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BARHL1 gene
Known as:
BARH-LIKE 1
, BARHL1
, BarH like homeobox 1
National Institutes of Health
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Papers overview
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2011
2011
The role of the transcription factor BARHL1 in medulloblastoma
J. Pöschl
2011
Corpus ID: 160498812
Das Medulloblastom ist der haufigste maligne Hirntumor des Kindesalters, und die Entwicklung von zielgerichteten…
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2008
2008
Barhl1 Regulatory Sequences Required for Cell-Specific Gene Expression and Autoregulation in the Inner Ear and Central Nervous System
Ramesh Chellappa
,
Shengguo Li
,
S. Pauley
,
I. Jahan
,
Kangxin Jin
,
M. Xiang
Molecular and Cellular Biology
2008
Corpus ID: 5312320
ABSTRACT The development of the nervous system requires the concerted actions of multiple transcription factors, yet the…
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2006
2006
Barhl1 is required for maintenance of a large population of neurons in the zonal layer of the superior colliculus
Shengguo Li
,
M. Xiang
Developmental Dynamics
2006
Corpus ID: 15277252
The mammalian superior colliculus of the midbrain is a brainstem center that integrates sensorimotor signals involved in the…
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2005
2005
Transcriptional regulation by Barhl1 and Brn-3c in organ-of-Corti-derived cell lines.
R. Sud
,
Chrisopher Jones
,
S. Banfi
,
S. Dawson
Brain Research. Molecular Brain Research
2005
Corpus ID: 43464964
2004
2004
Mutational analysis of BARHL1 and BARX1 in three new patients with Joubert syndrome
D. Gould
,
M. Walter
American Journal of Medical Genetics. Part A
2004
Corpus ID: 39365849
Joubert syndrome (JS) (OMIM no. 213300) is a serious central nervous system disorder that primarily affects the cerebellum and…
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2002
2002
Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1.
I. Blair
,
Roxanne R Gibson
,
C. Bennett
,
P. Chance
American journal of medical genetics
2002
Corpus ID: 26082601
Joubert syndrome (JS) is a rare autosomal recessive malformation syndrome involving agenesis or dysgenesis of the cerebellar…
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