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Items: 1 to 50 of 498

1.

Correction: A Golgi-associated protein 4.1B variant is required for assimilation of proteins in the membrane (doi:10.1242/jcs.039644).

Kang Q, Wang T, Zhang H, Mohandas N, An X.

J Cell Sci. 2019 Oct 21;132(20). pii: jcs240002. doi: 10.1242/jcs.240002. No abstract available.

PMID:
31636159
2.

A Unique Epigenomic Landscape Defines Human Erythropoiesis.

Schulz VP, Yan H, Lezon-Geyda K, An X, Hale J, Hillyer CD, Mohandas N, Gallagher PG.

Cell Rep. 2019 Sep 10;28(11):2996-3009.e7. doi: 10.1016/j.celrep.2019.08.020.

3.

Cutaneous and systemic IgG4-related disease: a review for dermatologists.

Shenoy A, Mohandas N, Gottlieb A.

Dermatol Online J. 2019 Jun 15;25(6). pii: 13030/qt9w91m8dz.

4.

Deciphering the role of epigenetics in self-limited epilepsy with centrotemporal spikes.

Mohandas N, Loke YJ, Mackenzie L, Bennett C, Berkovic SF, Craig JM, Vadlamudi L.

Epilepsy Res. 2019 Oct;156:106163. doi: 10.1016/j.eplepsyres.2019.106163. Epub 2019 Jul 4.

PMID:
31310899
5.

International Survey of Physicians' Perspectives on Percutaneous Endoscopic Gastrostomy Tube Feeding in Patients with Dementia and Review of Literature.

Mohandas N, Kumar R, Leelakrishnan V, Sharma S, Aparanji K.

Cureus. 2019 Apr 30;11(4):e4578. doi: 10.7759/cureus.4578.

6.

Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis.

Ludwig LS, Lareau CA, Bao EL, Nandakumar SK, Muus C, Ulirsch JC, Chowdhary K, Buenrostro JD, Mohandas N, An X, Aryee MJ, Regev A, Sankaran VG.

Cell Rep. 2019 Jun 11;27(11):3228-3240.e7. doi: 10.1016/j.celrep.2019.05.046.

7.

Evidence for type-specific DNA methylation patterns in epilepsy: a discordant monozygotic twin approach.

Mohandas N, Loke YJ, Hopkins S, Mackenzie L, Bennett C, Berkovic SF, Vadlamudi L, Craig JM.

Epigenomics. 2019 Jun;11(8):951-968. doi: 10.2217/epi-2018-0136. Epub 2019 Jun 5.

PMID:
31166810
8.

Anemia lurking in introns.

Mohandas N.

J Clin Invest. 2019 Jun 4;129(7):2655-2657. doi: 10.1172/JCI129443. eCollection 2019 Jun 4.

9.

Expression of Concern: A Golgi-associated protein 4.1B variant is required for assimilation of proteins in the membrane (doi:10.1242/jcs.039644).

Kang Q, Wang T, Zhang H, Mohandas N, An X.

J Cell Sci. 2019 May 2;132(9). pii: jcs233080. doi: 10.1242/jcs.233080. No abstract available. Erratum in: J Cell Sci. 2019 Oct 21;132(20):.

PMID:
31048547
10.

Deubiquitylase USP7 regulates human terminal erythroid differentiation by stabilizing GATA1.

Liang L, Peng Y, Zhang J, Zhang Y, Roy M, Han X, Xiao X, Sun S, Liu H, Nie L, Kuang Y, Zhu Z, Deng J, Xia Y, Sankaran VG, Hillyer CD, Mohandas N, Ye M, An X, Liu J.

Haematologica. 2019 Mar 14. pii: haematol.2018.206227. doi: 10.3324/haematol.2018.206227. [Epub ahead of print]

11.

Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1.

Rio S, Gastou M, Karboul N, Derman R, Suriyun T, Manceau H, Leblanc T, El Benna J, Schmitt C, Azouzi S, Larghéro J, Karim Z, Macias-Garcia A, Chen JJ, Hermine O, Courtois G, Puy H, Gouya L, Mohandas N, Da Costa L.

Blood. 2019 Mar 21;133(12):1358-1370. doi: 10.1182/blood-2018-09-875674. Epub 2019 Jan 30.

