引用次数
引用: 9,571
H-指数: 41
I10-指数 : 62
出版物: 121
A novel mutation in the gene encoding noggin is not causative in human neural tube defects.
Rolf W. Stottmann , Marcy C. Speer , Elizabeth C. Melvin , Michael A. Hauser
Journal of Neurogenetics 16 ( 1) 65 -71
10
2002
T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families.
Marcy C. Speer , Elizabeth C. Melvin , Kristi D. Viles , Kim A. Bauer
American Journal of Medical Genetics 110 ( 3) 215 -218
19
2002
Topiramate (TPM) dosages when used as initial therapy in children/adolescents with epilepsy
ML Zupanc , S Arroyo , MD Privitera , R Guerrini
ANNALS OF NEUROLOGY 58 S119 -S119
2005
CMSPNL
JP Nye , JB Cathey , JG Sawyer , AC Hare
Pacific Northwest Lab., Richland, WA (United States) ( ESTSC-000730SEQSM00)
1993
CMSPNL. Chemical Management System Lab-Wide Electronic Chemical Inventory Tracking
JP Nye , JB Cathey , JG Sawyer , AC Hare
Pacific Northwest Lab., Richland, WA (United States) ( ESTSC-000730SEQSM00)
1993
High-affinity cannabinoid binding site in brain: A possible marijuana receptor
Jeffrey Scott Nye
Johns Hopkins Univ., Baltimore, MD (USA)
1988
Spatiotemporal selectivity of response to Notch1 signals in mammalian forebrain precursors
Nicholas Gaiano , Gord Fishell , Jeffrey S. Nye , Christopher B. Chambers
Development 128 ( 5) 689 -702
237
2001
The intracellular domain of mouse Notch: a constitutively activated repressor of myogenesis directed at the basic helix-loop-helix region of MyoD
Raphael Kopan , Harold Weintraub , Jeffrey S. Nye
Development 120 ( 9) 2385 -2396
459
1994
Severe Variant of Waardenburg Syndrome with Meningomyelocele in Patients with Interstitial Deletion of 2q35 and the PAX3 Gene † 1747
Jeffrey S. Nye , Nancy E. Balkin , Heather Lucas , Paul A. Knepper
Pediatric Research 41 ( 4) 294 -294
1997
Possible association of NTDs with a polyhistidine tract polymorphism in the ZIC2 gene.
L�cia Y. Brown , Susan E. Hodge , William G. Johnson , Sandra G. Guy
American Journal of Medical Genetics 108 ( 2) 128 -131
32
2002
Alzheimer's disease research and development: a call for a new research roadmap
Howard H. Feldman , Magali Haas , Sam Gandy , Darryle D. Schoepp
Annals of the New York Academy of Sciences 1313 ( 1) 1 -16
25
2014
Deletion of PBP/PPARBP, the gene for nuclear receptor coactivator peroxisome proliferator-activated receptor-binding protein, results in embryonic lethality.
Yijun Zhu , Chao Qi , Yuzhi Jia , Jeffrey S. Nye
Journal of Biological Chemistry 275 ( 20) 14779 -14782
158
2000
Effects of galantamine in a 2-year, randomized, placebo-controlled study in Alzheimer's disease.
Klaus Hager , Alan S Baseman , Jeffrey S Nye , H Robert Brashear
Neuropsychiatric Disease and Treatment 10 391 -401
40
2014
Effects of galantamine in a 2-year, randomized, placebo-controlled study in Alzheimer’s disease [Corrigendum]
K Hager , AS Baseman , JS Nye , J Han
Neuropsychiatric Disease and Treatment 10 1997 -1998
1
2014
Myelin Basic Protein Is an Endogenous Inhibitor of the High‐Affinity Cannabinoid Binding Site in Brain
Jeffrey S. Nye , Susan Voglmaier , Russell E. Martenson , Solomon H. Snyder
Journal of Neurochemistry 50 ( 4) 1170 -1178
18
1988
High-affinity cannabinoid binding site: regulation by ions, ascorbic acid, and nucleotides.
Jeffrey S. Nye , Adele M. Snowman , Susan Voglmaier , Solomon H. Snyder
Journal of Neurochemistry 52 ( 6) 1892 -1897
3
1989
Regulation of amyloid precursor protein processing by presenilin 1 (PS1) and PS2 in PS1 knockout cells.
James J. Palacino , Bridget E. Berechid , Prince Alexander , Christopher Eckman
Journal of Biological Chemistry 275 ( 1) 215 -222
43
2000
Intracellular Retention of Caveolin 1 in Presenilin-deficient Cells
Douglas R. Wood , Jeffrey S. Nye , Ned J. C. Lamb , Anne Fernandez
Journal of Biological Chemistry 280 ( 8) 6663 -6668
25
2005
Neural tube defects and the 13q deletion syndrome: evidence for a critical region in 13q33-34.
Jeffrey Luo , Nancy Balkin , Julie F Stewart , John F Sarwark
American Journal of Medical Genetics 91 ( 3) 227 -230
46
2000
Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect.
Jeffrey S Nye , Nancy Balkin , Heather Lucas , Paul A Knepper
American Journal of Medical Genetics 75 ( 4) 401 -408
37
1998