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Outi Elomaa

Showing results (1-10 of 28) with videos related to

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Trends in Molecular Medicine|June 18, 2002
Healing a natural knockout of epithelial organogenesisJuha Kere, Outi Elomaa
Journal of Immunology (Baltimore, Md. : 1950)|December 13, 2005
Defective microarchitecture of the spleen marginal zone and impaired response to a thymus-independent type 2 antigen in mice lacking scavenger receptors MARCO and SR-AYunying Chen, Timo Pikkarainen, Outi Elomaa, et al.
Nephron. Experimental Nephrology|June 16, 2005
SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidneyMinna Kujala, Jukka Tienari, Hannes Lohi, et al.
Scientific Reports|December 15, 2019
Discovery of increased epidermal DNAH10 expression after regeneration of dermis in a randomized with-in person trial - reflections on psoriatic inflammationHeli Lagus, Mariliis Klaas, Susanna Juteau, et al.
Gene|December 20, 2002
Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancerKatja Ahokas, Jouko Lohi, Hannes Lohi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 3, 2025
SERPINB8-associated peeling skin with palmoplantar keratoderma-A new variant and phenotypic expansionEveliina Brandt, Kaisa Kettunen, Outi Elomaa, et al.
The Journal of Investigative Dermatology|December 17, 2003
HCR, a candidate gene for psoriasis, is expressed differently in psoriasis and other hyperproliferative skin disorders and is downregulated by interferon-gamma in keratinocytesSari Suomela, Outi Elomaa, Kati Asumalahti, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 24, 2003
Matrix metalloproteinase-21 is expressed epithelially during development and in cancer and is up-regulated by transforming growth factor-beta1 in keratinocytesKatja Ahokas, Jouko Lohi, Sara A Illman, et al.
American Journal of Medical Genetics. Part A|October 11, 2025
The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome FeaturesNikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, et al.
Human Mutation|January 1, 2008
Somatic FGF9 mutations in colorectal and endometrial carcinomas associated with membranous beta-cateninWael M Abdel-Rahman, Juliya Kalinina, Soheir Shoman, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Trends in Molecular Medicine|June 18, 2002
Healing a natural knockout of epithelial organogenesisJuha Kere, Outi Elomaa
Journal of Immunology (Baltimore, Md. : 1950)|December 13, 2005
Defective microarchitecture of the spleen marginal zone and impaired response to a thymus-independent type 2 antigen in mice lacking scavenger receptors MARCO and SR-AYunying Chen, Timo Pikkarainen, Outi Elomaa, et al.
Nephron. Experimental Nephrology|June 16, 2005
SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidneyMinna Kujala, Jukka Tienari, Hannes Lohi, et al.
Scientific Reports|December 15, 2019
Discovery of increased epidermal DNAH10 expression after regeneration of dermis in a randomized with-in person trial - reflections on psoriatic inflammationHeli Lagus, Mariliis Klaas, Susanna Juteau, et al.
Gene|December 20, 2002
Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancerKatja Ahokas, Jouko Lohi, Hannes Lohi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 3, 2025
SERPINB8-associated peeling skin with palmoplantar keratoderma-A new variant and phenotypic expansionEveliina Brandt, Kaisa Kettunen, Outi Elomaa, et al.
The Journal of Investigative Dermatology|December 17, 2003
HCR, a candidate gene for psoriasis, is expressed differently in psoriasis and other hyperproliferative skin disorders and is downregulated by interferon-gamma in keratinocytesSari Suomela, Outi Elomaa, Kati Asumalahti, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 24, 2003
Matrix metalloproteinase-21 is expressed epithelially during development and in cancer and is up-regulated by transforming growth factor-beta1 in keratinocytesKatja Ahokas, Jouko Lohi, Sara A Illman, et al.
American Journal of Medical Genetics. Part A|October 11, 2025
The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome FeaturesNikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, et al.
Human Mutation|January 1, 2008
Somatic FGF9 mutations in colorectal and endometrial carcinomas associated with membranous beta-cateninWael M Abdel-Rahman, Juliya Kalinina, Soheir Shoman, et al.
Pageof 3