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Michael Knapp

Showing results (151-160 of 209) with videos related to

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United European Gastroenterology Journal|February 22, 2019
First genotype-phenotype study reveals HLA-DQβ1 insertion heterogeneity in high-resolution manometry achalasia subtypesZuzana Vackova, Stefan Niebisch, Tania Triantafyllou, et al.
HGG Advances|January 20, 2022
Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palateJulia Welzenbach, Nigel L Hammond, Miloš Nikolić, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.
European Journal of Oral Sciences|March 27, 2009
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palateStefanie Birnbaum, Heiko Reutter, Meinhard Mende, et al.
Genomics|April 23, 2003
High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseasesNicole Herbon, Monika Werner, Christine Braig, et al.
International Journal of Pediatric Otorhinolaryngology|July 10, 2009
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descentHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.
International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.
Nature Communications|December 3, 2014
Identification of the remains of King Richard IIITuri E King, Gloria Gonzalez Fortes, Patricia Balaresque, et al.
Gut|September 18, 2013
Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndromeMira M Wouters, Diether Lambrechts, Michael Knapp, et al.
ACS Nano|October 22, 2025
Unlocking the Potential of Cobalt-Free Lithium-Ion Cathodes via Lithium-Rich Disorder DomainsHao Liu, Hang Li, Weibo Hua, et al.
Pageof 21

Showing results (151-160 of 209) with videos related to

Sort By:
Pageof 21
United European Gastroenterology Journal|February 22, 2019
First genotype-phenotype study reveals HLA-DQβ1 insertion heterogeneity in high-resolution manometry achalasia subtypesZuzana Vackova, Stefan Niebisch, Tania Triantafyllou, et al.
HGG Advances|January 20, 2022
Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palateJulia Welzenbach, Nigel L Hammond, Miloš Nikolić, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.
European Journal of Oral Sciences|March 27, 2009
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palateStefanie Birnbaum, Heiko Reutter, Meinhard Mende, et al.
Genomics|April 23, 2003
High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseasesNicole Herbon, Monika Werner, Christine Braig, et al.
International Journal of Pediatric Otorhinolaryngology|July 10, 2009
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descentHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.
International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.
Nature Communications|December 3, 2014
Identification of the remains of King Richard IIITuri E King, Gloria Gonzalez Fortes, Patricia Balaresque, et al.
Gut|September 18, 2013
Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndromeMira M Wouters, Diether Lambrechts, Michael Knapp, et al.
ACS Nano|October 22, 2025
Unlocking the Potential of Cobalt-Free Lithium-Ion Cathodes via Lithium-Rich Disorder DomainsHao Liu, Hang Li, Weibo Hua, et al.
Pageof 21