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MAB21L1 gene
Known as:
CAGR1
, MAB21, C. ELEGANS, HOMOLOG-LIKE 1
, mab-21 like 1
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
An exploration of the role of MAB21l1 in MAC-Spectrum Anomalies
Sarah DeBehnke
,
Brett Deml
,
L. Reis
,
R. Jamieson
,
E. Semina
2017
Corpus ID: 90838657
2016
2016
Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB 21 L 1
C. O. Mann
,
R. Kiefersauer
,
G. Witte
,
K. Hopfner
2016
Corpus ID: 9047918
The exceptionally conserved metazoan MAB21 proteins are implicated in cell fate decisions and share considerable sequence…
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2009
2009
Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3‐month‐old with severe pediatric gastroesophageal reflux
N. Champaigne
,
Nicole A. Laird
,
J. Northup
,
G. Velagaleti
American Journal of Medical Genetics. Part A
2009
Corpus ID: 7541470
Gastroesophageal reflux (GER) occurs when gastric contents travel back into the esophagus through the esophageal sphincter. GER…
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2002
2002
PII: S0925-4773(02)00012-6
Yau-Ming Wong
,
King L. Chow
2002
Corpus ID: 235314011
Mab21 homolog in Caenorhabditis elegans is expressed in the sensory ray cells and determines the ray identity (Dev. Dyn. 221…
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2000
2000
Refined localization of a gene for pediatric gastroesophageal reflux makes HTR2A an unlikely candidate gene
F. Hu
,
J. Post
,
Sandra Johnson
,
G. Ehrlich
,
R. Preston
Human Genetics
2000
Corpus ID: 6483404
Abstract. Our objective in this study was to determine whether mutations in the gene for the 5-hydroxytryptamine receptor 2A…
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1999
1999
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expression
R. Margolis
,
Colin Stine
,
+8 authors
Dr Margolis
Journal of Medical Genetics
1999
Corpus ID: 33990458
MAB21L1, originally termed CAGR1, is the human homologue of the C elegans cell fate determining genemab21. MAB21L1, mapped to…
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1997
1997
Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13.
N. Potter
Journal of Medical Genetics
1997
Corpus ID: 2892909
CAGR1 is a recently characterised polymorphic trinucleotide repeat localised to 13q13, which has been suggested as a possible…
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