Zobrazeno 1 - 10
of 445
pro vyhledávání: '"D A, Figlewicz"'
Publikováno v:
Journal of Lipid Research, Vol 26, Iss 1, Pp 140-144 (1985)
Pre-packed reverse phase columns (Bond Elut) were used for the separation of complex lipids, such as phosphatidylcholine, cerebrosides, sulfatides, and gangliosides, from their respective water-soluble radioactive precursors after their in vitro bios
Externí odkaz:
https://doaj.org/article/39adab232d7f4032a50e96f01335a11f
Autor:
J. K. Fink, T. Heiman-Patterson, T. Bird, F. Cambi, M.-P. Dube, D. A. Figlewicz, J. L. Haines, A. Hentati, M. A. Pericak-Vance, W. Raskind, G. A. Rouleau, T. Siddique
Publikováno v:
Neurology. 46:1507-1514
Hereditary spastic paraplegia (HSP) is a diverse group of inherited disorders characterized by progressive lower-extremity spasticity and weakness. Insight into the genetic basis of these disorders is expanding rapidly. Uncomplicated autosomal domina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccb5cda779835b8258fd1fb448359b52
https://doi.org/10.1212/wnl.46.6.1507
https://doi.org/10.1212/wnl.46.6.1507
Autor:
Madadi, Ahmad Khalid1 (AUTHOR) khalidmadadi@yahoo.com, Sohn, Moon-Jun1,2 (AUTHOR) mjsohn@paik.ac.kr
Publikováno v:
Pharmaceuticals (14248247). Aug2024, Vol. 17 Issue 8, p1070. 33p.
Publikováno v:
Teratology. 62(6)
Family studies have demonstrated that the autism spectrum disorders (ASDs) have a major genetic etiologic component, but expression and penetrance of the phenotype are variable. Mice with null mutations of Hoxa1 or Hoxb1, two genes critical to hindbr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b16d5f5ecf20620c5def571e7e8a5e8
https://pubmed.ncbi.nlm.nih.gov/11091361
https://pubmed.ncbi.nlm.nih.gov/11091361
Publikováno v:
Annals of the New York Academy of Sciences. 919
In order to investigate how mutant SOD1 protein or environmental exogenous stressors lead to the death of motor neurons, we have established several in vitro model systems. We describe some features of the various models in order to demonstrate the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df61b9352ef61cebf9b8fe22ecd72c5c
https://pubmed.ncbi.nlm.nih.gov/11083103
https://pubmed.ncbi.nlm.nih.gov/11083103
Publikováno v:
Annals of neurology. 43(3)
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common inherited diseases of muscle. Until recently, FSHD had received little attention because of its relatively benign course and the perception that it represented a syndrome rather
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad0d300c8b2de4acfffecb9877539481
https://pubmed.ncbi.nlm.nih.gov/9506542
https://pubmed.ncbi.nlm.nih.gov/9506542
Autor:
D A Figlewicz, R. Hamill, Marcy E. MacDonald, Ira Shoulson, K. Steinberg, James M. Powers, A. Rubio, T. Greenamyre
Publikováno v:
Acta neuropathologica. 92(4)
We present the clinical, molecular genetic and neuropathological findings of an 81-year-old man with concurrent Huntington's disease (HD) and familial amyotrophic lateral sclerosis (FALS). His mother had been diagnosed clinically as having ALS. There
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::126218b3c5a92f90e99a7fb935d3c86d
https://pubmed.ncbi.nlm.nih.gov/8891076
https://pubmed.ncbi.nlm.nih.gov/8891076
Autor:
J K, Fink, T, Heiman-Patterson, T, Bird, F, Cambi, M P, Dubé, D A, Figlewicz, J L, Haines, A, Hentati, M A, Pericak-Vance, W, Raskind, G A, Rouleau, T, Siddique
Publikováno v:
Neurology. 46(6)
Hereditary spastic paraplegia (HSP) is a diverse group of inherited disorders characterized by progressive lower-extremity spasticity and weakness. Insight into the genetic basis of these disorders is expanding rapidly. Uncomplicated autosomal domina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c24ea8f5af17aa19c55b636c14eeb79f
https://pubmed.ncbi.nlm.nih.gov/8649538
https://pubmed.ncbi.nlm.nih.gov/8649538
Publikováno v:
Behavioral neuroscience. 109(3)
Chronic intraventricular (IVT) insulin infusion suppresses food intake and body weight in the baboon. It has been hypothesized that one mechanism of this action may be enhancement of the effectiveness of satiety factors that regulate meal size. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df1155a65680fb3888bdd7bc91195839
https://pubmed.ncbi.nlm.nih.gov/7662167
https://pubmed.ncbi.nlm.nih.gov/7662167
Autor:
A, Pramatarova, D A, Figlewicz, A, Krizus, F Y, Han, I, Ceballos-Picot, A, Nicole, M, Dib, V, Meininger, R H, Brown, G A, Rouleau
Publikováno v:
American journal of human genetics. 56(3)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder affecting motor neurons. Although most cases of ALS are sporadic, approximately 10% are inherited as an autosomal dominant trait. Mutations in the Cu/Zn superoxide dismutase ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7cc284890096c2231cb733ab1e43d1c1
https://pubmed.ncbi.nlm.nih.gov/7887412
https://pubmed.ncbi.nlm.nih.gov/7887412