Search Results - "Dehejia, Anindya"

The ubiquitin pathway in Parkinson's disease by Leroy, Elisabeth, Boyer, Rebecca, Auburger, Georg, Leube, Barbara, Ulm, Gudrun, Mezey, Eva, Harta, Gyongyi, Brownstein, Michael J, Jonnalagada, Sobhanadditya, Chernova, Tanya, Dehejia, Anindya, Lavedan, Christian, Gasser, Thomas, Steinbach, Peter J, Wilkinson, Keith D, Polymeropoulos, Mihael H

“…Mutations of the α-synuclein gene, have been identified in some familial forms of Parkinson's disease, and α-synuclein protein has been shown to accumulate in…”
Get full text

Alpha-synuclein immunoreactivity of huntingtin polyglutamine aggregates in striatum and cortex of Huntington's disease patients and transgenic mouse models by Charles, Vinod, Mezey, Eva, Reddy, P.Hemachandra, Dehejia, Anindya, Young, Theresa A, Polymeropoulos, Mihail H, Brownstein, Michael J, Tagle, Danilo A

“…Polyglutamine expansions in proteins are implicated in at least eight inherited neurodegenerative disorders, including Huntington's disease. These mutant…”
Get full text

The genexpress IMAGE knowledge base of the human muscle transcriptome: a resource of structural, functional, and positional candidate genes for muscle physiology and pathologies by Piétu, G, Eveno, E, Soury-Segurens, B, Fayein, N A, Mariage-Samson, R, Matingou, C, Leroy, E, Dechesne, C, Krieger, S, Ansorge, W, Reguigne-Arnould, I, Cox, D, Dehejia, A, Polymeropoulos, M H, Devignes, M D, Auffray, C

“…Sequence, gene mapping, and expression data corresponding to 910 genes transcribed in human skeletal muscle have been integrated to form the muscle module of…”
Get full text

Mutation in the α-synuclein gene identified in families with Parkinson's disease by POLYMEROPOULOS, M. H, LAVEDAN, C, STENROOS, E. S, CHANDRASEKHARAPPA, S, ATHANASSIADOU, A, PAPAPETROPOULOS, T, JOHNSON, W. G, LAZZARINI, A. M, DUVOISIN, R. C, DI LORIO, G, GOLBE, L. I, NUSSBAUM, R. L, LEROY, E, IDE, S. E, DEHEJIA, A, DUTRA, A, PIKE, B, ROOT, H, RUBENSTEIN, J, BOYER, R

“…Parkinson's disease (PD) is a common neurodegenerative disorder with a lifetime incidence of approximately 2 percent. A pattern of familial aggregation has…”
Get full text

Molecular Cloning and Mapping of a Novel Human KRAB Domain-Containing C2H2-Type Zinc Finger to Chromosome 7q36.1 by Becker, Kevin G, Nagle, James W, Canning, Rachel D, Dehejia, Anindya M, Polymeropoulos, Mihael H, Gado, Ameer M, Biddison, William E, Drew, Paul D

“…C2H2 zinc finger proteins constitute the largest family of transcription factors known with an estimated 300-500 genes encoding these proteins in the human…”
Get full text

Characterization of the human extracellular matrix protein 1 gene on chromosome 1q21 by Johnson, Maureen R., Wilkin, Douglas J., Vos, Hans L., Ortiz De Luna, Rosa Isela, Dehejia, Anindya M., Polymeropoulos, Mihael H., Francomano, Clair A.

“…Ecm1, the mouse gene encoding extracellular matrix protein 1, is highly expressed in bone and cartilage as well as in osteogenic, preosteoblastic and…”
Get full text

Molecular cloning and mapping of a novel developmentally regulated human C2H2-type zinc finger by Becker, K G, Canning, R D, Nagle, J W, Dehejia, A M, Polymeropoulos, M H, Lee, I J, Gado, A M, Biddison, W E, Drew, P D

“…Zinc finger domains are found in a variety of protein families including steroid receptor, ring finger, and C2H2-type zinc finger proteins. C2H2-type zinc…”
Get full text

Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element by Touchman, J W, Dehejia, A, Chiba-Falek, O, Cabin, D E, Schwartz, J R, Orrison, B M, Polymeropoulos, M H, Nussbaum, R L

“…The human alpha-synuclein gene (SNCA) encodes a presynaptic nerve terminal protein that was originally identified as a precursor of the non-beta-amyloid…”
Get full text

Identification, localization and characterization of the human γ-synuclein gene by LAVEDAN, C, LEROY, E, DEHEJIA, A, BUCHHOLTZ, S, DUTRA, A, NUSSBAUM, R. L, POLYMEROPOULOS, M. H

“…We have identified and characterized a new member of the human synuclein gene family, gamma-synuclein (SNCG). This gene is composed of five exons, which encode…”
Get full text

Serine phosphorylation, chromosomal localization, and transforming growth factor-beta signal transduction by human bsp-1 by Lechleider, R J, de Caestecker, M P, Dehejia, A, Polymeropoulos, M H, Roberts, A B

“…The transforming growth factor-beta (TGF-beta) superfamily regulates a multitude of cellular and developmental events. TGF-beta family ligands signal through…”
Get full text

Genomic Organization and Expression of the Human β-Synuclein Gene (SNCB) by Lavedan, Christian, Leroy, Elisabeth, Torres, Rosarelis, Dehejia, Anindya, Dutra, Amalia, Buchholtz, Stephanie, Nussbaum, Robert L., Polymeropoulos, Mihael H.

