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The Journal of Pathology
|
November 25, 2024
Proteomic analysis of non-muscle invasive and muscle invasive bladder cancer highlights distinct subgroups with metabolic, matrisomal, and immune hallmarks and emphasizes importance of the stromal compartment
Thien-Ly Julia Dinh, Manuel Rogg, Miguel Cosenza-Contreras, et al.
Human Genetics
|
June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract
Daw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
American Journal of Human Genetics
|
April 9, 2022
Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations
John Devane, Elisabeth Ott, Eric G Olinger, et al.
The Journal of Clinical Investigation
|
April 4, 2023
Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy
Fabian Braun, Ahmed Abed, Dominik Sellung, et al.
The Journal of Experimental Medicine
|
May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
JCI Insight
|
May 20, 2025
Loss of genome maintenance is linked to mTORC1 signaling and accelerates podocyte damage
Fabian Braun, Amrei M Mandel, Linda Blomberg, et al.
The Journal of Experimental Medicine
|
May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
Nature Genetics
|
June 25, 2013
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3
Sylvia Hoff, Jan Halbritter, Daniel Epting, et al.
Cancer Cell
|
February 11, 2025
Adiponectin reduces immune checkpoint inhibitor-induced inflammation without blocking anti-tumor immunity
Lukas M Braun, Sophie Giesler, Geoffroy Andrieux, et al.
Kidney International
|
December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
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Search research articles
Search
Showing results (71-80 of 80) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 80 results.
The Journal of Pathology
|
November 25, 2024
Proteomic analysis of non-muscle invasive and muscle invasive bladder cancer highlights distinct subgroups with metabolic, matrisomal, and immune hallmarks and emphasizes importance of the stromal compartment
Thien-Ly Julia Dinh, Manuel Rogg, Miguel Cosenza-Contreras, et al.
Human Genetics
|
June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract
Daw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
American Journal of Human Genetics
|
April 9, 2022
Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations
John Devane, Elisabeth Ott, Eric G Olinger, et al.
The Journal of Clinical Investigation
|
April 4, 2023
Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy
Fabian Braun, Ahmed Abed, Dominik Sellung, et al.
The Journal of Experimental Medicine
|
May 21, 2024
Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
JCI Insight
|
May 20, 2025
Loss of genome maintenance is linked to mTORC1 signaling and accelerates podocyte damage
Fabian Braun, Amrei M Mandel, Linda Blomberg, et al.
The Journal of Experimental Medicine
|
May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.
Nature Genetics
|
June 25, 2013
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3
Sylvia Hoff, Jan Halbritter, Daniel Epting, et al.
Cancer Cell
|
February 11, 2025
Adiponectin reduces immune checkpoint inhibitor-induced inflammation without blocking anti-tumor immunity
Lukas M Braun, Sophie Giesler, Geoffroy Andrieux, et al.
Kidney International
|
December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
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of 8