Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Nature Genetics|July 16, 2002
Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)Katrin Hoffmann, Christine K Dreger, Ada L Olins, et al.
Circulation|August 4, 2011
Pilot study of extracorporeal removal of soluble fms-like tyrosine kinase 1 in preeclampsiaRavi Thadhani, Tuelay Kisner, Henning Hagmann, et al.
Clinical Kidney Journal|July 2, 2026
Clinical impact of genetic testing in inherited kidney diseasesLea M Merz, Sarah Stopp, Ilona Krey, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 20, 2024
Deceased donor urinary Dickkopf-3 associates with future allograft function following kidney transplantationJonathan de Fallois, Anna Günzel, Christoph Daniel, et al.
American Journal of Human Genetics|July 19, 2011
Faulty initiation of proteoglycan synthesis causes cardiac and joint defectsSevjidmaa Baasanjav, Lihadh Al-Gazali, Taishi Hashiguchi, et al.
Vaccines|July 27, 2024
Hybrid Immunity Protects against Antibody Fading after SARS-CoV-2mRNA Vaccination in Kidney Transplant Recipients, Dialysis Patients, and Medical Personnel: 9 Months Data from the Prospective, Observational Dia-Vacc StudyJulian Stumpf, Torsten Siepmann, Jörg Schwöbel, et al.
Kidney International Reports|June 9, 2025
<i>COL4A5</i>-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome PhenotypeBastian M Krüger, Annika Jens, Anna Neuhaus, et al.
American Journal of Human Genetics|August 5, 2008
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndromeVincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, et al.
Pageof 4