PMID:
30700418
12.

Inherited hemolytic anemia: a possessive beginner's guide.

Mohandas N.

Hematology Am Soc Hematol Educ Program. 2018 Nov 30;2018(1):377-381. doi: 10.1182/asheducation-2018.1.377. Review.

PMID:
30504335
13.

Absolute proteome quantification of highly purified populations of circulating reticulocytes and mature erythrocytes.

Gautier EF, Leduc M, Cochet S, Bailly K, Lacombe C, Mohandas N, Guillonneau F, El Nemer W, Mayeux P.

Blood Adv. 2018 Oct 23;2(20):2646-2657. doi: 10.1182/bloodadvances.2018023515.

14.

Sensing of red blood cells with decreased membrane deformability by the human spleen.

Safeukui I, Buffet PA, Deplaine G, Perrot S, Brousse V, Sauvanet A, Aussilhou B, Dokmak S, Couvelard A, Cazals-Hatem D, Mercereau-Puijalon O, Milon G, David PH, Mohandas N.

Blood Adv. 2018 Oct 23;2(20):2581-2587. doi: 10.1182/bloodadvances.2018024562.

15.

TET2 deficiency leads to stem cell factor-dependent clonal expansion of dysfunctional erythroid progenitors.

Qu X, Zhang S, Wang S, Wang Y, Li W, Huang Y, Zhao H, Wu X, An C, Guo X, Hale J, Li J, Hillyer CD, Mohandas N, Liu J, Yazdanbakhsh K, Vinchi F, Chen L, Kang Q, An X.

Blood. 2018 Nov 29;132(22):2406-2417. doi: 10.1182/blood-2018-05-853291. Epub 2018 Sep 25.

PMID:
30254129
16.

Fyn kinase is a novel modulator of erythropoietin signaling and stress erythropoiesis.

Beneduce E, Matte A, De Falco L, Mbiandjeu S, Chiabrando D, Tolosano E, Federti E, Petrillo S, Mohandas N, Siciliano A, Babu W, Menon V, Ghaffari S, Iolascon A, De Franceschi L.

Am J Hematol. 2019 Jan;94(1):10-20. doi: 10.1002/ajh.25295. Epub 2018 Oct 25.

PMID:
30252956
17.

An update on the pathogenesis and diagnosis of Diamond-Blackfan anemia.

Da Costa L, Narla A, Mohandas N.

F1000Res. 2018 Aug 29;7. pii: F1000 Faculty Rev-1350. doi: 10.12688/f1000research.15542.1. eCollection 2018. Review.

18.

Prognostic factors of disease severity in infants with sickle cell anemia: A comprehensive longitudinal cohort study.

Brousse V, El Hoss S, Bouazza N, Arnaud C, Bernaudin F, Pellegrino B, Guitton C, Odièvre-Montanié MH, Mames D, Brouzes C, Picard V, Nguyen-Khoa T, Pereira C, Lapouméroulie C, Pissard S, Gardner K, Menzel S, Le Van Kim C, Colin-Aronovicz Y, Buffet P, Mohandas N, Elie C, Maier-Redelsperger M, El Nemer W, de Montalembert M.

Am J Hematol. 2018 Nov;93(11):1411-1419. doi: 10.1002/ajh.25260. Epub 2018 Sep 21.

PMID:
30132969
19.

Severely impaired terminal erythroid differentiation as an independent prognostic marker in myelodysplastic syndromes.

Ali AM, Huang Y, Pinheiro RF, Xue F, Hu J, Iverson N, Hoehn D, Coutinho D, Kayani J, Chernak B, Lane J, Hillyer C, Galili N, Jurcic J, Mohandas N, An X, Raza A.

Blood Adv. 2018 Jun 26;2(12):1393-1402. doi: 10.1182/bloodadvances.2018018440.

20.

Function and dysfunction.

Mohandas N.

Blood. 2018 May 17;131(20):2179-2180. doi: 10.1182/blood-2018-04-840827. No abstract available.

21.

miR-326 regulates HbF synthesis by targeting EKLF in human erythroid cells.

