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List of works by Suely K Marie

A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation.

scientific article published on 10 November 2017

A Caucasian Family with the 3271 Mutation in Mitochondrial DNA

scientific article published on 01 August 1994

A comparison of the prevalence of the metabolic syndrome and its components among native Japanese and Japanese Brazilians residing in Japan and Brazil.

scientific article

A novel type of C11orf95-LOC-RELA fusion in a grade II supratentorial ependymoma: report of a case with literature review

scientific article published on 10 January 2019

ADAM23 methylation and expression analysis in brain tumors

scientific article (publication date: 3 June 2005)

ASPM gene expression in medulloblastoma.

scientific article

Adult neurogenesis and glial oncogenesis: when the process fails.

scientific article published on 11 March 2014

Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?

scientific article published on 01 March 1995

Angiotensin-converting enzyme insertion/deletion gene polymorphism is associated with dermatomyositis

scientific article published on 3 March 2014

Anti-C1q antibodies in juvenile-onset systemic lupus erythematosus.

scientific article published in September 2009

Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.

scientific article published in May 1994

Association of Lewis and Secretor gene polymorphisms and Helicobacter pylori seropositivity among Japanese-Brazilians

article

Atypical and Malignant Meningiomas: Neurooncologic Management in a Brazilian cohort.

scientific article published on 28 November 2017

Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy.

scientific article

Bioinformatics construction of the human cell surfaceome.

scientific article published on 15 September 2009

Bite force and handgrip force in patients with molecular diagnosis of myotonic dystrophy.

scientific article published in March 2007

Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: Analysis of muscle beta 1 syntrophin

article

CD99 is upregulated in placenta and astrocytomas with a differential subcellular distribution according to the malignancy stage

scientific article published on 6 May 2014

Cellular Model of Malignant Transformation of Primary Human Astrocytes Induced by Deadhesion/Readhesion Cycles

scientific article published on 19 April 2022

Changes in the expression of proteins associated with aerobic glycolysis and cell migration are involved in tumorigenic ability of two glioma cell lines

scientific article published on 3 September 2012

Clinical Outcome, Tumor Recurrence, and Causes of Death: A Long-Term Follow-Up of Surgically Treated Meningiomas

scientific article

Comparison of motor strength and function in patients with Duchenne muscular dystrophy with or without steroid therapy.

scientific article published on October 2010

Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region

article

Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency

scientific article published on 01 January 1996

Correlation of MGMT promoter methylation status with gene and protein expression levels in glioblastoma

scientific article

Current perspectives in stem cell therapy for spinal cord repair in humans: a review of work from the past 10 years.

scientific article published on June 2014

Cyclooxygenase-2 gene polymorphisms and susceptibility to colorectal cancer in a Brazilian population.

scientific article published on August 2017

Decreased AKT1/mTOR pathway mRNA expression in short-term bipolar disorder.

scientific article

Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy

scientific article published on 01 August 1997

Difference in adhesion molecule expression (ICAM-1 and VCAM-1) in juvenile and adult dermatomyositis, polymyositis and inclusion body myositis.

scientific article

Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families

article

Differential expression of ID4 and its association with TP53 mutation, SOX2, SOX4 and OCT-4 expression levels.

scientific article

Disruption of prion protein-HOP engagement impairs glioblastoma growth and cognitive decline and improves overall survival

scientific article published on 25 August 2014

Double Pathology in Rasmussen's Encephalitis: Etiologic Considerations

scientific article published on 01 May 1996

Effects of high adherence to mediterranean or low-fat diets in medicated secondary prevention patients

scientific article published on 03 September 2011

Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families

article

Expression of tissue factor signaling pathway elements correlates with the production of vascular endothelial growth factor and interleukin-8 in human astrocytoma patients.

scientific article published on 28 November 2013

Factors of morbidity in hemispherectomies: Surgical technique×pathology

scientific article published on 20 December 2005

Frequency of parafunctional oral habits in patients with cerebral palsy

scientific article published on 01 May 2007

Frequency of temporomandibular disorder signs in individuals with cerebral palsy

scientific article published on 01 March 2008

Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin–glycoprotein complex

article

Gene expression profile analysis of primary glioblastomas and non-neoplastic brain tissue: identification of potential target genes by oligonucleotide microarray and real-time quantitative PCR

scientific article

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

scientific article published on November 1993

Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

scientific journal article

Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy.

scientific article published in June 1994

Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases.

scientific article published on March 2000

Histopathological findings in skeletal muscle used in human dynamic cardiomyoplasty

scientific article published on 01 May 2001

Homozygotic intronic GAA mutation in three siblings with late-onset Pompe's disease.

scientific article published in April 2010

ICAM-1 (Lys469Glu) and PECAM-1 (Leu125Val) polymorphisms in diffuse astrocytomas.

scientific article published on 21 March 2009

IDH1 mutations in a Brazilian series of Glioblastoma.

scientific article

Identification of FAM46D as a novel cancer/testis antigen using EST data and serological analysis.

scientific article published on 18 June 2009

Immunohistochemical expression of cyclin D1 is higher in supratentorial ependymomas and predicts relapses in gross total resection cases.

