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Frank Baas

Showing results (121-130 of 231) with videos related to

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Acta Neuropathologica|November 14, 2009
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNPCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Genes, Chromosomes & Cancer|January 23, 2016
Type 1 papillary renal cell carcinoma in a patient with schwannomatosis: Mosaic versus loss of SMARCB1 expression in respectively schwannoma and renal tumor cellsTheo J M Hulsebos, Susan Kenter, Frank Baas, et al.
Diabetologia|February 10, 2019
Diurnal rhythms in the white adipose tissue transcriptome are disturbed in obese individuals with type 2 diabetes compared with lean control individualsDirk Jan Stenvers, Aldo Jongejan, Sadaf Atiqi, et al.
The Journal of Infection|October 17, 2012
Common polymorphisms in the complement system and susceptiblity to bacterial meningitisKirsten S Adriani, Matthijs C Brouwer, Madelijn Geldhoff, et al.
Human Genetics|January 11, 2003
Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotypeValérie Biancalana, Olivier Caron, Sabina Gallati, et al.
Molecular Biosystems|June 23, 2010
Utilization of unlocked nucleic acid (UNA) to enhance siRNA performance in vitro and in vivoMaria B Laursen, Malgorzata M Pakula, Shan Gao, et al.
Frontiers in Cellular Neuroscience|August 24, 2023
Corrigendum: Ldlr-/-.Leiden mice develop neurodegeneration, age-dependent astrogliosis and obesity-induced changes in microglia immunophenotype which are partly reversed by complement component 5 neutralizing antibodyFlorine Seidel, Kees Fluiter, Robert Kleemann, et al.
Hepatology (Baltimore, Md.)|January 10, 2013
Immunoglobulin G4+ clones identified by next-generation sequencing dominate the B cell receptor repertoire in immunoglobulin G4 associated cholangitisLucas J Maillette de Buy Wenniger, Marieke E Doorenspleet, Paul L Klarenbeek, et al.
Annals of Surgery|January 11, 2021
Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute PancreatitisFons F van den Berg, Yama Issa, Jeroen P Vreijling, et al.
Human Molecular Genetics|May 17, 2014
Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2Megan Hwa Brewer, Ki Hwan Ma, Gary W Beecham, et al.
Pageof 24

Showing results (121-130 of 231) with videos related to

Sort By:
Pageof 24
Acta Neuropathologica|November 14, 2009
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNPCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Genes, Chromosomes & Cancer|January 23, 2016
Type 1 papillary renal cell carcinoma in a patient with schwannomatosis: Mosaic versus loss of SMARCB1 expression in respectively schwannoma and renal tumor cellsTheo J M Hulsebos, Susan Kenter, Frank Baas, et al.
Diabetologia|February 10, 2019
Diurnal rhythms in the white adipose tissue transcriptome are disturbed in obese individuals with type 2 diabetes compared with lean control individualsDirk Jan Stenvers, Aldo Jongejan, Sadaf Atiqi, et al.
The Journal of Infection|October 17, 2012
Common polymorphisms in the complement system and susceptiblity to bacterial meningitisKirsten S Adriani, Matthijs C Brouwer, Madelijn Geldhoff, et al.
Human Genetics|January 11, 2003
Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotypeValérie Biancalana, Olivier Caron, Sabina Gallati, et al.
Molecular Biosystems|June 23, 2010
Utilization of unlocked nucleic acid (UNA) to enhance siRNA performance in vitro and in vivoMaria B Laursen, Malgorzata M Pakula, Shan Gao, et al.
Frontiers in Cellular Neuroscience|August 24, 2023
Corrigendum: Ldlr-/-.Leiden mice develop neurodegeneration, age-dependent astrogliosis and obesity-induced changes in microglia immunophenotype which are partly reversed by complement component 5 neutralizing antibodyFlorine Seidel, Kees Fluiter, Robert Kleemann, et al.
Hepatology (Baltimore, Md.)|January 10, 2013
Immunoglobulin G4+ clones identified by next-generation sequencing dominate the B cell receptor repertoire in immunoglobulin G4 associated cholangitisLucas J Maillette de Buy Wenniger, Marieke E Doorenspleet, Paul L Klarenbeek, et al.
Annals of Surgery|January 11, 2021
Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute PancreatitisFons F van den Berg, Yama Issa, Jeroen P Vreijling, et al.
Human Molecular Genetics|May 17, 2014
Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2Megan Hwa Brewer, Ki Hwan Ma, Gary W Beecham, et al.
Pageof 24