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Items: 1 to 50 of 78

1.

Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach.

Kedar PS, Harigae H, Ito E, Muramatsu H, Kojima S, Okuno Y, Fujiwara T, Dongerdiye R, Warang PP, Madkaikar MR.

Int J Hematol. 2019 Aug 10. doi: 10.1007/s12185-019-02716-9. [Epub ahead of print]

PMID:
31401766
2.

Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction.

Kedar PS, Dongerdiye R, Chilwirwar P, Gupta V, Chiddarwar A, Devendra R, Warang P, Prasada H, Sampagar A, Bhat S, Chandrakala S, Madkaikar M.

Indian J Pediatr. 2019 Aug;86(8):692-699. doi: 10.1007/s12098-019-02928-1. Epub 2019 Apr 27.

PMID:
31030358
3.

A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant.

Devendra R, Warang P, Gupta V, Chiddarwar A, Kedar P, Agarwal MB, Mukherjee MB.

Indian J Hematol Blood Transfus. 2019 Apr;35(2):399-401. doi: 10.1007/s12288-018-1049-3. Epub 2018 Dec 6. No abstract available.

PMID:
30988594
4.

Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).

Dongerdiye R, Kamat P, Jain P, Warang P, Devendra R, Wasekar N, Sharma R, Mhaskar K, Madkaikar MR, Manglani MV, Kedar PS.

J Clin Pathol. 2019 Jun;72(6):393-398. doi: 10.1136/jclinpath-2019-205718. Epub 2019 Mar 27.

PMID:
30918013
5.

Hereditary Elliptocytosis: A Rare Red Cell Membrane Disorder.

Warang P, Kedar P.

Indian J Hematol Blood Transfus. 2018 Oct;34(4):754-755. doi: 10.1007/s12288-018-0986-1. Epub 2018 Aug 2. No abstract available.

PMID:
30369757
6.

Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients.

Kedar PS, Gupta V, Dongerdiye R, Chiddarwar A, Warang P, Madkaikar MR.

J Clin Pathol. 2019 Jan;72(1):81-85. doi: 10.1136/jclinpath-2018-205420. Epub 2018 Oct 18.

PMID:
30337328
7.

Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.

Kedar PS, Gupta V, Warang P, Chiddarwar A, Madkaikar M.

Hematology. 2018 Sep;23(8):567-573. doi: 10.1080/10245332.2018.1444920. Epub 2018 Feb 27.

PMID:
29482478
8.

Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation.

Zaidi AU, Kedar P, Koduri PR, Goyette GW Jr, Buck S, Paglia DE, Ravindranath Y.

Pediatr Hematol Oncol. 2017 Nov;34(8):449-454. doi: 10.1080/08880018.2017.1383541. Epub 2017 Dec 11.

PMID:
29227722
9.

Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.

Kedar P, Parmar V, Devendra R, Gupta V, Warang P, Madkaikar M.

Ann Hematol. 2017 Dec;96(12):2135-2139. doi: 10.1007/s00277-017-3116-5. Epub 2017 Sep 7. No abstract available.

PMID:
28879554
10.

Does novel P5'N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?

Warang P, Devendra R, Chiddarwar A, Gupta V, Mirgal D, Jadli A, Mohite A, Kedar P, Mukherjee M.

Blood Cells Mol Dis. 2017 Jul;66:8-10. doi: 10.1016/j.bcmd.2017.07.002. Epub 2017 Jul 20. No abstract available.

PMID:
28756180
11.

A microplate reader-based method to quantify NADH-cytochrome b5 reductase activity for diagnosis of recessive congenital methaemoglobinemia.

Kedar P, Desai A, Warang P, Colah R.

Hematology. 2017 May;22(4):252-257. doi: 10.1080/10245332.2016.1252873. Epub 2016 Nov 18.

PMID:
27863456
12.

A novel nine base deletion mutation in NADH-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-II.

Warang P, Kedar P, Sivanandam S, Jothilakshmi K, Sumathi R, Colah R.

Mol Genet Metab Rep. 2015 Oct 22;5:44-47. doi: 10.1016/j.ymgmr.2015.10.002. eCollection 2015 Dec.

13.

