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Jeshurun C Kalanithy

Showing results (1-10 of 7) with videos related to

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Scientific Reports|October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formationEnrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
Journal of Neuroscience Research|September 14, 2021
Effect of modulating glutamate signaling on myelinating oligodendrocytes and their development-A study in the zebrafish modelFunda Turan, Öznur Yilmaz, Lena Schünemann, 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.
European Journal of Human Genetics : EJHG|December 20, 2024
Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish modelsNina 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 anomaliesJeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, 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 anomaliesGabriel 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 anomaliesJil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Scientific Reports|October 2, 2024
EZH2 specifically regulates ISL1 during embryonic urinary tract formationEnrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, et al.
Journal of Neuroscience Research|September 14, 2021
Effect of modulating glutamate signaling on myelinating oligodendrocytes and their development-A study in the zebrafish modelFunda Turan, Öznur Yilmaz, Lena Schünemann, 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.
European Journal of Human Genetics : EJHG|December 20, 2024
Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish modelsNina 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 anomaliesJeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, 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 anomaliesGabriel 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 anomaliesJil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, et al.
Pageof 1