Protein 4.1R–deficient Mice Are Viable but Have Erythroid Membrane Skeleton Abnormalities

Journal of Clinical Investigation - United States
doi 10.1172/jci3858
Full Text
Abstract

Available in full text

Categories
Medicine
Date
Authors
Publisher

American Society for Clinical Investigation

Related search

The Human Kell Blood Group Binds the Erythroid 4.1R Protein: New Insights Into the 4.1r-Dependent Red Cell Membrane Complex

Blood
BiochemistryImmunologyCell BiologyHematology
2015English

Zebrafish Sin3b Mutants Are Viable but Have Size, Skeletal and Locomotor Defects

Developmental Dynamics
Developmental Biology
2017English

Behavioral Abnormalities Observed in Zfhx2-Deficient Mice

PLoS ONE
Multidisciplinary
2012English

Glutamate Transporter EAAC-1-deficient Mice Develop Dicarboxylic Aminoaciduria and Behavioral Abnormalities but No Neurodegeneration

EMBO Journal
ImmunologyMolecular BiologyBiochemistryMicrobiology NeuroscienceMedicineGenetics
1997English

CD73-Deficient Mice Have Increased Antitumor Immunity and Are Resistant to Experimental Metastasis

Cancer Research
Cancer ResearchOncology
2011English

Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice

Neurobiology of Disease
Neurology
2002English

FGFR3 Deficient Mice Have Accelerated Fracture Repair

International Journal of Biological Sciences
Applied MicrobiologyEvolutionEcologyDevelopmental BiologyCell BiologyMolecular BiologySystematicsBehaviorBiotechnology
2017English

Gonadotropin and Kisspeptin Gene Expression, but Not GnRH, Are Impaired in cFOS Deficient Mice

Molecular and Cellular Endocrinology
BiochemistryEndocrinologyMolecular Biology
2015English

APRIL-Deficient Mice Have Normal Immune System Development

Molecular and Cellular Biology
Cell BiologyMolecular Biology
2004English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy