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Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibers

American Journal of Physiology: Cell Physiology, 2015-01, Vol.308 (2), p.C123-C138

2015

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Mutations in a NIMA-Related Kinase Gene, Nek1, Cause Pleiotropic Effects including a Progressive Polycystic Kidney Disease in Mice

Proceedings of the National Academy of Sciences - PNAS, 2000-01, Vol.97 (1), p.217-221

2000

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Na,K-ATPase in skeletal muscle: two populations of beta-spectrin control localization in the sarcolemma but not partitioning between the sarcolemma and the transverse tubules

Journal of cell science, 2001-02, Vol.114 (Pt 4), p.751-762

2001

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Small, Membrane-Bound, Alternatively Spliced Forms of Ankyrin 1 Associated with the Sarcoplasmic Reticulum of Mammalian Skeletal Muscle

The Journal of cell biology, 1997-02, Vol.136 (3), p.621-631

1997

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An Alternative First Exon in the Distal End of the Erythroid Ankyrin Gene Leads to Production of a Small Isoform Containing an NH2-Terminal Membrane Anchor

Genomics (San Diego, Calif.), 1998-05, Vol.50 (1), p.79-88

1998

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Complex patterns of sequence variation and multiple 5' and 3' ends are found among transcripts of the erythroid ankyrin gene

The Journal of biological chemistry, 1993-05, Vol.268 (13), p.9533-9540

1993

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Ankyrin and the Hemolytic Anemia Mutation, nb, Map to Mouse Chromosome 8: Presence of the nb Allele is Associated with a Truncated Erythrocyte Ankyrin

Proceedings of the National Academy of Sciences - PNAS, 1990-04, Vol.87 (8), p.3117-3121

1990

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Purkinje Cell Degeneration Associated with Erythroid Ankyrin Deficiency in nb/nb Mice

The Journal of cell biology, 1991-09, Vol.114 (6), p.1233-1241

1991

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Complete nucleotide sequence of the murine erythroid β-spectrin cDNA and tissue-specific expression in normal and jaundiced mice

Blood, 1993-11, Vol.82 (9), p.2906-2914

1993

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Chromosomal Location of Three Spectrin Genes: Relationship to the Inherited Hemolytic Anemias of Mouse and Man

Proceedings of the National Academy of Sciences - PNAS, 1988-11, Vol.85 (21), p.8121-8125

1988

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Fetal compensation of the hemolytic anemia in mice homozygous for the normoblastosis (nb) mutation

Blood, 1992-10, Vol.80 (8), p.2122-2127

1992

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Remarkable Homology among the Internal Repeats of Erythroid and Nonerythroid Spectrin

Proceedings of the National Academy of Sciences - PNAS, 1985-09, Vol.82 (17), p.5671-5675

1985

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Inhibition of intractable, nucleases with ribonucleoside-vanadyl complexes: isolation of messenger ribonucleic acid from resting lymphocytes

Biochemistry (Easton), 1979-11, Vol.18 (23), p.5143-5149

1979

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The Murine Mutation Jaundiced is Caused by Replacement of an Arginine with a Stop Codon in the mRNA Encoding the Ninth Repeat of β-Spectrin

Proceedings of the National Academy of Sciences - PNAS, 1994-10, Vol.91 (21), p.10099-10103

1994

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Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins

The Journal of pathology, 2004-11, Vol.204 (4), p.450-459

2004

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Changing Patterns in Cytoskeletal mRNA Expression and Protein Synthesis During Murine Erythropoiesis in vivo

Proceedings of the National Academy of Sciences - PNAS, 1992-07, Vol.89 (13), p.5749-5753

1992

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Urogenital syndrome (us): a developmental mutation on chromosome 2 of the mouse

Mammalian genome, 1993-01, Vol.4 (9), p.481-484

1993

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Distinct fetal Ank-1 and Ank-2 related proteins and mRNAs in normal and nb/nb mice