Li Y, Liu D, Zhang X, Li Z, Ye Y, Liu Q, Shen J, Chen Z, Huang H, Liang Y, Han X, Liu J, An X, Mohandas N, Xu X.

Exp Hematol. 2018 Jul;63:33-40.e2. doi: 10.1016/j.exphem.2018.03.004. Epub 2018 Mar 27.

PMID:
29601850
22.

Epigenome-wide analysis in newborn blood spots from monozygotic twins discordant for cerebral palsy reveals consistent regional differences in DNA methylation.

Mohandas N, Bass-Stringer S, Maksimovic J, Crompton K, Loke YJ, Walstab J, Reid SM, Amor DJ, Reddihough D, Craig JM.

Clin Epigenetics. 2018 Feb 23;10:25. doi: 10.1186/s13148-018-0457-4. eCollection 2018.

23.

Role of tissue-specific promoter DNA methylation in regulating the human EKLF gene.

Li Y, Liu D, Li Z, Zhang X, Ye Y, Liu Q, Shen J, Chen Z, Huang H, Liang Y, Han X, Liu J, An X, Mohandas N, Xu X.

Blood Cells Mol Dis. 2018 Jul;71:16-22. doi: 10.1016/j.bcmd.2018.01.004. Epub 2018 Feb 15.

PMID:
29475801
24.

Role of noninvasive markers to predict the presence of esophageal varices in cirrhosis: Pilot study.

Vegiraju VK, Shetty S, Leelakrishnan V, Janarthanan K, Mohandas N, Balakshmoji D.

Indian J Gastroenterol. 2018 Jan;37(1):74-75. doi: 10.1007/s12664-018-0834-0. No abstract available.

PMID:
29455439
25.

SF3B1 deficiency impairs human erythropoiesis via activation of p53 pathway: implications for understanding of ineffective erythropoiesis in MDS.

Huang Y, Hale J, Wang Y, Li W, Zhang S, Zhang J, Zhao H, Guo X, Liu J, Yan H, Yazdanbakhsh K, Huang G, Hillyer CD, Mohandas N, Chen L, Sun L, An X.

J Hematol Oncol. 2018 Feb 12;11(1):19. doi: 10.1186/s13045-018-0558-8.

26.

Protein 4.1N is required for the formation of the lateral membrane domain in human bronchial epithelial cells.

Wang Y, Zhang H, Kang Q, Liu J, Weng H, Li W, Mohandas N, An X, Chen L.

Biochim Biophys Acta Biomembr. 2018 May;1860(5):1143-1151. doi: 10.1016/j.bbamem.2018.02.009. Epub 2018 Feb 8.

27.

Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry.

Parrow NL, Violet PC, Tu H, Nichols J, Pittman CA, Fitzhugh C, Fleming RE, Mohandas N, Tisdale JF, Levine M.

J Vis Exp. 2018 Jan 12;(131). doi: 10.3791/56910.

28.

Remodeling of the malaria parasite and host human red cell by vesicle amplification that induces artemisinin resistance.

Bhattacharjee S, Coppens I, Mbengue A, Suresh N, Ghorbal M, Slouka Z, Safeukui I, Tang HY, Speicher DW, Stahelin RV, Mohandas N, Haldar K.

Blood. 2018 Mar 15;131(11):1234-1247. doi: 10.1182/blood-2017-11-814665. Epub 2018 Jan 23.

29.

The severe phenotype of Diamond-Blackfan anemia is modulated by heat shock protein 70.

Gastou M, Rio S, Dussiot M, Karboul N, Moniz H, Leblanc T, Sevin M, Gonin P, Larghéro J, Garrido C, Narla A, Mohandas N, Vainchenker W, Hermine O, Solary E, Da Costa L; French Society of Hematology (SFH); French Society of Immunology and Hematology (SHIP).

Blood Adv. 2017 Oct 10;1(22):1959-1976. doi: 10.1182/bloodadvances.2017008078. eCollection 2017 Oct 10.

30.

Developmental differences between neonatal and adult human erythropoiesis.

Yan H, Hale J, Jaffray J, Li J, Wang Y, Huang Y, An X, Hillyer C, Wang N, Kinet S, Taylor N, Mohandas N, Narla A, Blanc L.

