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M Bocian

Showing results (21-30 of 34) with videos related to

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American Journal of Medical Genetics|December 20, 2000
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13M Smith, P A Filipek, C Wu, et al.
Journal of Inherited Metabolic Disease|January 7, 2004
Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidationJ J Gargus, K Boyle, M Bocian, et al.
Actas Dermo-Sifiliograficas|May 15, 2013
Nevoid basal cell carcinoma syndrome: our experience in a pediatric hospitalP C Samela, V Tosi, A B Cervini, et al.
Actas Dermo-Sifiliograficas|March 17, 2012
Perianal ulcers on a segmental hemangioma with minimal or arrested growthA Lanoel, V Tosi, M Bocian, et al.
Actas Dermo-Sifiliograficas|December 17, 2010
[Paraneoplastic pemphigus or paraneoplastic autoimmune multiorgan syndrome. Report of 2 cases in children and a review of the literature]A B Cervini, V Tosi, S H Kim, et al.
Cell|July 29, 1994
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasiaR Shiang, L M Thompson, Y Z Zhu, et al.
American Journal of Medical Genetics|August 1, 1986
Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunkC O Reid, J G Hall, C Anderson, et al.
Frontiers in Microbiology|August 11, 2016
Engineering of Helicobacter pylori Dimeric Oxidoreductase DsbK (HP0231)Katarzyna M Bocian-Ostrzycka, Magdalena J Grzeszczuk, Anna M Banaś, et al.
International Journal of Medical Microbiology : IJMM|August 23, 2018
Thioloxidoreductase HP0231 of Helicobacter pylori impacts HopQ-dependent CagA translocationMagdalena J Grzeszczuk, Katarzyna M Bocian-Ostrzycka, Anna M Banaś, et al.
American Journal of Medical Genetics|June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type IIH J Stern, J M Graham, R S Lachman, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|December 20, 2000
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13M Smith, P A Filipek, C Wu, et al.
Journal of Inherited Metabolic Disease|January 7, 2004
Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidationJ J Gargus, K Boyle, M Bocian, et al.
Actas Dermo-Sifiliograficas|May 15, 2013
Nevoid basal cell carcinoma syndrome: our experience in a pediatric hospitalP C Samela, V Tosi, A B Cervini, et al.
Actas Dermo-Sifiliograficas|March 17, 2012
Perianal ulcers on a segmental hemangioma with minimal or arrested growthA Lanoel, V Tosi, M Bocian, et al.
Actas Dermo-Sifiliograficas|December 17, 2010
[Paraneoplastic pemphigus or paraneoplastic autoimmune multiorgan syndrome. Report of 2 cases in children and a review of the literature]A B Cervini, V Tosi, S H Kim, et al.
Cell|July 29, 1994
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasiaR Shiang, L M Thompson, Y Z Zhu, et al.
American Journal of Medical Genetics|August 1, 1986
Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunkC O Reid, J G Hall, C Anderson, et al.
Frontiers in Microbiology|August 11, 2016
Engineering of Helicobacter pylori Dimeric Oxidoreductase DsbK (HP0231)Katarzyna M Bocian-Ostrzycka, Magdalena J Grzeszczuk, Anna M Banaś, et al.
International Journal of Medical Microbiology : IJMM|August 23, 2018
Thioloxidoreductase HP0231 of Helicobacter pylori impacts HopQ-dependent CagA translocationMagdalena J Grzeszczuk, Katarzyna M Bocian-Ostrzycka, Anna M Banaś, et al.
American Journal of Medical Genetics|June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type IIH J Stern, J M Graham, R S Lachman, et al.
Pageof 4