Lista de obras - Suely K Marie - Dominio Público Uruguay

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

artículo científico publicado en 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.

artículo científico publicado en 2007

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

artículo científico publicado en 2005

ASPM gene expression in medulloblastoma.

artículo científico publicado en 2010

Adult neurogenesis and glial oncogenesis: when the process fails.

artículo científico publicado en 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

artículo científico publicado en 2014

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

artículo científico publicado en 2009

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

artículo científico publicado en 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.

artículo científico publicado en 2017

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

artículo científico publicado en 2005

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.

artículo científico publicado en 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

artículo científico publicado en 2014

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

artículo científico publicado en 2022

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

artículo científico publicado en 2012

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

artículo científico publicado en 2017

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

artículo científico publicado en 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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 1997

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

artículo científico publicado en 2005

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.

artículo científico publicado en 2013

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

artículo científico publicado en 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

artículo científico publicado en 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.

artículo científico publicado en 2013

Factors of morbidity in hemispherectomies: Surgical technique×pathology

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2008

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

artículo científico publicado en 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.

artículo científico publicado en 1994

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

artículo científico publicado en 2000

Histopathological findings in skeletal muscle used in human dynamic cardiomyoplasty

artículo científico publicado en 2001

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

artículo científico publicado en 2010

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

artículo científico publicado en 2009

IDH1 mutations in a Brazilian series of Glioblastoma.

artículo científico publicado en 2011

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

artículo científico publicado en 2009

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

artículo científico publicado en 2015

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

artículo científico publicado en 2007

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

artículo científico publicado en 2014

Isolation and characterization of novel RECK tumor suppressor gene splice variants

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 2019

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

artículo científico publicado en 2002

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

artículo científico publicado en 2021

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

artículo científico publicado en 2009

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

artículo científico publicado en 2013

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

artículo científico publicado en 2007

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

artículo científico publicado en 1996

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

artículo científico publicado en 2008

Melanocyte transformation associated with substrate adhesion impediment.

artículo científico publicado en 2006

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

artículo científico publicado en 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.

artículo científico publicado en 2010

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

artículo científico publicado en 2013

Molecular alterations in meningiomas: Literature review

artículo científico publicado en 2018

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

artículo científico publicado en 1995

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

artículo científico publicado en 2017

Nebulin expression in patients with nemaline myopathy

artículo científico publicado en 2001

Neuroinflammatory responses to traumatic brain injury

artículo científico publicado en 2015

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

artículo científico publicado en 2003

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.

artículo científico publicado en 2006

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

artículo científico publicado en 2007

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.

artículo científico publicado en 2010

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

artículo científico

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.

artículo científico publicado en 2015

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

artículo científico publicado en 2010

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.

artículo científico publicado en 2012

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

artículo científico publicado en 2009

Serum amyloid A1 is upregulated in human glioblastoma.

artículo científico publicado en 2017

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

artículo científico publicado en 2012

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

artículo científico publicado en 2016

Stem cells in neurology--current perspectives.

artículo científico

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.

artículo científico publicado en 2009

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

artículo científico publicado en 2001

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

artículo científico publicado en 2021

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

artículo científico publicado en 2012

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Lista de obras de 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.

A Caucasian Family with the 3271 Mutation in Mitochondrial DNA

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

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

ADAM23 methylation and expression analysis in brain tumors

ASPM gene expression in medulloblastoma.

Adult neurogenesis and glial oncogenesis: when the process fails.

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

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

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

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

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

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

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

Bioinformatics construction of the human cell surfaceome.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Double Pathology in Rasmussen's Encephalitis: Etiologic Considerations

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

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

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

Factors of morbidity in hemispherectomies: Surgical technique×pathology

Frequency of parafunctional oral habits in patients with cerebral palsy

Frequency of temporomandibular disorder signs in individuals with cerebral palsy

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

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

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

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

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

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

Histopathological findings in skeletal muscle used in human dynamic cardiomyoplasty

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

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

IDH1 mutations in a Brazilian series of Glioblastoma.

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

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

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

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

Isolation and characterization of novel RECK tumor suppressor gene splice variants

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

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

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

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

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

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

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

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

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

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

Melanocyte transformation associated with substrate adhesion impediment.

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

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

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

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

Molecular alterations in meningiomas: Literature review

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

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

Nebulin expression in patients with nemaline myopathy

Neuroinflammatory responses to traumatic brain injury

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

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

PIK3CA gene mutations in pediatric and adult glioblastoma multiforme.

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