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CARACTERIZAÇÃO de Mutações da Osteogênese imperfeita em Pacientes do Espírito Santo: Estudo Dos genes Ifitm5, Col1a1 e Col1a2

PAULA, F.; NOGUEIRA, B. V.; MARANDUBA, C. M. C.; GUIMARAES, M. C. C. (Universidade Federal do Espírito SantoBRPrograma de Pós-Graduação em BiotecnologiaUFESMestrado em Biotecnologia, 2018-02-27)

Novel genes and mutations in patients affected by recurrent pregnancy loss

Quintero-Ronderos, Paula; Mercier, Eric; Fukuda, Michiko; González, Ronald; Suárez, Carlos Fernando; Alfonso Patarroyo, Manuel; Vaiman, Daniel; Gris, Jean-Christophe; Laissue, Paul (2017)

Identification of COL6A1 as a differentially expressed gene in human astrocytomas

FUJITA, A.; SATO, J. R.; FESTA, F.; GOMES, L. R.; OBA-SHINJO, S. M.; MARIE, S. K. N.; FERREIRA, C. E.; SOGAYAR, M. C. (FUNPEC-EDITORA, 2008)

Diffuse infiltrating gliomas are the most common tumors of the central nervous system. Gliomas are classified by the WHO according to their histopathological and clinical characteristics into four classes: grade I (pilocytic ...

COL1A1 and miR-29b show lower expression levels during osteoblast differentiation of bone marrow stromal cells from Osteogenesis Imperfecta patients

Kaneto, Carla M; Lima, Patrícia S; Zanette, Dalila L; Prata, Karen L; Pina Neto, João M; Paula, Francisco J de; Silva, Wilson A (BioMed Central, 2014-04-27)

Abstract Background The majority of Osteogenesis Imperfecta (OI) cases are caused by mutations in one of the two genes, COL1A1 and COL1A2 encoding for the two chains that ...

Estudo das mutações no gene COL2A1 em uma coorte de pacientes com displasias esqueléticas do grupo colagenopatia tipo II segundo critérios clínico-radiológicosStudy of mutations in the COL2A1 gene in a cohort of patients with skeletal dysplasias of type 2 collagenopathy group according to clinical and radiological criteria

Silveira, Karina da Costa, 1989- ([s.n.], 2014)

COL1A1 Sp1-binding site polymorphism as a risk factor for genital prolapse

RODRIGUES, Andrea Moura; GIRAO, Manoel Joao Batista Castello; SILVA, Ismael Dale Cotrim Guerreiro da; SARTORI, Marair Gracio Ferreira; MARTINS, Karina de Falco; CASTRO, Rodrigo de Aquino (SPRINGER LONDON LTD, 2008)

The objective of this study was to verify the possible association between the Sp1-binding site polymorphism and genital prolapse. A case-control study was conducted in 107 patients with stages III and IV genital prolapse. ...

HR4 gene is induced in the Arabidopsis-Trichoderma atroviride beneficial interaction

JORGE SAENZ MATA; JUAN FRANCISCO JIMENEZ BREMONT (MDPI AG, 2012)

Influencia do polimorfismo D104N do gene COL18A1 na susceptilidade ao cancer de mama esporadicoInfluence of the D104N do gene COL18A1 gene in sporadic breast cancer susceptibility

Lourenço, Gustavo Jacob, 1978- ([s.n.], 2006)

MUTAÇÕES NA REGIÃO AMINOTERMINAL DO GENE COL1A2 E A MANIFESTAÇÃO DA OSTEOGÊNESE IMPERFEITA 2011

PAULA, F. (Universidade Federal do Espírito SantoBRPrograma de Pós-Graduação em BiotecnologiaUFESMestrado em Biotecnologia, 2011-04-29)

A Osteogênese Imperfeita (OI) é uma doença genética associada a alterações na molécula do colágeno tipo I. Caracteriza-se clinicamente por fragilidade e deformidade ósseas. A grande maioria dos casos relatados são alterações ...

Equine tendonitis therapy using mesenchymal stem cells and platelet concentrates: A randomized controlled trial

Universidade Estadual Paulista (UNESP) (2013-07-25)

Introduction. Tendon injury is a major cause of lameness and decreased performance in athletic equines. Various therapies for tendonitis have been described; however, none of these therapies results in complete tissue ...

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