Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Yolanda Narain"'
Autor:
Karl Fredga, Yolanda Narain
Publikováno v:
Hereditas. 125:137-145
Karyotypes of 319 common shrews from the area of Surahammar, central Sweden, were studied. A G-banding technique revealed the presence of two chromosome races: the Hallefors race (SM) and the Uppsa ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::893d3dc2bc2f0164ff4352189fa2ee64
https://doi.org/10.1111/j.1601-5223.1996.00137.x
https://doi.org/10.1111/j.1601-5223.1996.00137.x
Autor:
Bernardino Ghetti, Bradley S. Glazier, Yolanda Narain, Maria Grazia Spillantini, Pedro Piccardo, Jill R. Murrell, R. Anthony Crowther, Ross Jakes, Michel Goedert, Atsuo Koto, Hirotaka Yoshida, Miho Tsutsui, Masaki Takao, Ruben Vidal
Publikováno v:
Brain Pathol
The clinical and neuropathological characteristics of an atypical form of dementia with Lewy bodies (DLB) are described. The proband experienced difficulties in her school performance at 13 years of age. Neurological examination revealed cognitive dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b525a0b41b7a4bb4d0198f4df6a60725
https://doi.org/10.1111/j.1750-3639.2004.tb00046.x
https://doi.org/10.1111/j.1750-3639.2004.tb00046.x
Publikováno v:
Molecular Ecology. 13:1205-1215
The common shrew, Sorex araneus, exhibits an unusually high level of karyotypic variation. Populations with identical or similar karyotypes are defined as chromosome races, which are, in turn, grouped into larger evolutionary units, karyotypic groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7bc29f21849a149eb7807ebb0e8cf57
https://doi.org/10.1111/j.1365-294x.2004.02146.x
https://doi.org/10.1111/j.1365-294x.2004.02146.x
Autor:
Louise C. Serpell, Yolanda Narain, Robert Layfield, Della C. David, Michel Goedert, Maria Grazia Spillantini
Publikováno v:
Journal of Neurochemistry. 83:176-185
Filamentous inclusions composed of the microtubule-associated protein tau are a defining characteristic of a large number of neurodegenerative diseases. Here we show that tau degradation in stably transfected and non-transfected SH-SY5Y cells is bloc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6271297267f9e5120c3b12d96610f3a2
https://doi.org/10.1046/j.1471-4159.2002.01137.x
https://doi.org/10.1046/j.1471-4159.2002.01137.x
Autor:
Karl Fredga, Yolanda Narain
Publikováno v:
Biological Journal of the Linnean Society. 70:285-307
Six chromosome races of the common shrew occur in Sweden, each with its characteristic arm combination of metacentric chromosomes. G-banded karyotypes were analysed from 201 common shrews in 14 localities of the northern hybrid zone in Sweden. Analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45e3e8dbf14e705f0f603f0b00a3bc51
https://doi.org/10.1111/j.1095-8312.2000.tb00211.x
https://doi.org/10.1111/j.1095-8312.2000.tb00211.x
Autor:
Julia Rankin, Yolanda Narain, Robert A. Furlong, Andreas Wyttenbach, Jina Swartz, David C. Rubinsztein, Jenny Carmichael
Publikováno v:
Proceedings of the National Academy of Sciences. 97:2898-2903
Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations. A feature of these diseases is ubiquitinated intraneuronal inclusions derived
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb22e93ddf077f13e8a48ae9cf976ead
https://doi.org/10.1073/pnas.97.6.2898
https://doi.org/10.1073/pnas.97.6.2898
Publikováno v:
Biochemical Journal. 346:577-581
Protein aggregates are a neuropathological feature of Huntington's disease and Parkinson's disease. Mutant huntingtin exon 1 with 72 CAG repeats fused to enhanced green fluorescent protein (EGFP) forms hyperfluorescent inclusions in PC12 cells. Inclu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a47183bb562885e7dd1765e9f1d9451c
https://doi.org/10.1042/bj3460577
https://doi.org/10.1042/bj3460577
Publikováno v:
Journal of Medical Genetics. 36:739-746
Huntington's disease (HD) is thought to show true dominance, since subjects with two mutant alleles have been reported to have similar ages at onset of disease compared to heterozygous sibs. We have investigated this phenomenon using a cell culture m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba06912de4248f622c19725824a768d8
https://doi.org/10.1136/jmg.36.10.739
https://doi.org/10.1136/jmg.36.10.739
Autor:
Della C, David, Robert, Layfield, Louise, Serpell, Yolanda, Narain, Michel, Goedert, Maria Grazia, Spillantini
Publikováno v:
Journal of neurochemistry. 83(1)
Filamentous inclusions composed of the microtubule-associated protein tau are a defining characteristic of a large number of neurodegenerative diseases. Here we show that tau degradation in stably transfected and non-transfected SH-SY5Y cells is bloc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::040d16c4f10dea81f1e69a33f0163be6
https://pubmed.ncbi.nlm.nih.gov/12358741
https://pubmed.ncbi.nlm.nih.gov/12358741
Autor:
Robert A. Furlong, Douglas F. Easton, Agustin G. Yip, Nigel J. Cairns, Yolanda Narain, David C. Rubinsztein, John Grimley Evans, Carol Brayne, John H. Xuereb, Margaret M. Esiri, Terence Murphy
Publikováno v:
Journal of medical genetics. 37(9)
A recent study suggested that the insertion (I) allele in intron 16 of the angiotensin converting enzyme gene (ACE) is associated with Alzheimer's disease (AD) risk. In our series of 239 necropsy confirmed late onset AD cases and 342 elderly non-deme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da7919da0b76b5d704a3b50ec2825d8
https://pubmed.ncbi.nlm.nih.gov/10978362
https://pubmed.ncbi.nlm.nih.gov/10978362