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Human Mutation|August 3, 2000
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutationsN Bogdanova, M McCluskey, K Sikmann, et al.Nanotechnology|October 6, 2009
Use of self-actuating and self-sensing cantilevers for imaging biological samples in fluidG E Fantner, W Schumann, R J Barbero, et al.Neoplasma|January 1, 1986
The results of clinical trial within the framework of CMEA on surgical methods of mammary gland carcinoma treatmentV V Vishnyakova, S Kirov, V Todorov, et al.Folia Medica|July 1, 2021
L3 rootlet recurrent melanocytic schwannoma - case report and literature reviewGeorgi K Georgiev, Ivan V Todorov, Todor P Shamov, et al.Molecular Metabolism|December 10, 2025
Sustained diabetes remission induced by FGF1 involves a shift in transcriptionally distinct AgRP neuron subpopulationsNadia N Aalling, Petar V Todorov, Shad Hassan, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 26, 2001
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney diseaseT Schiavello, V Burke, N Bogdanova, et al.Nature Human Behaviour|August 24, 2021
Genetic analysis of dietary intake identifies new loci and functional links with metabolic traitsJordi Merino, Hassan S Dashti, Chloé Sarnowski, et al.Nature Genetics|September 7, 2023
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratificationVasiliki Lagou, Longda Jiang, Anna Ulrich, et al.Pageof 4