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Scientific Reports
|
October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formation
Enrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Impact of the Voltage-Gated Calcium Channel Antagonist Nimodipine on the Development of Oligodendrocyte Precursor Cells
Michael Enders, Alicia Weier, Rittika Chunder, et al.
Glia
|
November 9, 2019
CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch
Bhuvaneswari Nagarajan, Alexander Harder, Anna Japp, et al.
Cell Chemical Biology
|
September 20, 2022
Humanized zebrafish as a tractable tool for in vivo evaluation of pro-myelinating drugs
Felix Häberlein, Enrico Mingardo, Nicole Merten, et al.
Biomolecules
|
July 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates <i>LZTR1</i> in Disease Formation
Ricarda Köllges, Jil Stegmann, Sophia Schneider, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2024
Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish models
Nina Ishorst, Selina Hölzel, Carola Greve, et al.
Journal of Medical Genetics
|
December 23, 2024
<i>TFAP2E</i> is implicated in central nervous system, orofacial and maxillofacial anomalies
Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, et al.
Communications Biology
|
November 9, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Enrico Mingardo, Glenda Beaman, Philip Grote, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2021
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, et al.
NPJ Genomic Medicine
|
March 1, 2024
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
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of 1
Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Scientific Reports
|
October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formation
Enrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
International Journal of Molecular Sciences
|
February 25, 2023
Impact of the Voltage-Gated Calcium Channel Antagonist Nimodipine on the Development of Oligodendrocyte Precursor Cells
Michael Enders, Alicia Weier, Rittika Chunder, et al.
Glia
|
November 9, 2019
CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch
Bhuvaneswari Nagarajan, Alexander Harder, Anna Japp, et al.
Cell Chemical Biology
|
September 20, 2022
Humanized zebrafish as a tractable tool for in vivo evaluation of pro-myelinating drugs
Felix Häberlein, Enrico Mingardo, Nicole Merten, et al.
Biomolecules
|
July 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates <i>LZTR1</i> in Disease Formation
Ricarda Köllges, Jil Stegmann, Sophia Schneider, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2024
Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish models
Nina Ishorst, Selina Hölzel, Carola Greve, et al.
Journal of Medical Genetics
|
December 23, 2024
<i>TFAP2E</i> is implicated in central nervous system, orofacial and maxillofacial anomalies
Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, et al.
Communications Biology
|
November 9, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Enrico Mingardo, Glenda Beaman, Philip Grote, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2021
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, et al.
NPJ Genomic Medicine
|
March 1, 2024
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
Page
of 1