Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 128 entries
Sorted by: Best Match Show Resources per page
The trajectory of gray matter development in Broca's area is abnormal in people who stutter.

Frontiers in human neuroscience

Beal DS, Lerch JP, Cameron B, Henderson R, Gracco VL, De Nil LF.
PMID: 25784869
Front Hum Neurosci. 2015 Mar 03;9:89. doi: 10.3389/fnhum.2015.00089. eCollection 2015.

The acquisition and mastery of speech-motor control requires years of practice spanning the course of development. People who stutter often perform poorly on speech-motor tasks thereby calling into question their ability to establish the stable neural motor programs required...

Is metabotropic glutamate receptor 5 upregulated in prefrontal cortex in fragile X syndrome?.

Molecular autism

Lohith TG, Osterweil EK, Fujita M, Jenko KJ, Bear MF, Innis RB.
PMID: 23706040
Mol Autism. 2013 May 24;4(1):15. doi: 10.1186/2040-2392-4-15.

BACKGROUND: Fragile X syndrome (FXS) is a common inherited form of intellectual disability caused by loss of function of the fragile X mental retardation protein. Recent animal studies suggest that upregulated downstream signaling by metabotropic glutamate receptor 5 (mGluR5)...

Laparoscopic hepatectomy for hepatocellular carcinoma: are oncologic outcomes truly superior to an open approach?.

Hepatobiliary surgery and nutrition

Moris D, Burkhart RA, Beal EW, Pawlik TM.
PMID: 28653005
Hepatobiliary Surg Nutr. 2017 Jun;6(3):200-202. doi: 10.21037/hbsn.2017.03.09.

No abstract available.

Profile of collagen gene expression in the glenohumeral capsule of patients with traumatic anterior instability of the shoulder.

Revista brasileira de ortopedia

Belangero PS, Leal MF, de Castro Pochini A, Andreoli CV, Ejnisman B, Cohen M.
PMID: 26229875
Rev Bras Ortop. 2014 Oct 23;49(6):642-6. doi: 10.1016/j.rboe.2014.10.008. eCollection 2014.

OBJECTIVE: To evaluate the expression of the genes COL1A1, COL1A2, COL3A1 and COL5A1 in the glenohumeral capsule of patients with traumatic anterior instability of the shoulder.METHODS: Samples from the glenohumeral capsule of 18 patients with traumatic anterior instability of...

Response:Model of Huntington's disease.

Science (New York, N.Y.)

Beal MF, Kowall NW, Swartz KJ, Ferrante RJ, Martin JB.
PMID: 17792612
Science. 1988 Jul 22;241(4864):475. doi: 10.1126/science.241.4864.475.

No abstract available.

Prognostic import of a large Q3 deflection: a mortality study.

Transactions of the Association of Life Insurance Medical Directors of America

BOLT W, BELL MF.
PMID: 14835766
Trans Assoc Life Insur Med Dir Am. 1950;34:87-98.

No abstract available.

Drug delivery to the cochlea after implantation: consideration of the risk factors.

Cochlear implants international

Garnham C, Reetz G, Jolly C, Miller J, Salt A, Beal F.
PMID: 18792345
Cochlear Implants Int. 2005 Sep;6:12-4. doi: 10.1179/cim.2005.6.Supplement-1.12.

No abstract available.

Excitotoxicity.

Handbook of clinical neurology

Henchcliffe C, Beal MF.
PMID: 18808934
Handb Clin Neurol. 2007;83:553-69. doi: 10.1016/S0072-9752(07)83027-2.

No abstract available.

Hunting-ton for new proteases: MMPs as the new target?.

Neuron

Johri A, Beal MF.
PMID: 20670824
Neuron. 2010 Jul 29;67(2):171-3. doi: 10.1016/j.neuron.2010.07.011.

Mutant huntingtin proteolysis mediated by various proteases plays a key role in Huntington's disease (HD) pathogenesis. In this issue of Neuron, Miller et al. have identified 11 proteases, including matrix metalloproteinases (MMPs), that when inhibited reduce huntingtin proteolysis and...

Metabolomic analysis and signatures in motor neuron disease.

Metabolomics : Official journal of the Metabolomic Society

Rozen S, Cudkowicz ME, Bogdanov M, Matson WR, Kristal BS, Beecher C, Harrison S, Vouros P, Flarakos J, Vigneau-Callahan K, Matson TD, Newhall KM, Beal MF, Brown RH, Kaddurah-Daouk R.
PMID: 18820733
Metabolomics. 2005;1(2):101-108. doi: 10.1007/s11306-005-4810-1.

Motor neuron diseases (MND) are a heterogeneous group of disorders that includes amyotrophic lateral sclerosis (ALS) and result in death of motor neurons. These diseases may produce characteristic perturbations of the metabolome, the collection of small-molecules (metabolites) present in...

Muscling in on PGC-1α for improved quality of life in ALS.

Cell metabolism

Johri A, Beal MF.
PMID: 22560208
Cell Metab. 2012 May 02;15(5):567-9. doi: 10.1016/j.cmet.2012.04.015.

Impaired activity of peroxisome proliferator-activated receptor (PPAR)-γ coactivator (PGC)-1α has been implicated in the pathophysiology of several neurodegenerative disorders. In this issue, Da Cruz et al. (2012) show improved muscle function, but not survival, with increased PGC-1α activity in...

Diffusion imaging of cerebral white matter in persons who stutter: evidence for network-level anomalies.

Frontiers in human neuroscience

Cai S, Tourville JA, Beal DS, Perkell JS, Guenther FH, Ghosh SS.
PMID: 24611042
Front Hum Neurosci. 2014 Feb 11;8:54. doi: 10.3389/fnhum.2014.00054. eCollection 2014.

Deficits in brain white matter have been a main focus of recent neuroimaging studies on stuttering. However, no prior study has examined brain connectivity on the global level of the cerebral cortex in persons who stutter (PWS). In the...

Showing 1 to 12 of 128 entries