UB Paderborn / Katalog / Suche / in CDI

Retrovirology : Research and Treatment, 2008-11, Vol.2008 (Recent Developments in Retrovirology: Research and Treatment Special Issue (2008)), p.17-24

2008

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UTILIZATION OF WHOLE EXOME SEQUENCING DATA TO IDENTIFY CLINICALLY RELEVANT PHARMACOGENOMIC VARIANTS IN INFLAMMATORY BOWEL DISEASE

Inflammatory bowel diseases, 2021-01, Vol.27 (Supplement_1), p.S32-S32

2021

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Localization of heat shock protein HSPA 6 ( HSP 70B') to sites of transcription in cultured differentiated human neuronal cells following thermal stress

Journal of neurochemistry, 2014-12, Vol.131 (6), p.743-754

2014

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Stress-induced localization of HSPA6 (HSP70B') and HSPA1A (HSP70-1) proteins to centrioles in human neuronal cells

Cell stress & chaperones, 2014-05, Vol.19 (3), p.321-327

2014

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Genetic testing for Lynch syndrome in the province of Ontario

Cancer, 2016-06, Vol.122 (11), p.1672-1679

2016

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Abstract A34: BRCA1 and BRCA2 mutation spectrum across 5, 509 high-risk individuals identifies pathogenic variants associated with ethnicity, age of diagnosis, and type of cancer

Molecular cancer research, 2016-02, Vol.14 (2_Supplement), p.A34-A34

2016

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Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations

Journal of medical genetics, 2015-07, Vol.52 (7), p.438-445

2015

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Selective Pressure Against AUG Triplets in the 5´ Untranslated Region of Human Immunodeficiency Virus Type 1 Supports Cap-Dependent Translation Initiation Mechanism

Retrovirology : Research and Treatment, 2008-01, Vol.Recent Developments, p.17

2008

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Identification of a New Genetic Determinant Controlling Human Hematopoietic Stem Cell Engraftment

Blood, 2007-11, Vol.110 (11), p.175-175

2007

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Bioinformatic Approach to Identify Penultimate Amino Acids Efficient for N-Terminal Methionine Excision

2007 1st International Conference on Bioinformatics and Biomedical Engineering, 2007, Vol.1, p.386-389

2007

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Polymorphism in Sirpa modulates engraftment of human hematopoietic stem cells

Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings

Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity

Utilization of Whole Exome Sequencing Data to Identify Clinically Relevant Pharmacogenomic Variants in Pediatric Inflammatory Bowel Disease

A Machine Learning Approach to Identifying Causal Monogenic Variants in Inflammatory Bowel Disease

Increased Light Intensity Induces Heat Shock Protein Hsp60 in Coral Species

Molecular-based classification algorithm for endometrial carcinoma categorizes ovarian endometrioid carcinoma into prognostically significant groups

Heteromeric complexes of heat shock protein 70 (HSP70) family members, including Hsp70B', in differentiated human neuronal cells

Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center

Genetic risk assessment and prevention: the role of genetic testing panels in breast cancer

Localization of heat shock protein HSPA6 (HSP70B') to sites of transcription in cultured differentiated human neuronal cells following thermal stress

UTILIZATION OF WHOLE EXOME SEQUENCING DATA TO IDENTIFY CLINICALLY RELEVANT PHARMACOGENOMIC VARIANTS IN INFLAMMATORY BOWEL DISEASE

Selective Pressure Against AUG Triplets in the 5´ Untranslated Region of Human Immunodeficiency Virus Type 1 Supports Cap-Dependent Translation Initiation Mechanism

UTILIZATION OF WHOLE EXOME SEQUENCING DATA TO IDENTIFY CLINICALLY RELEVANT PHARMACOGENOMIC VARIANTS IN INFLAMMATORY BOWEL DISEASE

Localization of heat shock protein HSPA 6 ( HSP 70B') to sites of transcription in cultured differentiated human neuronal cells following thermal stress

Stress-induced localization of HSPA6 (HSP70B') and HSPA1A (HSP70-1) proteins to centrioles in human neuronal cells

Genetic testing for Lynch syndrome in the province of Ontario

Abstract A34: BRCA1 and BRCA2 mutation spectrum across 5, 509 high-risk individuals identifies pathogenic variants associated with ethnicity, age of diagnosis, and type of cancer

Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations

Selective Pressure Against AUG Triplets in the 5´ Untranslated Region of Human Immunodeficiency Virus Type 1 Supports Cap-Dependent Translation Initiation Mechanism

Identification of a New Genetic Determinant Controlling Human Hematopoietic Stem Cell Engraftment

Bioinformatic Approach to Identify Penultimate Amino Acids Efficient for N-Terminal Methionine Excision

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