Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Keith Slifer"'
Autor:
Zixuan Lin, Tiffany McIntyre, Dengrong Jiang, Alicia Cannon, Peiying Liu, Aylin Tekes, James F. Casella, Keith Slifer, Hanzhang Lu, Eboni Lance
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Sickle cell disease (SCD) is an inherited hemoglobinopathy with an increased risk of neurological complications. Due to anemia and other factors related to the underlying hemoglobinopathy, cerebral blood flow (CBF) increases as compensation; however,
Externí odkaz:
https://doaj.org/article/7fcb0bb33bf144d9809f925ac31b63b1
Autor:
James Robert Brašić, Jack Alexander Goodman, Ayon Nandi, David S. Russell, Danna Jennings, Olivier Barret, Samuel D. Martin, Keith Slifer, Thomas Sedlak, Anil Kumar Mathur, John P. Seibyl, Elizabeth M. Berry-Kravis, Dean F. Wong, Dejan B. Budimirovic
Publikováno v:
Brain Sciences, Vol 12, Iss 3, p 314 (2022)
Multiple lines of evidence suggest that a deficiency of Fragile X Mental Retardation Protein (FMRP) mediates dysfunction of the metabotropic glutamate receptor subtype 5 (mGluR5) in the pathogenesis of fragile X syndrome (FXS), the most commonly know
Externí odkaz:
https://doaj.org/article/a1c24f10d046468782c1830dbc4bd8a5
Autor:
James R. Brašić, Ayon Nandi, David S. Russell, Danna Jennings, Olivier Barret, Anil Mathur, Keith Slifer, Thomas Sedlak, Samuel D. Martin, Zabecca Brinson, Pankhuri Vyas, John P. Seibyl, Elizabeth M. Berry-Kravis, Dean F. Wong, Dejan B. Budimirovic
Publikováno v:
Brain Sciences, Vol 10, Iss 12, p 899 (2020)
Glutamatergic receptor expression is mostly unknown in adults with fragile X syndrome (FXS). Favorable behavioral effects of negative allosteric modulators (NAMs) of the metabotropic glutamate receptor subtype 5 (mGluR5) in fmr1 knockout (KO) mouse m
Externí odkaz:
https://doaj.org/article/db437a126ef0462aaf2bf7f51b8ed8e6
Autor:
James Robert Brašić, Jack Alexander Goodman, Ayon Nandi, David S. Russell, Danna Jennings, Olivier Barret, Samuel D. Martin, Keith Slifer, Thomas Sedlak, Anil Kumar Mathur, John P. Seibyl, Elizabeth M. Berry-Kravis, Dean F. Wong, Dejan B. Budimirovic
Publikováno v:
Brain Sciences; Volume 12; Issue 3; Pages: 314
Multiple lines of evidence suggest that a deficiency of Fragile X Mental Retardation Protein (FMRP) mediates dysfunction of the metabotropic glutamate receptor subtype 5 (mGluR5) in the pathogenesis of fragile X syndrome (FXS), the most commonly know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf5f57cf1516c388fb92f5a40d8bb65a
https://pubmed.ncbi.nlm.nih.gov/35326270
https://pubmed.ncbi.nlm.nih.gov/35326270
Autor:
Zixuan Lin, Tiffany McIntyre, Dengrong Jiang, Alicia Cannon, Peiying Liu, Aylin Tekes, James F. Casella, Keith Slifer, Hanzhang Lu, Eboni Lance
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Sickle cell disease (SCD) is an inherited hemoglobinopathy with an increased risk of neurological complications. Due to anemia and other factors related to the underlying hemoglobinopathy, cerebral blood flow (CBF) increases as compensation; however,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05fe5cc7525edd8ef97a301e26e8dabe
https://pubmed.ncbi.nlm.nih.gov/35222083
https://pubmed.ncbi.nlm.nih.gov/35222083
