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Biomed Research International
|
June 16, 2015
Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss
Ana Paula Grillo, Flávia Marcorin de Oliveira, Gabriela Queila de Carvalho, et al.
Genetic Testing and Molecular Biomarkers
|
September 1, 2009
Screening for the GJB2 c.-3170 G>A (IVS 1+1 G>A) mutation in Brazilian deaf individuals using multiplex ligation-dependent probe amplification
Sueli Matilde da Silva-Costa, Fernanda Borchers Coeli, Carolina Rodrigues Lincoln-de-Carvalho, et al.
BMC Medical Genetics
|
May 28, 2016
Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry
Rogério Marins Alves, Sueli Matilde da Silva Costa, Paulo Mauricio do Amôr Divino Miranda, et al.
Ophthalmic Genetics
|
August 29, 2017
Association of HTRA1 rs11200638 with age-related macular degeneration (AMD) in Brazilian patients
Tamires Prates Lana, Sueli Matilde da Silva Costa, Galina Ananina, et al.
Molecular Vision
|
September 2, 2016
Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy
Paulo Maurício do Amôr Divino Miranda, Sueli Matilde da Silva-Costa, Juliane Cristina Balieiro, et al.
Plos One
|
September 21, 2022
Epigenetic analysis in placentas from sickle cell disease patients reveals a hypermethylation profile
Gislene Pereira Gil, Galina Ananina, Mariana Maschietto, et al.
Annals of Hematology
|
February 22, 2024
Comparative transcriptomic analysis of circulating endothelial cells in sickle cell stroke
Júlia Nicoliello Pereira de Castro, Sueli Matilde da Silva Costa, Ana Carolina Lima Camargo, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
April 4, 2023
Comparative transcriptome analysis of endothelial progenitor cells of HbSS patients with and without proliferative retinopathy
Victor de Haidar E Bertozzo, Sueli Matilde da Silva Costa, Mirta Tomie Ito, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
August 8, 2024
The molecular mechanism responsible for HbSC retinopathy may depend on the action of the angiogenesis-related genes <i>ROBO1</i> and <i>SLC38A5</i>
Sueli Matilde da Silva Costa, Mirta Tomie Ito, Pedro Rodrigues Sousa da Cruz, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Biomed Research International
|
June 16, 2015
Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss
Ana Paula Grillo, Flávia Marcorin de Oliveira, Gabriela Queila de Carvalho, et al.
Genetic Testing and Molecular Biomarkers
|
September 1, 2009
Screening for the GJB2 c.-3170 G>A (IVS 1+1 G>A) mutation in Brazilian deaf individuals using multiplex ligation-dependent probe amplification
Sueli Matilde da Silva-Costa, Fernanda Borchers Coeli, Carolina Rodrigues Lincoln-de-Carvalho, et al.
BMC Medical Genetics
|
May 28, 2016
Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry
Rogério Marins Alves, Sueli Matilde da Silva Costa, Paulo Mauricio do Amôr Divino Miranda, et al.
Ophthalmic Genetics
|
August 29, 2017
Association of HTRA1 rs11200638 with age-related macular degeneration (AMD) in Brazilian patients
Tamires Prates Lana, Sueli Matilde da Silva Costa, Galina Ananina, et al.
Molecular Vision
|
September 2, 2016
Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy
Paulo Maurício do Amôr Divino Miranda, Sueli Matilde da Silva-Costa, Juliane Cristina Balieiro, et al.
Plos One
|
September 21, 2022
Epigenetic analysis in placentas from sickle cell disease patients reveals a hypermethylation profile
Gislene Pereira Gil, Galina Ananina, Mariana Maschietto, et al.
Annals of Hematology
|
February 22, 2024
Comparative transcriptomic analysis of circulating endothelial cells in sickle cell stroke
Júlia Nicoliello Pereira de Castro, Sueli Matilde da Silva Costa, Ana Carolina Lima Camargo, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
April 4, 2023
Comparative transcriptome analysis of endothelial progenitor cells of HbSS patients with and without proliferative retinopathy
Victor de Haidar E Bertozzo, Sueli Matilde da Silva Costa, Mirta Tomie Ito, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
August 8, 2024
The molecular mechanism responsible for HbSC retinopathy may depend on the action of the angiogenesis-related genes <i>ROBO1</i> and <i>SLC38A5</i>
Sueli Matilde da Silva Costa, Mirta Tomie Ito, Pedro Rodrigues Sousa da Cruz, et al.
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of 1