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Results: 1-17 |
Results: 17
GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE (GSS) WITH A MUTATION AT PRIONPROTEIN (PRP) RESIDUE-212
Authors: YOUNG K PICCARDO P KISH SJ ANG LC DLOUHY S GHETTI B
Citation: K. Young et al., GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE (GSS) WITH A MUTATION AT PRIONPROTEIN (PRP) RESIDUE-212, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 195-195
ALTERED RESPONSES TO POTASSIUM IN CEREBELLAR NEURONS FROM WEAVER HETEROZYGOTE MICE
Authors: FOX AP DLOUHY S GHETTI B HURLEY JH NUCIFORA PGP NELSON DJ WON L HELLER A
Citation: Ap. Fox et al., ALTERED RESPONSES TO POTASSIUM IN CEREBELLAR NEURONS FROM WEAVER HETEROZYGOTE MICE, Experimental Brain Research, 123(3), 1998, pp. 298-306
PROTEOLIPID PROTEIN (PLP) EXPRESSION IS CRITICAL FOR PNS AS WELL AS CNS MYELINATION - MOLECULAR AND PATHOLOGICAL CHARACTERIZATION OF A FAMILY WITH A NOVEL PLP MUTATION
Authors: GARBERN JY CAMBI F LEWIS R SHY ME HODES ME DLOUHY S PRATT V SIMA A BIRD T KAMHOLZ J
Citation: Jy. Garbern et al., PROTEOLIPID PROTEIN (PLP) EXPRESSION IS CRITICAL FOR PNS AS WELL AS CNS MYELINATION - MOLECULAR AND PATHOLOGICAL CHARACTERIZATION OF A FAMILY WITH A NOVEL PLP MUTATION, Neurology, 48(3), 1997, pp. 6093-6093
HYPOTHALAMIC-PITUITARY FUNCTION IS UNAFFECTED BY THE WEAVER (WV) MOUSE MUTATION
Authors: SCHWARTZ NB SZABO M VERINA T WEI JJ DLOUHY S WON L HELLER A GHETTI B
Citation: Nb. Schwartz et al., HYPOTHALAMIC-PITUITARY FUNCTION IS UNAFFECTED BY THE WEAVER (WV) MOUSE MUTATION, Biology of reproduction, 56, 1997, pp. 565-565
THE MURINE GENE TIAM1 IS DIFFERENTIALLY EXPRESSED IN MOUSE-BRAIN AND DEVELOPMENTALLY-REGULATED IN CEREBELLAR GRANULE NEURONS
Authors: DLOUHY S WEI J FENG Y WANG Y GHETTI B HODES M
Citation: S. Dlouhy et al., THE MURINE GENE TIAM1 IS DIFFERENTIALLY EXPRESSED IN MOUSE-BRAIN AND DEVELOPMENTALLY-REGULATED IN CEREBELLAR GRANULE NEURONS, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 41-41
MULTIPLE ISOFORMS OF ALTERNATIVELY-SPLICED GIRK2 TRANSCRIPTS ARE DIFFERENTIALLY EXPRESSED IN MURINE CNS AND TESTIS
Authors: WEI J HODES M PIVA R WANG Y FENG Y GHETTI B DLOUHY S
Citation: J. Wei et al., MULTIPLE ISOFORMS OF ALTERNATIVELY-SPLICED GIRK2 TRANSCRIPTS ARE DIFFERENTIALLY EXPRESSED IN MURINE CNS AND TESTIS, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 42-42
MODALITIES OF CELL-DEATH IN WEAVER MUTANT MICE
Authors: MIGHELI A ATTANASIO A PIVA R WEI JJ HODES ME DLOUHY S GHETTI B
Citation: A. Migheli et al., MODALITIES OF CELL-DEATH IN WEAVER MUTANT MICE, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 63-63
PROTEINASE-K (PK) RESISTANT PRION PROTEIN (PRP) ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (GSS) F198S
Authors: PICCARDO P SEILER C DLOUHY S YOUNG K FARLOW M PRELLI F FRANGIONE B BUGIANI O TAGLIAVINI F GHETTI B
Citation: P. Piccardo et al., PROTEINASE-K (PK) RESISTANT PRION PROTEIN (PRP) ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (GSS) F198S, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 125-125
GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH MUTATION AT CODON-102 ANDMETHIONINE AT CODON-129 OF PRNP IN PREVIOUSLY UNREPORTED PATIENTS
