Results
|
61.
|
A Pkd1-Fbn1 genetic interaction implicates TGF-β signaling in the pathogenesis of vascular complications in autosomal dominant polycystic kidney disease. [electronic resource] by
- Liu, Dongyan
- Wang, Connie J
- Judge, Daniel P
- Halushka, Marc K
- Ni, Jie
- Habashi, Jennifer P
- Moslehi, Javid
- Bedja, Djahida
- Gabrielson, Kathleen L
- Xu, Hangxue
- Qian, Feng
- Huso, David
- Dietz, Harry C
- Germino, Gregory G
- Watnick, Terry
Producer: 20140225
In:
Journal of the American Society of Nephrology : JASN vol. 25
Availability: No items available.
|
|
62.
|
The mTOR pathway is regulated by polycystin-1, and its inhibition reverses renal cystogenesis in polycystic kidney disease. [electronic resource] by
- Shillingford, Jonathan M
- Murcia, Noel S
- Larson, Claire H
- Low, Seng Hui
- Hedgepeth, Ryan
- Brown, Nicole
- Flask, Chris A
- Novick, Andrew C
- Goldfarb, David A
- Kramer-Zucker, Albrecht
- Walz, Gerd
- Piontek, Klaus B
- Germino, Gregory G
- Weimbs, Thomas
Producer: 20060606
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 103
Availability: No items available.
|
|
63.
|
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 repeats. [electronic resource] by
- Onuchic, Luiz F
- Furu, Laszlo
- Nagasawa, Yasuyuki
- Hou, Xiaoying
- Eggermann, Thomas
- Ren, Zhiyong
- Bergmann, Carsten
- Senderek, Jan
- Esquivel, Ernie
- Zeltner, Raoul
- Rudnik-Schöneborn, Sabine
- Mrug, Michael
- Sweeney, William
- Avner, Ellis D
- Zerres, Klaus
- Guay-Woodford, Lisa M
- Somlo, Stefan
- Germino, Gregory G
Producer: 20020523
In:
American journal of human genetics vol. 70
Availability: No items available.
|
|
64.
|
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). [electronic resource] by
- Bergmann, Carsten
- Senderek, Jan
- Küpper, Fabian
- Schneider, Frank
- Dornia, Christian
- Windelen, Ellen
- Eggermann, Thomas
- Rudnik-Schöneborn, Sabine
- Kirfel, Jutta
- Furu, Laszlo
- Onuchic, Luiz F
- Rossetti, Sandro
- Harris, Peter C
- Somlo, Stefan
- Guay-Woodford, Lisa
- Germino, Gregory G
- Moser, Markus
- Büttner, Reinhard
- Zerres, Klaus
Producer: 20040917
In:
Human mutation vol. 23
Availability: No items available.
|
|
65.
|
TRPP2 and TRPV4 form a polymodal sensory channel complex. [electronic resource] by
- Köttgen, Michael
- Buchholz, Björn
- Garcia-Gonzalez, Miguel A
- Kotsis, Fruzsina
- Fu, Xiao
- Doerken, Mara
- Boehlke, Christopher
- Steffl, Daniel
- Tauber, Robert
- Wegierski, Tomasz
- Nitschke, Roland
- Suzuki, Makoto
- Kramer-Zucker, Albrecht
- Germino, Gregory G
- Watnick, Terry
- Prenen, Jean
- Nilius, Bernd
- Kuehn, E Wolfgang
- Walz, Gerd
Producer: 20080905
In:
The Journal of cell biology vol. 182
Availability: No items available.
|
|
66.
|
Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function. [electronic resource] by
- Tan, Perciliz L
- Barr, Travis
- Inglis, Peter N
- Mitsuma, Norimasa
- Huang, Susan M
- Garcia-Gonzalez, Miguel A
- Bradley, Brian A
- Coforio, Stephanie
- Albrecht, Phillip J
- Watnick, Terry
- Germino, Gregory G
- Beales, Philip L
- Caterina, Michael J
- Leroux, Michel R
- Rice, Frank L
- Katsanis, Nicholas
Producer: 20071227
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 104
Availability: No items available.
|
|
67.
|
A cleavage product of Polycystin-1 is a mitochondrial matrix protein that affects mitochondria morphology and function when heterologously expressed. [electronic resource] by
- Lin, Cheng-Chao
- Kurashige, Mahiro
- Liu, Yi
- Terabayashi, Takeshi
- Ishimoto, Yu
- Wang, Tanchun
- Choudhary, Vineet
- Hobbs, Ryan
- Liu, Li-Ka
- Lee, Ping-Hsien
- Outeda, Patricia
- Zhou, Fang
- Restifo, Nicholas P
- Watnick, Terry
- Kawano, Haruna
- Horie, Shigeo
- Prinz, William
- Xu, Hong
- Menezes, Luis F
- Germino, Gregory G
Producer: 20190920
In:
Scientific reports vol. 8
Availability: No items available.
|
|
68.
|
NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology. [electronic resource] by
- Kaimori, Jun-Ya
- Lin, Cheng-Chao
- Outeda, Patricia
- Garcia-Gonzalez, Miguel A
- Menezes, Luis F
- Hartung, Erum A
- Li, Ao
- Wu, Guanqing
- Fujita, Hideaki
- Sato, Yasunori
- Nakanuma, Yasuni
- Yamamoto, Satoko
- Ichimaru, Naotsugu
- Takahara, Shiro
- Isaka, Yoshitaka
- Watnick, Terry
- Onuchic, Luiz F
- Guay-Woodford, Lisa M
- Germino, Gregory G
Producer: 20190225
In:
Scientific reports vol. 7
Availability: No items available.
|
|
69.
|
Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference. [electronic resource] by
- Gunay-Aygun, Meral
- Avner, Ellis D
- Bacallao, Robert L
- Choyke, Peter L
- Flynn, Joseph T
- Germino, Gregory G
- Guay-Woodford, Lisa
- Harris, Peter
- Heller, Theo
- Ingelfinger, Julie
- Kaskel, Frederick
- Kleta, Robert
- LaRusso, Nicholas F
- Mohan, Parvathi
- Pazour, Gregory J
- Shneider, Benjamin L
- Torres, Vicente E
- Wilson, Patricia
- Zak, Colleen
- Zhou, Jing
- Gahl, William A
Producer: 20060907
In:
The Journal of pediatrics vol. 149
Availability: No items available.
|
|
70.
|
Multiple-laboratory comparison of microarray platforms. [electronic resource] by
- Irizarry, Rafael A
- Warren, Daniel
- Spencer, Forrest
- Kim, Irene F
- Biswal, Shyam
- Frank, Bryan C
- Gabrielson, Edward
- Garcia, Joe G N
- Geoghegan, Joel
- Germino, Gregory
- Griffin, Constance
- Hilmer, Sara C
- Hoffman, Eric
- Jedlicka, Anne E
- Kawasaki, Ernest
- Martínez-Murillo, Francisco
- Morsberger, Laura
- Lee, Hannah
- Petersen, David
- Quackenbush, John
- Scott, Alan
- Wilson, Michael
- Yang, Yanqin
- Ye, Shui Qing
- Yu, Wayne
Producer: 20050516
In:
Nature methods vol. 2
Availability: No items available.
|