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G Germino

Showing results (111-120 of 124) with videos related to

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Journal of the American Society of Nephrology : JASN|August 23, 2002
Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD geneYasuyuki Nagasawa, Sonja Matthiesen, Luiz F Onuchic, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2006
The mTOR pathway is regulated by polycystin-1, and its inhibition reverses renal cystogenesis in polycystic kidney diseaseJonathan M Shillingford, Noel S Murcia, Claire H Larson, et al.
Journal of the American Society of Nephrology : JASN|May 9, 2015
The Future of Polycystic Kidney Disease Research--As Seen By the 12 Kaplan AwardeesCorinne Antignac, James P Calvet, Gregory G Germino, et al.
Human Molecular Genetics|September 25, 2012
Polycystin-1 regulates the stability and ubiquitination of transcription factor Jade-1Rebecca L Foy, Vipul C Chitalia, Maria V Panchenko, et al.
Journal of the American Society of Nephrology : JASN|November 30, 1999
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney diseaseD M Reynolds, T Hayashi, Y Cai, et al.
Genomics|May 1, 1997
An integrated genetic and physical map of the autosomal recessive polycystic kidney disease regionX M Lens, L F Onuchic, G Wu, et al.
The Journal of Cell Biology|August 13, 2008
TRPP2 and TRPV4 form a polymodal sensory channel complexMichael Köttgen, Björn Buchholz, Miguel A Garcia-Gonzalez, et al.
American Journal of Human Genetics|March 19, 2002
PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeatsLuiz F Onuchic, Laszlo Furu, Yasuyuki Nagasawa, et al.
Human Mutation|April 27, 2004
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)Carsten Bergmann, Jan Senderek, Fabian Küpper, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2007
Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and functionPerciliz L Tan, Travis Barr, Peter N Inglis, et al.
Pageof 13

Showing results (111-120 of 124) with videos related to

Sort By:
Pageof 13
Journal of the American Society of Nephrology : JASN|August 23, 2002
Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD geneYasuyuki Nagasawa, Sonja Matthiesen, Luiz F Onuchic, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2006
The mTOR pathway is regulated by polycystin-1, and its inhibition reverses renal cystogenesis in polycystic kidney diseaseJonathan M Shillingford, Noel S Murcia, Claire H Larson, et al.
Journal of the American Society of Nephrology : JASN|May 9, 2015
The Future of Polycystic Kidney Disease Research--As Seen By the 12 Kaplan AwardeesCorinne Antignac, James P Calvet, Gregory G Germino, et al.
Human Molecular Genetics|September 25, 2012
Polycystin-1 regulates the stability and ubiquitination of transcription factor Jade-1Rebecca L Foy, Vipul C Chitalia, Maria V Panchenko, et al.
Journal of the American Society of Nephrology : JASN|November 30, 1999
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney diseaseD M Reynolds, T Hayashi, Y Cai, et al.
Genomics|May 1, 1997
An integrated genetic and physical map of the autosomal recessive polycystic kidney disease regionX M Lens, L F Onuchic, G Wu, et al.
The Journal of Cell Biology|August 13, 2008
TRPP2 and TRPV4 form a polymodal sensory channel complexMichael Köttgen, Björn Buchholz, Miguel A Garcia-Gonzalez, et al.
American Journal of Human Genetics|March 19, 2002
PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeatsLuiz F Onuchic, Laszlo Furu, Yasuyuki Nagasawa, et al.
Human Mutation|April 27, 2004
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)Carsten Bergmann, Jan Senderek, Fabian Küpper, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2007
Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and functionPerciliz L Tan, Travis Barr, Peter N Inglis, et al.
Pageof 13