Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia-Reference-Cited by-同舟云学术

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Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia

Published:2004-02-19 Issue:9 Volume:101 Page:2894-2899
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Chubanov V.,Waldegger S.,Schnitzler M. M. y,Vitzthum H.,Sassen M. C.,Seyberth H. W.,Konrad M.,Gudermann T.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference26 articles.

1. Phototransduction in Drosophila melanogaster

2. International Union of Pharmacology. XLIII. Compendium of Voltage-Gated Ion Channels: Transient Receptor Potential Channels

3. TRP channels as cellular sensors

4. TRPs Make Sense

5. Subunit composition of mammalian transient receptor potential channels in living cells

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1. Characterization of intestine-specific TRPM6 knockout C57BL/6 J mice: effects of short-term omeprazole treatment;Pflügers Archiv - European Journal of Physiology;2024-09-13

2. Hypomagnesaemia leading to parathyroid dysfunction, hypocalcaemia, and hypokalaemia as a complication of long-term treatment with a proton pump inhibitor — a literature review;Endokrynologia Polska;2024-07-24

3. The odyssey of the TR(i)P journey to the cellular membrane;Frontiers in Cell and Developmental Biology;2024-07-23

4. Magnesium biology;Nephrology Dialysis Transplantation;2024-06-13

5. TRPM7 in neurodevelopment and therapeutic prospects for neurodegenerative disease;Cell Calcium;2024-06

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