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Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

Molecular psychiatry, 2005-10, Vol.10 (10), p.950-960

2005

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GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

Heart rhythm, 2014-11, Vol.11 (11), p.2133-2133

2014

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Effectiveness of acoustic cameras as tools for assessing biogenic structures formed by Sabellaria in highly turbid environments

Aquatic conservation, 2020-06, Vol.30 (6), p.1121-1136

2020

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Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease

Blood, 2018-08, Vol.132 (5), p.469-483

2018

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Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians

European journal of human genetics : EJHG, 2017-08, Vol.25 (8), p.995-1003

2017

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Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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Leu351Arg in apoB, a new missense variant causing familial hypobetalipoproteinemia

Atherosclerosis, 2022-08, Vol.355, p.153

2022

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Risk factors for anastomotic leak and postoperative morbidity and mortality after elective right colectomy for cancer: results from a prospective, multicentric study of 1102 patients

International journal of colorectal disease, 2016-01, Vol.31 (1), p.105-114

2016

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Identification of a gain-of-function LIPC variant as a novel cause of familial combined hypocholesterolemia

Atherosclerosis, 2022-08, Vol.355, p.49

2022

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P2864A novel mechanism of sinus node dysfunction: intergenic deletion between PITX2 and ANK2 disrupts chromatin structure in pacemaker cell differentiation

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

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In vivo and in vitro phosphorylation of rotavirus NSP5 correlates with its localization in viroplasms

Journal of Virology, 1997-01, Vol.71 (1), p.34-41

1997

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Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Publishers’ Booklists in Late Seventeenth-Century London

Library, 2010-12, Vol.11 (4), p.381-404

Lindenbaum, Peter

2010

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Nomograms for morbidity and mortality after oncologic colon resection in the enhanced recovery era: results from a multicentric prospective national study

International journal of colorectal disease, 2020-12, Vol.35 (12), p.2227-2238

2020

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Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder

Archives of cardiovascular diseases supplements, 2023-01, Vol.15 (1), p.115-116

2023

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Identification by Whole Genome Sequencing of a New Gene Causing Hereditary Sinus Node and Atrioventricular Conduction Dysfunction

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.263-263

2020

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Relevance and diagnostic performance of genes involved in arrhythmogenic cardiomyopathy

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.261-261

2020

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P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder

Cardiovascular research, 2014-07, Vol.103 (suppl 1), p.S61-S61

2014

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2014-A-33-CES - GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

Heart rhythm, 2014-11, Vol.11 (11), p.2133-2133

2014

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RoXaN, a Novel Cellular Protein Containing TPR, LD, and Zinc Finger Motifs, Forms a Ternary Complex with Eukaryotic Initiation Factor 4G and Rotavirus NSP3

Journal of Virology, 2004-04, Vol.78 (8), p.3851-3862

2004

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CloneIT: finding cloning strategies, in-frame deletions and frameshifts

Bioinformatics (Oxford, England), 1998-06, Vol.14 (5), p.465-466

Lindenbaum, P

1998

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Clonelt : finding cloning strategies, in-frame deletions and frameshifts

Bioinformatics (Oxford, England), 1998, Vol.14 (5), p.465-466

LINDENBAUM, P

1998

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Authors and Publishers in the Late Seventeenth Century, II: Brabazon Aylmer and the Mysteries of the Trade

Library, 2002-03, Vol.3 (1), p.32-57

LINDENBAUM, P.

2002

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Dispatches from the Archives

Milton quarterly, 2002-03, Vol.36 (1), p.46-54

Lindenbaum, Peter

2002

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The Shattering of an Illusion: The Problem of Competition in Lesbian Relationships

Feminist studies, 1985-04, Vol.11 (1), p.85-103

Lindenbaum, Joyce P.

1985

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Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

Effectiveness of acoustic cameras as tools for assessing biogenic structures formed by Sabellaria in highly turbid environments

Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease

Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians

Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation

Leu351Arg in apoB, a new missense variant causing familial hypobetalipoproteinemia

Risk factors for anastomotic leak and postoperative morbidity and mortality after elective right colectomy for cancer: results from a prospective, multicentric study of 1102 patients

Identification of a gain-of-function LIPC variant as a novel cause of familial combined hypocholesterolemia

P2864A novel mechanism of sinus node dysfunction: intergenic deletion between PITX2 and ANK2 disrupts chromatin structure in pacemaker cell differentiation

In vivo and in vitro phosphorylation of rotavirus NSP5 correlates with its localization in viroplasms

Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

Publishers’ Booklists in Late Seventeenth-Century London

Nomograms for morbidity and mortality after oncologic colon resection in the enhanced recovery era: results from a multicentric prospective national study

Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder

Identification by Whole Genome Sequencing of a New Gene Causing Hereditary Sinus Node and Atrioventricular Conduction Dysfunction

Relevance and diagnostic performance of genes involved in arrhythmogenic cardiomyopathy

P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder

2014-A-33-CES - GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

RoXaN, a Novel Cellular Protein Containing TPR, LD, and Zinc Finger Motifs, Forms a Ternary Complex with Eukaryotic Initiation Factor 4G and Rotavirus NSP3

CloneIT: finding cloning strategies, in-frame deletions and frameshifts

Clonelt : finding cloning strategies, in-frame deletions and frameshifts

Authors and Publishers in the Late Seventeenth Century, II: Brabazon Aylmer and the Mysteries of the Trade

Dispatches from the Archives

The Shattering of an Illusion: The Problem of Competition in Lesbian Relationships

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