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Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD)
Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD)
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Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD)

Rachel Gallagher Ernie Esquivel; Xin Tian; Tiffany Samaroo; Dhanpat Jain; Luiz Onuchie; Lisa Guay Woodford; Gregory Germino; Stefan Somlo; Abstracts issue journal of the american Society of Nephrology - JASN 2004 St. Louis

Journal of the American Society of Nephrology Baltimore v. 15, Abstracts issue, p. 56A res. SU-FC061, 2004

Baltimore 2004

Localização: FM - Fac. Medicina    (BCSEP 236 2004 ) e outros locais(Acessar)

2
Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1
Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1
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Artigo 		Adicionar ao Meu Espaço

Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1

Gallagher,Anna-Rachel Ernie L Esquivel; Tiffany S Briere; Xin Tian; Michihiro Mitobe; Luis F Menezes; Glen S Markowitz; Dhanpat Jain; Luiz F Onuchic; Stefan Somlo

American Journal of Pathology New York v. 172, n. 2, p. 417-429, 2011

New York 2008

Acesso online. A biblioteca também possui exemplares impressos.

3
Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1
Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1
Material Type:
Artigo 		Adicionar ao Meu Espaço

Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1

Gallagher,Anna-Rachel Ernie L Esquivel; Tiffany S Briere; Xin Tian; Michihiro Mitobe; Luis F Menezes; Glen S Markowitz; Dhanpat Jain; Luiz F Onuchic; Stefan Somlo

American Journal of Pathology New York v. 172, n. 2, p. 417-429, 2011

New York 2008

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

  1. Esquivel, E
  2. Tian, X
  3. Somlo, S
  4. Jain, D
  5. Briere, T

Neste Assunto:

  1. Rim (Patologia)
  2. Cistos
  3. Doenças Hereditárias (Genética)
  4. Fibrose Cística
  5. Camundongos

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

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