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Human Mutation|December 14, 2007
Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencingEdgar A Otto, Juliana Helou, Susan J Allen, et al.Cancer Chemotherapy and Pharmacology|November 13, 2023
Relative bioavailability of fedratinib through various alternative oral administration methods in healthy adultsYizhe Chen, David Wyatt, Massimo Attanasio, et al.JCI Insight|May 14, 2021
Loss of diacylglycerol kinase ε causes thrombotic microangiopathy by impairing endothelial VEGFA signalingDingxiao Liu, Qiong Ding, Dao-Fu Dai, et al.American Journal of Physiology. Renal Physiology|August 21, 2015
Hedgehog signaling indirectly affects tubular cell survival after obstructive kidney injuryAlysha A Rauhauser, Chongyu Ren, Dongmei Lu, et al.Scientific Reports|April 23, 2021
Detection of pro angiogenic and inflammatory biomarkers in patients with CKDDiana Jalal, Bridget Sanford, Brandon Renner, et al.Human Genetics|June 2, 2006
Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharingMatthias T F Wolf, Bettina E Mucha, Hans C Hennies, et al.European Journal of Internal Medicine|June 24, 2018
β-Thalassemia heterozygote state detrimentally affects health expectationLuciano Graffeo, Angela Vitrano, Salvatore Scondotto, et al.BMC Oral Health|February 4, 2023
MRONJ in breast cancer patients under bone modifying agents for cancer treatment-induced bone loss (CTIBL): a multi-hospital-based case seriesRodolfo Mauceri, Martina Coppini, Massimo Attanasio, et al.Redox Biology|October 9, 2018
Persistent increase in mitochondrial superoxide mediates cisplatin-induced chronic kidney diseaseKranti A Mapuskar, Hsiang Wen, Danniele G Holanda, et al.Journal of Medical Genetics|July 10, 2007
Mutation analysis of NPHP6/CEP290 in patients with Joubert syndrome and Senior-Løken syndromeJuliana Helou, Edgar A Otto, Massimo Attanasio, et al.Pageof 7