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Items: 17

1.

The ubiquitin ligase HECTD1 promotes retinoic acid signaling required for development of the aortic arch.

Sugrue KF, Sarkar AA, Leatherbury L, Zohn IE.

Dis Model Mech. 2019 Jan 11;12(1). pii: dmm036491. doi: 10.1242/dmm.036491.

2.

AutDB: a platform to decode the genetic architecture of autism.

Pereanu W, Larsen EC, Das I, Estévez MA, Sarkar AA, Spring-Pearson S, Kollu R, Basu SN, Banerjee-Basu S.

Nucleic Acids Res. 2018 Jan 4;46(D1):D1049-D1054. doi: 10.1093/nar/gkx1093.

3.

Abnormal labyrinthine zone in the Hectd1-null placenta.

Sarkar AA, Sabatino JA, Sugrue KF, Zohn IE.

Placenta. 2016 Feb;38:16-23. doi: 10.1016/j.placenta.2015.12.002. Epub 2015 Dec 13.

4.

Role of Cholesterol and Phospholipids in Amylin Misfolding, Aggregation and Etiology of Islet Amyloidosis.

Singh S, Trikha S, Bhowmick DC, Sarkar AA, Jeremic AM.

Adv Exp Med Biol. 2015;855:95-116. doi: 10.1007/978-3-319-17344-3_4. Review.

5.

Hectd1 is required for development of the junctional zone of the placenta.

Sarkar AA, Nuwayhid SJ, Maynard T, Ghandchi F, Hill JT, Lamantia AS, Zohn IE.

Dev Biol. 2014 Aug 15;392(2):368-80. doi: 10.1016/j.ydbio.2014.05.007. Epub 2014 May 20.

6.

An explant assay for assessing cellular behavior of the cranial mesenchyme.

Sarkar AA, Zohn IE.

J Vis Exp. 2013 Jan 20;(71). pii: 4245. doi: 10.3791/4245.

7.

HectD1 E3 ligase modifies adenomatous polyposis coli (APC) with polyubiquitin to promote the APC-axin interaction.

Tran H, Bustos D, Yeh R, Rubinfeld B, Lam C, Shriver S, Zilberleyb I, Lee MW, Phu L, Sarkar AA, Zohn IE, Wertz IE, Kirkpatrick DS, Polakis P.

J Biol Chem. 2013 Feb 8;288(6):3753-67. doi: 10.1074/jbc.M112.415240. Epub 2012 Dec 31.

8.

Does the cranial mesenchyme contribute to neural fold elevation during neurulation?

Zohn IE, Sarkar AA.

Birth Defects Res A Clin Mol Teratol. 2012 Oct;94(10):841-8. doi: 10.1002/bdra.23073. Epub 2012 Sep 3. Review.

9.

Hectd1 regulates intracellular localization and secretion of Hsp90 to control cellular behavior of the cranial mesenchyme.

Sarkar AA, Zohn IE.

J Cell Biol. 2012 Mar 19;196(6):789-800. doi: 10.1083/jcb.201105101.

10.

The visceral yolk sac endoderm provides for absorption of nutrients to the embryo during neurulation.

Zohn IE, Sarkar AA.

Birth Defects Res A Clin Mol Teratol. 2010 Aug;88(8):593-600. doi: 10.1002/bdra.20705. Review.

PMID:
20672346
11.

Modeling neural tube defects in the mouse.

Zohn IE, Sarkar AA.

Curr Top Dev Biol. 2008;84:1-35. doi: 10.1016/S0070-2153(08)00601-7. Review.

PMID:
19186242
12.

Polymerase chain reaction-based search for two alpha-globin gene mutations in India.

Bhattacharya G, Sarkar AA, Banerjee D, Chandra S, Das M, Dasgupta UB.

Hemoglobin. 2008;32(5):485-90. doi: 10.1080/03630260802341620.

PMID:
18932074
13.

Expression of Hand2 is sufficient for neurogenesis and cell type-specific gene expression in the enteric nervous system.

Hendershot TJ, Liu H, Sarkar AA, Giovannucci DR, Clouthier DE, Abe M, Howard MJ.

Dev Dyn. 2007 Jan;236(1):93-105.

14.
15.

A novel 33.3 kb deletion (- -KOL) in the alpha-globin gene cluster: a brief report on deletional alpha-thalassaemia in the heterogeneous eastern Indian population.

Sarkar AA, Banerjee S, Chandra S, Ghosh M, Banerjee D, Choudhury MD, Das M, Dasgupta UB.

Br J Haematol. 2005 Aug;130(3):454-7.

PMID:
16042697
16.

Co-inheritance of the Hb Sun Prairie mutation with a point mutation at 5'-UTR in the eastern Indian population.

Sarkar AA, Mukhopadhyay C, Chandra S, Banerjee S, Das MK, Dasgupta UB.

Br J Haematol. 2005 Apr;129(2):282-6.

PMID:
15813858
17.

Profile of beta-thalassemia in eastern India and its prenatal diagnosis.

Bandyopadhyay A, Bandyopadhyay S, Basak J, Mondal BC, Sarkar AA, Majumdar S, Das MK, Chandra S, Mukhopadhyay A, Sanghamita M, Ghosh K, Dasgupta UB.

Prenat Diagn. 2004 Dec 15;24(12):992-6.

PMID:
15614841

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