Am J Hematol. 2018 Aug;93(4):494-503. doi: 10.1002/ajh.25015. Epub 2018 Jan 9.

31.

Case series supporting heme detoxification via therapeutic plasma exchange in acute multiorgan failure syndrome resistant to red blood cell exchange in sickle cell disease.

Louie JE, Anderson CJ, Fayaz M Fomani K, Henry A, Killeen T, Mohandas N, Yazdanbakhsh K, Belcher JD, Vercellotti GM, Shi PA.

Transfusion. 2018 Feb;58(2):470-479. doi: 10.1111/trf.14407. Epub 2017 Nov 27.

PMID:
29193101
32.

Unraveling Macrophage Heterogeneity in Erythroblastic Islands.

Seu KG, Papoin J, Fessler R, Hom J, Huang G, Mohandas N, Blanc L, Kalfa TA.

Front Immunol. 2017 Sep 20;8:1140. doi: 10.3389/fimmu.2017.01140. eCollection 2017.

33.

Enhancing diversity in the hematology biomedical research workforce: A mentoring program to improve the odds of career success for early stage investigators.

Pace BS, Makala LH, Sarkar R, Liu L, Takezaki M, Mohandas N, Dixon G, Werner EM, Jeffe DB, Rice TK, Maihle NJ, González J.

Am J Hematol. 2017 Dec;92(12):1275-1279. doi: 10.1002/ajh.24899. Epub 2017 Sep 25. No abstract available.

34.

Peroxiredoxin-2: A Novel Regulator of Iron Homeostasis in Ineffective Erythropoiesis.

Matte A, De Falco L, Federti E, Cozzi A, Iolascon A, Levi S, Mohandas N, Zamo A, Bruno M, Lebouef C, Janin A, Siciliano A, Ganz T, Federico G, Carlomagno F, Mueller S, Silva I, Carbone C, Melisi D, Kim DW, Choi SY, De Franceschi L.

Antioxid Redox Signal. 2018 Jan 1;28(1):1-14. doi: 10.1089/ars.2017.7051. Epub 2017 Sep 6.

PMID:
28793778
35.

Circulating primitive erythroblasts establish a functional, protein 4.1R-dependent cytoskeletal network prior to enucleating.

Huang YS, Delgadillo LF, Cyr KH, Kingsley PD, An X, McGrath KE, Mohandas N, Conboy JG, Waugh RE, Wan J, Palis J.

Sci Rep. 2017 Jul 12;7(1):5164. doi: 10.1038/s41598-017-05498-4.

36.

Confounding in ex vivo models of Diamond-Blackfan anemia.

Ulirsch JC, Lareau C, Ludwig LS, Mohandas N, Nathan DG, Sankaran VG.

Blood. 2017 Aug 31;130(9):1165-1168. doi: 10.1182/blood-2017-05-783191. Epub 2017 Jun 14. No abstract available.

37.

Measurements of red cell deformability and hydration reflect HbF and HbA2 in blood from patients with sickle cell anemia.

Parrow NL, Tu H, Nichols J, Violet PC, Pittman CA, Fitzhugh C, Fleming RE, Mohandas N, Tisdale JF, Levine M.

Blood Cells Mol Dis. 2017 Jun;65:41-50. doi: 10.1016/j.bcmd.2017.04.005. Epub 2017 Apr 18.

PMID:
28472705
38.

Red cell membrane disorders.

Narla J, Mohandas N.

Int J Lab Hematol. 2017 May;39 Suppl 1:47-52. doi: 10.1111/ijlh.12657. Review.

PMID:
28447420
39.

Distinct roles for TET family proteins in regulating human erythropoiesis.

Yan H, Wang Y, Qu X, Li J, Hale J, Huang Y, An C, Papoin J, Guo X, Chen L, Kang Q, Li W, Schulz VP, Gallagher PG, Hillyer CD, Mohandas N, An X.

Blood. 2017 Apr 6;129(14):2002-2012. doi: 10.1182/blood-2016-08-736587. Epub 2017 Feb 6.

40.

Decreasing TfR1 expression reverses anemia and hepcidin suppression in β-thalassemic mice.

