المؤلفون: Simonetti L; Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., Ferreira LGA; Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.; Department of Biochemistry, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., Vidi AC; Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.; Department of Biochemistry, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., de Souza JS; Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., Kunii IS; Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., Melaragno MI; Department of Morphology and Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., de Mello CB; Department of Psychobiology, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., Carvalheira G; Department of Morphology and Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., Dias da Silva MR; Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.; Department of Biochemistry, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.

المصدر: Frontiers in genetics [Front Genet] 2021 Sep 20; Vol. 12, pp. 724625. Date of Electronic Publication: 2021 Sep 20 (Print Publication: 2021).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE

المؤلفون: Melo MCC; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil., de Souza JS; Biological Sciences, Universidade Federal de São Paulo, Diadema, 09972-270, Brazil., Kizys MML; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil., Vidi AC; Molecular Biology Program, Universidade Federal de São Paulo, São Paulo, 04044-020, Brazil., Dorta HS; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil., Kunii IS; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil., Giannocco G; Molecular Biology Program, Universidade Federal de São Paulo, São Paulo, 04044-020, Brazil., Carvalheira G; Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil., Dias-da-Silva MR; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil.; Biological Sciences, Universidade Federal de São Paulo, Diadema, 09972-270, Brazil.

المصدر: Journal of the Endocrine Society [J Endocr Soc] 2017 Feb 28; Vol. 1 (7), pp. 809-815. Date of Electronic Publication: 2017 Feb 28 (Print Publication: 2017).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Endocrine Society Country of Publication: United States NLM ID: 101697997 Publication Model: eCollection Cited Medium: Print ISSN: 2472-1972 (Print) Linking ISSN: 24721972 NLM ISO Abbreviation: J Endocr Soc Subsets: PubMed not MEDLINE

المؤلفون: Paninka RM; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 669, 11° andar, São Paulo, SP, 04039-032, Brazil.; Laboratory of Structural and Functional Neurobiology, Department of Biophysics, Universidade Federal de São Paulo, São Paulo, Brazil., Mazzotti DR; Department of Psychobiology, Universidade Federal de São Paulo, São Paulo, Brazil., Kizys MM; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 669, 11° andar, São Paulo, SP, 04039-032, Brazil., Vidi AC; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 669, 11° andar, São Paulo, SP, 04039-032, Brazil., Rodrigues H; Department of Psychobiology, Universidade Federal de São Paulo, São Paulo, Brazil., Silva SP; Laboratory of Integrative Biology and Metabolism, Department of Biophysics, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil., Kunii IS; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 669, 11° andar, São Paulo, SP, 04039-032, Brazil., Furuzawa GK; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 669, 11° andar, São Paulo, SP, 04039-032, Brazil., Arcisio-Miranda M; Laboratory of Structural and Functional Neurobiology, Department of Biophysics, Universidade Federal de São Paulo, São Paulo, Brazil., Dias-da-Silva MR; Laboratory of Molecular and Translational Endocrinology, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Pedro de Toledo, 669, 11° andar, São Paulo, SP, 04039-032, Brazil. mrdsilva@unifesp.br.

المصدر: Molecular genetics and genomics : MGG [Mol Genet Genomics] 2016 Aug; Vol. 291 (4), pp. 1535-44. Date of Electronic Publication: 2016 Mar 23.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101093320 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1617-4623 (Electronic) Linking ISSN: 16174623 NLM ISO Abbreviation: Mol Genet Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Channelopathies/*genetics , Potassium Channels, Inwardly Rectifying/*genetics , Sequence Analysis, DNA/*methods, Chromosome Mapping/methods ; Exome ; Genetic Predisposition to Disease ; Genome, Human ; HEK293 Cells ; Humans ; Polymorphism, Single Nucleotide ; Protein Isoforms/genetics ; Sequence Alignment

المؤلفون: Sisdelli L; Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, 04023-900, Brazil., Vidi AC; Department of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil.; Department of Medicine, Universidade Federal de São Paulo, São Paulo, Brazil., Moysés-Oliveira M; Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, 04023-900, Brazil., Di Battista A; Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, 04023-900, Brazil., Bortolai A; Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, 04023-900, Brazil., Moretti-Ferreira D; Department of Genetics, Instituto de Biociências de Botucatu, São Paulo State University, São Paulo, 18618-970, Brazil., da Silva MR; Department of Biochemistry, Universidade Federal de São Paulo, São Paulo, Brazil.; Department of Medicine, Universidade Federal de São Paulo, São Paulo, Brazil., Melaragno MI; Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, 04023-900, Brazil., Carvalheira G; Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, 04023-900, Brazil. carvalheira@unifesp.br.

المصدر: Human genetics [Hum Genet] 2016 Feb; Vol. 135 (2), pp. 185-92. Date of Electronic Publication: 2015 Dec 15.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Gene Rearrangement* , X Chromosome Inactivation*, Chromosomes, Human, X/*genetics , Deoxyuridine/*analogs & derivatives, Chromosome Disorders/genetics ; Cytogenetic Analysis ; DNA Replication ; Deoxyuridine/metabolism ; Female ; Humans ; Male ; Translocation, Genetic