scientific article

International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trials.

scientific article published on October 2007

Intraoperative assistive technologies and extent of resection in glioma surgery: a systematic review of prospective controlled studies

scientific article

Isolation and characterization of novel RECK tumor suppressor gene splice variants

scientific article published on 28 September 2015

Knobloch syndrome in a large Brazilian consanguineous family: Confirmation of autosomal recessive inheritance

article

LOX expression and functional analysis in astrocytomas and impact of IDH1 mutation

scientific article published on 19 March 2015

LOXL3 Function Beyond Amino Oxidase and Role in Pathologies, Including Cancer

scientific article published on 23 July 2019

Lack of the C-terminal domain of nebulin in a patient with nemaline myopathy

scientific article published on 01 May 2002

Late p65 nuclear translocation in glioblastoma cells indicates non-canonical TLR4 signaling and activation of DNA repair genes

scientific article published on 14 January 2021

Limited Ca2+ and PKA-pathway dependent neurogenic differentiation of human adult mesenchymal stem cells as compared to fetal neuronal stem cells.

scientific article published on 15 August 2009

Low-grade astrocytoma: surgical outcomes in eloquent versus non-eloquent brain areas.

scientific article published on 8 January 2013

Lower HDL-cholesterol among healthy middle-aged Japanese-Brazilians in São Paulo compared to Natives and Japanese-Brazilians in Japan.

scientific article published on 17 January 2007

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.

scientific article

Maternal embryonic leucine zipper kinase transcript abundance correlates with malignancy grade in human astrocytomas.

scientific article published in February 2008

Melanocyte transformation associated with substrate adhesion impediment.

scientific article

Melatonergic system-based two-gene index is prognostic in human gliomas

scientific article published on 29 October 2015

Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI

article

Mitochondrial DNA depletion and its correlation with TFAM, TFB1M, TFB2M and POLG in human diffusely infiltrating astrocytomas.

scientific article published on 17 July 2010

Modulation of HJURP (Holliday Junction-Recognizing Protein) levels is correlated with glioblastoma cells survival

scientific article

Molecular alterations in meningiomas: Literature review

scientific article published on 07 December 2018

Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian families.

scientific article

N-acetylcysteine Counteracts Adipose Tissue Macrophage Infiltration and Insulin Resistance Elicited by Advanced Glycated Albumin in Healthy Rats.

scientific article published on 22 September 2017

Nebulin expression in patients with nemaline myopathy

scientific article published on 01 March 2001

Neuroinflammatory responses to traumatic brain injury

scientific article published on 19 March 2015

New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype

scientific article

No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy familes (FSHD) with 4q markers

article

PIK3CA gene mutations in pediatric and adult glioblastoma multiforme.

scientific article published in October 2006

Phenotypic and immunohistochemical characterization of sarcoglycanopathies

scientific article published on January 1, 2011

Pleiotrophin expression in astrocytic and oligodendroglial tumors and it's correlation with histological diagnosis, microvascular density, cellular proliferation and overall survival.

scientific article

Pompe disease in a Brazilian series: clinical and molecular analyses with identification of nine new mutations

article

Pompe disease: further challenges to pursue

scientific article published on 01 May 2013

Proteomic analysis of low- to high-grade astrocytomas reveals an alteration of the expression level of raf kinase inhibitor protein and nucleophosmin.

scientific article

Quantitative proteomic analysis and functional studies reveal that nucleophosmin is involved in cell death in glioblastoma cell line transfected with siRNA.

scientific article published on August 2012

Quantitative proteomic analysis shows differentially expressed HSPB1 in glioblastoma as a discriminating short from long survival factor and NOVA1 as a differentiation factor between low-grade astrocytoma and oligodendroglioma.

scientific article published on 25 June 2015

Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: role of the C2a splice variant.

scientific article

Report of the first Brazilian infantile Pompe disease patient to be treated with recombinant human acid alpha-glucosidase

article

Resistance to EGF receptor inhibitors in glioblastoma mediated by phosphorylation of the PTEN tumor suppressor at tyrosine 240.

scientific article

SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas

scientific article

Serum amyloid A1 is upregulated in human glioblastoma.

scientific article

Skeletal muscle major histocompatibility complex class I and II expression differences in adult and juvenile dermatomyositis.

scientific article

Stathmin involvement in the maternal embryonic leucine zipper kinase pathway in glioblastoma.

scientific article published on 11 March 2016

Stem cells in neurology--current perspectives.

scientific article published on June 2014

Targeted Assessment of G0S2 Methylation Identifies a Rapidly Recurrent, Routinely Fatal Molecular Subtype of Adrenocortical Carcinoma

scientific article published on 15 February 2019

The Brazilian consensus on the management of Pompe disease.

scientific article published on October 2009

The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome.

scientific article

Transcriptional profiling of macaque microglia reveals an evolutionary preserved gene expression program

scientific article published on 07 May 2021

Transcriptional response to GAA deficiency (Pompe disease) in infantile-onset patients

scientific article published on 14 May 2012

Transcriptomic analysis of purified human cortical microglia reveals age-associated changes

scientific article

Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of disease

scientific article

Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma.

scientific article