Corrigendum: Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in Xenopus laevis

Corrigendum: Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in Xenopus laevis

Bibliographic Details
Main Authors:	Alexandra Mills, Elizabeth Bearce, Rachael Cella, Seung Woo Kim, Megan Selig, Sangmook Lee, Laura Anne Lowery
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2021-02-01
Series:	Frontiers in Physiology
Subjects:	craniofacial development developmental disorders Wolf-Hirschhorn Syndrome WHSC1 WHSC2 LETM1
Online Access:	https://www.frontiersin.org/articles/10.3389/fphys.2020.644596/full

Similar Items

Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in Xenopus laevis
by: Alexandra Mills, et al.
Published: (2019-04-01)

The Many Faces of Xenopus: Xenopus laevis as a Model System to Study Wolf–Hirschhorn Syndrome
by: Micaela Lasser, et al.
Published: (2019-06-01)

Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature
by: Mona K. Mekkawy, et al.
Published: (2021-02-01)

Low expression of NSD1, NSD2, and NSD3 define a subset of human papillomavirus-positive oral squamous carcinomas with unfavorable prognosis
by: Steven F. Gameiro, et al.
Published: (2021-02-01)

Structure, Activity and Function of the NSD3 Protein Lysine Methyltransferase
by: Philipp Rathert
Published: (2021-07-01)

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review
by: Eva-Cristiana Gavril, et al.
Published: (2021-08-01)

Anaesthetic management of a child with Wolf–Hirschhorn syndrome
by: Priyanka Das, et al.
Published: (2024-12-01)

Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity
by: Ermis Hayri, et al.
Published: (2003-01-01)

Wolf-Hirschhorn Syndrome: Report of two Cases in Bosnia and Herzegovina
by: Heljić S, et al.
Published: (2007-01-01)

Technical research on engine cycle constructing based on transformation model
by: Hu Xi, et al.
Published: (2021-01-01)

16p12.1 Deletion Orthologs are Expressed in Motile Neural Crest Cells and are Important for Regulating Craniofacial Development in Xenopus laevis
by: Micaela Lasser, et al.
Published: (2022-03-01)

WHSC1 monomethylates histone H1 and induces stem-cell like features in squamous cell carcinoma of the head and neck
by: Vassiliki Saloura, et al.
Published: (2020-08-01)

Early Postnatal Seizures in a Neonate with Wolf–Hirschhorn Syndrome
by: Hayato Go, et al.
Published: (2016-10-01)

Experience of the diagnosis and observation of a child with wolf-hirschhorn syndrome
by: L.V. Besh, et al.
Published: (2017-02-01)

Características clínicas y citogenéticas en el síndrome de Wolf-Hirschhorn. Serie de casos
by: Francisco Cammarata-Scalisi, et al.
Published: (2015-10-01)

LETM1 couples mitochondrial DNA metabolism and nutrient preference
by: Romina Durigon, et al.
Published: (2018-07-01)

Wolf-Hirschhorn syndrome presenting with cardiac manifestations at birth
by: Sudhir D Malwade, et al.
Published: (2016-01-01)

Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene
by: Khouloud Rjiba, et al.
Published: (2021-02-01)

De novo truncating variant in NSD2gene leading to atypical Wolf-Hirschhorn syndrome phenotype
by: Yanrui Jiang, et al.
Published: (2019-08-01)

Anesthetic considerations for an adult with Wolf-Hirschhorn syndrome - A case report -
by: Hye-Jin Kim, et al.
Published: (2020-01-01)

Targeted Next-Generation Sequencing Identifies Actionable Targets in Estrogen Receptor Positive and Estrogen Receptor Negative Endometriod Endometrial Cancer
by: Siti Syazani Suhaimi, et al.
Published: (2018-07-01)

Circular RNA circWHSC1 facilitates colorectal cancer cell proliferation by targeting miR-130a-5p/zeb1 signaling in vitro and in vivo
by: Lei Shi, et al.
Published: (2023-10-01)

Single port laparoscopic splenectomy for wandering spleen with splenomegaly in a patient with Wolf-Hirschhorn syndrome
by: Ricardo Zorron, et al.
Published: (2017-01-01)

Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes
by: Juliana F. Mazzeu, et al.
Published: (2007-03-01)

Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant to Young Teenager
by: Popescu D.E., et al.
Published: (2023-07-01)

Prenatal sonographic findings in confirmed cases of Wolf-Hirschhorn syndrome
by: Corinna Simonini, et al.
Published: (2022-04-01)

Activating transcription factor 2 promotes the progression of hepatocellular carcinoma by inducing the activation of the WHSC1‐mediated TOP2A/PI3K/AKT axis
by: Zhong‐Ming Bao, et al.
Published: (2022-07-01)

Critical laboratory : the writings of Thomas Hirschhorn /
by: Hirschhorn, Thomas, author, et al.
Published: (2013)

Síndrome de Wolf-Hirschhorn: variante de localización cromosómica clásica, primer caso reportado en población pediátrica colombiana
by: Pedro José Baquero Marín, et al.
Published: (2023-05-01)

Anesthetic experience using total intra-venous anesthesia for a patient with Wolf-Hirschhorn syndrome -A case report-
by: Jae Ho Choi, et al.
Published: (2011-02-01)

Prenatal phenotype of Wolf–Hirschhorn syndrome: A case series and literature review
by: Feng Tang, et al.
Published: (2023-06-01)

Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization
by: Wen-Xu Yang, et al.
Published: (2016-01-01)

Epilepsy combined with Wolf-Hirschhorn syndrome: a literature review and description of clinical cases
by: M. B. Mironov, et al.
Published: (2019-03-01)

From Wolf-Hirschhorn syndrome to NSD2 haploinsufficiency: a shifting paradigm through the description of a new case and a review of the literature
by: Luisa Cortellazzo Wiel, et al.
Published: (2022-05-01)

Habilidades comunicativas y lingüísticas del síndrome de Wolf-Hirschhorn: estudio de caso con fenotipo atenuado. Un estudio de caso
by: Verónica Martínez López, et al.
Published: (2020-01-01)

Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones
by: Chih-Ping Chen, et al.
Published: (2017-12-01)

Wolf-Hirschhorn Syndrome Candidate 1 Is Necessary for Correct Hematopoietic and B Cell Development
by: Elena Campos-Sanchez, et al.
Published: (2017-05-01)

Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature
by: Sifakis Stavros, et al.
Published: (2012-02-01)

Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf–Hirschhorn syndrome
by: Wen-Xu Yang, et al.
Published: (2016-02-01)

EEG in Wolf-Hirschhorn/Pitt-Rogers-Danks Syndromes
by: J Gordon Millichap
Published: (2001-04-01)