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Journal of Molecular Medicine (Berlin, Germany)
|
December 18, 2025
Preclinical evaluation of [<sup>11</sup>C]CHDI-009R for quantification of mutant huntingtin aggregates
Franziska Zajicek, Liesbeth Everix, Annemie Van Eetveldt, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 1, 2007
Thiophene substituted acylguanidines as BACE1 inhibitors
William F Fobare, William R Solvibile, Albert J Robichaud, et al.
Journal of Medicinal Chemistry
|
September 18, 2009
Aminoimidazoles as potent and selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
November 19, 2016
Longitudinal Small-Animal PET Imaging of the zQ175 Mouse Model of Huntington Disease Shows In Vivo Changes of Molecular Targets in the Striatum and Cerebral Cortex
Jenny Häggkvist, Miklós Tóth, Lenke Tari, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
August 24, 2022
Biodistribution and dosimetry in human healthy volunteers of the PET radioligands [<sup>11</sup>C]CHDI-00485180-R and [<sup>11</sup>C]CHDI-00485626, designed for quantification of cerebral aggregated mutant huntingtin
Aline Delva, Michel Koole, Kim Serdons, et al.
Journal of Medicinal Chemistry
|
December 9, 2009
Design and synthesis of 5,5'-disubstituted aminohydantoins as potent and selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Aging Cell
|
August 24, 2024
Age-related increase of CD38 directs osteoclastogenic potential of monocytic myeloid-derived suppressor cells through mitochondrial dysfunction in male mice
Ramkumar Thiyagarajan, Lixia Zhang, Omar D Glover, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
June 17, 2025
PET imaging with [¹¹C]CHDI-00485180-R, designed as radioligand for aggregated mutant huntingtin, in people with Huntington's disease
Aline Delva, Michel Koole, Kim Serdons, et al.
Bioorganic & Medicinal Chemistry
|
January 5, 2010
Di-substituted pyridinyl aminohydantoins as potent and highly selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Keith Barnes, Matthew Johnson, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 13, 2011
New pyrazolyl and thienyl aminohydantoins as potent BACE1 inhibitors: exploring the S2' region
Michael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 79) with videos related to
Sort By:
Page
of 8
Journal of Molecular Medicine (Berlin, Germany)
|
December 18, 2025
Preclinical evaluation of [<sup>11</sup>C]CHDI-009R for quantification of mutant huntingtin aggregates
Franziska Zajicek, Liesbeth Everix, Annemie Van Eetveldt, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 1, 2007
Thiophene substituted acylguanidines as BACE1 inhibitors
William F Fobare, William R Solvibile, Albert J Robichaud, et al.
Journal of Medicinal Chemistry
|
September 18, 2009
Aminoimidazoles as potent and selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
November 19, 2016
Longitudinal Small-Animal PET Imaging of the zQ175 Mouse Model of Huntington Disease Shows In Vivo Changes of Molecular Targets in the Striatum and Cerebral Cortex
Jenny Häggkvist, Miklós Tóth, Lenke Tari, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
August 24, 2022
Biodistribution and dosimetry in human healthy volunteers of the PET radioligands [<sup>11</sup>C]CHDI-00485180-R and [<sup>11</sup>C]CHDI-00485626, designed for quantification of cerebral aggregated mutant huntingtin
Aline Delva, Michel Koole, Kim Serdons, et al.
Journal of Medicinal Chemistry
|
December 9, 2009
Design and synthesis of 5,5'-disubstituted aminohydantoins as potent and selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Aging Cell
|
August 24, 2024
Age-related increase of CD38 directs osteoclastogenic potential of monocytic myeloid-derived suppressor cells through mitochondrial dysfunction in male mice
Ramkumar Thiyagarajan, Lixia Zhang, Omar D Glover, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
June 17, 2025
PET imaging with [¹¹C]CHDI-00485180-R, designed as radioligand for aggregated mutant huntingtin, in people with Huntington's disease
Aline Delva, Michel Koole, Kim Serdons, et al.
Bioorganic & Medicinal Chemistry
|
January 5, 2010
Di-substituted pyridinyl aminohydantoins as potent and highly selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Keith Barnes, Matthew Johnson, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 13, 2011
New pyrazolyl and thienyl aminohydantoins as potent BACE1 inhibitors: exploring the S2' region
Michael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Page
of 8