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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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L L Peters

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The Journal of Clinical Investigation|June 8, 1999

Mild spherocytosis and altered red cell ion transport in protein 4. 2-null miceL L Peters, H K Jindel, B Gwynn, et al.

American Journal of Physiology. Cell Physiology|October 31, 2014

Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibersE Giacomello, M Quarta, C Paolini, et al.

The Journal of Clinical Investigation|February 2, 1999

Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalitiesZ T Shi, V Afzal, B Coller, et al.

Cell|September 20, 1996

Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeletonL L Peters, R A Shivdasani, S C Liu, et al.

Blood|December 9, 2000

Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanismB Gwynn, S L Ciciotte, S J Hunter, et al.

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Search research articles

Showing results (51-60 of 55) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 55 results.

The Journal of Clinical Investigation|June 8, 1999

Mild spherocytosis and altered red cell ion transport in protein 4. 2-null miceL L Peters, H K Jindel, B Gwynn, et al.

American Journal of Physiology. Cell Physiology|October 31, 2014

Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibersE Giacomello, M Quarta, C Paolini, et al.

The Journal of Clinical Investigation|February 2, 1999

Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalitiesZ T Shi, V Afzal, B Coller, et al.

Cell|September 20, 1996

Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeletonL L Peters, R A Shivdasani, S C Liu, et al.

Blood|December 9, 2000

Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanismB Gwynn, S L Ciciotte, S J Hunter, et al.

Pageof 6