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Select item 81839021.

Clinical and molecular genetic analysis of a Chinese family with hereditary elliptocytosis caused by a novel mutation in the EPB41 gene

Manxiong Cao, Zhanqin Huang, Huanbing Zhou, Jinghua Lin, Dongqing Zhang

J Clin Lab Anal. 2021 Jun; 35(6): e23781. Published online 2021 May 4. doi: 10.1002/jcla.23781

PMCID:: PMC8183902

Article PDF–895K

Select item 69526072.

Epithelial-specific isoforms of protein 4.1R promote adherens junction assembly in maturing epithelia

Shu-Ching Huang, Jia Y. Liang, Long V. Vu, Faye H. Yu, Alexander C. Ou, Jennie Park Ou, Henry S. Zhang, Kimberly M. Burnett, Edward J. Benz, Jr.

J Biol Chem. 2020 Jan 3; 295(1): 191–211. Published online 2019 Nov 27. doi: 10.1074/jbc.RA119.009650

PMCID:: PMC6952607

Article PDF–4.8M

Select item 61637323.

Lnc-EPB41-Protein Interactions Associated with Congenital Pouch Colon

Sonal Gupta, Nidhi Gupta, Pradeep Tiwari, Saji Menon, Praveen Mathur, Shanker Lal Kothari, Sivaramaiah Nallapeta, Krishna Mohan Medicherla, Prashanth Suravajhala

Biomolecules. 2018 Sep; 8(3): 95. Published online 2018 Sep 17. doi: 10.3390/biom8030095

PMCID:: PMC6163732

Article PDF–2.6M

Select item 53247474.

Alternative polyadenylation in a family of paralogous EPB41 genes generates protein 4.1 diversity

Laura Rangel, Eva Lospitao, Ana Ruiz-Sáenz, Miguel A. Alonso, Isabel Correas

RNA Biol. 2017; 14(2): 236–244. Published online 2016 Dec 16. doi: 10.1080/15476286.2016.1270003

PMCID:: PMC5324747

Article PDF–891K

Select item 49740665.

Integrative Functional Genomics Implicates EPB41 Dysregulation in Hepatocellular Carcinoma Risk

Xinyu Yang, Dianke Yu, Yanli Ren, Jinyu Wei, Wenting Pan, Changchun Zhou, Liqing Zhou, Yu Liu, Ming Yang

Am J Hum Genet. 2016 Aug 4; 99(2): 275–286. Published online 2016 Jul 21. doi: 10.1016/j.ajhg.2016.05.029

PMCID:: PMC4974066

Article PDF–2.3M

Select item 22684236.

Downregulation of Protein 4.1R, a Mature Centriole Protein, Disrupts Centrosomes, Alters Cell Cycle Progression, and Perturbs Mitotic Spindles and Anaphase

Sharon Wald Krauss, Jeffrey R. Spence, Shirin Bahmanyar, Angela I. M. Barth, Minjoung M. Go, Debra Czerwinski, Adam J. Meyer

Mol Cell Biol. 2008 Apr; 28(7): 2283–2294. Published online 2008 Jan 22. doi: 10.1128/MCB.02021-07

PMCID:: PMC2268423

Article PDF–754K

Select item 22061387.

Intrasplicing coordinates alternative first exons with alternative splicing in the protein 4.1R gene

Marilyn K Parra, Jeff S Tan, Narla Mohandas, John G Conboy

EMBO J. 2008 Jan 9; 27(1): 122–131. Published online 2007 Dec 13. doi: 10.1038/sj.emboj.7601957

PMCID:: PMC2206138

Article PDF–433K

Select item 18054528.

Neuroacanthocytosis associated with a defect of the 4.1R membrane protein

Antonio Orlacchio, Paolo Calabresi, Adriana Rum, Anna Tarzia, Anna Maria Salvati, Toshitaka Kawarai, Alessandro Stefani, Antonio Pisani, Giorgio Bernardi, Paolo Cianciulli, Patrizia Caprari

BMC Neurol. 2007; 7: 4. Published online 2007 Feb 13. doi: 10.1186/1471-2377-7-4

PMCID:: PMC1805452

Article PDF–637K

Select item 16986089.

Protein 4.1R self-association: identification of the binding domain

Carmen M. Pérez-Ferreiro, Eva Lospitao, Isabel Correas

Biochem J. 2006 Dec 15; 400(Pt 3): 457–465. Prepublished online 2006 Aug 2. Published online 2006 Nov 28. doi: 10.1042/BJ20060644

PMCID:: PMC1698608

Article PDF–753K

Select item 163572410.

The 10 kDa domain of human erythrocyte protein 4.1 binds the Plasmodium falciparum EBA-181 protein

Roberto Lanzillotti, Theresa L Coetzer

Malar J. 2006; 5: 100. Published online 2006 Nov 6. doi: 10.1186/1475-2875-5-100

PMCID:: PMC1635724

Article PDF–1.4M

Select item 32999711.

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

Summary Page Browse PDF–1.6M

Select item 29675512.

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

Summary Page Browse PDF–1.3M

Select item 28266313.

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

Summary Page Browse PDF–807K

Select item 28028814.

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

Summary Page Browse PDF–1.4M

Select item 19687515.

Nuclear actin and protein 4.1: Essential interactions during nuclear assembly in vitro

Sharon Wald Krauss, Cynthia Chen, Sheldon Penman, Rebecca Heald

Proc Natl Acad Sci U S A. 2003 Sep 16; 100(19): 10752–10757. Published online 2003 Sep 5. doi: 10.1073/pnas.1934680100

PMCID:: PMC196875

Article PDF–690K

Select item 2381516.

Structural protein 4.1 is located in mammalian centrosomes

Sharon Wald Krauss, Joel Anne Chasis, Catherine Rogers, Narla Mohandas, Gabriela Krockmalnic, Sheldon Penman

Proc Natl Acad Sci U S A. 1997 Jul 8; 94(14): 7297–7302. doi: 10.1073/pnas.94.14.7297

PMCID:: PMC23815

Article PDF–823K

Select item 509880117.

Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis

Omar Niss, Satheesh Chonat, Neha Dagaonkar, Marya O. Almansoori, Karol Kerr, Zora R. Rogers, Patrick T. McGann, Maa-Ohui Quarmyne, Mary Risinger, Kejian Zhang, Theodosia A. Kalfa

Blood Cells Mol Dis. Author manuscript; available in PMC 2017 Oct 1.

Published in final edited form as: Blood Cells Mol Dis. 2016 Oct; 61: 4–9. Published online 2016 Jul 17. doi: 10.1016/j.bcmd.2016.07.003