A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6 (1999)
- Authors:
- Autor USP: ONUCHIC, LUIZ FERNANDO - FM
- Unidade: FM
- Subjects: GENÉTICA; GENÉTICA
- Language: Inglês
- Source:
-
ABNT
PARK, Jong Hoon et al. A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics, v. 57, p. 249-255, 1999Tradução . . Acesso em: 11 jan. 2026. -
APA
Park, J. H., Dixit, M. P., Onuchic, L. F., Wu, G., Goncharuk, A. N., Kneitz, S., et al. (1999). A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics, 57, 249-255. -
NLM
Park JH, Dixit MP, Onuchic LF, Wu G, Goncharuk AN, Kneitz S, Santarine LB, Hayashi T, Avner ED, Guay-Woodford L, Zerres K, Germino GG, Somlo S. A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics. 1999 ; 57 249-255.[citado 2026 jan. 11 ] -
Vancouver
Park JH, Dixit MP, Onuchic LF, Wu G, Goncharuk AN, Kneitz S, Santarine LB, Hayashi T, Avner ED, Guay-Woodford L, Zerres K, Germino GG, Somlo S. A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6. Genomics. 1999 ; 57 249-255.[citado 2026 jan. 11 ] - Expression of polyductin, the PKHD1 gene product, during normal and abnormal fetal development of the intrahepatic billiary sytem, billiary atresia, paucity of the intrahepatic biliary system and liver tumors
- Polyductin undergoes notch-like processing and regulated release from primary cilia
- Molecular and cellular pathogenesis of autosomal recessive polycystic kidney disease
- Haploinsufficiency for PKD1 results in increased tubularization of the bowman´s capsule and overexpression of COX-2
- Development of in vitro espression system of autosomal ressive polycystic kidney disease responsible gene (PKIID1) product, polydutin
- Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD)
- Dendrogram Analyses of Relative Expression Between Bladder Cancers and Controls Identify PTEN-HIF1α Association as an Alteration Characteristic of Malignancy
- Infundibular stenosis in Bardet–Biedl syndrome
- Clinical aspects of autosomal recessive polycystic kidney disease
- Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
