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MYT1L gene
Known as:
myelin transcription factor 1 like
, MYT1L
, Myelin Transcription Factor 1-Like Gene
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This gene is involved in transcriptional regulation and neuronal development.
National Institutes of Health
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Related topics
Related topics
6 relations
Homo sapiens
MYT2 gene
Neurogenesis
Schizophrenia
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
microarray data for "MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus" Published in PLoS Genetics…
M. Alisdair
2017
Corpus ID: 90872754
2016
2016
Insights on the function of MyT1L in Ascl1 mediated neuronal reprogramming
Diogo M. Tomaz
2016
Corpus ID: 55893828
2016
2016
Exosome-Based Transfection
Michael Homsy
2016
Corpus ID: 73637529
Exosomes are mammalian extracellular vesicles that are involved in intracellular communication. The discovery of RNA in exosomes…
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2014
2014
Abstracts from the 12 th meeting of the International Society for Neural Transplantation and Restoration
A. Álvarez-Buylla
,
Luis Azmitia
,
P. Capetian
,
M. Klett
,
M. Döbrössy
,
G. Nikkhah
2014
Corpus ID: 14732178
s from the 12th meeting of the International Society for Neural Transplantation and Restoration NeuroReport 2014, 25:139–163 Note…
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Review
2014
Review
2014
Immunogenetic studies of Guillain - Barré syndrome and chronic inflammatory demyelinating polyradiculoneuropathy
S. Blum
2014
Corpus ID: 53783640
Guillain-Barre syndrome (GBS) is an acute inflammatory neuropathy that is frequently triggered by an infectious illness. It is…
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2014
2014
The use of lentivirus-mediated gene delivery to investigate the role of the brain specific transcription factor MYT1L in-vitro and in-vivo
Lourdes Martínez Medina
2014
Corpus ID: 83134318
2013
2013
Detecting the structure of haplotypes, local ancestry and excessive local European ancestry in Mexicans
Yongtao Guan
2013
Corpus ID: 18680374
We present a two-layer hidden Markov model to detect structure of haplotypes for unrelated individuals. This allows modeling two…
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2013
2013
Bases moléculaires et physiopathologiques de syndromes avec anomalies du développement et déficience intellectuelle
J. Thevenon
2013
Corpus ID: 190351522
La deficience intellectuelle (DI) correspond a un defaut des performances intellectuelles et des fonctions adaptatives, debutant…
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2012
2012
MYT1L, a new candidate gene for non-syndromic intellectual disability
N. D. Rocker
,
Sarah Vergult
,
+19 authors
B. Menten
2012
Corpus ID: 151953752
2008
2008
Genome Wide Association analysis for Borderline Personality Disorder Characteristics
J. Hottenga
,
M. Distel
,
+4 authors
D. Boomsma
2008
Corpus ID: 148832613
Acknowledgements The Netherlands Organization for Scientific Research, The Center for Cognitive and Neurological Research…
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