Blood, 1993-04, Vol.81 (8), p.2144-2149

1993

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Rh-RhAG/Ankyrin-R, a New Interaction Site between the Membrane Bilayer and the Red Cell Skeleton, Is Impaired by Rh sub(null)-associated Mutation

The Journal of biological chemistry, 2003-07, Vol.278 (28), p.25526-25533

2003

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Mutations in the murine erythroid α-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton

Blood, 2003-01, Vol.101 (1), p.325-330

2003

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Murine erythrocyte ankyrin cDNA: highly conserved regions of the regulatory domain

Mammalian genome, 1992-01, Vol.3 (5), p.281-285

1992

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Characterization of interferon messenger RNA synthesis in Namalva cells

The Journal of biological chemistry, 1980-04, Vol.255 (7), p.2955-2961

1980

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Brain beta spectrin isoform 235 (Spnb-2) maps to mouse chromosome 11

Mammalian genome, 1992-01, Vol.3 (5), p.293-295

1992

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Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene

The hematology journal : the official journal of the European Haematology Association, 2000, Vol.1 (4), p.235-242

2000

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Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse

Mammalian genome, 1993-09, Vol.4 (9), p.481-484

1993

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Deletion of small ankyrin 1 (sAnk1) isoforms results in structural and functional alterations in aging skeletal muscle fibers

Mutations in a NIMA-Related Kinase Gene, Nek1, Cause Pleiotropic Effects including a Progressive Polycystic Kidney Disease in Mice

Na,K-ATPase in skeletal muscle: two populations of beta-spectrin control localization in the sarcolemma but not partitioning between the sarcolemma and the transverse tubules

Small, Membrane-Bound, Alternatively Spliced Forms of Ankyrin 1 Associated with the Sarcoplasmic Reticulum of Mammalian Skeletal Muscle

An Alternative First Exon in the Distal End of the Erythroid Ankyrin Gene Leads to Production of a Small Isoform Containing an NH2-Terminal Membrane Anchor

Complex patterns of sequence variation and multiple 5' and 3' ends are found among transcripts of the erythroid ankyrin gene

Ankyrin and the Hemolytic Anemia Mutation, nb, Map to Mouse Chromosome 8: Presence of the nb Allele is Associated with a Truncated Erythrocyte Ankyrin

Purkinje Cell Degeneration Associated with Erythroid Ankyrin Deficiency in nb/nb Mice

Complete nucleotide sequence of the murine erythroid β-spectrin cDNA and tissue-specific expression in normal and jaundiced mice

Chromosomal Location of Three Spectrin Genes: Relationship to the Inherited Hemolytic Anemias of Mouse and Man

Fetal compensation of the hemolytic anemia in mice homozygous for the normoblastosis (nb) mutation

Remarkable Homology among the Internal Repeats of Erythroid and Nonerythroid Spectrin

Inhibition of intractable, nucleases with ribonucleoside-vanadyl complexes: isolation of messenger ribonucleic acid from resting lymphocytes

The Murine Mutation Jaundiced is Caused by Replacement of an Arginine with a Stop Codon in the mRNA Encoding the Ninth Repeat of β-Spectrin

Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins

Changing Patterns in Cytoskeletal mRNA Expression and Protein Synthesis During Murine Erythropoiesis in vivo

Urogenital syndrome (us): a developmental mutation on chromosome 2 of the mouse

Distinct fetal Ank-1 and Ank-2 related proteins and mRNAs in normal and nb/nb mice

Rh-RhAG/Ankyrin-R, a New Interaction Site between the Membrane Bilayer and the Red Cell Skeleton, Is Impaired by Rh sub(null)-associated Mutation

Mutations in the murine erythroid α-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton

Murine erythrocyte ankyrin cDNA: highly conserved regions of the regulatory domain

Characterization of interferon messenger RNA synthesis in Namalva cells

Brain beta spectrin isoform 235 (Spnb-2) maps to mouse chromosome 11

Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene

Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse

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