Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Christopher Kerfoot"'
Publikováno v:
Journal of Histochemistry & Cytochemistry. 52:419-422
Forty-six advanced-stage human breast carcinoma specimens were evaluated by immunohistochemistry for PKCα expression and compared with 25 samples of normal adjacent breast tissue. For normal tissue, the median staining of ductal epithelia was of mod
Publikováno v:
Modern Pathology. 14:202-210
Tuberous sclerosis (TSC) is a bigenic autosomal dominant disease caused by mutations in one of two tumor-suppressor genes, TSC1 and TSC2, resulting in benign hamartomas and low grade neoplasms in multiple organs including brain, heart, kidney, and sk
Autor:
Sung Hye Park, Christopher Kerfoot, Michael Catania, Michael W. Johnson, Harry V. Vinters, Paul S. Mischel
Publikováno v:
Developmental Neuroscience. 21:248-259
Cortical dysplasia (CD) represents a common neuropathologic substrate of pediatric epilepsy, one frequently encountered in surgical resection specimens from infants and children with intractable seizure disorders, including infantile spasms. Severe C
Publikováno v:
Science. 346:1131-1131
Concerns about incorrectly or insufficiently characterized antibodies employed in biomedical research have been raised by recent reports of nonreproducible research studies. Reproducibility issues have resulted in loss of time, resources, and scienti
Publikováno v:
Developmental neuroscience. 21(3-5)
Cerebral cortical dysplasia (CD) is a common cause of intractable childhood epilepsy. Five cases of CD were analyzed for GABAA receptor subunit β (GABAAβ), glutamate decarboxylase, AMPA receptor subunit 1 (GluR1) and subunit 2/3 (GluR2/3), and NMDA
Autor:
Jessica K. Emelin, Jeffrey E. DeClue, Christopher Kerfoot, Steven N. Roper, Michael Catania, Harry V. Vinters
Publikováno v:
Epilepsy research. 32(1-2)
Cortical dysplasia (CD) broadly defines a complex cerebral malformative lesion associated clinically with intractable, pharmacoresistant epilepsy (including infantile spasms), especially in infants and children. In CD, the spectrum of structural brai
Autor:
Jeffrey E. DeClue, Harry V. Vinters, Michael J. De Rosa, Vadims Poukens, Ralf Wienecke, Samuel H. Pepkowitz, Christopher Kerfoot, Sung Hye Park
Publikováno v:
Acta neuropathologica. 94(2)
We report an autopsy case of tuberous sclerosis complex (TSC) in a 20-week gestational age female fetus. The brain showed lesions suggestive of early cortical tubers and subependymal hamartomatous nodules. The large cells within these nodular cluster
Autor:
Cynthia T. Welsh, Ralf Wienecke, John C. Maize, Michael Menchine, Margaret G. Norman, Harry V. Vinters, Jeffrey E. DeClue, Christopher Kerfoot, Jessica K. Emelin
Publikováno v:
Brain pathology (Zurich, Switzerland). 6(4)
Tuberous sclerosis (TSC), an autosomal dominant disorder, is characterized by malformations, hamartomas and tumors in various organs including the brain. TSC is genetically linked to two loci: TSC1 on chromosome 9q34 and TSC2 on 16p13.3. TSC2 has bee
Publikováno v:
Annals of Neurology. 42:270-271