1.
The SLC38 family of sodium–amino acid co-transporters
by Broer, Stefan
Pflügers Archiv, 2013, Vol.466 (1), p.155-172
2.
Amino acids regulate mTOR pathway and milk protein synthesis in a mouse mammary epithelial cell line is partly mediated by T1R1/T1R3
by Wang, YanHong
European journal of nutrition, 2016, Vol.56 (8), p.2467-2474
3.
Allosteric inhibition of lysyl oxidase-like-2 impedes the development of a pathologic microenvironment
by Smith, Victoria
Nature medicine, 2010, Vol.16 (9), p.1009-1017
4.
Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway
by Hart, Claire E
American journal of human genetics, 2007, Vol.80 (5), p.931-937
5.
Amino acid changes during transition to a vegan diet supplemented with fish in healthy humans
by Elshorbagy, Amany
European journal of nutrition, 2016, Vol.56 (5), p.1953-1962
6.
Imaging Patients with Psychosis and a Mouse Model Establishes a Spreading Pattern of Hippocampal Dysfunction and Implicates Glutamate as a Driver
by Schobel, Scott A
Neuron (Cambridge, Mass.), 2013, Vol.78 (1), p.81-93
7.
Plasma branched chain/aromatic amino acids, enriched Mediterranean diet and risk of type 2 diabetes: case-cohort study within the PREDIMED Trial
by Ruiz-Canela, Miguel
Diabetologia, 2018, Vol.61 (7), p.1560-1571
8.
Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency
by Banka, Siddharth
American journal of human genetics, 2011, Vol.88 (2), p.216-225
9.
Sarcopenia impairs prognosis of patients with liver cirrhosis
by Hanai, Tatsunori, M.D
Nutrition (Burbank, Los Angeles County, Calif.), 2015, Vol.31 (1), p.193-199
10.
Genetic evidence of a causal effect of insulin resistance on branched-chain amino acid levels
by Mahendran, Yuvaraj
Diabetologia, 2017, Vol.60 (5), p.873-878
11.
Late-onset episodic ataxia associated with SLC1A3 mutation
by Choi, Kwang-Dong
Journal of human genetics, 2017, Vol.62 (3), p.443-446
12.
DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria
by Danhauser, Katharina
American journal of human genetics, 2012, Vol.91 (6), p.1082-1087
13.
Cell-type-specific metabolic labeling of nascent proteomes in vivo
by Alvarez-Castelao, Beatriz
Nature biotechnology, 2017, Vol.35 (12), p.1196-1201
14.
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-Coa dehydrogenase deficiency
by KÖLKER, Stefan
Pediatric research, 2006, Vol.59 (6), p.840-847
15.
Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome
by Pierce, Sarah B
American journal of human genetics, 2013, Vol.92 (4), p.614-620
16.
Branched-chain amino acid levels are associated with improvement in insulin resistance with weight loss
by Shah, S. H
Diabetologia, 2011, Vol.55 (2), p.321-330
17.
Elevation of circulating branched-chain amino acids is an early event in human pancreatic adenocarcinoma development
by Mayers, Jared R
Nature medicine, 2014, Vol.20 (10), p.1193-1198
18.
Metabolite profiles and the risk of developing diabetes
by Wang, Thomas J
Nature medicine, 2011, Vol.17 (4), p.448-453
19.
Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease
by Porath, Binu
American journal of human genetics, 2016, Vol.98 (6), p.1193-1207
20.
Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut- , cblA, cblB)
by HÖRSTER, Friederike
Pediatric research, 2007, Vol.62 (2), p.225-230
Filter electronic articles 10.272 Hits
Remove Filters
- Subjects
- Female
- Science & Technology (8.512)
- Life Sciences & Biomedicine (8.281)
- more ...