Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.
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| Title: | Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract. |
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| Authors: | Kesdiren E; Department of Human Genetics, Hannover Medical School, Hannover, Germany., Martens H; Department of Human Genetics, Hannover Medical School, Hannover, Germany., Brand F; Department of Human Genetics, Hannover Medical School, Hannover, Germany., Werfel L; Department of Human Genetics, Hannover Medical School, Hannover, Germany.; Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany., Wedekind L; Institute of Molecular Biology, Hannover Medical School, Hannover, Germany., Trowe MO; Institute of Molecular Biology, Hannover Medical School, Hannover, Germany., Schmitz J; Nephropathology, Department of Pathology, Hannover Medical School, Hannover, Germany., Hennies I; Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany., Geffers R; Genome Analytics Research Group, Helmholtz Centre for Infection Research, Braunschweig, Germany., Gucev Z; Pediatric Nephrology, University Children's Hospital, Skopje, Macedonia., Seeman T; Department of Pediatrics, 2nd Faculty of Medicine, Charles University, Prague, Czech Republic.; Department of Pediatrics, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic., Schmidt S; Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany., Tasic V; Pediatric Nephrology, University Children's Hospital, Skopje, Macedonia., Fasano L; Aix-Marseille Univ, CNRS, IBDM UMR7288, Marseille, France., Bräsen JH; Nephropathology, Department of Pathology, Hannover Medical School, Hannover, Germany., Kispert A; Institute of Molecular Biology, Hannover Medical School, Hannover, Germany., Christians A; Department of Human Genetics, Hannover Medical School, Hannover, Germany., Haffner D; Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany., Weber RG; Department of Human Genetics, Hannover Medical School, Hannover, Germany. weber.ruthild@mh-hannover.de. |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2025 Jan; Vol. 33 (1), pp. 44-55. Date of Electronic Publication: 2024 Oct 17. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39420202 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Kesdiren+E%22">Kesdiren E</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Martens+H%22">Martens H</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Brand+F%22">Brand F</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Werfel+L%22">Werfel L</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.; Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Wedekind+L%22">Wedekind L</searchLink>; Institute of Molecular Biology, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Trowe+MO%22">Trowe MO</searchLink>; Institute of Molecular Biology, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Schmitz+J%22">Schmitz J</searchLink>; Nephropathology, Department of Pathology, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Hennies+I%22">Hennies I</searchLink>; Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Geffers+R%22">Geffers R</searchLink>; Genome Analytics Research Group, Helmholtz Centre for Infection Research, Braunschweig, Germany.<br /><searchLink fieldCode="AU" term="%22Gucev+Z%22">Gucev Z</searchLink>; Pediatric Nephrology, University Children's Hospital, Skopje, Macedonia.<br /><searchLink fieldCode="AU" term="%22Seeman+T%22">Seeman T</searchLink>; Department of Pediatrics, 2nd Faculty of Medicine, Charles University, Prague, Czech Republic.; Department of Pediatrics, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Schmidt+S%22">Schmidt S</searchLink>; Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.<br /><searchLink fieldCode="AU" term="%22Tasic+V%22">Tasic V</searchLink>; Pediatric Nephrology, University Children's Hospital, Skopje, Macedonia.<br /><searchLink fieldCode="AU" term="%22Fasano+L%22">Fasano L</searchLink>; Aix-Marseille Univ, CNRS, IBDM UMR7288, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Bräsen+JH%22">Bräsen JH</searchLink>; Nephropathology, Department of Pathology, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Kispert+A%22">Kispert A</searchLink>; Institute of Molecular Biology, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Christians+A%22">Christians A</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Haffner+D%22">Haffner D</searchLink>; Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.<br /><searchLink fieldCode="AU" term="%22Weber+RG%22">Weber RG</searchLink>; Department of Human Genetics, Hannover Medical School, Hannover, Germany. weber.ruthild@mh-hannover.de. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229302235%22">European journal of human genetics : EJHG</searchLink> [Eur J Hum Genet] 2025 Jan; Vol. 33 (1), pp. 44-55. <i>Date of Electronic Publication: </i>2024 Oct 17. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9302235 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1476-5438 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210184813%22">10184813 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39420202 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41431-024-01710-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 44 Titles: – TitleFull: Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kesdiren E – PersonEntity: Name: NameFull: Martens H – PersonEntity: Name: NameFull: Brand F – PersonEntity: Name: NameFull: Werfel L – PersonEntity: Name: NameFull: Wedekind L – PersonEntity: Name: NameFull: Trowe MO – PersonEntity: Name: NameFull: Schmitz J – PersonEntity: Name: NameFull: Hennies I – PersonEntity: Name: NameFull: Geffers R – PersonEntity: Name: NameFull: Gucev Z – PersonEntity: Name: NameFull: Seeman T – PersonEntity: Name: NameFull: Schmidt S – PersonEntity: Name: NameFull: Tasic V – PersonEntity: Name: NameFull: Fasano L – PersonEntity: Name: NameFull: Bräsen JH – PersonEntity: Name: NameFull: Kispert A – PersonEntity: Name: NameFull: Christians A – PersonEntity: Name: NameFull: Haffner D – PersonEntity: Name: NameFull: Weber RG IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: 2025 Jan Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1476-5438 Numbering: – Type: volume Value: 33 – Type: issue Value: 1 Titles: – TitleFull: European journal of human genetics : EJHG Type: main |
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