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Solute Carrier Family
Known as:
SLC Family
, Solute Carrier Group
A large group of integral membrane proteins that are involved in either facilitated or secondary active transport of solutes across cellular…
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National Institutes of Health
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Related topics
Related topics
50 relations
Adenosine 3'-phospho 5'-phosphosulfate Transporter 1
Anion Exchange Protein 1, Erythrocyte
B(0,+)-Type Amino Acid Transporter 1
Cellular Membrane
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Association of solute carrier family 2, member 9 (SLC2A9) genetic variant rs3733591 with gout in a Malay sample set.
W. Taib
,
Mahfudzah Adanan
,
+5 authors
T. Merriman
The Medical journal of Malaysia
2018
Corpus ID: 53036242
INTRODUCTION Gout is one of the most common inflammatory arthritis in Malaysia. It is due to persistent hyperuricemia that leads…
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2017
2017
Upregulated solute carrier family 37 member 1 in colorectal cancer is associated with poor patient outcome and metastasis
Daiki Kikuchi
,
M. Saito
,
+10 authors
S. Takenoshita
Oncology Letters
2017
Corpus ID: 3304733
Solute carrier (SLC) drug transporters exchange various molecules without energy from adenosine triphosphate hydrolysis…
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2017
2017
Leptin (rs7799039) and solute carrier family 30 zinc transporter (rs13266634) polymorphisms in Euro-Brazilian pregnant women with gestational diabetes.
A. Teleginski
,
M. Welter
,
+5 authors
G. Picheth
Genetics and Molecular Research
2017
Corpus ID: 44674155
Leptin (LEP), a protein that plays a fundamental role in the metabolism of energy reserves, and the solute carrier family 30 A8…
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2016
2016
RAPID COMMUNICATION: Isolation of glucose transporters and in bovine uteroplacental tissues from days 16 to 50 of gestation.
M. Crouse
,
J. Caton
,
+5 authors
A. Ward
Journal of Animal Science
2016
Corpus ID: 24781661
Glucose transporter solute carrier family 2 member 14 () is a duplicon of glucose transporter solute carrier family 2 member 3…
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2014
2014
Tag polymorphisms of solute carrier family 12 member 3 gene modify the risk of hypertension in northeastern Han Chinese
Y-L Wang
,
Y. Qi
,
+9 authors
W. Niu
Journal of Human Hypertension
2014
Corpus ID: 24894582
Converging evidence suggests that the gene encoding solute carrier family 12 member 3 (SLC12A3) is a logical candidate involved…
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2010
2010
Large-scale medical resequencing for X-linked mental retardation.
Yiping Shen
,
Bai-Lin Wu
,
J. Gusella
Clinical Chemistry
2010
Corpus ID: 1555762
Severe intellectual disability (ID),1 commonly referred to as mental retardation (MR), comprises a large collection of clinical…
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2007
2007
Mutations in the SLC30A8 gene are not a major cause of MODY or other forms of early-onset, autosomal dominant type 2 diabetes
M. Borowiec
,
R. Thompson
,
C. Powers
,
R. Xu
,
T. Dickey
,
A. Doria
Diabetologia
2007
Corpus ID: 28160631
Maturity onset diabetes of the young or MODY is a relatively rare type of familial diabetescharacterized by a young age of onset…
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2005
2005
Assignment of the solute carrier family 27 member 1 (SLC27A1) gene to bovine chromosome 7.
L. Ordovás
,
R. Roy
,
Pilar Zaragoza
,
Hélène Hayes
,
André Eggen
,
C. Rodellar
Animal Genetics
2005
Corpus ID: 26148881
Source/description: Long chain fatty acids (LCFAs) are an important source of energy for most organisms and are also involved in…
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2004
2004
Assignment of solute carrier family 26 (sulfate transporter), member 2 (SLC26a2) to river buffalo (Bubalus bubalis, 2n = 50) chromosome 9q26 (BBU9q26) by fluorescence in situ hybridization and R…
G. Kierstein
,
L. Iannuzzi
,
A. Silva
,
M. Schneider
,
B.G. Baumgartne
,
B. Brenig
Cytogenetic and Genome Research
2004
Corpus ID: 46849606
a International Livestock Research Institute, Nairobi (Kenya); b National Research Council (CNR), ISPAAM, Laboratory of Animal…
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2002
2002
Lack of Plasma Membrane Targeting of a G172D Mutant Thiamine Transporter Derived from Rogers Syndrome Family
D. Baron
,
Y. Assaraf
,
N. Cohen
,
A. Aronheim
Molecular Medicine
2002
Corpus ID: 36651840
BackgroundRogers syndrome, also known as thiamine responsive megaloblastic anemia (TRMA), is an autosomal recessive disorder…
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