Left Aberrant Gastric Vein Causing Isolated Left Hepatic Portal Venous Gas Secondary to an Incarcerated Diaphragmatic Hernia.

Mittal K, Anandpara K, Dey AK, Kedar P, Hira P, Kale S.

Pol J Radiol. 2015 Jul 21;80:364-7. doi: 10.12659/PJR.894103. eCollection 2015.

14.

Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experience.

Warang P, Kedar P, Ghosh K, Colah RB.

Clin Chem Lab Med. 2015 Mar;53(4):e105-8. doi: 10.1515/cclm-2014-0648. No abstract available.

PMID:
25246706
15.

Erythrocytosis, methemoglobinemia, and the saturation gap.

Koduri PR, Kedar PS, Warang P.

Ann Hematol. 2015 Mar;94(3):509-10. doi: 10.1007/s00277-014-2179-9. Epub 2014 Aug 5. No abstract available.

PMID:
25091522
16.

Hb M Hyde Park and Hb M Boston in two Indian families - a rare cause of methaemoglobinemia.

Upadhye D, Koduri P, Tarakeshwari S, Mehta P, Surve R, Warang P, Kedar P, Nadkarni A, Ghosh K, Colah R.

Int J Lab Hematol. 2015 Apr;37(2):e40-3. doi: 10.1111/ijlh.12281. Epub 2014 Jul 31. No abstract available.

PMID:
25079170
17.

Primaquine-induced severe methemoglobinemia developed during treatment of Plasmodium vivax malarial infection in an Indian family associated with a novel mutation (p.Agr57Trp) in the CYB5R3 gene.

Kedar P, Warang P, Sanyal S, Devendra R, Ghosh K, Colah R.

Clin Chim Acta. 2014 Nov 1;437:103-5. doi: 10.1016/j.cca.2014.07.015. Epub 2014 Jul 21. No abstract available.

PMID:
25058800
18.

Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?

Warang P, Devendra R, D'Silva S, Chiddarwar A, Kedar P, Ghosh K, Colah R, Mukherjee MB.

Ann Hematol. 2015 Jan;94(1):169-71. doi: 10.1007/s00277-014-2123-z. Epub 2014 Jun 20. No abstract available.

PMID:
24947795
19.

Base excision repair defects invoke hypersensitivity to PARP inhibition.

Horton JK, Stefanick DF, Prasad R, Gassman NR, Kedar PS, Wilson SH.

Mol Cancer Res. 2014 Aug;12(8):1128-39. doi: 10.1158/1541-7786.MCR-13-0502. Epub 2014 Apr 25.

20.

Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.

Warang PP, Kedar PS, Shanmukaiah C, Ghosh K, Colah RB.

Clin Genet. 2015;87(1):62-7. doi: 10.1111/cge.12326. Epub 2013 Dec 20.

PMID:
24266649
21.

Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: the first report from India.

Warang P, Nair S, Nadkarni A, Kedar P, Bhave A, Ghosh K, Colah R.

Hematology. 2014 Jun;19(4):199-201. doi: 10.1179/1607845413Y.0000000116. Epub 2013 Nov 25.

PMID:
24074398
22.

Preventing oxidation of cellular XRCC1 affects PARP-mediated DNA damage responses.

Horton JK, Stefanick DF, Gassman NR, Williams JG, Gabel SA, Cuneo MJ, Prasad R, Kedar PS, Derose EF, Hou EW, London RE, Wilson SH.

DNA Repair (Amst). 2013 Sep;12(9):774-85. doi: 10.1016/j.dnarep.2013.06.004. Epub 2013 Jul 18.

23.

Interaction between DNA Polymerase β and BRCA1.

Masaoka A, Gassman NR, Horton JK, Kedar PS, Witt KL, Hobbs CA, Kissling GE, Tano K, Asagoshi K, Wilson SH.

PLoS One. 2013 Jun 27;8(6):e66801. doi: 10.1371/journal.pone.0066801. Print 2013.

24.

Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.

Warang P, Kedar P, Ghosh K, Colah R.

Blood Cells Mol Dis. 2013 Oct;51(3):133-7. doi: 10.1016/j.bcmd.2013.05.006. Epub 2013 Jun 14.

PMID:
23770304
25.

Hyperactivation of PARP triggers nonhomologous end-joining in repair-deficient mouse fibroblasts.

