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Endothelial expression of PD-L1 and PD-L2 down-regulates CD8+ T cell activation and cytolysis. [electronic resource] by
- Rodig, Nancy
- Ryan, Timothy
- Allen, Jessica A
- Pang, Hong
- Grabie, Nir
- Chernova, Tatyana
- Greenfield, Edward A
- Liang, Spencer C
- Sharpe, Arlene H
- Lichtman, Andrew H
- Freeman, Gordon J
Producer: 20031218
In:
European journal of immunology vol. 33
Availability: No items available.
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15.
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New England BK consortium: Regional survey of BK screening and management protocols in comparison to published consensus guidelines. [electronic resource] by
- Gabardi, Steven
- Pavlakis, Martha
- Tan, Chen
- Francis, Jean
- Cardarelli, Francesca
- Asch, William
- Bodziak, Kenneth
- Chobanian, Michael
- Gilligan, Hannah
- Gohh, Reginald
- Kung, Shiang-Cheng
- Inker, Lesley
- Martin, Spencer
- Rodig, Nancy
- Rossi, Ana
- Chandraker, Anil
Producer: 20190111
In:
Transplant infectious disease : an official journal of the Transplantation Society vol. 20
Availability: No items available.
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16.
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Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. [electronic resource] by
- Tan, Weizhen
- Lovric, Svjetlana
- Ashraf, Shazia
- Rao, Jia
- Schapiro, David
- Airik, Merlin
- Shril, Shirlee
- Gee, Heon Yung
- Baum, Michelle
- Daouk, Ghaleb
- Ferguson, Michael A
- Rodig, Nancy
- Somers, Michael J G
- Stein, Deborah R
- Vivante, Asaf
- Warejko, Jillian K
- Widmeier, Eugen
- Hildebrandt, Friedhelm
Producer: 20190107
In:
Pediatric nephrology (Berlin, Germany) vol. 33
Availability: No items available.
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17.
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Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome. [electronic resource] by
- Warejko, Jillian K
- Schueler, Markus
- Vivante, Asaf
- Tan, Weizhen
- Daga, Ankana
- Lawson, Jennifer A
- Braun, Daniela A
- Shril, Shirlee
- Amann, Kassaundra
- Somers, Michael J G
- Rodig, Nancy M
- Baum, Michelle A
- Daouk, Ghaleb
- Traum, Avram Z
- Kim, Heung Bae
- Vakili, Khashayar
- Porras, Diego
- Lock, James
- Rivkin, Michael J
- Chaudry, Gulraiz
- Smoot, Leslie B
- Singh, Michael N
- Smith, Edward R
- Mane, Shrikant M
- Lifton, Richard P
- Stein, Deborah R
- Ferguson, Michael A
- Hildebrandt, Friedhelm
Producer: 20190123
In:
Hypertension (Dallas, Tex. : 1979) vol. 71
Availability: No items available.
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18.
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Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. [electronic resource] by
- Mann, Nina
- Braun, Daniela A
- Amann, Kassaundra
- Tan, Weizhen
- Shril, Shirlee
- Connaughton, Dervla M
- Nakayama, Makiko
- Schneider, Ronen
- Kitzler, Thomas M
- van der Ven, Amelie T
- Chen, Jing
- Ityel, Hadas
- Vivante, Asaf
- Majmundar, Amar J
- Daga, Ankana
- Warejko, Jillian K
- Lovric, Svjetlana
- Ashraf, Shazia
- Jobst-Schwan, Tilman
- Widmeier, Eugen
- Hugo, Hannah
- Mane, Shrikant M
- Spaneas, Leslie
- Somers, Michael J G
- Ferguson, Michael A
- Traum, Avram Z
- Stein, Deborah R
- Baum, Michelle A
- Daouk, Ghaleb H
- Lifton, Richard P
- Manzi, Shannon
- Vakili, Khashayar
- Kim, Heung Bae
- Rodig, Nancy M
- Hildebrandt, Friedhelm
Producer: 20191104
In:
Journal of the American Society of Nephrology : JASN vol. 30
Availability: No items available.
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19.
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Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. [electronic resource] by
- Daga, Ankana
- Majmundar, Amar J
- Braun, Daniela A
- Gee, Heon Yung
- Lawson, Jennifer A
- Shril, Shirlee
- Jobst-Schwan, Tilman
- Vivante, Asaf
- Schapiro, David
- Tan, Weizhen
- Warejko, Jillian K
- Widmeier, Eugen
- Nelson, Caleb P
- Fathy, Hanan M
- Gucev, Zoran
- Soliman, Neveen A
- Hashmi, Seema
- Halbritter, Jan
- Halty, Margarita
- Kari, Jameela A
- El-Desoky, Sherif
- Ferguson, Michael A
- Somers, Michael J G
- Traum, Avram Z
- Stein, Deborah R
- Daouk, Ghaleb H
- Rodig, Nancy M
- Katz, Avi
- Hanna, Christian
- Schwaderer, Andrew L
- Sayer, John A
- Wassner, Ari J
- Mane, Shrikant
- Lifton, Richard P
- Milosevic, Danko
- Tasic, Velibor
- Baum, Michelle A
- Hildebrandt, Friedhelm
Producer: 20181211
In:
Kidney international vol. 93
Availability: No items available.
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20.
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Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database. [electronic resource] by
- Bower, Matthew
- Salomon, Rémi
- Allanson, Judith
- Antignac, Corinne
- Benedicenti, Francesco
- Benetti, Elisa
- Binenbaum, Gil
- Jensen, Uffe B
- Cochat, Pierre
- DeCramer, Stephane
- Dixon, Joanne
- Drouin, Regen
- Falk, Marni J
- Feret, Holly
- Gise, Robert
- Hunter, Alasdair
- Johnson, Kisha
- Kumar, Rajiv
- Lavocat, Marie Pierre
- Martin, Laura
- Morinière, Vincent
- Mowat, David
- Murer, Luisa
- Nguyen, Hiep T
- Peretz-Amit, Gabriela
- Pierce, Eric
- Place, Emily
- Rodig, Nancy
- Salerno, Ann
- Sastry, Sujatha
- Sato, Tadashi
- Sayer, John A
- Schaafsma, Gerard C P
- Shoemaker, Lawrence
- Stockton, David W
- Tan, Wen-Hann
- Tenconi, Romano
- Vanhille, Philippe
- Vats, Abhay
- Wang, Xinjing
- Warman, Berta
- Weleber, Richard G
- White, Susan M
- Wilson-Brackett, Carolyn
- Zand, Dina J
- Eccles, Michael
- Schimmenti, Lisa A
- Heidet, Laurence
Producer: 20120608
In:
Human mutation vol. 33
Availability: No items available.
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