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Cell Communication and Signaling : CCS
|
February 3, 2025
Dynamic changes of extracellular vesicles during zebrafish organogenesis
Linda-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 complex
Lihong 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 malformations
Stefanie 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 Pneumonia
Alisa 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 anomalies
Eberhard 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-complex
Heiko 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 omphalocele
Caroline 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 chylothorax
Sophia 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 gene
Markus Draaken, Wiebke Prins, Claudia Zeidler, et al.
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of 21
Search research articles
Search
Showing results (111-120 of 209) with videos related to
Sort By:
Page
of 21
Cell Communication and Signaling : CCS
|
February 3, 2025
Dynamic changes of extracellular vesicles during zebrafish organogenesis
Linda-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 complex
Lihong 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 malformations
Stefanie 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 Pneumonia
Alisa 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 anomalies
Eberhard 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-complex
Heiko 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 omphalocele
Caroline 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 chylothorax
Sophia 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 gene
Markus Draaken, Wiebke Prins, Claudia Zeidler, et al.
Page
of 21