Gassman NR, Stefanick DF, Kedar PS, Horton JK, Wilson SH.

PLoS One. 2012;7(11):e49301. doi: 10.1371/journal.pone.0049301. Epub 2012 Nov 7.

26.

New missense homozygous mutation (Q270Ter) in the pyrimidine 5' nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia.

Warang P, Kedar P, Kar R, Ghosh K, Colah R.

Ann Hematol. 2013 May;92(5):715-7. doi: 10.1007/s00277-012-1616-x. Epub 2012 Nov 9. No abstract available.

PMID:
23139015
27.

Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family.

Kedar P, Warang P, Ghosh K, Colah R.

Ann Hematol. 2012 Dec;91(12):1985-6. doi: 10.1007/s00277-012-1513-3. Epub 2012 Jul 15. No abstract available.

PMID:
22797852
28.

Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.

Warang P, Kedar P, Ghosh K, Colah RB.

Int J Hematol. 2012 Aug;96(2):263-7. doi: 10.1007/s12185-012-1122-x. Epub 2012 Jul 11.

PMID:
22782259
29.

HMGN1 protein regulates poly(ADP-ribose) polymerase-1 (PARP-1) self-PARylation in mouse fibroblasts.

Masaoka A, Gassman NR, Kedar PS, Prasad R, Hou EW, Horton JK, Bustin M, Wilson SH.

J Biol Chem. 2012 Aug 10;287(33):27648-58. doi: 10.1074/jbc.M112.370759. Epub 2012 Jun 26.

30.

Increased PARP-1 association with DNA in alkylation damaged, PARP-inhibited mouse fibroblasts.

Kedar PS, Stefanick DF, Horton JK, Wilson SH.

Mol Cancer Res. 2012 Mar;10(3):360-8. doi: 10.1158/1541-7786.MCR-11-0477. Epub 2012 Jan 13.

31.

A new simple approach for the determination of pyrimidine 5'-nucleotidase activity in human erythrocytes using an ELISA reader.

Warang P, Kedar P, Ghosh K, Colah R.

Int J Lab Hematol. 2012 Jun;34(3):232-6. doi: 10.1111/j.1751-553X.2011.01381.x. Epub 2011 Nov 14.

PMID:
22078096
32.

Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutations.

Kedar PS, Warang P, Ghosh K, Colah RB.

Am J Hematol. 2011 Mar;86(3):327-9. doi: 10.1002/ajh.21956. Epub 2011 Feb 15. No abstract available.

33.

Flow cytometric osmotic fragility--an effective screening approach for red cell membranopathies.

Warang P, Gupta M, Kedar P, Ghosh K, Colah R.

Cytometry B Clin Cytom. 2011 May;80(3):186-90. doi: 10.1002/cyto.b.20583. Epub 2011 Feb 4.

34.

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.

Stewart AK, Kedar PS, Shmukler BE, Vandorpe DH, Hsu A, Glader B, Rivera A, Brugnara C, Alper SL.

Am J Physiol Cell Physiol. 2011 May;300(5):C1034-46. doi: 10.1152/ajpcell.00447.2010. Epub 2011 Jan 5.

35.

Base excision repair and design of small molecule inhibitors of human DNA polymerase β.

Wilson SH, Beard WA, Shock DD, Batra VK, Cavanaugh NA, Prasad R, Hou EW, Liu Y, Asagoshi K, Horton JK, Stefanick DF, Kedar PS, Carrozza MJ, Masaoka A, Heacock ML.

Cell Mol Life Sci. 2010 Nov;67(21):3633-47. doi: 10.1007/s00018-010-0489-1. Epub 2010 Sep 16. Review.

36.

DNA polymerases beta and lambda mediate overlapping and independent roles in base excision repair in mouse embryonic fibroblasts.

Braithwaite EK, Kedar PS, Stumpo DJ, Bertocci B, Freedman JH, Samson LD, Wilson SH.

PLoS One. 2010 Aug 18;5(8):e12229. doi: 10.1371/journal.pone.0012229.

37.

Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D.

Shmukler BE, Kedar PS, Warang P, Desai M, Madkaikar M, Ghosh K, Colah RB, Alper SL.

