Kết quả tìm kiếm - Hartmut Cuny
- Đang hiển thị 1 - 11 kết quả của 11
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The two-pore channel TPCN2 mediates NAADP-dependent Ca2+-release from lysosomal stores Bằng Xiangang Zong, Michael Schieder, Hartmut Cuny, Stefanie Fenske, Christian Grüner, Katrin Rötzer, Oliver Griesbeck, Hartmann Harz, Martin Biel, Christian Wahl‐Schott
Được phát hành 2009Artigo -
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Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders Bằng Justin O. Szot, Carla Campagnolo, Ye Cao, Kavitha R. Iyer, Hartmut Cuny, Thomas A. Drysdale, Josue Flores-Daboub, Weimin Bi, Lauren Westerfield, Pengfei Liu, Tse Ngong Leung, Kwong Wai Choy, Gavin Chapman, Rui Xiao, Victoria Mok Siu, Sally L. Dunwoodie
Được phát hành 2019Artigo -
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A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data Bằng Justin O. Szot, Hartmut Cuny, Gillian M. Blue, David T. Humphreys, Eddie Ip, Katrina Harrison, Gary F. Sholler, Eleni Giannoulatou, Paul Leo, Emma L. Duncan, Duncan B. Sparrow, Joshua W. K. Ho, Robert M. Graham, Nicholas Pachter, Gavin Chapman, David S. Winlaw, Sally L. Dunwoodie
Được phát hành 2018Artigo -
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Identification of clinically actionable variants from genome sequencing of families with congenital heart disease Bằng Dimuthu Alankarage, Eddie Ip, Justin O. Szot, Jacob E. Munro, Gillian M. Blue, Katrina Harrison, Hartmut Cuny, Annabelle Enriquez, Michael Troup, David T. Humphreys, Meredith Wilson, Richard P. Harvey, Gary F. Sholler, Robert M. Graham, Joshua W. K. Ho, Edwin P. Kirk, Nicholas Pachter, Gavin Chapman, David S. Winlaw, Eleni Giannoulatou, Sally L. Dunwoodie
Được phát hành 2018Artigo -
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High susceptibility to fatty liver disease in two-pore channel 2-deficient mice Bằng Christian Grimm, Lesca M. Holdt, Cheng‐Chang Chen, Sami Hassan, Christoph Müller, Simone Jörs, Hartmut Cuny, Sandra Kissing, Bernd Schröder, Elisabeth Butz, Bernd H. Northoff, Jan Castonguay, Christian A. Luber, Markus Moser, Saskia Spahn, Renate Lüllmann‐Rauch, Christina Fendel, Norbert Klugbauer, Oliver Griesbeck, Albert Haas, Matthias Mann, Franz Bracher, Daniel Teupser, Paul Säftig, Martin Biel, Christian Wahl‐Schott
Được phát hành 2014Artigo -
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A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder Bằng Justin O. Szot, Hartmut Cuny, Ella MMA Martin, Delicia Z Sheng, Kavitha R. Iyer, Stephanie Portelli, Vivien Nguyen, Jessica Gereis, Dimuthu Alankarage, David Chitayat, Karen Chong, Ingrid M. Wentzensen, Catherine Vincent‐Delorme, Alban Lermine, Emma Burkitt‐Wright, Weizhen Ji, Lauren Jeffries, Lynn Pais, Tiong Yang Tan, James Pitt, C. Wise, Helen Wright, Israel D. Andrews, Brianna Pruniski, Theresa A. Grebe, Nicole Corsten‐Janssen, Katelijne Bouman, Cathryn Poulton, Supraja Prakash, Boris Keren, Natasha J. Brown, Matthew F. Hunter, Oliver Heath, Saquib A. Lakhani, John McDermott, David B. Ascher, Gavin Chapman, Kayleigh Bozon, Sally L. Dunwoodie
Được phát hành 2024Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Biochemistry
Chemistry
Enzyme
Gene
Genetics
Receptor
Internal medicine
Medicine
NAD+ kinase
Biophysics
Calcium
Calcium channel
Cell biology
Disease
N-type calcium channel
Organic chemistry
Phenotype
T-type calcium channel
Voltage-dependent calcium channel
Bioinformatics
Endocrinology
GABAB receptor
Genotype
Heart disease
Intracellular
Nicotinamide adenine dinucleotide
Pharmacology
Agonist
Allele