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Parkinson'S Disease|September 9, 2015
Plasma Prolidase Activity and Oxidative Stress in Patients with Parkinson's DiseaseAkhilesh Kumar Verma, Janak Raj, Vivek Sharma, et al.
Dental Research Journal|July 24, 2013
Analysis of the immunoexpression of Ki-67 and Bcl-2 in the pericoronal tissues of impacted teeth, dentigerous cysts and gingiva using software image analysisFarzan Rahman, Akshay Bhargava, Shoaib R Tippu, et al.
Biochemistry Research International|October 3, 2014
Serum prolidase activity and oxidative stress in diabetic nephropathy and end stage renal disease: a correlative study with glucose and creatinineAkhilesh Kumar Verma, Subhash Chandra, Rana Gopal Singh, et al.
Clinical Kidney Journal|August 8, 2015
Successful treatment of hypercalcaemia associated with a CYP24A1 mutation with fluconazoleJudith Sayers, Ann Marie Hynes, Shalabh Srivastava, et al.
Frontiers in Nephrology|September 7, 2023
Outcomes from the Northeast England cohort of autosomal dominant polycystic kidney disease (ADPKD) patients on tolvaptanEleftherios Gkekas, Tsz Yau Tiffany Tang, Alan Green, et al.
Biological Trace Element Research|September 15, 2015
Prolidase-Associated Trace Elements (Mn, Zn, Co, and Ni) in the Patients with Parkinson's DiseaseAkhilesh Kumar Verma, Anand Kumar Keshari, Janak Raj, et al.
Human Molecular Genetics|October 4, 2017
A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapiesShalabh Srivastava, Simon A Ramsbottom, Elisa Molinari, et al.
Physiological Reports|January 9, 2014
Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicityShalabh Srivastava, Dimin Li, Noel Edwards, et al.
Scientific Reports|July 27, 2019
Targeted exon skipping rescues ciliary protein composition defects in Joubert syndrome patient fibroblastsElisa Molinari, Simon A Ramsbottom, Shalabh Srivastava, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 18, 2018
Targeted exon skipping of a CEP290 mutation rescues Joubert syndrome phenotypes in vitro and in a murine modelSimon A Ramsbottom, Elisa Molinari, Shalabh Srivastava, et al.
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