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SLC17A5 gene
Known as:
AST
, SLC17A5
, SIALIN
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National Institutes of Health
Create Alert
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Related topics
Related topics
3 relations
Infantile Sialic Acid Storage Disease
SBDS gene
Standard deviation
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
Language Disorders Are Learning Disabilities: Challenges on the Divergent and Diverse Paths to Language Learning Disability
Lei Sun
,
Geraldine P. Wallach
2014
Corpus ID: 149690793
This article takes readers along the pathway of language learning and disorders across childhood and adolescence, highlighting…
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Review
2013
Review
2013
Lysosomal diseases: biochemical pathways and investigations.
M. Vanier
Handbook of Clinical Neurology
2013
Corpus ID: 41109280
2012
2012
10-Gb/s direct modulation of polymer-based tunable external cavity lasers
Byung-Seok Choi
,
S. Oh
,
+8 authors
Y. Chung
European Conference and Exhibition on Optical…
2012
Corpus ID: 16905806
We demonstrate a directly-modulated 10-Gb/s tunable external cavity laser with a polymer Bragg reflector and a high speed…
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2011
2011
Postnatal expression of sialin in the mouse submandibular gland.
Miao He
,
F. Lin
,
+4 authors
Songlin Wang
Archives of Oral Biology
2011
Corpus ID: 6799767
2010
2010
A vesicular transporter that mediates aspartate and glutamate neurotransmission.
T. Miyaji
,
H. Omote
,
Y. Moriyama
Biological and Pharmaceutical Bulletin
2010
Corpus ID: 31779810
Aspartate, an excitatory amino acid, is known to be stored in synaptic vesicles and exocytosed from some neurons to perform…
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2009
2009
Toward Simple Learning Design 2.0
G. Durand
,
S. Downes
International Conference on Crowd Science and…
2009
Corpus ID: 2429190
In 2003, based on the work done by the OUNL on Educational Modeling Language, IMS-LD was released and brought to the research…
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2007
2007
G328E and G409E sialin missense mutations similarly impair transport activity, but differentially affect trafficking.
Nathaniel J Myall
,
C. Wreden
,
Marcin Wlizla
,
R. Reimer
Molecular Genetics and Metabolism
2007
Corpus ID: 31416406
2005
2005
Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla disease
R. Biancheri
,
A. Rossi
,
+7 authors
M. Filocamo
Neurogenetics
2005
Corpus ID: 7570187
Lysosomal free sialic acid storage diseases are recessively inherited allelic neurodegenerative disorders that include Salla…
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1986
1986
Genetic-Dependent Alterations in Adrenal Stress Response and Adrenocortical Cell Function of the Domestic Fowl (Gallus domesticus) 1
R. Carsia
,
H. Weber
Proceedings of the Society for Experimental…
1986
Corpus ID: 24711130
Strain-dependent differences in adrenocortical function were investigated in male White Leghorn domestic fowl. Adrenocortical…
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1983
1983
A comparison of the acid-base metabolisms of pooled human dental plaque and salivary sediment.
D. Singer
,
R. Chatterjee
,
L. Denepitiya
,
I. Kleinberg
Archives of Oral Biology
1983
Corpus ID: 2028791
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