Zobrazeno 1 - 10
of 147
pro vyhledávání: '"Wade Hamilton"'
Autor:
Jordi Creus-Muncunill, Jean Vianney Haure-Mirande, Daniele Mattei, Joanna Bons, Angie V. Ramirez, B. Wade Hamilton, Chuhyon Corwin, Sarah Chowdhury, Birgit Schilling, Lisa M. Ellerby, Michelle E. Ehrlich
Publikováno v:
Journal of Neuroinflammation, Vol 21, Iss 1, Pp 1-26 (2024)
Abstract Introduction Huntington’s disease (HD) is a fatal neurodegenerative disorder caused by an expansion of the CAG trinucleotide repeat in the Huntingtin gene (HTT). Immune activation is abundant in the striatum of HD patients. Detection of ac
Externí odkaz:
https://doaj.org/article/b2af945c340e484f850a0185183190e3
Autor:
Sicheng Song, Jordi Creus Muncunill, Carlos Galicia Aguirre, Kizito-Tshitoko Tshilenge, B. Wade Hamilton, Akos A. Gerencser, Houda Benlhabib, Maria-Daniela Cirnaru, Mark Leid, Sean D. Mooney, Lisa M. Ellerby, Michelle E. Ehrlich
Publikováno v:
Biomedicines, Vol 10, Iss 10, p 2377 (2022)
The dysregulation of striatal gene expression and function is linked to multiple diseases, including Huntington’s disease (HD), Parkinson’s disease, X-linked dystonia-parkinsonism (XDP), addiction, autism, and schizophrenia. Striatal medium spiny
Externí odkaz:
https://doaj.org/article/4bd87685543d46c2b0b873499ca2ac64
Autor:
Emilie L. Castranio, Philip Hasel, Jean‐Vianney Haure‐Mirande, Angie V. Ramirez Jimenez, B. Wade Hamilton, Rachel D. Kim, Charles G. Glabe, Minghui Wang, Bin Zhang, Sam Gandy, Shane A. Liddelow, Michelle E. Ehrlich
Publikováno v:
Alzheimer's & Dementia.
The inositol polyphosphate-5-phosphatase D (INPP5D) gene encodes a dual-specificity phosphatase that can dephosphorylate both phospholipids and phosphoproteins. Single nucleotide polymorphisms in INPP5D impact risk for developing late onset sporadic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4818097de544fc665949b91f0b448a3
https://doi.org/10.1002/alz.12821
https://doi.org/10.1002/alz.12821
Autor:
Jordi Creus-Muncunill, Daniele Mattei, Joanna Bons, Angie V. Ramirez-Jimenez, B. Wade Hamilton, Chuhyon Corwin, Sarah Chowdhury, Birgit Schilling, Lisa Ellerby, Michelle E. Ehrlich
BACKGROUNDHuntington’s disease (HD) is a fatal neurodegenerative disorder caused by an expansion of the CAG trinucleotide repeat in the huntingtin gene. Immune activation is abundant in the striatum of HD patients. Detection of active microglia at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bce1fd1e242772557d07b5d5971fea0d
https://doi.org/10.1101/2022.02.18.480944
https://doi.org/10.1101/2022.02.18.480944
Autor:
Shears, Jeremy, Poyner, Gary
Publikováno v:
Journal of the British Astronomical Association. Apr2024, Vol. 134 Issue 2, p136-141. 6p.
Autor:
Creus-Muncunill, Jordi1 (AUTHOR), Haure-Mirande, Jean Vianney1 (AUTHOR), Mattei, Daniele2 (AUTHOR), Bons, Joanna3 (AUTHOR), Ramirez, Angie V.1 (AUTHOR), Hamilton, B. Wade1 (AUTHOR), Corwin, Chuhyon1 (AUTHOR), Chowdhury, Sarah1 (AUTHOR), Schilling, Birgit3 (AUTHOR), Ellerby, Lisa M.3 (AUTHOR), Ehrlich, Michelle E.1 (AUTHOR) michelle.ehrlich@mssm.edu
Publikováno v:
Journal of Neuroinflammation. 3/8/2024, Vol. 21 Issue 1, p1-26. 26p.
Autor:
Paul Francis, Edward D. Helton, Wade Hamilton, James V. Prochazka, Susan Winter, Kenneth L. Jue, Lawrence S. Linn
Publikováno v:
Journal of Child Neurology. 10:2S45-2S51
Metabolic and genetic factors underlie some forms of cardiomyopathy in childhood. A variety of inborn errors of metabolism can impair mitochondrial energy production, or β-oxidation, in the heart and lead to myocardial dysfunction. L-Carnitine, an e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f5f7dd7e9e063a635f7b3f329bf74ac
https://doi.org/10.1177/0883073895010002s07
https://doi.org/10.1177/0883073895010002s07
Publikováno v:
The Journal of Pediatrics. 92:603-607
Correction of essential fatty acid deficiency by transcutaneous absorption of topically applied EFA-rich oil has been reported. We measured serum EFA levels in two groups of neonates receiving fat-free total parenteral nutrition: nine control patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d304d480673326b78b3d7e1c8192d122
https://doi.org/10.1016/s0022-3476(78)80303-5
https://doi.org/10.1016/s0022-3476(78)80303-5
Publikováno v:
Journal of Pediatric Hematology/Oncology. 10:35-38
A 7-week-old infant with methemoglobinemia, hemolytic anemia, and inadequate weight gain was found to have a Campylobacter jejuni gastrointestinal tract infection. Known etiologies of methemoglobinemia such as oxidative drug exposure, deficiency of N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44fc96031c4da6382f91febd58f9b904
https://doi.org/10.1097/00043426-198821000-00007
https://doi.org/10.1097/00043426-198821000-00007
Publikováno v:
Pediatrics. 61(6)
A 7-year-old black boy with sickle cell disease, Wolff-Parkinson-White syndrome, mild left ventricular dysfunction, and normal coronary arteries developed angina pectoris five months after cessation of hypertransfusion therapy. Exercise-induced ECG S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58882fc144245ea35de997eead855017
https://pubmed.ncbi.nlm.nih.gov/673556
https://pubmed.ncbi.nlm.nih.gov/673556