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Spatial Attention Modulates Neuronal Interactions between Simple and Complex Cells in V1

International journal of molecular sciences, 2023-05, Vol.24 (9), p.8229

2023

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A proposed explanation for female predominance in alveolar soft part sarcoma: Noninactivation of X: autosome translocation fusion gene?

Cancer, 2005-03, Vol.103 (6), p.1245-1253

2005

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Body mass index is associated with barrett esophagus and cardiac mucosal metaplasia

Digestive diseases and sciences, 2006-09, Vol.51 (9), p.1589-1594

2006

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Sentinel lymph node identification using NIR-II ultrabright Raman nanotags on preclinical models

Biomaterials, 2024-07, Vol.308, p.122538-122538, Article 122538

2024

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Systemic mastocytosis with associated clonal hematological non‐mast‐cell lineage disease: Analysis of clinicopathologic features and activating c‐kit mutations

American journal of hematology, 2003-05, Vol.73 (1), p.12-17

2003

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Modulation of Spike Count Correlations Between Macaque Primary Visual Cortex Neurons by Difficulty of Attentional Task

Neuroscience bulletin, 2022-05, Vol.38 (5), p.489-504

2022

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T-cell lymphoma in HIV-infected patients

Journal of acquired immune deficiency syndromes (1999), 2004-08, Vol.36 (5), p.1020-1027

2004

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Feature-based attention elicited by precueing in an orientation discrimination task

Vision research (Oxford), 2018-07, Vol.148, p.15-25

2018

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X Chromosome-Linked and Mitochondrial Gene Control of Leber Hereditary Optic Neuropathy: Evidence from Segregation Analysis for Dependence on X Chromosome Inactivation

Proceedings of the National Academy of Sciences - PNAS, 1991-09, Vol.88 (18), p.8198-8202

1991

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Multilocus genetic determinants of LDL particle size in coronary artery disease families

American journal of human genetics, 1996-03, Vol.58 (3), p.585-594

1996

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Wolfram syndrome: a mitochondrial-mediated disorder?

The Lancet (British edition), 1993-09, Vol.342 (8871), p.598-600

1993

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A proposed explanation for female predominance in alveolar soft part sarcoma

Cancer, 2005-03, Vol.103 (6), p.1245-1253

2005

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Sensorineural deafness inherited as a tissue specific mitochondrial disorder

Journal of medical genetics, 1992-02, Vol.29 (2), p.86-90

1992

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Linkage analysis of the genetic determinants of high density lipoprotein concentrations and composition : evidence for involvement of the apolipoprotein A-II and cholesteryl ester transfer protein loci

Human genetics, 1994-06, Vol.93 (6), p.639-648

1994

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Evidence for Linkage of the Apolipoprotein A-II Locus to Plasma Apolipoprotein A-II and Free Fatty Acid Levels in Mice and Humans

Proceedings of the National Academy of Sciences - PNAS, 1993-11, Vol.90 (22), p.10886-10890

1993

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Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

Nature genetics, 1993-07, Vol.4 (3), p.289-294

1993

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The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the α-globin complex on 16p : evidence for locus homogeneity

American journal of human genetics, 1992-12, Vol.51 (6), p.1349-1354

1992

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Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community

American journal of medical genetics, 1992-09, Vol.44 (1), p.1-6

1992

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A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: Evidence from pedigree segregation analysis

Genetic epidemiology, 1993, Vol.10 (1), p.3-15

1993

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Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22

The Journal of clinical investigation, 1996-05, Vol.97 (9), p.2111-2118

1996

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Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness

Pharmacogenetics (London), 1995-06, Vol.5 (3), p.165-172

1995

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Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus

American journal of human genetics, 1995, Vol.56 (1), p.287-293

1995

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Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

American journal of otolaryngology, 1993-11, Vol.14 (6), p.399-403

1993

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Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation

American journal of medical genetics, 1998-06, Vol.77 (5), p.421-426

1998

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Evidence for linkage of the apolipoprotein A-11 locus to plasma apolipoprotein A-II and free fatty acid levels in mice and humans

Proceedings of the National Academy of Sciences - PNAS, 1993-11, Vol.90 (22), p.10886

1993

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Spatial Attention Modulates Neuronal Interactions between Simple and Complex Cells in V1

A proposed explanation for female predominance in alveolar soft part sarcoma: Noninactivation of X: autosome translocation fusion gene?

Body mass index is associated with barrett esophagus and cardiac mucosal metaplasia

Sentinel lymph node identification using NIR-II ultrabright Raman nanotags on preclinical models

Systemic mastocytosis with associated clonal hematological non‐mast‐cell lineage disease: Analysis of clinicopathologic features and activating c‐kit mutations

Modulation of Spike Count Correlations Between Macaque Primary Visual Cortex Neurons by Difficulty of Attentional Task

T-cell lymphoma in HIV-infected patients

Feature-based attention elicited by precueing in an orientation discrimination task

X Chromosome-Linked and Mitochondrial Gene Control of Leber Hereditary Optic Neuropathy: Evidence from Segregation Analysis for Dependence on X Chromosome Inactivation

Multilocus genetic determinants of LDL particle size in coronary artery disease families

Wolfram syndrome: a mitochondrial-mediated disorder?

A proposed explanation for female predominance in alveolar soft part sarcoma

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

Linkage analysis of the genetic determinants of high density lipoprotein concentrations and composition : evidence for involvement of the apolipoprotein A-II and cholesteryl ester transfer protein loci

Evidence for Linkage of the Apolipoprotein A-II Locus to Plasma Apolipoprotein A-II and Free Fatty Acid Levels in Mice and Humans

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the α-globin complex on 16p : evidence for locus homogeneity

Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community

A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: Evidence from pedigree segregation analysis

Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22

Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness

Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation

Evidence for linkage of the apolipoprotein A-11 locus to plasma apolipoprotein A-II and free fatty acid levels in mice and humans

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