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Results: 1 to 20 of 23

1.

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.

PMID:
24524654
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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.

PMID:
23323973
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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.

PMID:
21943378
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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.

PMID:
18703765
[PubMed - indexed for MEDLINE]
Free Article
5.

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.

PMID:
16940433
[PubMed - indexed for MEDLINE]
Free Article
6.

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
[PubMed - indexed for MEDLINE]
7.

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.

PMID:
15252187
[PubMed - indexed for MEDLINE]
Free Article
8.

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
[PubMed - indexed for MEDLINE]
9.

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.

PMID:
11093279
[PubMed - indexed for MEDLINE]
Free Article
10.

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
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
9285800
[PubMed - indexed for MEDLINE]
Free Article
12.

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.

PMID:
8193372
[PubMed - indexed for MEDLINE]
Free Article
13.

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
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

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.

PMID:
1688723
[PubMed - indexed for MEDLINE]
Free Article
16.

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
[PubMed - indexed for MEDLINE]
17.

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.

PMID:
2905048
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH.

Surrey S, Delgrosso K, Malladi P, Schwartz E.

Blood. 1988 Mar;71(3):807-10.

PMID:
2449926
[PubMed - indexed for MEDLINE]
Free Article
19.

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.

PMID:
3601670
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

DNA sequence changes in the 5'-flanking region of G gamma-globin genes in a black with beta S and a non-deletional form of G gamma-beta+ HPFH.

Schwartz E, Month S, Delgrosso K, Rappaport E, Orchowski P, Malladi P, Surrey S.

Prog Clin Biol Res. 1987;251:363-71. No abstract available.

PMID:
2448806
[PubMed - indexed for MEDLINE]

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