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Ramadevi

Showing results (251-260 of 258) with videos related to

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Journal of Medical Genetics|June 21, 2015
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneityR Bachmann-Gagescu, J C Dempsey, I G Phelps, et al.
Molecular & Cellular Proteomics : MCP|February 14, 2016
Bacterial Interactomes: Interacting Protein Partners Share Similar Function and Are Validated in Independent Assays More Frequently Than Previously ReportedMaxim Shatsky, Simon Allen, Barbara L Gold, et al.
Journal of the American Chemical Society|February 18, 2020
Two Distinct Mechanisms of Inhibition of LpxA Acyltransferase Essential for Lipopolysaccharide BiosynthesisWooseok Han, Xiaolei Ma, Carl J Balibar, et al.
European Journal of Human Genetics : EJHG|March 26, 2015
Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in ItalyMartina Nemethova, Jan Radvanszky, Ludevit Kadasi, et al.
Bioorganic & Medicinal Chemistry Letters|January 17, 2018
Optimization of novel monobactams with activity against carbapenem-resistant Enterobacteriaceae - Identification of LYS228Folkert Reck, Alun Bermingham, Johanne Blais, et al.
JCO Global Oncology|November 19, 2025
Practice Patterns and Outcomes in Advanced Colorectal Cancers From a Multi-Institutional Analysis: Real-World Evidence From IndiaAnant Ramaswamy, Ramjas Prajapati, Vivek Agarwala, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosisSonja A de Munnik, Louise S Bicknell, Salim Aftimos, et al.
American Journal of Medical Genetics. Part A|October 2, 2012
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorderSonja A de Munnik, Barto J Otten, Jeroen Schoots, et al.
Pageof 26

Showing results (251-260 of 258) with videos related to

Sort By:
Pageof 26
You have reached the last page of results.This site can display upto 258 results.
Journal of Medical Genetics|June 21, 2015
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneityR Bachmann-Gagescu, J C Dempsey, I G Phelps, et al.
Molecular & Cellular Proteomics : MCP|February 14, 2016
Bacterial Interactomes: Interacting Protein Partners Share Similar Function and Are Validated in Independent Assays More Frequently Than Previously ReportedMaxim Shatsky, Simon Allen, Barbara L Gold, et al.
Journal of the American Chemical Society|February 18, 2020
Two Distinct Mechanisms of Inhibition of LpxA Acyltransferase Essential for Lipopolysaccharide BiosynthesisWooseok Han, Xiaolei Ma, Carl J Balibar, et al.
European Journal of Human Genetics : EJHG|March 26, 2015
Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in ItalyMartina Nemethova, Jan Radvanszky, Ludevit Kadasi, et al.
Bioorganic & Medicinal Chemistry Letters|January 17, 2018
Optimization of novel monobactams with activity against carbapenem-resistant Enterobacteriaceae - Identification of LYS228Folkert Reck, Alun Bermingham, Johanne Blais, et al.
JCO Global Oncology|November 19, 2025
Practice Patterns and Outcomes in Advanced Colorectal Cancers From a Multi-Institutional Analysis: Real-World Evidence From IndiaAnant Ramaswamy, Ramjas Prajapati, Vivek Agarwala, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosisSonja A de Munnik, Louise S Bicknell, Salim Aftimos, et al.
American Journal of Medical Genetics. Part A|October 2, 2012
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorderSonja A de Munnik, Barto J Otten, Jeroen Schoots, et al.
Pageof 26