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Frank Baas

Showing results (111-120 of 231) with videos related to

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Plos One|December 22, 2006
Monitoring the T-cell receptor repertoire at single-clone resolutionHendrik P J Bonarius, Frank Baas, Ester B M Remmerswaal, et al.
The New England Journal of Medicine|July 12, 2002
Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidismJosé C Moreno, Hennie Bikker, Marlies J E Kempers, et al.
European Journal of Human Genetics : EJHG|June 19, 2009
A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR)Janina Hantke, David Chandler, Rosalind King, et al.
Hemoglobin|March 31, 2025
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel <i>SUPT5H</i> VariantsNik Fatma Fairuz Nik Mohd Hasan, Ahlem Achour, Tamara Koopmann, et al.
Blood|April 8, 2009
Changes in gene expression of granulocytes during in vivo granulocyte colony-stimulating factor/dexamethasone mobilization for transfusion purposesAgata Drewniak, Bram J van Raam, Judy Geissler, et al.
Plos One|December 24, 2011
Deep sequencing whole transcriptome exploration of the σE regulon in Neisseria meningitidisRobert Antonius Gerhardus Huis in 't Veld, Antonius Marcellinus Willemsen, Antonius Hubertus Cornelis van Kampen, et al.
Genome Announcements|April 23, 2016
First Complete Genome Sequence of the Dutch Veterinary Coxiella burnetii Strain NL3262, Originating from the Largest Global Q Fever Outbreak, and Draft Genome Sequence of Its Epidemiologically Linked Chronic Human Isolate NLhu3345937Runa Kuley, Hilde E Smith, Ingmar Janse, et al.
Synapse (New York, N.Y.)|April 6, 2011
COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndromeErik Boot, Jan Booij, Janneke R Zinkstok, et al.
Frontiers in Cellular Neuroscience|July 17, 2023
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.
Annals of Clinical and Translational Neurology|February 23, 2016
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's diseaseMarjolein B Aerts, Marian A J Weterman, Marialuisa Quadri, et al.
Pageof 24

Showing results (111-120 of 231) with videos related to

Sort By:
Pageof 24
Plos One|December 22, 2006
Monitoring the T-cell receptor repertoire at single-clone resolutionHendrik P J Bonarius, Frank Baas, Ester B M Remmerswaal, et al.
The New England Journal of Medicine|July 12, 2002
Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidismJosé C Moreno, Hennie Bikker, Marlies J E Kempers, et al.
European Journal of Human Genetics : EJHG|June 19, 2009
A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR)Janina Hantke, David Chandler, Rosalind King, et al.
Hemoglobin|March 31, 2025
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel <i>SUPT5H</i> VariantsNik Fatma Fairuz Nik Mohd Hasan, Ahlem Achour, Tamara Koopmann, et al.
Blood|April 8, 2009
Changes in gene expression of granulocytes during in vivo granulocyte colony-stimulating factor/dexamethasone mobilization for transfusion purposesAgata Drewniak, Bram J van Raam, Judy Geissler, et al.
Plos One|December 24, 2011
Deep sequencing whole transcriptome exploration of the σE regulon in Neisseria meningitidisRobert Antonius Gerhardus Huis in 't Veld, Antonius Marcellinus Willemsen, Antonius Hubertus Cornelis van Kampen, et al.
Genome Announcements|April 23, 2016
First Complete Genome Sequence of the Dutch Veterinary Coxiella burnetii Strain NL3262, Originating from the Largest Global Q Fever Outbreak, and Draft Genome Sequence of Its Epidemiologically Linked Chronic Human Isolate NLhu3345937Runa Kuley, Hilde E Smith, Ingmar Janse, et al.
Synapse (New York, N.Y.)|April 6, 2011
COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndromeErik Boot, Jan Booij, Janneke R Zinkstok, et al.
Frontiers in Cellular Neuroscience|July 17, 2023
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.
Annals of Clinical and Translational Neurology|February 23, 2016
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's diseaseMarjolein B Aerts, Marian A J Weterman, Marialuisa Quadri, et al.
Pageof 24