Li H, Choesang T, Bao W, Chen H, Feola M, Garcia-Santos D, Li J, Sun S, Follenzi A, Pham P, Liu J, Zhang J, Ponka P, An X, Mohandas N, Fleming RE, Rivella S, Li G, Ginzburg YZ.

Blood. 2017 Mar 16;129(11):1514-1526. doi: 10.1182/blood-2016-09-742387. Epub 2017 Feb 1. Erratum in: Blood. 2017 Dec 21;130(25):2809.

41.

Characterization, regulation, and targeting of erythroid progenitors in normal and disordered human erythropoiesis.

Dulmovits BM, Hom J, Narla A, Mohandas N, Blanc L.

Curr Opin Hematol. 2017 May;24(3):159-166. doi: 10.1097/MOH.0000000000000328. Review.

42.

Unexpected role for p19INK4d in posttranscriptional regulation of GATA1 and modulation of human terminal erythropoiesis.

Han X, Zhang J, Peng Y, Peng M, Chen X, Chen H, Song J, Hu X, Ye M, Li J, Sankaran VG, Hillyer CD, Mohandas N, An X, Liu J.

Blood. 2017 Jan 12;129(2):226-237. doi: 10.1182/blood-2016-09-739268. Epub 2016 Nov 22.

43.

Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia.

Lacy JN, Ulirsch JC, Grace RF, Towne MC, Hale J, Mohandas N, Lux SE 4th, Agrawal PB, Sankaran VG.

Cold Spring Harb Mol Case Stud. 2016 Jul;2(4):a000885. doi: 10.1101/mcs.a000885.

44.

The road not taken?

Narla A, Mohandas N.

Blood. 2016 Aug 18;128(7):886-8. doi: 10.1182/blood-2016-07-722413. No abstract available.

PMID:
27539995
45.

Sustained treatment of sickle cell mice with haptoglobin increases HO-1 and H-ferritin expression and decreases iron deposition in the kidney without improvement in kidney function.

Shi PA, Choi E, Chintagari NR, Nguyen J, Guo X, Yazdanbakhsh K, Mohandas N, Alayash AI, Manci EA, Belcher JD, Vercellotti GM.

Br J Haematol. 2016 Nov;175(4):714-723. doi: 10.1111/bjh.14280. Epub 2016 Aug 10.

46.

Comprehensive Proteomic Analysis of Human Erythropoiesis.

Gautier EF, Ducamp S, Leduc M, Salnot V, Guillonneau F, Dussiot M, Hale J, Giarratana MC, Raimbault A, Douay L, Lacombe C, Mohandas N, Verdier F, Zermati Y, Mayeux P.

Cell Rep. 2016 Aug 2;16(5):1470-1484. doi: 10.1016/j.celrep.2016.06.085. Epub 2016 Jul 21.

47.

An Unrecognized Function of Cholesterol: Regulating the Mechanism Controlling Membrane Phospholipid Asymmetry.

Arashiki N, Saito M, Koshino I, Kamata K, Hale J, Mohandas N, Manno S, Takakuwa Y.

Biochemistry. 2016 Jun 28;55(25):3504-3513. doi: 10.1021/acs.biochem.6b00407. Epub 2016 Jun 13.

48.

Malaria Parasite Proteins and Their Role in Alteration of the Structure and Function of Red Blood Cells.

Proellocks NI, Coppel RL, Mohandas N, Cooke BM.

Adv Parasitol. 2016;91:1-86. doi: 10.1016/bs.apar.2015.09.002. Epub 2015 Dec 14. Review.

PMID:
27015947
49.

A dynamic intron retention program in the mammalian megakaryocyte and erythrocyte lineages.

Edwards CR, Ritchie W, Wong JJ, Schmitz U, Middleton R, An X, Mohandas N, Rasko JE, Blobel GA.

Blood. 2016 Apr 28;127(17):e24-e34. doi: 10.1182/blood-2016-01-692764. Epub 2016 Mar 9.

50.

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia.

Arashiki N, Takakuwa Y, Mohandas N, Hale J, Yoshida K, Ogura H, Utsugisawa T, Ohga S, Miyano S, Ogawa S, Kojima S, Kanno H.

Haematologica. 2016 May;101(5):559-65. doi: 10.3324/haematol.2016.142273. Epub 2016 Mar 4.

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