Results 101 to 110 of about 2,755 (211)

Effect of ELX-02 in CTNSY226X/Y226X mice.

open access: yes, 2019
A. Half-cystine measurements show decrease pathologic accumulation in kidneys of CtnsY226X/Y226X mice treated with 7 injections of ELX-02 (10 mg/kg) over a 3-week period. B. Serum creatinine levels show no toxic effect of repeated ELX-02 treatment (50 mg/
Pedro Huertas (4891903)   +9 more
core   +1 more source

Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells

open access: yes
Cystinosis is an autosomal recessive disease caused by mutations in the CTNS gene encoding a protein called cystinosine, which is a lysosomal cystine transporter.
Gok-Topak, Elif Damla Go   +12 more
core   +1 more source

CTNS mutations in publicly-available human cystinosis cell lines

open access: yes, 2015
Patient samples play an important role in the study of inherited metabolic disorders. Open-access biorepositories distribute such samples. Unfortunately, not all clinically-characterized samples come with reliable genotype information.
Renee Kinkade   +3 more
core   +1 more source

Cadenas globales de suministro y activos intangibles en las industrias del automóvil y aeronáutica [PDF]

open access: yesOla Financiera, 2019
La relocalización de las corporaciones transnacionales (CTNs) de las actividades de alta generación de valor ya sea en el más alto nivel (diseño, desarrollo, marcas y propiedad intelectual) o en el más bajo (comercialización, mantenimiento y servicios ...
Claude Serfati , Catherine Sauviat
doaj  

Mutational Spectrum of the CTNS Gene in Egyptian Patients with Nephropathic Cystinosis

open access: yes, 2014
Nephropathic cystinosis is a rare autosomal recessive disorder caused by mutations in the CTNS gene, encoding for cystinosin, a carrier protein transporting cystine out of lysosomes.
Levtchenko, Elena   +7 more
core   +1 more source

Gyrfalcons Falco rusticolus adjust CTNS expression to food abundance: a possible contribution to cysteine homeostasis

open access: yes, 2017
© Springer-Verlag GmbH Germany 2017Melanins form the basis of animal pigmentation. When the sulphurated form of melanin, termed pheomelanin, is synthesized, the sulfhydryl group of cysteine is incorporated to the pigment structure.
Inácio, Ângela   +5 more
core   +1 more source

Nlrp2 deletion ameliorates kidney damage in a mouse model of cystinosis

open access: yesFrontiers in Immunology
Cystinosis is a rare autosomal recessive disorder caused by mutations in the CTNS gene that encodes cystinosin, a ubiquitous lysosomal cystine/H+ antiporter.
Marianna Nicoletta Rossi   +13 more
doaj   +1 more source

Mutation analysis of the CTNS gene in Iranian patients with infantile nephropathic cystinosis: identification of two novel mutations

open access: yes, 2017
Nephropathic cystinosis is an inherited lysosomal transport disorder caused by mutations in the CTNS gene that encodes for a lysosomal membrane transporter, cystinosin.
Majid Fardaei   +3 more
core   +1 more source

CTN Multiple Comparisons Procedures SOP

open access: yes, 2016
This procedure is intended for the Lead Investigator and Protocol Development Team within the Clinical Trials Network as guidance for the consideration of multiple statistical comparisons within a protocol.  The Statistics Workgroup of the Data Management and Analysis Subcommittee will examine the proposed rationale for addressing multiple comparisons ...
openaire   +1 more source

Inducible nitric oxide synthase inhibitor 1400W increases Na+ ,K+ -ATPase levels and activity and ameliorates mitochondrial dysfunction in Ctns null kidney proximal tubular epithelial cells

open access: yes, 2018
Nitric oxide (NO) has been shown to play an important role in renal physiology and pathophysiology partly through its influence on various transport systems in the kidney proximal tubule.
Tara McMorrow   +5 more
core   +1 more source

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