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H Annika Siitonen

Showing results (1-10 of 9) with videos related to

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Archives of Dermatology|May 18, 2005
A patient with Rothmund-Thomson syndrome and all features of RAPADILINORichard Kellermayer, H Annika Siitonen, Kinga Hadzsiev, et al.
Neuromuscular Disorders : NMD|March 24, 2004
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)Henna Haravuori, H Annika Siitonen, Ibrahim Mahjneh, et al.
Human Molecular Genetics|September 4, 2003
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseasesH Annika Siitonen, Outi Kopra, Helena Kääriäinen, et al.
European Journal of Pediatrics|March 21, 2007
Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromesYves Sznajer, H Annika Siitonen, Gaia Roversi, et al.
BMC Genomics|June 6, 2018
Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomesMari H Tervaniemi, Shintaro Katayama, Tiina Skoog, et al.
Plos One|November 29, 2012
Centrosomal localization of the psoriasis candidate gene product, CCHCR1, supports a role in cytoskeletal organizationMari H Tervaniemi, H Annika Siitonen, Cilla Söderhäll, et al.
Scientific Reports|March 16, 2016
NOD-like receptor signaling and inflammasome-related pathways are highlighted in psoriatic epidermisMari H Tervaniemi, Shintaro Katayama, Tiina Skoog, et al.
BMC Genomics|June 26, 2015
Gene expression analysis of skin grafts and cultured keratinocytes using synthetic RNA normalization reveals insights into differentiation and growth controlShintaro Katayama, Tiina Skoog, Eeva-Mari Jouhilahti, et al.
European Journal of Human Genetics : EJHG|August 22, 2008
The mutation spectrum in RECQL4 diseasesH Annika Siitonen, Jenni Sotkasiira, Martine Biervliet, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Archives of Dermatology|May 18, 2005
A patient with Rothmund-Thomson syndrome and all features of RAPADILINORichard Kellermayer, H Annika Siitonen, Kinga Hadzsiev, et al.
Neuromuscular Disorders : NMD|March 24, 2004
Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)Henna Haravuori, H Annika Siitonen, Ibrahim Mahjneh, et al.
Human Molecular Genetics|September 4, 2003
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseasesH Annika Siitonen, Outi Kopra, Helena Kääriäinen, et al.
European Journal of Pediatrics|March 21, 2007
Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromesYves Sznajer, H Annika Siitonen, Gaia Roversi, et al.
BMC Genomics|June 6, 2018
Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomesMari H Tervaniemi, Shintaro Katayama, Tiina Skoog, et al.
Plos One|November 29, 2012
Centrosomal localization of the psoriasis candidate gene product, CCHCR1, supports a role in cytoskeletal organizationMari H Tervaniemi, H Annika Siitonen, Cilla Söderhäll, et al.
Scientific Reports|March 16, 2016
NOD-like receptor signaling and inflammasome-related pathways are highlighted in psoriatic epidermisMari H Tervaniemi, Shintaro Katayama, Tiina Skoog, et al.
BMC Genomics|June 26, 2015
Gene expression analysis of skin grafts and cultured keratinocytes using synthetic RNA normalization reveals insights into differentiation and growth controlShintaro Katayama, Tiina Skoog, Eeva-Mari Jouhilahti, et al.
European Journal of Human Genetics : EJHG|August 22, 2008
The mutation spectrum in RECQL4 diseasesH Annika Siitonen, Jenni Sotkasiira, Martine Biervliet, et al.
Pageof 1