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Heiko Reutter

Showing results (111-120 of 209) with videos related to

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Cell Communication and Signaling : CCS|February 3, 2025
Dynamic changes of extracellular vesicles during zebrafish organogenesisLinda-Marie Mulzer, Tim Felger, Luis E Muñoz, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 6, 2013
Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complexLihong Qi, Mei Wang, Garima Yagnik, et al.
Pediatric Surgery International|July 28, 2011
German network for congenital uro-rectal malformations: first evaluation and interpretation of postoperative urological complications in anorectal malformationsStefanie Maerzheuser, Ekkehart Jenetzky, Nadine Zwink, et al.
Antibiotics (Basel, Switzerland)|February 25, 2023
Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and PneumoniaAlisa Bär, Sabina Schmitt-Grohé, Jürgen Held, et al.
Pediatric Surgery International|July 24, 2012
Unexpected results of a nationwide, treatment-independent assessment of fecal incontinence in patients with anorectal anomaliesEberhard Schmiedeke, Nadine Zwink, Nicole Schwarzer, et al.
American Journal of Medical Genetics. Part A|October 17, 2006
Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complexHeiko Reutter, Tim Becker, Michael Ludwig, et al.
Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
American Journal of Medical Genetics. Part A|January 7, 2022
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothoraxSophia Schneider, Ricarda Köllges, Jil D Stegmann, et al.
American Journal of Medical Genetics. Part A|September 14, 2006
Bladder exstrophy and Epstein type congenital macrothrombocytopenia: evidence for a common cause?Boris Utsch, Analisa DiFeo, Annegret Kujat, et al.
International Journal of Molecular Medicine|September 11, 2012
Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T geneMarkus Draaken, Wiebke Prins, Claudia Zeidler, et al.
Pageof 21

Showing results (111-120 of 209) with videos related to

Sort By:
Pageof 21
Cell Communication and Signaling : CCS|February 3, 2025
Dynamic changes of extracellular vesicles during zebrafish organogenesisLinda-Marie Mulzer, Tim Felger, Luis E Muñoz, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 6, 2013
Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complexLihong Qi, Mei Wang, Garima Yagnik, et al.
Pediatric Surgery International|July 28, 2011
German network for congenital uro-rectal malformations: first evaluation and interpretation of postoperative urological complications in anorectal malformationsStefanie Maerzheuser, Ekkehart Jenetzky, Nadine Zwink, et al.
Antibiotics (Basel, Switzerland)|February 25, 2023
Evaluating the Use of Neonatal Colonization Screening for Empiric Antibiotic Therapy of Sepsis and PneumoniaAlisa Bär, Sabina Schmitt-Grohé, Jürgen Held, et al.
Pediatric Surgery International|July 24, 2012
Unexpected results of a nationwide, treatment-independent assessment of fecal incontinence in patients with anorectal anomaliesEberhard Schmiedeke, Nadine Zwink, Nicole Schwarzer, et al.
American Journal of Medical Genetics. Part A|October 17, 2006
Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complexHeiko Reutter, Tim Becker, Michael Ludwig, et al.
Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
American Journal of Medical Genetics. Part A|January 7, 2022
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothoraxSophia Schneider, Ricarda Köllges, Jil D Stegmann, et al.
American Journal of Medical Genetics. Part A|September 14, 2006
Bladder exstrophy and Epstein type congenital macrothrombocytopenia: evidence for a common cause?Boris Utsch, Analisa DiFeo, Annegret Kujat, et al.
International Journal of Molecular Medicine|September 11, 2012
Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T geneMarkus Draaken, Wiebke Prins, Claudia Zeidler, et al.
Pageof 21