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1
Transcriptome reveals miRNA-mRNA signatures associated with three conditions of azoospermia
Transcriptome reveals miRNA-mRNA signatures associated with three conditions of azoospermia
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Artigo de Congresso 		Adicionar ao Meu Espaço

Transcriptome reveals miRNA-mRNA signatures associated with three conditions of azoospermia

J. V. W Cachay Wester C Dias; Wilson Araújo da Silva Júnior; Alfredo Ribeiro da Silva; João Monteiro de Pina Neto; International Congress of Genetics (22. 2018 Foz do Iguaçu)

Abstracts Foz do Iguaçu : SBG, 2018

Foz do Iguaçu SBG 2018

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2937476 Estantes Deslizantes )(Acessar)

2
Haplotypes linked to the X chromosome in paternity investigation in incomplete cases
Haplotypes linked to the X chromosome in paternity investigation in incomplete cases
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Haplotypes linked to the X chromosome in paternity investigation in incomplete cases

I. C. D. Alcarás Aguinaldo Luiz Simões; Brazilian-International Congress of Genetics (62. 2016 Caxambu)

Abstracts Caxambu : SBG, 2016

Caxambu SBG 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2875788 Estantes Deslizantes )(Acessar)

3
Synthetic biology in the high school in Brazil
Synthetic biology in the high school in Brazil
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Artigo de Congresso 		Adicionar ao Meu Espaço

Synthetic biology in the high school in Brazil

C Paris L. M Bimbati; Aparecida Maria Fontes; International Congress of Genetics (22. 2018 Foz do Iguaçu)

Abstracts Foz do Iguaçu : SBG, 2018

Foz do Iguaçu SBG 2018

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2937482 Estantes Deslizantes )(Acessar)

4
O4 Amino acid substitution in genotype 3a hepatitis C virus polymerase protein affects responses to sofosbuvir and interferon alpha and inhibits apoptosis
O4 Amino acid substitution in genotype 3a hepatitis C virus polymerase protein affects responses to sofosbuvir and interferon alpha and inhibits apoptosis
Material Type:
Artigo 		Adicionar ao Meu Espaço

O4 Amino acid substitution in genotype 3a hepatitis C virus polymerase protein affects responses to sofosbuvir and interferon alpha and inhibits apoptosis

Lee, Wing-yiu Jason ; Jones, Meleri ; Wing, Peter AC ; Rajagopal, Swathi ; Foster, Graham R

Gut, 2020-09, Vol.69 (Suppl 1), p.A2-A3 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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5
966 Genetic variations causing neonatal diabetes mellitus
966 Genetic variations causing neonatal diabetes mellitus
Material Type:
Artigo 		Adicionar ao Meu Espaço

966 Genetic variations causing neonatal diabetes mellitus

Elemam, Hazem Helmy ; Allman, Anneli ; Hawkes, Davida

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A177-A178 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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6
1373 Rapid exome sequencing for acutely unwell children: experiences from Yorkshire regional genetics service
1373 Rapid exome sequencing for acutely unwell children: experiences from Yorkshire regional genetics service
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Artigo 		Adicionar ao Meu Espaço

1373 Rapid exome sequencing for acutely unwell children: experiences from Yorkshire regional genetics service

Lerou, Dimitra-Ilektra ; Meng Yin Chen, Jasmine ; Redman, Melody ; Lam, Zena ; Hartill, Verity ; Campbell, Jennifer

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A343-A344 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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7
359 A novel COL4A4 mutation in the proband initially diagnosed as IgAN with autosomal recessive Alport syndrome
359 A novel COL4A4 mutation in the proband initially diagnosed as IgAN with autosomal recessive Alport syndrome
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359 A novel COL4A4 mutation in the proband initially diagnosed as IgAN with autosomal recessive Alport syndrome

Altun, Ilayda ; Saygılı, Seha ; Canpolat, Nur ; Çalışkan, Salim ; Sever, Lale

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A151-A151 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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8
91 Fabry’s disease with minimal manifestations in girls (clinical cases)
91 Fabry’s disease with minimal manifestations in girls (clinical cases)
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91 Fabry’s disease with minimal manifestations in girls (clinical cases)

Gadzhikerimov, Gadzhikerim ; Gumeniuk, Olga

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A38-A38 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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9
159 Severe presentation of Netherton syndrome: a case report
159 Severe presentation of Netherton syndrome: a case report
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159 Severe presentation of Netherton syndrome: a case report

Gagro, Alenka ; Pustišek, Nives ; Ožanić, Suzana Bulić ; Niseteo, Tena ; Sila, Sara ; Kolaček, Sanja ; Barišić, Ingeborg

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A67-A68 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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10
1165 The wales infants’ and children’s genome service’ (WINGS): diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis
1165 The wales infants’ and children’s genome service’ (WINGS): diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis
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1165 The wales infants’ and children’s genome service’ (WINGS): diagnostic rapid whole genome sequencing for unwell children with a suspected rare genetic diagnosis

Murch, Oliver ; Jezkova, Jana ; Halstead, Joseph ; Burke, Katherine ; Oruganti, Siva ; Calvert, Jennifer ; Evans, Jennifer ; Williams, Hywel ; Sansbury, Francis ; Corrin, Sian ; Sloper, Emily

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 1), p.A256-A256 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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Deste Autor:

  1. International Congress of Genetics
  2. Dias, C
  3. Alcarás, I
  4. Silva, A
  5. Bimbati, L

Neste Assunto:

  1. Pediatrics
  2. Abstracts
  3. Patients
  4. Mutation
  5. Genetic Disorders

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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