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Items: 11

1.
Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation
Marcela Salomao, Ke Chen, Jonathan Villalobos, Narla Mohandas, Xiuli An, Joel Anne Chasis
Blood. 2010 Jul 15; 116(2): 267–269. Prepublished online 2010 Mar 25. doi: 10.1182/blood-2010-02-264127
PMCID:
PMC2910610
AbstractArticle
2.
Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene.
N Dalla Venezia, F Gilsanz, N Alloisio, M T Ducluzeau, E J Benz, Jr, J Delaunay
J Clin Invest. 1992 Nov; 90(5): 1713–1717. doi: 10.1172/JCI116044
PMCID:
PMC443228
SummaryPage BrowsePDF–1.1M
3.
Protein 4.1R–deficient mice are viable but have erythroid membrane skeleton abnormalities
Zheng-Tao Shi, Veena Afzal, Barry Coller, Dipti Patel, Joel A. Chasis, Marilyn Parra, Gloria Lee, Chris Paszty, Mary Stevens, Loren Walensky, Luanne L. Peters, Narla Mohandas, Edward Rubin, John G. Conboy
J Clin Invest. 1999 Feb 1; 103(3): 331–340. doi: 10.1172/JCI3858
PMCID:
PMC407893
AbstractArticlePDF–599K
4.
Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton.
J Conboy, Y W Kan, S B Shohet, N Mohandas
Proc Natl Acad Sci U S A. 1986 Dec; 83(24): 9512–9516. doi: 10.1073/pnas.83.24.9512
PMCID:
PMC387170
SummaryPage BrowsePDF–1.2M
5.
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability.
G Tchernia, N Mohandas, S B Shohet
J Clin Invest. 1981 Aug; 68(2): 454–460. doi: 10.1172/JCI110275
PMCID:
PMC370818
SummaryPage BrowsePDF–1.6M
6.
An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.
J G Conboy, J A Chasis, R Winardi, G Tchernia, Y W Kan, N Mohandas
J Clin Invest. 1993 Jan; 91(1): 77–82. doi: 10.1172/JCI116203
PMCID:
PMC329997
SummaryPage BrowsePDF–1.6M
7.
Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1.
Y Takakuwa, G Tchernia, M Rossi, M Benabadji, N Mohandas
J Clin Invest. 1986 Jul; 78(1): 80–85. doi: 10.1172/JCI112577
PMCID:
PMC329534
SummaryPage BrowsePDF–1.3M
8.
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
J Conboy, S Marchesi, R Kim, P Agre, Y W Kan, N Mohandas
J Clin Invest. 1990 Aug; 86(2): 524–530. doi: 10.1172/JCI114739
PMCID:
PMC296755
SummaryPage BrowsePDF–1.3M
9.
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations.
S L Marchesi, J Conboy, P Agre, J T Letsinger, V T Marchesi, D W Speicher, N Mohandas
J Clin Invest. 1990 Aug; 86(2): 516–523. doi: 10.1172/JCI114738
PMCID:
PMC296754
SummaryPage BrowsePDF–2.2M
10.
Multiple protein 4.1 isoforms produced by alternative splicing in human erythroid cells.
J G Conboy, J Chan, N Mohandas, Y W Kan
Proc Natl Acad Sci U S A. 1988 Dec; 85(23): 9062–9065. doi: 10.1073/pnas.85.23.9062
PMCID:
PMC282663
SummaryPage BrowsePDF–807K
11.
Selective expression of an erythroid-specific isoform of protein 4.1.
T K Tang, T L Leto, I Correas, M A Alonso, V T Marchesi, E J Benz, Jr
Proc Natl Acad Sci U S A. 1988 Jun; 85(11): 3713–3717. doi: 10.1073/pnas.85.11.3713
PMCID:
PMC280288
SummaryPage BrowsePDF–1.4M

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