis, Allele, Promoter Regions, Genetic, Molecular Biology, Allele frequency, Melanoma, Aged, Skin, PTGS2, promoter polymorphisms, Haplotype, Promoter, Fibroblasts, Middle Aged, medicine.disease, Molecular biology, PTGS2 Gene, Haplotypes, Italy, Cyclooxygenase 2, Case-Control Studies, Cancer research, Female, Carcinogenesis, PTGS2, expression analysis, malignant melanoma, promoter polymorphisms
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10
المؤلفون: Carla Taveggia, Claudio Bordignon, Alessandro Salviati, Lawrence Wrabetz, Antonella Sangalli, Giovanni Maria Severini
المساهمون: Sangalli, A., Taveggia, C., Salviati, A., Wrabetz, L., Bordignon, Claudio, G. M., Severini
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Arylsulfatase A, Genetic Vectors, Biology, Transduction (genetics), Transduction, Genetic, Genetics, medicine, Lysosomal storage disease, Humans, Lymphocytes, Molecular Biology, Cerebroside-Sulfatase, Gene Transfer Techniques, Genetic Therapy, Leukodystrophy, Metachromatic, Fibroblasts, medicine.disease, Molecular biology, In vitro, Lysosomal Storage Diseases, Metachromatic leukodystrophy, Oligodendroglia, Retroviridae, surgical procedures, operative, medicine.anatomical_structure, Cell culture, Pseudodeficiency alleles, Immunology, Molecular Medicine, Neuroglia, Schwann Cells
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11
المؤلفون: M C Digilio, Antonella Sangalli, Macarena Gomez-Lira, E Carnevale, A Giannotti, P.F. Pignatti, Monica Mottes
المصدر: Journal of Medical Genetics. 31:965-968
مصطلحات موضوعية: Heterozygote, COL1A2, Molecular Sequence Data, Mutant, Glycine, Biology, medicine.disease_cause, Exon, Nucleic acid thermodynamics, Pregnancy, Prenatal Diagnosis, Allele-specific oligonucleotide, Genetics, medicine, Humans, Point Mutation, Cysteine, Transversion, Genetics (clinical), Mutation, Base Sequence, osteogenesis imperfecta, prenatal diagnosis, Point mutation, Nucleic Acid Hybridization, DNA, Osteogenesis Imperfecta, Molecular biology, Collagen, type I, alpha 2, Female, Collagen, Research Article
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12
المؤلفون: Antonella Sangalli, S. Mirandola, Monica Mottes
المصدر: Molecular and Cellular Probes. 16:73-75
مصطلحات موضوعية: Genetic Markers, Sp1 Transcription Factor, COL1A1 gene, polymorphism, osteoporosis, Biology, Polymerase Chain Reaction, Collagen Type I, law.invention, Bone Density, law, Humans, Binding site, Molecular Biology, Genotyping, Polyacrylamide gel electrophoresis, Polymerase chain reaction, DNA Primers, Bone mineral, Genetics, Binding Sites, Polymorphism, Genetic, Intron, Cell Biology, Molecular biology, Collagen Type I, alpha 1 Chain, genomic DNA, Genetic marker, Electrophoresis, Polyacrylamide Gel, Collagen
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13
المؤلفون: Erica Diani, Maria Romanelli, Antonella Sangalli, Monica Mottes, Pamela Lorenzi
مصطلحات موضوعية: Molecular Sequence Data, 5' flanking region, farnesyl diphospate synthase, Biology, Gene Expression Regulation, Enzymologic, Farnesyl Pyrophosphate Synthetase, Farnesyl diphosphate synthase, Gene expression, Genetics, Consensus sequence, Animals, Humans, Promoter Regions, Genetic, OCT-1, Transcription factor, Gene, Conserved Sequence, Pax5, Base Sequence, promoter analysis, PAX5 Transcription Factor, Promoter, Geranyltranstransferase, Dimethylallyltranstransferase, Chromatin immunoprecipitation, Reporter gene, farnesyl pyrophosphate synthetase, Biochemistry, biology.protein, FDPS, FPP, 5' Untranslated Regions, Sequence Alignment, HeLa Cells, Octamer Transcription Factor-1
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14
المؤلفون: Antonella Sangalli, Antonella Delmarco, Maurizio Rossini, Carlo Castellani, Elena Petrelli, Baroukh M. Assael, Monica Mottes, Giovanni Malerba
مصطلحات موضوعية: Adult, Genetic Markers, Male, Pulmonary and Respiratory Medicine, Candidate gene, medicine.medical_specialty, Osteoporosis, Cystic Fibrosis Transmembrane Conductance Regulator, Cystic fibrosis, Calcitriol receptor, Collagen Type I, cystic fibrosis, modifier genes, Internal medicine, Medicine, Humans, Pediatrics, Perinatology, and Child Health, Calcitonin receptor, osteoporosis, Polymorphism, Genetic, biology, business.industry, Haplotype, Estrogen Receptor alpha, Receptors, Calcitonin, medicine.disease, Cystic fibrosis transmembrane conductance regulator, Spine, Radiography, Endocrinology, Phenotype, Pediatrics, Perinatology and Child Health, biology.protein, Receptors, Calcitriol, Female, business, Estrogen receptor alpha, Densitometry
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15
