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Nina Ishorst

Showing results (11-20 of 19) with videos related to

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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.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
American Journal of Human Genetics|March 29, 2016
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft PalateElisabeth Mangold, Anne C Böhmer, Nina Ishorst, et al.
Molecular Genetics & Genomic Medicine|December 5, 2022
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scoresNina Ishorst, Leonie Henschel, Frederic Thieme, et al.
Nature Biotechnology|July 19, 2022
Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, et al.
Nature Biotechnology|June 30, 2021
LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, 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|March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesisCharlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, 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 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
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.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
American Journal of Human Genetics|March 29, 2016
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft PalateElisabeth Mangold, Anne C Böhmer, Nina Ishorst, et al.
Molecular Genetics & Genomic Medicine|December 5, 2022
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scoresNina Ishorst, Leonie Henschel, Frederic Thieme, et al.
Nature Biotechnology|July 19, 2022
Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, et al.
Nature Biotechnology|June 30, 2021
LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcodingKerstin U Ludwig, Ricarda M Schmithausen, David Li, 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|March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesisCharlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, 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 2