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Agm1/Pgm3-Mediated Sugar Nucleotide Synthesis Is Essential for Hematopoiesis and Development

Molecular and Cellular Biology, 2007-08, Vol.27 (16), p.5849-5859

2007

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ALG13 X‐linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes

Journal of inherited metabolic disease, 2021-07, Vol.44 (4), p.1001-1012

2021

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Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling

Journal of Genetic Counseling, 2016-12, Vol.25 (6), p.1171-1178

2016

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Control of basal ganglia output by direct and indirect pathway projection neurons

The Journal of neuroscience, 2013-11, Vol.33 (47), p.18531-18539

2013

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Dissecting the molecular organization of the translocon-associated protein complex

Nature communications, 2017-02, Vol.8 (1), p.14516-14516, Article 14516

2017

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Expanding the molecular and clinical phenotypes of FUT8‐CDG

Journal of inherited metabolic disease, 2020-07, Vol.43 (4), p.871-879

2020

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Facing the challenge of democracy: explorations in the analysis of public opinion and political participation

1, 2011

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Federation on the History of Russia in the Nineteenth and Early Twentieth Centuries

The American Historical Review, 1997, Vol.102 (2), p.486-487

Ransel, David L.

1997

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Food Recovery Efforts for Upstream and Downstream Benefits (I1.A2)

Data & Analytics for Good Journal, 2021

2021

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The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of Services

Journal of genetic counseling, 2018-06, Vol.27 (3), p.558-564

2018

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Genetic Evaluation and Use of Chromosome Microarray in Patients with Isolated Heart Defects: Benefits and Challenges of a New Model in Cardiovascular Care

Frontiers in cardiovascular medicine, 2016-06, Vol.3, p.19-19

2016

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HNF4α Antagonists Discovered by a High-Throughput Screen for Modulators of the Human Insulin Promoter

Chemistry & biology, 2012-07, Vol.19 (7), p.806-818

2012

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Modeling seeding and neuroanatomic spread of pathology in amyotrophic lateral sclerosis

NeuroImage (Orlando, Fla.), 2022-05, Vol.251, p.118968-118968, Article 118968

2022

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Network mediation of pathology pattern in sporadic Creutzfeldt–Jakob disease

Brain communications, 2020-01, Vol.2 (1), p.fcaa060-fcaa060

2020

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New Diagnosis and Treatment of Congenital Hepatic Fibrosis

Journal of pediatric gastroenterology and nutrition, 1999, Vol.29 (1), p.104-106

Freeze, Hudson H.

1999

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Optogenetic dissection of pathway-specific processing in the basal ganglia

Freeze, Benjamin

2012

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Origins of atrophy in Parkinson linked to early onset and local transcription patterns

Brain communications, 2020-01, Vol.2 (2), p.fcaa065-fcaa065

2020

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Political Participation, Polarization, and Public Opinion: Activism and the Merging of Partisan and Ideological Polarization

Facing the Challenge of Democracy, 2015, p.185-206

2015

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Political Participation, Polarization, and Public Opinion: ACTIVISM AND THE MERGING OF PARTISAN AND IDEOLOGICAL POLARIZATION

Facing the Challenge of Democracy, 2011, p.185

2011

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Regional expression of genes mediating trans-synaptic alpha-synuclein transfer predicts regional atrophy in Parkinson disease

NeuroImage clinical, 2018-01, Vol.18, p.456-466

2018

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Regional transcriptional architecture of Parkinson's disease pathogenesis and network spread

Brain (London, England : 1878), 2019-10, Vol.142 (10), p.3072-3085

2019

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Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry

Nature (London), 2010-07, Vol.466 (7306), p.622-626

2010

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Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry

Nature (London), 2010-08, p.S19

2010

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The Russian Archive Series

The Russian Review, 1996, Vol.55 (4), p.692-698

Raleigh, Donald J.

1996

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State-Dependent Verapamil Block of the Cloned Human Ca sub(v)3.1 T-Type Ca super(2+) Channel

Molecular pharmacology, 2006-08, Vol.70 (2), p.718-726

2006

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Agm1/Pgm3-Mediated Sugar Nucleotide Synthesis Is Essential for Hematopoiesis and Development

ALG13 X‐linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes

Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling

Control of basal ganglia output by direct and indirect pathway projection neurons

Dissecting the molecular organization of the translocon-associated protein complex

Expanding the molecular and clinical phenotypes of FUT8‐CDG

Facing the challenge of democracy: explorations in the analysis of public opinion and political participation

Federation on the History of Russia in the Nineteenth and Early Twentieth Centuries

Food Recovery Efforts for Upstream and Downstream Benefits (I1.A2)

The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of Services

Genetic Evaluation and Use of Chromosome Microarray in Patients with Isolated Heart Defects: Benefits and Challenges of a New Model in Cardiovascular Care

HNF4α Antagonists Discovered by a High-Throughput Screen for Modulators of the Human Insulin Promoter

Modeling seeding and neuroanatomic spread of pathology in amyotrophic lateral sclerosis

Network mediation of pathology pattern in sporadic Creutzfeldt–Jakob disease

New Diagnosis and Treatment of Congenital Hepatic Fibrosis

Optogenetic dissection of pathway-specific processing in the basal ganglia

Origins of atrophy in Parkinson linked to early onset and local transcription patterns

Political Participation, Polarization, and Public Opinion: Activism and the Merging of Partisan and Ideological Polarization

Political Participation, Polarization, and Public Opinion: ACTIVISM AND THE MERGING OF PARTISAN AND IDEOLOGICAL POLARIZATION

Regional expression of genes mediating trans-synaptic alpha-synuclein transfer predicts regional atrophy in Parkinson disease

Regional transcriptional architecture of Parkinson's disease pathogenesis and network spread

Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry

Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry

The Russian Archive Series

State-Dependent Verapamil Block of the Cloned Human Ca sub(v)3.1 T-Type Ca super(2+) Channel

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