Am J Hematol. 2010 Oct;85(10):824-8. doi: 10.1002/ajh.21836.

38.

PARP inhibition during alkylation-induced genotoxic stress signals a cell cycle checkpoint response mediated by ATM.

Carrozza MJ, Stefanick DF, Horton JK, Kedar PS, Wilson SH.

DNA Repair (Amst). 2009 Nov 2;8(11):1264-72. doi: 10.1016/j.dnarep.2009.07.010. Epub 2009 Aug 31.

39.

Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypes.

Kedar P, Hamada T, Warang P, Nadkarni A, Shimizu K, Fujji H, Ghosh K, Kanno H, Colah R.

Clin Genet. 2009 Feb;75(2):157-62. doi: 10.1111/j.1399-0004.2008.01079.x. Epub 2008 Aug 28.

PMID:
18759866
40.

Interaction between PARP-1 and ATR in mouse fibroblasts is blocked by PARP inhibition.

Kedar PS, Stefanick DF, Horton JK, Wilson SH.

DNA Repair (Amst). 2008 Nov 1;7(11):1787-98. doi: 10.1016/j.dnarep.2008.07.006. Epub 2008 Aug 22.

41.

A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.

Chalvam R, Kedar PS, Colah RB, Ghosh K, Mukherjee MB.

J Hum Genet. 2008;53(2):181-4. Epub 2007 Nov 28.

PMID:
18043863
42.

A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.

Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K.

Blood Cells Mol Dis. 2008 May-Jun;40(3):323-7. Epub 2007 Oct 25.

PMID:
17964195
43.

First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation.

Kedar PS, Nampoothiri S, Sreedhar S, Ghosh K, Shimizu K, Kanno H, Colah RB.

Genet Mol Res. 2007 Jun 30;6(2):470-5.

PMID:
17952871
44.

HMGB1 is a cofactor in mammalian base excision repair.

Prasad R, Liu Y, Deterding LJ, Poltoratsky VP, Kedar PS, Horton JK, Kanno S, Asagoshi K, Hou EW, Khodyreva SN, Lavrik OI, Tomer KB, Yasui A, Wilson SH.

Mol Cell. 2007 Sep 7;27(5):829-41.

45.

Coordination of steps in single-nucleotide base excision repair mediated by apurinic/apyrimidinic endonuclease 1 and DNA polymerase beta.

Liu Y, Prasad R, Beard WA, Kedar PS, Hou EW, Shock DD, Wilson SH.

J Biol Chem. 2007 May 4;282(18):13532-41. Epub 2007 Mar 12.

46.

ATR signaling mediates an S-phase checkpoint after inhibition of poly(ADP-ribose) polymerase activity.

Horton JK, Stefanick DF, Kedar PS, Wilson SH.

DNA Repair (Amst). 2007 Jun 1;6(6):742-50. Epub 2007 Feb 9.

47.

Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family.

Gupta N, Bianchi P, Fermo E, Kabra M, Warang P, Kedar P, Gupta N, Colah R.

Prenat Diagn. 2007 Feb;27(2):117-8.

PMID:
17191259
48.

Red cell pyruvate kinase deficiency in neonatal jaundice cases in India.

Kedar PS, Warang P, Colah RB, Mohanty D.

Indian J Pediatr. 2006 Nov;73(11):985-8.

PMID:
17127778
49.

NEIL2-initiated, APE-independent repair of oxidized bases in DNA: Evidence for a repair complex in human cells.

Das A, Wiederhold L, Leppard JB, Kedar P, Prasad R, Wang H, Boldogh I, Karimi-Busheri F, Weinfeld M, Tomkinson AE, Wilson SH, Mitra S, Hazra TK.

DNA Repair (Amst). 2006 Dec 9;5(12):1439-48. Epub 2006 Sep 18.

50.

DNA polymerase lambda protects mouse fibroblasts against oxidative DNA damage and is recruited to sites of DNA damage/repair.

Braithwaite EK, Kedar PS, Lan L, Polosina YY, Asagoshi K, Poltoratsky VP, Horton JK, Miller H, Teebor GW, Yasui A, Wilson SH.

J Biol Chem. 2005 Sep 9;280(36):31641-7. Epub 2005 Jul 7.

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