D. Groth

Details der Publikationsliste

Zeitraum

1963 - 2008

Anzahl

27

Co-Autoren

Microsatellite Analysis of Genetic Diversity in Wild and Farmed Emus (Dromaius novaehollandiae) (2002)

Hammond, E. L., Lymbery, A. J., Martin, G. B., Groth, D., Wetherall, J. D.

The emu (Dromaius novaehollandiae) occupies most regions of the Australian continent and in recent times has been farmed for meat, oil, and leather. Very little is known about the genetic structure...

Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice.

Carlson, G A, Ebeling, C, Yang, S L, Telling, G, Torchia, M, Groth, D, ...

Different prion isolates, often referred to as "strains," present an enigma because considerable evidence argues that prions are devoid of nucleic acid. To investigate prion diversity, we inoculated...

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein.

Hsiao, K K, Groth, D, Scott, M, Yang, S L, Serban, H, Rapp, D, ...

Two lines of transgenic (Tg) mice expressing high (H) levels of the mutant P101L prion protein (PrP) developed a neurologic illness and central nervous system pathology indistinguishable from...

Attempts to restore scrapie prion infectivity after exposure to protein denaturants.

Prusiner, S B, Groth, D, Serban, A, Stahl, N, Gabizon, R

A wealth of experimental evidence argues that infectious prions are composed largely, if not entirely, of the scrapie isoform of the prion protein. We attempted to restore scrapie infectivity after...

Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform.

DeArmond, S J, Yang, S L, Lee, A, Bowler, R, Taraboulos, A, Groth, D, ...

To investigate the molecular basis of prion diversity, we inoculated transgenic mice expressing the Syrian hamster prion protein (PrP) with three distinct prion isolates. We compared the three...

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.

Prusiner, S B, Groth, D, Serban, A, Koehler, R, Foster, D, Torchia, M, ...

Mice, homozygous for prion protein (PrP) gene ablation (Prn-p0/0), develop normally and remain well > 500 days after inoculation with murine scrapie prions. In contrast, wild-type mice developed...

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins.

Pan, K M, Baldwin, M, Nguyen, J, Gasset, M, Serban, A, Groth, D, ...

Prions are composed largely, if not entirely, of prion protein (PrPSc in the case of scrapie). Although the formation of PrPSc from the cellular prion protein (PrPC) is a post-translational process,...

Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity.

Riesner, D, Kellings, K, Post, K, Wille, H, Serban, H, Groth, D, ...

An abnormal isoform of the prion protein (PrP) designated PrPSc is the major, or possibly the only, component of infectious prions. Structural studies of PrPSc have been impeded by its lack of...

Failure to transmit disease from gray tremor mutant mice.

Carlson, G A, Banks, S, Lund, D, Reichert, C, Groth, D, Torchia, M, ...

Mice homozygous for mutant alleles at the gray tremor (gt) locus develop a marked non-intention tremor beginning at 8 days of age. Most homozygous mice die by 3 months. Homozygotes exhibit intense...

Propagation of prion strains through specific conformers of the prion protein.

Scott, M R, Groth, D, Tatzelt, J, Torchia, M, Tremblay, P, DeArmond, S J, ...

Two prion strains with identical incubation periods in mice exhibited distinct incubation periods and different neuropathological profiles upon serial transmission to transgenic mice expressing...

Immunoaffinity purification and neutralization of scrapie prion infectivity.

Gabizon, R, McKinley, M P, Groth, D, Prusiner, S B

Prions are unusual infectious pathogens causing scrapie of sheep and goats as well as Creutzfeldt-Jakob disease of humans. Biochemical and genetic studies contend that the scrapie isoform of the...

Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice.

Carlson, G A, Ebeling, C, Yang, S L, Telling, G, Torchia, M, Groth, D, ...

Different prion isolates, often referred to as "strains," present an enigma because considerable evidence argues that prions are devoid of nucleic acid. To investigate prion diversity, we inoculated...

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein.

Hsiao, K K, Groth, D, Scott, M, Yang, S L, Serban, H, Rapp, D, ...

Two lines of transgenic (Tg) mice expressing high (H) levels of the mutant P101L prion protein (PrP) developed a neurologic illness and central nervous system pathology indistinguishable from...

Attempts to restore scrapie prion infectivity after exposure to protein denaturants.

Prusiner, S B, Groth, D, Serban, A, Stahl, N, Gabizon, R

A wealth of experimental evidence argues that infectious prions are composed largely, if not entirely, of the scrapie isoform of the prion protein. We attempted to restore scrapie infectivity after...

Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform.

DeArmond, S J, Yang, S L, Lee, A, Bowler, R, Taraboulos, A, Groth, D, ...

To investigate the molecular basis of prion diversity, we inoculated transgenic mice expressing the Syrian hamster prion protein (PrP) with three distinct prion isolates. We compared the three...

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.

Prusiner, S B, Groth, D, Serban, A, Koehler, R, Foster, D, Torchia, M, ...

Mice, homozygous for prion protein (PrP) gene ablation (Prn-p0/0), develop normally and remain well > 500 days after inoculation with murine scrapie prions. In contrast, wild-type mice developed...

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins.

Pan, K M, Baldwin, M, Nguyen, J, Gasset, M, Serban, A, Groth, D, ...

Prions are composed largely, if not entirely, of prion protein (PrPSc in the case of scrapie). Although the formation of PrPSc from the cellular prion protein (PrPC) is a post-translational process,...

Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity.

Riesner, D, Kellings, K, Post, K, Wille, H, Serban, H, Groth, D, ...

An abnormal isoform of the prion protein (PrP) designated PrPSc is the major, or possibly the only, component of infectious prions. Structural studies of PrPSc have been impeded by its lack of...

Failure to transmit disease from gray tremor mutant mice.

Carlson, G A, Banks, S, Lund, D, Reichert, C, Groth, D, Torchia, M, ...

Mice homozygous for mutant alleles at the gray tremor (gt) locus develop a marked non-intention tremor beginning at 8 days of age. Most homozygous mice die by 3 months. Homozygotes exhibit intense...

Propagation of prion strains through specific conformers of the prion protein.

Scott, M R, Groth, D, Tatzelt, J, Torchia, M, Tremblay, P, DeArmond, S J, ...

Two prion strains with identical incubation periods in mice exhibited distinct incubation periods and different neuropathological profiles upon serial transmission to transgenic mice expressing...

Immunoaffinity purification and neutralization of scrapie prion infectivity.

Gabizon, R, McKinley, M P, Groth, D, Prusiner, S B

Prions are unusual infectious pathogens causing scrapie of sheep and goats as well as Creutzfeldt-Jakob disease of humans. Biochemical and genetic studies contend that the scrapie isoform of the...