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06/2009
Although many advances in the treatment of schizophrenia have been made over the past decade, little is known about the process of recovery from a first... 
0347 | Sense of Self | Process of Recovery | Recovery | First Episode Schiophrenia
Dissertation
2009, ISBN 9780494713662
Although many advances in the treatment of schizophrenia have been made over the past decade, little is known about the process of recovery from a first... 
Psychology, Clinical
eBook
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2010, Volume 42, Issue 3, pp. 203 - 209
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 05/1998, Volume 273, Issue 21, pp. 12817 - 12826
Journal Article
Cell, ISSN 0092-8674, 08/2019, Volume 178, Issue 5, pp. 1159 - 1175.e17
Expansion of CAG trinucleotide repeats in causes spinocerebellar ataxia type 1 (SCA1), a neurodegenerative disease that impairs coordination and cognition.... 
axonal targeting | BACE1 | Alzheimer’s disease | ataxin-1 | amyloid precursor protein | CA2 | neurodegeneration | spinocerebellar ataxia type 1 | hippocampal neurogenesis
Journal Article
JOURNAL OF BIOLOGICAL CHEMISTRY, ISSN 0021-9258, 05/1998, Volume 273, Issue 21, pp. 12817 - 12826
The cortical deposition of A beta is an event that occurs in Alzheimer's disease, Down's syndrome, head injury, and normal aging. Previously, in appraising the... 
C-REACTIVE PROTEIN | AMYLOID PROTEIN DEPOSITION | HUMAN TRANSFERRIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | SEVERE HEAD-INJURY | DENSITY-LIPOPROTEIN | BINDING SITES | HIGH-AFFINITY | RAT-BRAIN | CEREBROSPINAL-FLUID | APOLIPOPROTEIN-E
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2005, Volume 280, Issue 15, pp. 15413 - 15421
Processing of the beta-amyloid precursor protein (APP) plays a key role in Alzheimer disease neuropathogenesis. APP is cleaved by beta- and alpha-secretase to... 
PRESENILIN | APP | GAMMA-SECRETASE COMPLEX | APH-1 | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | A-BETA | NICASTRIN | PEN-2 | CLEAVAGE | BINDING
Journal Article
Early Intervention in Psychiatry, ISSN 1751-7885, 08/2010, Volume 4, Issue 3, pp. 243 - 250
Although advances in the treatment of schizophrenia have been made, little is known about the process of recovery from first episode of schizophrenia (FES). To... 
Qualitative research | Self-concept | Recovery of function | Schizophrenia | Schizophrenia - diagnosis | Self Concept | Humans | Models, Psychological | Adult | Family | Female | Male | Psychological Theory | Remission, Spontaneous | Qualitative Research | Schizophrenic Psychology
Journal Article
Neuron, ISSN 0896-6273, 10/2013, Volume 80, Issue 2, p. 385
The generation of A[beta], the main component of senile plaques in Alzheimer's disease (AD), is precluded by [alpha]-secretase cleavage within the A[beta]... 
Genetic research | Nervous system diseases | Genetic aspects | Alzheimer's disease | Amyloid beta-protein | Mutation | Alzheimers disease | Transgenic animals | Rodents | Genes
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2006, Volume 281, Issue 43, pp. 32240 - 32253
Ubiquilin 1 (UBQLN1) is a ubiquitin-like protein, which has been shown to play a central role in regulating the proteasomal degradation of various proteins,... 
GAMMA | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | FAMILIAL ALZHEIMERS-DISEASE | CELL-SURFACE | DEGRADATION | PRESENILIN ENDOPROTEOLYSIS | GENERATION | IDENTIFICATION | MISSENSE MUTATIONS | ONSET
Journal Article
Journal Article
Journal of Molecular Neuroscience, ISSN 0895-8696, 01/2005, Volume 25, Issue 1, pp. 67 - 77
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2014, Volume 164, Issue 10, pp. 2557 - 2566
Mowat-Wilson syndrome(MWS) is characterized by moderate to severe intellectual disability and distinctive facial features in association with variable... 
CHARGE syndrome | minor malformations | Mowat–Wilson syndrome | craniosynostosis | intellectual disability | Mowat-Wilson syndrome | Intellectual disability | Minor malformations | Craniosynostosis | MENTAL RETARDATION SYNDROME | SMAD-INTERACTING PROTEIN-1 | CLINICAL-FEATURES | BOX 1B GENE | SYNDROME PHENOTYPE | GENETICS & HEREDITY | MISSENSE MUTATION | HIRSCHSPRUNG-DISEASE | PATIENT | CEREBELLAR HYPOPLASIA | ZFHX1B GENE | Microcephaly - genetics | Face - abnormalities | Humans | Hirschsprung Disease - genetics | Child, Preschool | Infant | Male | Zinc Finger E-box Binding Homeobox 2 | Intellectual Disability - genetics | Young Adult | Facies | Adult | Female | Child | Abnormalities, Multiple - genetics | Infant, Newborn | Craniosynostoses - genetics | Craniosynostoses - diagnosis | Genetic Association Studies - methods | Microcephaly - diagnosis | Repressor Proteins - genetics | CHARGE Syndrome - diagnosis | Mutation - genetics | Homeodomain Proteins - genetics | Hirschsprung Disease - diagnosis | Intellectual Disability - diagnosis | CHARGE Syndrome - genetics | Phenotypes | Congenital diseases | Congenital defects | Intellectual disabilities | Epilepsy | Pattern recognition | Coronary artery disease | Corpus callosum | Choanal atresia | Eye | Hirschsprung's disease | Missense mutation | Microencephaly | Children | Mutation | Heart diseases | Genotypes
Journal Article