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Simon Alfred
Simon Alfred
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Verifierad e-postadress på utoronto.ca
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Abscisic acid inhibits type 2C protein phosphatases via the PYR/PYL family of START proteins
SY Park, P Fung, N Nishimura, DR Jensen, H Fujii, Y Zhao, S Lumba, ...
science 324 (5930), 1068-1071, 2009
28532009
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
GN Mnatzakanian, H Lohi, I Munteanu, SE Alfred, T Yamada, ...
Nature genetics 36 (4), 339-341, 2004
4112004
Chemical genetic interrogation of natural variation uncovers a molecule that is glycoactivated
Y Zhao, TF Chow, RS Puckrin, SE Alfred, AK Korir, CK Larive, SR Cutler
Nature chemical biology 3 (11), 716-721, 2007
1362007
Incipient stem cell niche conversion in tissue culture: using a systems approach to probe early events in WUSCHEL‐dependent conversion of lateral root primordia …
SP Chatfield, R Capron, A Severino, PA Penttila, S Alfred, H Nahal, ...
The Plant Journal 73 (5), 798-813, 2013
1092013
Abscisic acid inhibits PP2Cs via the PYR/PYL family of ABA-binding START proteins
S Park, P Fung, N Nishimura, DR Jensen, H Fujii, Y Zhao, S Lumba, ...
Science (New York, NY) 324 (5930), 1068, 2009
952009
Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets
W Warnica, D Merico, G Costain, SE Alfred, J Wei, CR Marshall, ...
Biological psychiatry 77 (2), 158-166, 2015
762015
MicroRNA dysregulation, gene networks, and risk for schizophrenia in 22q11. 2 deletion syndrome
D Merico, G Costain, NJ Butcher, W Warnica, L Ogura, SE Alfred, ...
Frontiers in neurology 5, 118956, 2014
602014
Sequence variants within exon 1 of MECP2 occur in females with mental retardation
CG Harvey, SD Menon, B Stachowiak, A Noor, A Proctor, AK Mensah, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007
302007
A phenotypic screening platform to identify small molecule modulators of Chlamydomonas reinhardtiigrowth, motility and photosynthesis
SE Alfred, A Surendra, C Le, K Lin, A Mok, IM Wallace, M Proctor, ...
Genome biology 13, 1-12, 2012
192012
Characterization of a de novo translocation t (5; 18)(q33. 1; q12. 1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the …
JB Vincent, A Noor, C Windpassinger, PJ Gianakopoulos, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150 …, 2009
142009
In Planta Labeling Using a Clickable ER-Disrupting Probe Suggests a Role for Oleosins in Arabidopsis Seedling ER Integrity
W Dejonghe, AS Vaidya, SE Alfred, SR Cutler
ACS Chemical Biology 16 (11), 2151-2157, 2021
22021
Incipient stem cell niche conversion in tissue culture: using a systems approach to probe early events in WUSCHEL-dependent conversion of lateral root primordial into shoot …
SP Chatfield, R Capron, A Severino, PA Penttila, S Alfred, H Nahal, ...
PLANT JOURNAL 77 (4), 665-666, 2014
22014
MicroRNA target genes and risk for schizophrenia in 22q11. 2 deletion syndrome
D Merico, G Costain, N Butcher, W Warnica, L Ogura, SE Alfred, ...
Frontiers in Neurology 5 (OCT), 221, 2014
12014
Screening for mutations in exon 1 of MECP2, among individuals with either Rett syndrome, autism or mental retardation
C Harvey, SE Alfred, G Mnatzakanian, WS Roberts, NC Schanen, ...
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 130 (1 …, 2004
12004
The Identification and Characterization of New Small Molecule Probes of Cell Expansion and Cytokinesis
SE Alfred
Library and Archives Canada= Bibliothèque et Archives Canada, Ottawa, 2012
2012
Mutation analysis of the Rett syndrome gene (MECP2) exon 1 in autism and mental retardation, and genetic studies of the distal portion of chromosome Xq
B Stachowiak, C Harvey, SD Menon, AK Mensah, N Mnatzakanian, ...
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 138 (1 …, 2005
2005
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Artiklar 1–16