“…The β-synuclein protein is highly homologous to the α-synuclein protein for which two mutations were reported in some familial cases of Parkinson disease. It…”
Get full text

Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein : Identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects by STUMPO, D. J, EDDY, R. L, BLACKSHEAR, P. J, HALEY, L. L, SAIT, S, SHOWS, T. B, LAI, W. S, YOUNG, W. S, SPEER, M. C, DEHEJIA, A, POLYMEROPOULOS, M

“…The MARCKS-like protein (MLP), also known as F52, MacMARCKS, or MARCKS-related protein, is a widely distributed substrate for protein kinase C (PKC). Recent…”
Get full text

Serine Phosphorylation, Chromosomal Localization, and Transforming Growth Factor-β Signal Transduction by Human bsp-1 by Robert J. Lechleider, Mark P. de Caestecker, Anindya Dehejia, Mihael H. Polymeropoulos, Anita B. Roberts

“…The transforming growth factor-β (TGF-β) superfamily regulates a multitude of cellular and developmental events. TGF-β family ligands signal through…”
Get full text

Serine Phosphorylation, Chromosomal Localization, and Transforming Growth Factor-β Signal Transduction by Human by Lechleider, Robert J., de Caestecker, Mark P., Dehejia, Anindya, Polymeropoulos, Mihael H., Roberts, Anita B.

Get full text

Promoter Sequence, Expression, and Fine Chromosomal Mapping of the Human Gene (MLP) Encoding the MARCKS-like Protein: Identification of Neighboring and Linked Polymorphic Loci forMLPandMACSand Use in the Evaluation of Human Neural Tube Defects by Stumpo, Deborah J., Eddy, Roger L., Haley, Linda L., Sait, Sheila, Shows, Thomas B., Lai, Wi S., Young, W.Scott, Speer, Marcy C., Dehejia, Anindya, Polymeropoulos, Mihael, Blackshear, Perry J.

“…The MARCKS-like protein (MLP), also known as F52, MacMARCKS, or MARCKS-related protein, is a widely distributed substrate for protein kinase C (PKC). Recent…”
Get full text

Isolation of chromosome-specific ESTs by microdissection-mediated cDNA capture by Gracia, E, Ray, M E, Polymeropoulos, M H, Dehejia, A, Meltzer, P S, Trent, J M

“…Despite dramatic advances in the identification of human expressed sequence tags (ESTs), techniques that facilitate isolation of chromosome or chromosome…”
Get full text

The Magainin gene family in Xenopus laevis: Expansion of this gene family on the basis of its conserved structural framework by Dehejia, Anindya Makarand

“…The studies here detail the identification, isolation and characterization of a novel member of the Magainin gene family. The Magainin peptides are recently…”
Get full text

Contig map of the Parkinson's disease region on 4q21-q23 by Lavedan, C, Dehejia, A, Pike, B, Dutra, A, Leroy, E, Ide, S E, Root, H, Rubenstein, J, Boyer, R L, Chandrasekharappa, S, Makalowska, I, Nussbaum, R L, Polymeropoulos, M H

“…We have constructed a yeast artificial chromosome contig (YAC) map of human chromosome 4q21-q23 across the Parkinson's disease region by combining molecular…”
Get full text

Genomic distribution and gonadal mRNA expression of two human luteinizing hormone receptor exon 1 sequences in random populations by Tsai-Morris, C H, Geng, Y, Buczko, E, Dehejia, A, Dufau, M L

“…Exon 1 of the human luteinizing hormone receptor (LHR) gene coding region exhibits at least two forms of sequence heterogeneity between 37 and 60 bp, spanning…”
Get more information

Mutation in the α-Synuclein Gene Indentified in Families with Parkinson's Disease by Polymeropoulos, Mihael H., Lavedan, Christian, Leroy, Elisabeth, Ide, Susan E., Dehejia, Anindya, Dutra, Amalia, Pike, Brian, Root, Holly, Rubenstein, Jeffrey, Boyer, Rebecca, Stenroos, Edward S., Chandrasekharappa, Settara, Athanassiadou, Aglaia, Papapetropoulos, Theodore, Johnson, William G., Lazzarini, Alice M., Duvoisin, Roger C., Di Iorio, Giuseppe, Golbe, Lawrence I., Nussbaum, Robert L.

“…Parkinson's disease (PD) is a common neurodegenerative disorder with a lifetime incidence of approximately 2 percent. A pattern of familial aggregation has…”
Get full text