Detalhe da pesquisa
1.
Mutations in the TSGA14 gene in families with autism spectrum disorders.
Am J Med Genet B Neuropsychiatr Genet
; 156B(3): 303-11, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21438139
2.
Candidate gene for the chromosome 1 familial Alzheimer's disease locus.
Science
; 269(5226): 973-7, 1995 Aug 18.
Artigo
Inglês
| MEDLINE | ID: mdl-7638622
3.
Positional cloning of the Werner's syndrome gene.
Science
; 272(5259): 258-62, 1996 Apr 12.
Artigo
Inglês
| MEDLINE | ID: mdl-8602509
4.
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.
Brain
; 130(Pt 5): 1360-74, 2007 May.
Artigo
Inglês
| MEDLINE | ID: mdl-17439980
5.
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.
Genes Brain Behav
; 17(6): e12429, 2018 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29045054
6.
Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control study.
J Clin Epidemiol
; 49(10): 1143-8, 1996 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-8826994
7.
The c-fos gene and early-onset familial Alzheimer's disease.
Neurosci Lett
; 160(1): 33-6, 1993 Sep 17.
Artigo
Inglês
| MEDLINE | ID: mdl-8247328
8.
Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease.
Neurobiol Aging
; 32(3): 556.e13-23, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21196064
9.
Evidence for multiple loci from a genome scan of autism kindreds.
Mol Psychiatry
; 11(11): 1049-60, 979, 2006 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-16880825
10.
Frequency of the erythrogenic toxin B and C genes (speB and speC) among clinical isolates of group A streptococci.
Infect Immun
; 59(1): 211-5, 1991 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-1987034
11.
Molecular epidemiologic analysis of the type A streptococcal exotoxin (erythrogenic toxin) gene (speA) in clinical Streptococcus pyogenes strains.
Infect Immun
; 57(12): 3715-9, 1989 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-2553612
12.
Molecular characterization of new group A streptococcal bacteriophages containing the gene for streptococcal erythrogenic toxin A (speA).
Mol Gen Genet
; 231(1): 161-8, 1991 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-1753942
13.
Management of salt poisoning in an extremely low birth weight infant.
Pediatr Nephrol
; 8(2): 172-4, 1994 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-8018494
14.
Aging-associated neuropathology in Werner syndrome.
Acta Neuropathol
; 96(4): 421-4, 1998 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-9797008
15.
Inactivation of the streptococcal erythrogenic toxin B gene (speB) in Streptococcus pyogenes.
Infect Immun
; 61(9): 3719-23, 1993 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-8359893
16.
The Werner syndrome protein contributes to induction of p53 by DNA damage.
FASEB J
; 14(14): 2138-40, 2000 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-11023999
17.
A panel of radiation hybrids for human chromosome 8.
Genomics
; 21(1): 208-16, 1994 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-8088789
18.
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Genomics
; 35(3): 431-40, 1996 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-8812476
19.
Physical and functional interaction between p53 and the Werner's syndrome protein.
J Biol Chem
; 274(41): 29463-9, 1999 Oct 08.
Artigo
Inglês
| MEDLINE | ID: mdl-10506209
20.
Homozygosity mapping of the Werner syndrome locus (WRN).
Genomics
; 23(3): 600-8, 1994 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-7851888