Cargando…

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

Disrupted development of oropharyngeal structures as well as cranial nerve and brainstem circuits may lead to feeding and swallowing difficulties in children with 22q11. 2 deletion syndrome (22q11DS). We previously demonstrated aspiration-based dysphagia during early postnatal life in the LgDel mous...

Descripción completa

Detalles Bibliográficos
Autores principales:	Welby, Lauren, Caudill, Hailey, Yitsege, Gelila, Hamad, Ali, Bunyak, Filiz, Zohn, Irene E., Maynard, Thomas, LaMantia, Anthony-Samuel, Mendelowitz, David, Lever, Teresa E.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006055/ https://www.ncbi.nlm.nih.gov/pubmed/32082240 http://dx.doi.org/10.3389/fneur.2020.00004

Ejemplares similares

Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome
por: Yitsege, Gelila, et al.
Publicado: (2020)

Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome
por: Karpinski, Beverly A., et al.
Publicado: (2021)

Disrupted Coordination of Hypoglossal Motor Control in a Mouse Model of Pediatric Dysphagia in DiGeorge/22q11.2 Deletion Syndrome
por: Wang, Xin, et al.
Publicado: (2020)

In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
por: Motahari, Zahra, et al.
Publicado: (2019)

Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome
por: Paronett, Elizabeth M, et al.
Publicado: (2023)

Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome
por: Karpinski, Beverly A., et al.
Publicado: (2014)

Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome
por: Motahari, Zahra, et al.
Publicado: (2020)

Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome
por: Maynard, Thomas M, et al.
Publicado: (2020)

Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome
por: Maynard, Thomas M, et al.
Publicado: (2020)

Visual processing deficits in 22q11.2 Deletion Syndrome
por: Biria, Marjan, et al.
Publicado: (2017)

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
por: Heung, Tracy, et al.
Publicado: (2022)

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology
por: Morrison, Sinead, et al.
Publicado: (2020)

Obesity in adults with 22q11.2 deletion syndrome
por: Voll, S, et al.
Publicado: (2016)

Case Report: Autoimmune Psychosis in Chromosome 22q11.2 Deletion Syndrome
por: Ciano-Petersen, Nicolás Lundahl, et al.
Publicado: (2021)

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome
por: Niarchou, Maria, et al.
Publicado: (2019)

The clinical presentation of attention deficit‐hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome
por: Niarchou, Maria, et al.
Publicado: (2015)

An affected core drives network integration deficits of the structural connectome in 22q11.2 deletion syndrome
por: Váša, František, et al.
Publicado: (2015)

22q11.2 Deletion and Duplication Syndromes and COVID-19
por: Crowley, T. Blaine, et al.
Publicado: (2022)

Neural mechanisms of response inhibition and impulsivity in 22q11.2 deletion carriers and idiopathic attention deficit hyperactivity disorder()
por: Montojo, C.A., et al.
Publicado: (2015)

Disrupted anatomic networks in the 22q11.2 deletion syndrome
por: Schmitt, J. Eric, et al.
Publicado: (2016)

Hematological abnormalities and 22q11.2 deletion syndrome
por: Rosa, Rafael Fabiano Machado, et al.
Publicado: (2011)

Risk of malignancy in 22q11.2 deletion syndrome
por: Stevens, Toer, et al.
Publicado: (2017)

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
por: Du, Qiumei, et al.
Publicado: (2020)

Complement Activation in 22q11.2 Deletion Syndrome
por: Grinde, Dina, et al.
Publicado: (2020)

Laryngeal web with 22q11.2 deletion syndrome
por: Abe, Yasuhiro, et al.
Publicado: (2022)

Tonsillectomy in Children with 22q11.2 Deletion Syndrome
por: Arganbright, Jill M., et al.
Publicado: (2022)

Otologic and audiologic findings in 22q11.2 deletion syndrome
por: Verheij, E., et al.
Publicado: (2016)

Platybasia in 22q11.2 Deletion Syndrome Is Not Correlated with Speech Resonance
por: Spruijt, Nicole E, et al.
Publicado: (2014)

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
por: Schonherz, Yael, et al.
Publicado: (2014)

Evaluation of 22q11.2 deletion in Cleft Palate patients
por: Prabodha, L. B. Lahiru, et al.
Publicado: (2012)

Genotype-phenotype correlation in 22q11.2 deletion syndrome
por: Michaelovsky, Elena, et al.
Publicado: (2012)

Psychopathology and cognition in children with 22q11.2 deletion syndrome
por: Niarchou, Maria, et al.
Publicado: (2014)

Psychiatric Disorders Associated with 22q11.2 Deletion Syndrome
por: Gambini, Orsola
Publicado: (2016)

Clinical variability of chromosome 22q11.2 deletion syndrome
por: Boyarchuk, Oksana, et al.
Publicado: (2017)

22q11.2 Deletion Syndrome–Associated Parkinson's Disease
por: Boot, Erik, et al.
Publicado: (2018)

Dopaminergic neurons in chromosome 22q11.2 deletion syndrome
por: Inoue, Haruhisa
Publicado: (2021)

Deletion Syndrome 22q11.2: A Systematic Review
por: Cortés-Martín, Jonathan, et al.
Publicado: (2022)

Clinical management of psychosis in 22q11.2 deletion syndrome
por: Iftimovici, Anton, et al.
Publicado: (2022)

Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome
por: Palmer, Lisa D., et al.
Publicado: (2022)

Pediatric healthcare costs for patients with 22q11.2 deletion syndrome
por: Benn, Peter, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_jp6it9rnpieglr3hq5ecl4sq7a