Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 24

1.

Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- and tissue-specific microRNAs.

Londin E, Loher P, Telonis AG, Quann K, Clark P, Jing Y, Hatzimichael E, Kirino Y, Honda S, Lally M, Ramratnam B, Comstock CE, Knudsen KE, Gomella L, Spaeth GL, Hark L, Katz LJ, Witkiewicz A, Rostami A, Jimenez SA, Hollingsworth MA, Yeh JJ, Shaw CA, McKenzie SE, Bray P, Nelson PT, Zupo S, Van Roosbroeck K, Keating MJ, Calin GA, Yeo C, Jimbo M, Cozzitorto J, Brody JR, Delgrosso K, Mattick JS, Fortina P, Rigoutsos I.

Proc Natl Acad Sci U S A. 2015 Mar 10;112(10):E1106-15. doi: 10.1073/pnas.1420955112. Epub 2015 Feb 23.

2.

The human platelet: strong transcriptome correlations among individuals associate weakly with the platelet proteome.

Londin ER, Hatzimichael E, Loher P, Edelstein L, Shaw C, Delgrosso K, Fortina P, Bray PF, McKenzie SE, Rigoutsos I.

Biol Direct. 2014 Feb 14;9:3. doi: 10.1186/1745-6150-9-3.

3.

The complex transcriptional landscape of the anucleate human platelet.

Bray PF, McKenzie SE, Edelstein LC, Nagalla S, Delgrosso K, Ertel A, Kupper J, Jing Y, Londin E, Loher P, Chen HW, Fortina P, Rigoutsos I.

BMC Genomics. 2013 Jan 16;14:1. doi: 10.1186/1471-2164-14-1.

4.

Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor.

Londin ER, Keller MA, D'Andrea MR, Delgrosso K, Ertel A, Surrey S, Fortina P.

BMC Genomics. 2011 Sep 26;12:464. doi: 10.1186/1471-2164-12-464.

5.

Genotyping beta-globin gene mutations on copolymer-coated glass slides with the ligation detection reaction.

Battistella S, Damin F, Chiari M, Delgrosso K, Surrey S, Fortina P, Ferrari M, Cremonesi L.

Clin Chem. 2008 Oct;54(10):1657-63. doi: 10.1373/clinchem.2008.107870. Epub 2008 Aug 14.

6.

Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulators.

Keller MA, Addya S, Vadigepalli R, Banini B, Delgrosso K, Huang H, Surrey S.

Physiol Genomics. 2006 Dec 13;28(1):114-28. Epub 2006 Aug 29.

7.

Identification of APC gene mutations in colorectal cancer using universal microarray-based combinatorial sequencing-by-hybridization.

Cowie S, Drmanac S, Swanson D, Delgrosso K, Huang S, du Sart D, Drmanac R, Surrey S, Fortina P.

Hum Mutat. 2004 Sep;24(3):261-71.

PMID:
15300853
8.

Erythroid-induced commitment of K562 cells results in clusters of differentially expressed genes enriched for specific transcription regulatory elements.

Addya S, Keller MA, Delgrosso K, Ponte CM, Vadigepalli R, Gonye GE, Surrey S.

Physiol Genomics. 2004 Sep 16;19(1):117-30. Epub 2004 Jul 13.

9.

Interpretation of fetal hemoglobin only on newborn screening for hemoglobinopathy.

Heeney MM, Delgrosso K, Robinson R, Johnson CA, Daeschner CW, Campbell TA, Surrey S, Ware RE.

J Pediatr Hematol Oncol. 2002 Aug-Sep;24(6):499-502.

PMID:
12218602
10.

Simple two-color array-based approach for mutation detection.

Fortina P, Delgrosso K, Sakazume T, Santacroce R, Moutereau S, Su HJ, Graves D, McKenzie S, Surrey S.

Eur J Hum Genet. 2000 Nov;8(11):884-94.

11.

Identification of the nucleotide change (CAC-->CGC) responsible for Hb P-Galveston [BETA117(G19)His-->Arg].

Keller, Delgrosso K, Surrey S, Schwartz E.

Hemoglobin. 2000 May;24(2):165-7. No abstract available.

PMID:
10870891
12.

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

Zelante L, Gasparini P, Estivill X, Melchionda S, D'Agruma L, Govea N, Milá M, Monica MD, Lutfi J, Shohat M, Mansfield E, Delgrosso K, Rappaport E, Surrey S, Fortina P.

Hum Mol Genet. 1997 Sep;6(9):1605-9.

13.

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia.

Fortina P, Parrella T, Sartore M, Gottardi E, Gabutti V, Delgrosso K, Mansfield E, Rappaport E, Schwartz E, Camaschella C, et al.

Blood. 1994 Jun 1;83(11):3356-62.

14.

A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent.

Fortina P, Delgrosso K, Werner E, Haines K, Rappaport E, Schwartz E, Surrey S.

Hemoglobin. 1991;15(1-2):23-41.

PMID:
1717405
15.

Organization of the gene for platelet glycoprotein IIb.

Heidenreich R, Eisman R, Surrey S, Delgrosso K, Bennett JS, Schwartz E, Poncz M.

Biochemistry. 1990 Feb 6;29(5):1232-44.

PMID:
2322558
16.

The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factors.

Gumucio DL, Lockwood WK, Weber JL, Saulino AM, Delgrosso K, Surrey S, Schwartz E, Goodman M, Collins FS.

Blood. 1990 Feb 1;75(3):756-61.

17.

Large deletions encompassing the entire alpha- and beta-like globin gene clusters in humans.

Fortina P, Delgrosso K, Rappaport E, Werner E, Ballas S, Schwartz E, Surrey S.

Prog Clin Biol Res. 1989;316B:151-9. No abstract available.

PMID:
2575754
18.

A large deletion encompassing the entire alpha-like globin gene cluster in a family of northern European extraction.

Fortina P, Delgrosso K, Rappaport E, Poncz M, Ballas SK, Schwartz E, Surrey S.

Nucleic Acids Res. 1988 Dec 9;16(23):11223-35.

19.
20.

DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2).

Poncz M, Sutton M, Delgrosso K, Schwartz E, Surrey S.

Nucleic Acids Res. 1987 Jul 10;15(13):5169-79.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk