Search research articles
Contact Us
Filters
Showing results (41-50 of 56) with videos related to
Page
of 6
Sort By:
Pediatric Nephrology (Berlin, Germany)
|
September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families
Dalia Pantel, Nils D Mertens, Ronen Schneider, et al.
Leukemia
|
December 19, 2008
The candidate immunotherapeutical target, the receptor for hyaluronic acid-mediated motility, is associated with proliferation and shows prognostic value in B-cell chronic lymphocytic leukemia
K Giannopoulos, D Mertens, A Bühler, et al.
American Journal of Medical Genetics. Part A
|
January 24, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract
Caroline M Kolvenbach, Bixia Zheng, Lea M Merz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
April 10, 2022
Assessing the dynamic changes in vitiligo: reliability and validity of the Vitiligo Disease Activity Score (VDAS) and Vitiligo Disease Improvement Score (VDIS)
N van Geel, L Depaepe, V Vandaele, et al.
Deutsche Medizinische Wochenschrift (1946)
|
December 10, 2014
[Quality of life in pulmonal arterial hypertension and in chronic thromboembolic pulmonary hypertension]
M Halank, R Speich, D Petkova, et al.
Plos One
|
December 19, 2013
From knock-out phenotype to three-dimensional structure of a promising antibiotic target from Streptococcus pneumoniae
Con Dogovski, Michael A Gorman, Natalia E Ketaren, et al.
Scientific Reports
|
July 10, 2024
Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type
Katharina Lemberg, Nils D Mertens, Kirollos Yousef, et al.
American Journal of Physiology. Renal Physiology
|
March 14, 2024
Quantitative phenotyping of <i>Nphs1</i> knockout mice as a prerequisite for gene replacement studies
Florian Buerger, Lea M Merz, Ken Saida, et al.
Journal of Nephrology
|
August 8, 2024
Correction to: Phenotypic quantification of Nphs1‑deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of Nephrology
|
July 14, 2024
Phenotypic quantification of Nphs1-deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 56) with videos related to
Sort By:
Page
of 6
Pediatric Nephrology (Berlin, Germany)
|
September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families
Dalia Pantel, Nils D Mertens, Ronen Schneider, et al.
Leukemia
|
December 19, 2008
The candidate immunotherapeutical target, the receptor for hyaluronic acid-mediated motility, is associated with proliferation and shows prognostic value in B-cell chronic lymphocytic leukemia
K Giannopoulos, D Mertens, A Bühler, et al.
American Journal of Medical Genetics. Part A
|
January 24, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract
Caroline M Kolvenbach, Bixia Zheng, Lea M Merz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
April 10, 2022
Assessing the dynamic changes in vitiligo: reliability and validity of the Vitiligo Disease Activity Score (VDAS) and Vitiligo Disease Improvement Score (VDIS)
N van Geel, L Depaepe, V Vandaele, et al.
Deutsche Medizinische Wochenschrift (1946)
|
December 10, 2014
[Quality of life in pulmonal arterial hypertension and in chronic thromboembolic pulmonary hypertension]
M Halank, R Speich, D Petkova, et al.
Plos One
|
December 19, 2013
From knock-out phenotype to three-dimensional structure of a promising antibiotic target from Streptococcus pneumoniae
Con Dogovski, Michael A Gorman, Natalia E Ketaren, et al.
Scientific Reports
|
July 10, 2024
Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type
Katharina Lemberg, Nils D Mertens, Kirollos Yousef, et al.
American Journal of Physiology. Renal Physiology
|
March 14, 2024
Quantitative phenotyping of <i>Nphs1</i> knockout mice as a prerequisite for gene replacement studies
Florian Buerger, Lea M Merz, Ken Saida, et al.
Journal of Nephrology
|
August 8, 2024
Correction to: Phenotypic quantification of Nphs1‑deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Journal of Nephrology
|
July 14, 2024
Phenotypic quantification of Nphs1-deficient mice
Ronen Schneider, Bshara Mansour, Caroline M Kolvenbach, et al.
Page
of 6