Authors: YOUNG K JONES CK PICCARDO P LAZZARINI A GOLBE LI ZIMMERMAN TR DICKSON DW MCLACHLAN DC STGEORGEHYSLOP P LENNOX A PERLMAN S VINTERS HV HODES ME DLOUHY S GHETTI B
Citation: K. Young et al., GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH MUTATION AT CODON-102 ANDMETHIONINE AT CODON-129 OF PRNP IN PREVIOUSLY UNREPORTED PATIENTS, Neurology, 45(6), 1995, pp. 1127-1134
EVIDENCE OF GENE FOR CLEFT-LIP AND PALATE TO 4Q
Authors: BEIRAGHI S FOROUD T DLOUHY S BIXLER D CONNEALLY PM HODES ME
Citation: S. Beiraghi et al., EVIDENCE OF GENE FOR CLEFT-LIP AND PALATE TO 4Q, Journal of dental research, 74, 1995, pp. 64-64
FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH MUTATION AT CODON-200 OF THE PRNP GENE - CLINICAL AND PATHOLOGICAL-STUDIES ON A CASE
Authors: CATT KE PICCARDO P FARLOW MR MARKAND O JONES C YOUNG K DLOUHY S GHETTI B
Citation: Ke. Catt et al., FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH MUTATION AT CODON-200 OF THE PRNP GENE - CLINICAL AND PATHOLOGICAL-STUDIES ON A CASE, Annals of neurology, 36(2), 1994, pp. 314-314
CEREBROSPINAL-FLUID LEVELS OF AMYLOID BETA-PROTEIN PRECURSOR ARE LOW IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE, INDIANA KINDRED
Authors: FARLOW M GHETTI B DLOUHY S GIACCONE G BUGIANI O TAGLIAVINI F WAGNER S
Citation: M. Farlow et al., CEREBROSPINAL-FLUID LEVELS OF AMYLOID BETA-PROTEIN PRECURSOR ARE LOW IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE, INDIANA KINDRED, Neurology, 44(8), 1994, pp. 1508-1510
CEREBROSPINAL-FLUID LEVELS OF AMYLOID BETA-PROTEIN PRECURSOR ARE LOW IN AN INDIANA KINDRED WITH GERSTMANN-STRAUSSLER-SCHEINKER DISEASE
Authors: FARLOW MR GHETTI B DLOUHY S GIACCONE G BUGIANI O TAGLIAVINI F WAGNER S
Citation: Mr. Farlow et al., CEREBROSPINAL-FLUID LEVELS OF AMYLOID BETA-PROTEIN PRECURSOR ARE LOW IN AN INDIANA KINDRED WITH GERSTMANN-STRAUSSLER-SCHEINKER DISEASE, Neurology, 43(4), 1993, pp. 193-193
POSSIBLE LOCALIZATION OF A MAJOR GENE FOR CLEFT-LIP AND PALATE TO 4Q
Authors: BEIRAGHI S FOROUD T DLOUHY S WEBER J BIXLER D CONNEALLY PM HODES ME
Citation: S. Beiraghi et al., POSSIBLE LOCALIZATION OF A MAJOR GENE FOR CLEFT-LIP AND PALATE TO 4Q, American journal of human genetics, 53(3), 1993, pp. 975-975
PRNP CODON-129 POLYMORPHISM AND GERSTMANN-STRAUSSLER-SCHEINKER (GSS)WITH MUTATION AT CODON-102
Authors: YOUNG K JONES CK LAZZARINI A GOLBE LI ZIMMERMAN TR DICKSON DW VINTERS HV HODES ME DLOUHY S GHETTI B
Citation: K. Young et al., PRNP CODON-129 POLYMORPHISM AND GERSTMANN-STRAUSSLER-SCHEINKER (GSS)WITH MUTATION AT CODON-102, American journal of human genetics, 53(3), 1993, pp. 1258-1258
ISOLATION OF CHROMOSOME-16 CDNA CLONES FROM A MOUSE NEWBORN WV + CEREBELLAR LIBRARY/
Authors: DLOUHY S WANG Y SANGAMESWARAN L GHETTI B HODES ME
Citation: S. Dlouhy et al., ISOLATION OF CHROMOSOME-16 CDNA CLONES FROM A MOUSE NEWBORN WV + CEREBELLAR LIBRARY/, American journal of human genetics, 53(3), 1993, pp. 1598-1598
PELIZAEUS-MERZBACHER DISEASE IN A FAMILY OF PORTUGUESE ORIGIN CAUSED BY A POINT MUTATION IN EXON 5 OF THE PLP GENE
Authors: PRATT VM BOYADJEV S DLOUHY S SILVER K DERKALOUSTIAN V HODES ME
Citation: Vm. Pratt et al., PELIZAEUS-MERZBACHER DISEASE IN A FAMILY OF PORTUGUESE ORIGIN CAUSED BY A POINT MUTATION IN EXON 5 OF THE PLP GENE, American journal of human genetics, 53(3), 1993, pp. 1751-1751
Risultati: 1-17 |