E-LIB Suche - Ergebnisse für: Smith, Richard J. H.

1

Advancing Genetic Testing in Kidney Diseases: Report From a..:

Franceschini, Nora ; Feldman, David L. ; Berg, Jonathan S....
American Journal of Kidney Diseases. , 2024

Link: https://doi.org/10.1053/..

2

Renin and renin blockade have no role in complement activit:

Zhang, Yuzhou ; Martin, Bertha ; Spies, M. Ashley...
Kidney International. 105 (2024) 2 - p. 328-337 , 2024

Link: https://doi.org/10.1016/..

3

The role of complement in kidney disease: conclusions from ..:

Vivarelli, Marina ; Barratt, Jonathan ; Beck Jr., Laurence H....
Kidney International. , 2024

Link: https://doi.org/10.1016/..

4

Force Field X: A computational microscope to study genetic ..:

Gogal, Rose A. ; Nessler, Aaron J. ; Thiel, Andrew C....
The Journal of Chemical Physics. 161 (2024) 1 - p. , 2024

Link: https://doi.org/10.1063/..

5

WCN24-1146 SAFETY AND EFFICACY OF IPTACOPAN IN ADOLESCENT P..:

Webb, Nicholas ; Kavanagh, David ; Bomback, Andrew S....
Kidney International Reports. 9 (2024) 4 - p. S116-S117 , 2024

Link: https://doi.org/10.1016/..

6

Defining Nephritic Factors as Diverse Drivers of Systemic C..:

Hauer, Jill J. ; Zhang, Yuzhou ; Goodfellow, Renee...
Kidney International Reports. 9 (2024) 2 - p. 464-477 , 2024

Link: https://doi.org/10.1016/..

7

Iptacopan in Idiopathic Immune Complex–Mediated Membranopro..:

Vivarelli, Marina ; Bomback, Andrew S. ; Meier, Matthias...
Kidney International Reports. 9 (2024) 1 - p. 64-72 , 2024

Link: https://doi.org/10.1016/..

8

Assessing variants of uncertain significance implicated in ..:

Tollefson, Mallory R. ; Gogal, Rose A. ; Weaver, A. Monique...
Human Genetics. 142 (2023) 6 - p. 819-834 , 2023

Link: https://doi.org/10.1007/..

9

Modeling C3 glomerulopathies: C3 convertase regulation on a..:

Pisarenka, Sofiya ; Meyer, Nicole C. ; Xiao, Xue...
Frontiers in Immunology. 13 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

10

Single-cell RNA-sequencing of stria vascularis cells in the..:

Koh, Jin-Young ; Affortit, Corentin ; Ranum, Paul T....
BMC Medical Genomics. 16 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

11

Is Genetic Testing Indicated in a Pediatric Patient with Un..:

Kocharyan, Armine ; Schaefer, Amanda M. ; Smith, Richard J. H..
The Laryngoscope. 133 (2023) 9 - p. 2042-2043 , 2023

Link: https://doi.org/10.1002/..

12

De novo variants are a common cause of genetic hearing loss:

Klimara, Miles J. ; Nishimura, Carla ; Wang, Donghong...
Genetics in Medicine. 24 (2022) 12 - p. 2555-2567 , 2022

Link: https://doi.org/10.1016/..

13

Complement Factor I Variants in Complement-Mediated Renal D..:

Zhang, Yuzhou ; Goodfellow, Renee X. ; Ghiringhelli Borsa, Nicolo...
Frontiers in Immunology. 13 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

14

International Pediatric Otolaryngology Group (IPOG) consens..:

Sidell, Douglas R. ; Meister, Kara D. ; de Alarcon, Alessandro...
International Journal of Pediatric Otorhinolaryngology. 161 (2022) - p. 111251 , 2022

Link: https://doi.org/10.1016/..

15

Improving Clinical Trials for Anticomplement Therapies in C..:

Bomback, Andrew S. ; Appel, Gerald B. ; Gipson, Debbie S....
American Journal of Kidney Diseases. 79 (2022) 4 - p. 570-581 , 2022

Link: https://doi.org/10.1053/..