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Lars R Jensen

Showing results (31-40 of 44) with videos related to

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Experimental Hematology & Oncology|February 20, 2026
Molecular background of Philadelphia chromosome dependent enhancement of cellular growth and tyrosine kinase inhibitor sensitivityMd Faruq Hossain, Lisa Hagenau, Lars R Jensen, et al.
Human Genetics|June 20, 2006
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndromeBartlomiej Budny, Wei Chen, Heymut Omran, et al.
Human Mutation|February 26, 2017
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disabilityLuciana Musante, Lucia Püttmann, Kimia Kahrizi, et al.
BMC Genomics|June 30, 2014
Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7Grit Ebert, Anne Steininger, Robert Weißmann, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiencyLaura van Diepen, Falk F R Buettner, Dirk Hoffmann, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|November 11, 2020
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4qTiemo Grimm, Masoud Garshasbi, Lucia Puettmann, et al.
Pathogenetics|February 26, 2010
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5CLars R Jensen, Heinz Bartenschlager, Sinitdhorn Rujirabanjerd, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 31, 2026
White-Light Emission in Zeolitic Imidazolate Framework GlassesZhencai Li, Zihao Wang, Huotian Zhang, et al.
Nature Communications|July 30, 2025
Continuous structure modification of metal-organic framework glasses via halide saltsFengming Cao, Søren S Sørensen, Anders K R Christensen, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Experimental Hematology & Oncology|February 20, 2026
Molecular background of Philadelphia chromosome dependent enhancement of cellular growth and tyrosine kinase inhibitor sensitivityMd Faruq Hossain, Lisa Hagenau, Lars R Jensen, et al.
Human Genetics|June 20, 2006
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndromeBartlomiej Budny, Wei Chen, Heymut Omran, et al.
Human Mutation|February 26, 2017
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disabilityLuciana Musante, Lucia Püttmann, Kimia Kahrizi, et al.
BMC Genomics|June 30, 2014
Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7Grit Ebert, Anne Steininger, Robert Weißmann, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiencyLaura van Diepen, Falk F R Buettner, Dirk Hoffmann, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|November 11, 2020
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4qTiemo Grimm, Masoud Garshasbi, Lucia Puettmann, et al.
Pathogenetics|February 26, 2010
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5CLars R Jensen, Heinz Bartenschlager, Sinitdhorn Rujirabanjerd, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 31, 2026
White-Light Emission in Zeolitic Imidazolate Framework GlassesZhencai Li, Zihao Wang, Huotian Zhang, et al.
Nature Communications|July 30, 2025
Continuous structure modification of metal-organic framework glasses via halide saltsFengming Cao, Søren S Sørensen, Anders K R Christensen, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
Pageof 5