المؤلفون: Fulvio Parentin, Paolo Perissutti, Antonella Sangalli, Monica Mottes
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, genetic structures, DNA Mutational Analysis, Locus (genetics), Biology, Polymerase Chain Reaction, Cellular and Molecular Neuroscience, Chromosome Segregation, Myopia, medicine, Humans, Stickler syndrome, Child, Connective Tissue Diseases, Genetics, Genetic heterogeneity, Vitreoretinal degeneration, Retinal Degeneration, Chromosome Mapping, Retinal detachment, Eye Diseases, Hereditary, Syndrome, medicine.disease, Osteochondrodysplasia, Phenotype, eye diseases, Sensory Systems, Pedigree, Vitreous Body, Ophthalmology, Mutation, Female, Collagen, sense organs, Retinopathy
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16
المؤلفون: Antonella Sangalli, Maurizio Clementi, Remo Naccarato, Aldo Roda, Anna Baragiotta, Monica Mottes, Annarosa Floreani, Mariella Molaro
مصطلحات موضوعية: Adult, Male, Genotype, Genetic Linkage, Benign Recurrent Intrahepatic Cholestasis, Cholestasis, Intrahepatic, Biology, Chronic liver disease, Genetic determinism, Genetic Heterogeneity, Liver disease, Liver Function Tests, Cholestasis, Recurrence, Locus heterogeneity, medicine, Humans, Chromatography, High Pressure Liquid, Genetics (clinical), Genes, Dominant, Adenosine Triphosphatases, Genetics, Genetic heterogeneity, Haplotype, Chromosome Mapping, Middle Aged, medicine.disease, Pedigree, Haplotypes, Chromosomes, Human, Pair 2, Female, Chromosomes, Human, Pair 18, Cholangiography, Microsatellite Repeats
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17
المؤلفون: Macarena Gomez-Lira, Monica Mottes, Antonella Sangalli, Pier Franco Pignatti, Nicolo' Rizzuto, Chiara Perusi, Alessandro Salviati
المصدر: Human Genetics. 96
مصطلحات موضوعية: Adult, Male, Genetics, Base Sequence, Molecular Sequence Data, Sandhoff Disease, Gene mutation, Sandhoff disease, Biology, Gangliosidosis, medicine.disease, beta-N-Acetylhexosaminidases, Human genetics, Pedigree, Mutation, Genotype, Mutation (genetic algorithm), medicine, Humans, Gene, Genetics (clinical), Heteroduplex
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18
المؤلفون: Monica Mottes, Antonella Sangalli, Pier Franco Pignatti
المصدر: American journal of medical genetics. 45(2)
مصطلحات موضوعية: musculoskeletal diseases, Genetic Markers, Male, congenital, hereditary, and neonatal diseases and abnormalities, Population, Locus (genetics), macromolecular substances, Biology, Polymerase Chain Reaction, Gene Frequency, medicine, Humans, Allele, skin and connective tissue diseases, education, Allele frequency, Genetics (clinical), Genetics, education.field_of_study, integumentary system, Haplotype, Osteogenesis Imperfecta, medicine.disease, Pedigree, Minor allele frequency, Haplotypes, Osteogenesis imperfecta, Mutation, Female, Collagen, Restriction fragment length polymorphism, Polymorphism, Restriction Fragment Length
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19
المؤلفون: Maurizia Valli, Antonella Sangalli, Antonio Rossi, Pier Franco Pignatti, Antonella Forlino, Monica Mottes, Giuseppe Cetta, Ruggero Tenni
مصطلحات موضوعية: Mutant, osteogenesis imperfecta, type I collagen, mutations, Glycine, Biology, Peptide Mapping, Biochemistry, Deoxyribonuclease HpaII, medicine, Humans, Point Mutation, Trypsin, Cyanogen Bromide, Deoxyribonucleases, Type II Site-Specific, Fibroblast, Transversion, Alanine, Point mutation, Infant, Newborn, Sequence Analysis, DNA, Fibroblasts, medicine.disease, medicine.anatomical_structure, Osteogenesis imperfecta, Electrophoresis, Polyacrylamide Gel, Female, Collagen, Type I collagen, medicine.drug
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20
المؤلفون: Monica Mottes, Piera Buttitta, Ruggero Tenni, Antonella Sangalli, Maurizia Valli, Macarena Gomez Lira, Giuseppe Cetta, Pier Franco Pignatti
المصدر: Human Genetics. 89
مصطلحات موضوعية: molecular defect, Male, Proband, Collagen helix, DNA Mutational Analysis, Molecular Sequence Data, Glycine, Gene Expression, Biology, medicine.disease_cause, Polymerase Chain Reaction, Serine, triple helical domain, osteogenesis imperfecta, collagen triple helix, healthy family member, Genetics, medicine, Humans, RNA, Messenger, Child, Codon, Genetics (clinical), Genes, Dominant, Chromosome Aberrations, Mutation, Base Sequence, Transition (genetics), Genetic Variation, Middle Aged, Osteogenesis Imperfecta, medicine.disease, Molecular biology, Pedigree, Procollagen peptidase, Genes, Osteogenesis imperfecta, Female, Collagen, Procollagen
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