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SLC7A7 protein, human
Known as:
Y+LAT1
, Solute Carrier Family 7 Member 7
, solute-carrier family 7 (cationic amino acid transporter, y+ system), member 7 protein, human
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Y+L amino acid transporter 1 (511 aa, ~56 kDa) is encoded by the human SLC7A7 gene. This protein plays a role in the localization of cationic amino…
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National Institutes of Health
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Related topics
Related topics
12 relations
Amino Acid Transporter
Cellular Membrane
Integral Membrane Proteins
Ionophore activity
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
mRNA expression of amino acid transporters, aminopeptidase, and the di- and tri-peptide transporter PepT1 in the intestine and liver of posthatch broiler chicks.
K. Miska
,
R. Fetterer
,
E. Wong
Poultry Science
2015
Corpus ID: 40380545
Amino acid (AA) transporter proteins are responsible for the movement of amino acids in and out of cells. Aminopeptidase cleaves…
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2015
2015
Duodenum has the greatest potential to absorb soluble non-ammonia nitrogen in the nonmesenteric gastrointestinal tissues of dairy cows
Ying-ming Xie
,
Qing Xu
,
Yue-ming Wu
,
Xin-bei Huang
,
Jian-xin Liu
Journal of Zhejiang University SCIENCE B
2015
Corpus ID: 42344270
In cattle, dietary protein is gradually degraded into peptide-bound amino acids (PBAAs), free amino acids(FAAs), and ultimately…
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2015
2015
The effects of mutated cationic amino acid transporter y+LAT1 at the cellular and systemic level
M. Tringham
2015
Corpus ID: 59386412
2013
2013
Interactions of y+LAT1 and 4F2hc in the y+l amino acid transporter complex: consequences of lysinuric protein intolerance-causing mutations.
M. Toivonen
,
M. Tringham
,
+4 authors
J. Mykkänen
General Physiology and Biophysics
2013
Corpus ID: 32849865
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by recessive mutations in the SLC7A7 gene encoding y+L…
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2013
2013
Fluorescence-based imaging of cellular defect in lysinuric protein intolerance (LPI)
M. Toivonen
2013
Corpus ID: 51734555
Lysinuric protein intolerance is an autosomal recessive disease of Finnish disease heritage characterized by cationic amino acid…
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2012
2012
Nueva metodología del concepto de determinante en la asignatura de Matemáticas I del Curso de Orientación Universitaria
Isaías Uña Juárez
2012
Corpus ID: 179045885
En este trabajo se desarrolla una propuesta de metodologia docente para el concepto de determinante y sus propiedades en la…
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2005
2005
A y+LAT-1 mutant protein interferes with y+LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance
M. P. Sperandeo
,
S. Paladino
,
+5 authors
G. Sebastio
European Journal of Human Genetics
2005
Corpus ID: 26059243
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by defective cationic amino acid (CAA) transport at the…
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2003
2003
Regulation of L-leucine transport in rat kidney by dexamethasone and triiodothyronine
M. Schwertfeger
,
K. Pissowotzki
,
C. Fleck
,
P. Taylor
Amino Acids
2003
Corpus ID: 20335629
Summary. We have investigated the transport mechanisms involved in the stimulation of renal tubular reabsorption of large amino…
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