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Brain-derived neurotrophic factor Val66met polymorphism and volume of the hippocampal formation

Molecular psychiatry, 2005-07, Vol.10 (7), p.631-636

2005

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Correlates of posttraumatic epilepsy 35 years following combat brain injury

Neurology, 2010-07, Vol.75 (3), p.224-229

2010

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Differential actions of ethanol and trichloroethanol at sites in the M3 and M4 domains of the NMDA receptor GluN2A (NR2A) subunit

British journal of pharmacology, 2009-11, Vol.158 (5), p.1395-1404

2009

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Queueing Theory: A Linear Algebraic Approach

Lipsky, Lester

2, 2008

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Mutations at F637 in the NMDA receptor NR2A subunit M3 domain influence agonist potency, ion channel gating and alcohol action

British journal of pharmacology, 2007-07, Vol.151 (6), p.749-757

2007

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APOE genotype influences acquisition and recall following traumatic brain injury

Neurology, 2002-04, Vol.58 (7), p.1115-1118

2002

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The Met66 allele of the functional Val66Met polymorphism in the brain-derived neurotrophic factor gene confers protection against neurocognitive dysfunction in systemic lupus erythematosus

Annals of the rheumatic diseases, 2006-10, Vol.65 (10), p.1330-1335

2006

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DNA Melting Analysis for Detection of Single Nucleotide Polymorphisms

Clinical chemistry (Baltimore, Md.), 2001-04, Vol.47 (4), p.635-644

2001

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Nuclear factor κB is a critical determinant in N‐methyl‐d‐aspartate receptor‐mediated neuroprotection

Journal of neurochemistry, 2001-07, Vol.78 (2), p.254-264

2001

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Nucleotide sequence variation within the human tyrosine kinase B neurotrophin receptor gene: association with antisocial alcohol dependence

The pharmacogenomics journal, 2007-12, Vol.7 (6), p.368-379

2007

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The FKBP5 -Gene in Depression and Treatment Response—an Association Study in the Sequenced Treatment Alternatives to Relieve Depression (STARD) Cohort

Biological psychiatry (1969), 2008-06, Vol.63 (12), p.1103-1110

2008

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Sites in the fourth membrane-associated domain regulate alcohol sensitivity of the NMDA receptor

Neuropharmacology, 2004-04, Vol.46 (5), p.647-654

2004

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Search marketing traffic and performance models

Computer standards and interfaces, 2012-11, Vol.34 (6), p.517-526

2012

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Variation in the Gene Encoding the Serotonin 2A Receptor Is Associated with Outcome of Antidepressant Treatment

American journal of human genetics, 2006-05, Vol.78 (5), p.804-814

2006

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Isolation and characterization of platelet glycoprotein IV (CD36)

The Journal of biological chemistry, 1989-05, Vol.264 (13), p.7570-7575

1989

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Demographic, structural and genetic predictors of late cognitive decline after penetrating head injury

Brain (London, England : 1878), 2008-02, Vol.131 (2), p.543-558

2008

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Genomics and variation of ionotropic glutamate receptors: implications for neuroplasticity

Amino acids, 2005-03, Vol.28 (2), p.169-175

2005

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Identification of Molecular Defects in a Subject With Type I CD36 Deficiency

Blood, 1994-06, Vol.83 (12), p.3545-3552

1994

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The role of the Met66 brain-derived neurotrophic factor allele in the recovery of executive functioning after combat-related traumatic brain injury

The Journal of neuroscience, 2011-01, Vol.31 (2), p.598-606

2011

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Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder

American journal of human genetics, 2004-11, Vol.75 (5), p.862-872

2004

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A Platelet Membrane Glycoprotein (GP) Deficiency in Healthy Blood Donors: Naka Platelets Lack Detectable GPIV (CD36)

Blood, 1990-11, Vol.76 (9), p.1698-1703

1990

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Family studies of type II CD36 deficient subjects: linkage of a CD36 allele to a platelet-specific mRNA expression defect(s) causing type II CD36 deficiency

Thrombosis and haemostasis, 1995, Vol.74 (2), p.758-763

1995

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Mutations in PAX3 associated with waardenburg syndrome type I

Human mutation, 1994, Vol.3 (3), p.205-211

1994

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A dinucleotide repeat in the third intron of CD36

Human molecular genetics, 1994-01, Vol.3 (1), p.217-217

1994

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Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16

Neuron (Cambridge, Mass.), 2005-12, Vol.48 (5), p.702-703

2005

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Brain-derived neurotrophic factor Val66met polymorphism and volume of the hippocampal formation

Correlates of posttraumatic epilepsy 35 years following combat brain injury

Differential actions of ethanol and trichloroethanol at sites in the M3 and M4 domains of the NMDA receptor GluN2A (NR2A) subunit

Queueing Theory: A Linear Algebraic Approach

Mutations at F637 in the NMDA receptor NR2A subunit M3 domain influence agonist potency, ion channel gating and alcohol action

APOE genotype influences acquisition and recall following traumatic brain injury

The Met66 allele of the functional Val66Met polymorphism in the brain-derived neurotrophic factor gene confers protection against neurocognitive dysfunction in systemic lupus erythematosus

DNA Melting Analysis for Detection of Single Nucleotide Polymorphisms

Nuclear factor κB is a critical determinant in N‐methyl‐d‐aspartate receptor‐mediated neuroprotection

Nucleotide sequence variation within the human tyrosine kinase B neurotrophin receptor gene: association with antisocial alcohol dependence

The FKBP5 -Gene in Depression and Treatment Response—an Association Study in the Sequenced Treatment Alternatives to Relieve Depression (STARD) Cohort

Sites in the fourth membrane-associated domain regulate alcohol sensitivity of the NMDA receptor

Search marketing traffic and performance models

Variation in the Gene Encoding the Serotonin 2A Receptor Is Associated with Outcome of Antidepressant Treatment

Isolation and characterization of platelet glycoprotein IV (CD36)

Demographic, structural and genetic predictors of late cognitive decline after penetrating head injury

Genomics and variation of ionotropic glutamate receptors: implications for neuroplasticity

Identification of Molecular Defects in a Subject With Type I CD36 Deficiency

The role of the Met66 brain-derived neurotrophic factor allele in the recovery of executive functioning after combat-related traumatic brain injury

Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder

A Platelet Membrane Glycoprotein (GP) Deficiency in Healthy Blood Donors: Naka Platelets Lack Detectable GPIV (CD36)

Family studies of type II CD36 deficient subjects: linkage of a CD36 allele to a platelet-specific mRNA expression defect(s) causing type II CD36 deficiency

Mutations in PAX3 associated with waardenburg syndrome type I

A dinucleotide repeat in the third intron of CD36

Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16

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