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G Germino

Showing results (71-80 of 124) with videos related to

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Genomics|May 1, 1992
Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markersS Somlo, B Wirth, G G Germino, et al.
Lancet (London, England)|July 2, 1988
A second genetic locus for autosomal dominant polycystic kidney diseaseG Romeo, M Devoto, G Costa, et al.
American Journal of Human Genetics|May 1, 1990
Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16G G Germino, N J Barton, J Lamb, et al.
Kidney International|March 11, 2011
T-cell factor/β-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney diseaseMichelle M Miller, Diana M Iglesias, Zhao Zhang, et al.
Kidney International|January 16, 2009
Inactivation of Pkd1 in principal cells causes a more severe cystic kidney disease than in intercalated cellsKalani L Raphael, Kevin A Strait, Peter K Stricklett, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Studies of mice with a large deletion of the ARPKD-associated <i>Pkhd1</i> locus likely explain its GWAS association with glaucoma in humansYu Ishimoto, Luis F Menezes, Naoki Nakaya, et al.
Journal of the American Society of Nephrology : JASN|October 17, 2009
Pkd1 haploinsufficiency increases renal damage and induces microcyst formation following ischemia/reperfusionAna P Bastos, Klaus Piontek, Ana M Silva, et al.
American Journal of Human Genetics|January 13, 2001
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney diseaseY Pei, A D Paterson, K R Wang, et al.
Human Molecular Genetics|September 1, 1997
An unusual pattern of mutation in the duplicated portion of PKD1 is revealed by use of a novel strategy for mutation detectionT J Watnick, K B Piontek, T M Cordal, et al.
Journal of Medical Genetics|April 5, 2005
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohortsA M Sharp, L M Messiaen, G Page, et al.
Pageof 13

Showing results (71-80 of 124) with videos related to

Sort By:
Pageof 13
Genomics|May 1, 1992
Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markersS Somlo, B Wirth, G G Germino, et al.
Lancet (London, England)|July 2, 1988
A second genetic locus for autosomal dominant polycystic kidney diseaseG Romeo, M Devoto, G Costa, et al.
American Journal of Human Genetics|May 1, 1990
Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16G G Germino, N J Barton, J Lamb, et al.
Kidney International|March 11, 2011
T-cell factor/β-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney diseaseMichelle M Miller, Diana M Iglesias, Zhao Zhang, et al.
Kidney International|January 16, 2009
Inactivation of Pkd1 in principal cells causes a more severe cystic kidney disease than in intercalated cellsKalani L Raphael, Kevin A Strait, Peter K Stricklett, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Studies of mice with a large deletion of the ARPKD-associated <i>Pkhd1</i> locus likely explain its GWAS association with glaucoma in humansYu Ishimoto, Luis F Menezes, Naoki Nakaya, et al.
Journal of the American Society of Nephrology : JASN|October 17, 2009
Pkd1 haploinsufficiency increases renal damage and induces microcyst formation following ischemia/reperfusionAna P Bastos, Klaus Piontek, Ana M Silva, et al.
American Journal of Human Genetics|January 13, 2001
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney diseaseY Pei, A D Paterson, K R Wang, et al.
Human Molecular Genetics|September 1, 1997
An unusual pattern of mutation in the duplicated portion of PKD1 is revealed by use of a novel strategy for mutation detectionT J Watnick, K B Piontek, T M Cordal, et al.
Journal of Medical Genetics|April 5, 2005
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohortsA M Sharp, L M Messiaen, G Page, et al.
Pageof 13