Results
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101.
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B37 repeats are normal in most schizophrenic patients. [electronic resource] by
- Rubinsztein, D C
- Leggo, J
- Goodburn, S
- Barton, D E
- Ferguson-Smith, M A
- Ross, C A
- Li, S H
- Lofthouse, R
- Crow, T J
- DeLisi, L E
Producer: 19941129
In:
The British journal of psychiatry : the journal of mental science vol. 164
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102.
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Association analysis of dynamin-binding protein (DNMBP) on chromosome 10q with late onset Alzheimer's disease in a large caucasian UK sample. [electronic resource] by
- Morgan, A R
- Hollingworth, P
- Abraham, R
- Lovestone, S
- Brayne, C
- Rubinsztein, D C
- Lynch, A
- Lawlor, B
- Gill, M
- O'Donovan, M C
- Owen, M J
- Williams, J
Producer: 20090310
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 150B
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103.
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A 3-basepair deletion in repeat 1 of the LDL receptor promoter reduces transcriptional activity in a South African Pedi. [electronic resource] by
- Peeters, A V
- Kotze, M J
- Scholtz, C L
- De Waal, L F
- Rubinsztein, D C
- Coetzee, G A
- Zuliani, G
- Streiff, R
- Liu, J
- van der Westhuyzen, D R
Producer: 19980828
In:
Journal of lipid research vol. 39
Availability: No items available.
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104.
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Psychiatric symptoms and CAG repeats in neurologically asymptomatic Huntington's disease gene carriers. [electronic resource] by
- Berrios, G E
- Wagle, A C
- Marková, I S
- Wagle, S A
- Ho, L W
- Rubinsztein, D C
- Whittaker, J
- Ffrench-Constant, C
- Kershaw, A
- Rosser, A
- Bak, T
- Hodges, J R
Producer: 20010823
In:
Psychiatry research vol. 102
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105.
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Alzheimer disease is not associated with polymorphisms in the angiotensinogen and renin genes. [electronic resource] by
- Taylor, A
- Ezquerra, M
- Bagri, G
- Yip, A
- Goumidi, L
- Cottel, D
- Easton, D
- Evans, J G
- Xuereb, J
- Cairns, N J
- Amouyel, P
- Chartier-Harlin, M C
- Brayne, C
- Rubinsztein, D C
Producer: 20020305
In:
American journal of medical genetics vol. 105
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106.
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Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorder. [electronic resource] by
- Jain, S
- Leggo, J
- DeLisi, L E
- Crow, T J
- Margolis, R L
- Li, S H
- Goodburn, S
- Walsh, C
- Paykel, E S
- Ferguson-Smith, M A
- Ross, C A
- Rubinsztein, D C
Producer: 19961024
In:
American journal of medical genetics vol. 67
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107.
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Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease. [electronic resource] by
- Morgan, A R
- Turic, D
- Jehu, L
- Hamilton, G
- Hollingworth, P
- Moskvina, V
- Jones, L
- Lovestone, S
- Brayne, C
- Rubinsztein, D C
- Lawlor, B
- Gill, M
- O'Donovan, M C
- Owen, M J
- Williams, J
Producer: 20071107
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 144B
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108.
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Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation. [electronic resource] by
- Singleton, A B
- Hall, R
- Ballard, C G
- Perry, R H
- Xuereb, J H
- Rubinsztein, D C
- Tysoe, C
- Matthews, P
- Cordell, B
- Kumar-Singh, S
- De Jonghe, C
- Cruts, M
- van Broeckhoven, C
- Morris, C M
Producer: 20010104
In:
Brain : a journal of neurology vol. 123 Pt 12
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109.
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Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees. [electronic resource] by
- Becher, M W
- Rubinsztein, D C
- Leggo, J
- Wagster, M V
- Stine, O C
- Ranen, N G
- Franz, M L
- Abbott, M H
- Sherr, M
- MacMillan, J C
- Barron, L
- Porteous, M
- Harper, P S
- Ross, C A
Producer: 19971014
In:
Movement disorders : official journal of the Movement Disorder Society vol. 12
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110.
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Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias. [electronic resource] by
- Matilla-Dueñas, A
- Ashizawa, T
- Brice, A
- Magri, S
- McFarland, K N
- Pandolfo, M
- Pulst, S M
- Riess, O
- Rubinsztein, D C
- Schmidt, J
- Schmidt, T
- Scoles, D R
- Stevanin, G
- Taroni, F
- Underwood, B R
- Sánchez, I
Producer: 20140912
In:
Cerebellum (London, England) vol. 13
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111.
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Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. [electronic resource] by
- Morgan, A R
- Hamilton, G
- Turic, D
- Jehu, L
- Harold, D
- Abraham, R
- Hollingworth, P
- Moskvina, V
- Brayne, C
- Rubinsztein, D C
- Lynch, A
- Lawlor, B
- Gill, M
- O'Donovan, M
- Powell, J
- Lovestone, S
- Williams, J
- Owen, M J
Producer: 20081204
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 147B
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112.
