Results 111 to 120 of about 13,220 (172)

Rescue of myocytes and locomotion through AAV2/9-2YF intracisternal gene therapy in a rat model of creatine transporter deficiency. [PDF]

Mol Ther Methods Clin Dev
Fernandes-Pires G, Azevedo MD, Lanzillo M, Roux-Petronelli C, Binz PA, Cudalbu C, Sandi C, Tenenbaum L, Braissant O.   +8 more
europepmc   +1 more source

Mouse model for creatine transporter deficiency (CTD) [PDF]

Science-Business eXchange, 2012
openaire   +1 more source

Biogenesis of Organelles and Membrane Proteins. [PDF]

, 1988
Harmey, Matthew A., Neupert, Walter, Nicholson, Donald W., Stuart, Rosemary A.   +3 more
core   +1 more source

The Regulation and Expression of the Creatine Transporter: A Brief Review of Creatine Supplementation in Humans and Animals [PDF]

Ryan D Schoch, Darryn Willoughby, Mike Greenwood, JLM Mesa, A Chanutin, A Chanutin, RC Harris, AM Persky, RJ Snow, O Speer, B Walzel, ML Guerrero-Ontiveros, CD Fitch, R Murphy, W Wang, MJ Peral, JJ Brault, JJ Brault, GJ Pyne-Geithman, TJ DeGrauw, MA Tarnopolsky, ML Guerrero-Ontiveros, KKO Watt, RM Murphy, M Tarnopolsky, Z Argov, PL Greenhaff, DG Syrotuik, AL Green, JE Odoom   +29 more
core   +1 more source

A Nervous System-Specific Model of Creatine Transporter Deficiency Recapitulates the Cognitive Endophenotype of the Disease: a Longitudinal Study. [PDF]

Sci Rep, 2019
Molinaro A, Alessandrì MG, Putignano E, Leuzzi V, Cioni G, Baroncelli L, Pizzorusso T.   +6 more
europepmc   +1 more source

IS GLYCINE SUPPLEMENTATION USEFUL IN CREATINE TRANSPORTER DEFICIENCY? [PDF]

International Journal of Advanced Research, 2016
openaire   +1 more source

Creatine transporter deficiency leads to increased whole body and cellular metabolism. [PDF]

Amino Acids, 2016
Perna MK, Kokenge AN, Miles KN, Udobi KC, Clark JF, Pyne-Geithman GJ, Khuchua Z, Skelton MR.   +7 more
europepmc   +1 more source

Creatine Transporter Deficiency: Screening of Males with Neurodevelopmental Disorders and Neurocognitive Characterization of a Case. [PDF]

J Dev Behav Pediatr, 2016
Thurm A, Himelstein D, DʼSouza P, Rennert O, Jiang S, Olatunji D, Longo N, Pasquali M, Swedo S, Salomons GS, Carrillo N.   +10 more
europepmc   +1 more source

Processing of mitochondrial precursor proteins [PDF]

, 1984
Neupert, Walter, Schmidt, Bernd
core  

A novel SLC6A8 mutation associated with motor dysfunction in a child exhibiting creatine transporter deficiency. [PDF]

Hum Genome Var, 2015
Cervera-Acedo C, Lopez M, Aguirre-Lamban J, Santibañez P, Garcia-Oguiza A, Poch-Olive ML, Dominguez-Garrido E.   +6 more
europepmc   +1 more source