Witte DP - Search Results

1

Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder.

Szafranski P, Dharmadhikari AV, Brosens E, Gurha P, Kolodziejska KE, Zhishuo O, Dittwald P, Majewski T, Mohan KN, Chen B, Person RE, Tibboel D, de Klein A, Pinner J, Chopra M, Malcolm G, Peters G, Arbuckle S, Guiang SF 3rd, Hustead VA, Jessurun J, Hirsch R, Witte DP, Maystadt I, Sebire N, Fisher R, Langston C, Sen P, Stankiewicz P. Szafranski P, et al. Among authors: witte dp. Genome Res. 2013 Jan;23(1):23-33. doi: 10.1101/gr.141887.112. Epub 2012 Oct 3. Genome Res. 2013. PMID: 23034409 Free PMC article.

2

Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins.

Karolak JA, Liu Q, Xie NG, Wu LR, Rocha G, Fernandes S, Ho-Ming L, Lo IF, Mowat D, Fiorino EK, Edelman M, Fox J, Hayes DA, Witte D, Parrott A, Popek E, Szafranski P, Zhang DY, Stankiewicz P. Karolak JA, et al. J Mol Diagn. 2020 Apr;22(4):447-456. doi: 10.1016/j.jmoldx.2019.12.007. Epub 2020 Feb 7. J Mol Diagn. 2020. PMID: 32036090 Free PMC article.

3

Pulmonary arterial hypertension in pediatric patients with hematopoietic stem cell transplant-associated thrombotic microangiopathy.

Jodele S, Hirsch R, Laskin B, Davies S, Witte D, Chima R. Jodele S, et al. Biol Blood Marrow Transplant. 2013 Feb;19(2):202-7. doi: 10.1016/j.bbmt.2012.08.022. Epub 2012 Sep 6. Biol Blood Marrow Transplant. 2013. PMID: 22960385 Free article.

4

Isolation and characterization of the human prosaposin promoter.

Sun Y, Jin P, Witte DP, Grabowski GA. Sun Y, et al. Among authors: witte dp. Gene. 1998 Sep 18;218(1-2):37-47. doi: 10.1016/s0378-1119(98)00391-6. Gene. 1998. PMID: 9751800

5

Transcriptional profiles of intestinal tumors in Apc(Min) mice are unique from those of embryonic intestine and identify novel gene targets dysregulated in human colorectal tumors.

Reichling T, Goss KH, Carson DJ, Holdcraft RW, Ley-Ebert C, Witte D, Aronow BJ, Groden J. Reichling T, et al. Cancer Res. 2005 Jan 1;65(1):166-76. Cancer Res. 2005. PMID: 15665292

6

Chd7 cooperates with Sox10 and regulates the onset of CNS myelination and remyelination.

He D, Marie C, Zhao C, Kim B, Wang J, Deng Y, Clavairoly A, Frah M, Wang H, He X, Hmidan H, Jones BV, Witte D, Zalc B, Zhou X, Choo DI, Martin DM, Parras C, Lu QR. He D, et al. Nat Neurosci. 2016 May;19(5):678-689. doi: 10.1038/nn.4258. Epub 2016 Feb 29. Nat Neurosci. 2016. PMID: 26928066 Free PMC article.

7

Prosaposin: promoter analysis and central-nervous-system-preferential elements for expression in vivo.

Sun Y, Jin P, Witte DP, Grabowski GA. Sun Y, et al. Among authors: witte dp. Biochem J. 2000 Dec 1;352 Pt 2(Pt 2):549-56. Biochem J. 2000. PMID: 11085950 Free PMC article.

8

A submicroscopic deletion in Xq26 associated with familial situs ambiguus.

Ferrero GB, Gebbia M, Pilia G, Witte D, Peier A, Hopkin RJ, Craigen WJ, Shaffer LG, Schlessinger D, Ballabio A, Casey B. Ferrero GB, et al. Am J Hum Genet. 1997 Aug;61(2):395-401. doi: 10.1086/514857. Am J Hum Genet. 1997. PMID: 9311745 Free PMC article.

9

Early-lethal Costello syndrome due to rare HRAS Tandem Base substitution (c.35_36GC>AA; p.G12E)-associated pulmonary vascular disease.

Weaver KN, Wang D, Cnota J, Gardner N, Stabley D, Sol-Church K, Gripp KW, Witte DP, Bove KE, Hopkin RJ. Weaver KN, et al. Among authors: witte dp. Pediatr Dev Pathol. 2014 Nov-Dec;17(6):421-30. doi: 10.2350/14-05-1488-OA.1. Epub 2014 Aug 18. Pediatr Dev Pathol. 2014. PMID: 25133308 Free PMC article.

10

Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation.

George-Abraham JK, Zimmerman SL, Hinton RB, Marino BS, Witte DP, Hopkin RJ. George-Abraham JK, et al. Among authors: witte dp. Am J Med Genet A. 2012 Aug;158A(8):1971-6. doi: 10.1002/ajmg.a.35428. Epub 2012 Jun 18. Am J Med Genet A. 2012. PMID: 22711292

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