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Calpain inhibition mediates autophagy-dependent protection against polyglutamine toxicity. [electronic resource] by
- Menzies, F M
- Garcia-Arencibia, M
- Imarisio, S
- O'Sullivan, N C
- Ricketts, T
- Kent, B A
- Rao, M V
- Lam, W
- Green-Thompson, Z W
- Nixon, R A
- Saksida, L M
- Bussey, T J
- O'Kane, C J
- Rubinsztein, D C
Producer: 20151229
In:
Cell death and differentiation vol. 22
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113.
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Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion. [electronic resource] by
- De Jonghe, C
- Cruts, M
- Rogaeva, E A
- Tysoe, C
- Singleton, A
- Vanderstichele, H
- Meschino, W
- Dermaut, B
- Vanderhoeven, I
- Backhovens, H
- Vanmechelen, E
- Morris, C M
- Hardy, J
- Rubinsztein, D C
- St George-Hyslop, P H
- Van Broeckhoven, C
Producer: 19990914
In:
Human molecular genetics vol. 8
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114.
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Interaction between the ADAM12 and SH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease. [electronic resource] by
- Harold, D
- Jehu, L
- Turic, D
- Hollingworth, P
- Moore, P
- Summerhayes, P
- Moskvina, V
- Foy, C
- Archer, N
- Hamilton, B A
- Lovestone, S
- Powell, J
- Brayne, C
- Rubinsztein, D C
- Jones, L
- O'Donovan, M C
- Owen, M J
- Williams, J
Producer: 20070814
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 144B
Availability: No items available.
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115.
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Patients with features similar to Huntington's disease, without CAG expansion in huntingtin. [electronic resource] by
- Rosenblatt, A
- Ranen, N G
- Rubinsztein, D C
- Stine, O C
- Margolis, R L
- Wagster, M V
- Becher, M W
- Rosser, A E
- Leggo, J
- Hodges, J R
- ffrench-Constant, C K
- Sherr, M
- Franz, M L
- Abbott, M H
- Ross, C A
Producer: 19980730
In:
Neurology vol. 51
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116.
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A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD). [electronic resource] by
- Proitsi, P
- Hamilton, G
- Tsolaki, M
- Lupton, M
- Daniilidou, M
- Hollingworth, P
- Archer, N
- Foy, C
- Stylios, F
- McGuinness, B
- Todd, S
- Lawlor, B
- Gill, M
- Brayne, C
- Rubinsztein, D C
- Owen, M
- Williams, J
- Craig, D
- Passmore, P
- Lovestone, S
- Powell, J F
Producer: 20110719
In:
Neurobiology of aging vol. 32
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117.
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Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats. [electronic resource] by
- Rubinsztein, D C
- Leggo, J
- Coles, R
- Almqvist, E
- Biancalana, V
- Cassiman, J J
- Chotai, K
- Connarty, M
- Crauford, D
- Curtis, A
- Curtis, D
- Davidson, M J
- Differ, A M
- Dode, C
- Dodge, A
- Frontali, M
- Ranen, N G
- Stine, O C
- Sherr, M
- Abbott, M H
- Franz, M L
- Graham, C A
- Harper, P S
- Hedreen, J C
- Hayden, M R
Producer: 19960801
In:
American journal of human genetics vol. 59
Availability: No items available.
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118.
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Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element. [electronic resource] by
- Hoogendijk, C F
- Scholtz, C L
- Pimstone, S M
- Ehrenborg, E
- Kastelein, J J P
- Defesche, J C
- Thiart, R
- du Plessis, L
- de Villiers, J N P
- Zaahl, M G
- Delport, R
- Rubinsztein, D C
- Raffel, L J
- Grim, C E
- Mediene-Benchekor, S
- Amouyel, P
- Brousseau, T
- Steyn, K
- Lombard, C J
- Hayden, M R
- Kotze, M J
Producer: 20040416
In:
Molecular and cellular probes vol. 17
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119.
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cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat. [electronic resource] by
- Margolis, R L
- Stine, O C
- McInnis, M G
- Ranen, N G
- Rubinsztein, D C
- Leggo, J
- Brando, L V
- Kidwai, A S
- Loev, S J
- Breschel, T S
- Callahan, C
- Simpson, S G
- DePaulo, J R
- McMahon, F J
- Jain, S
- Paykel, E S
- Walsh, C
- DeLisi, L E
- Crow, T J
- Torrey, E F
- Ashworth, R G
- Macke, J P
- Nathans, J
- Ross, C A
Producer: 19970604
In:
Human molecular genetics vol. 5
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120.
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Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012. [electronic resource] by
- Galluzzi, L
- Vitale, I
- Abrams, J M
- Alnemri, E S
- Baehrecke, E H
- Blagosklonny, M V
- Dawson, T M
- Dawson, V L
- El-Deiry, W S
- Fulda, S
- Gottlieb, E
- Green, D R
- Hengartner, M O
- Kepp, O
- Knight, R A
- Kumar, S
- Lipton, S A
- Lu, X
- Madeo, F
- Malorni, W
- Mehlen, P
- Nuñez, G
- Peter, M E
- Piacentini, M
- Rubinsztein, D C
- Shi, Y
- Simon, H-U
- Vandenabeele, P
- White, E
- Yuan, J
- Zhivotovsky, B
- Melino, G
- Kroemer, G
Producer: 20120330
In:
Cell death and differentiation vol. 19
Availability: No items available.
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