Hensle TW - Search Results

1

CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors.

Li CM, Kim CE, Margolin AA, Guo M, Zhu J, Mason JM, Hensle TW, Murty VV, Grundy PE, Fearon ER, D'Agati V, Licht JD, Tycko B. Li CM, et al. Among authors: hensle tw. Am J Pathol. 2004 Dec;165(6):1943-53. doi: 10.1016/s0002-9440(10)63246-4. Am J Pathol. 2004. PMID: 15579438 Free PMC article.

2

Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors.

Chung WY, Yuan L, Feng L, Hensle T, Tycko B. Chung WY, et al. Hum Mol Genet. 1996 Aug;5(8):1101-8. doi: 10.1093/hmg/5.8.1101. Hum Mol Genet. 1996. PMID: 8842727

3

Genomic imprinting and Wilms' tumor.

Moulton T, Chung WY, Yuan L, Hensle T, Waber P, Nisen P, Tycko B. Moulton T, et al. Med Pediatr Oncol. 1996 Nov;27(5):476-83. doi: 10.1002/(SICI)1096-911X(199611)27:5<476::AID-MPO15>3.0.CO;2-8. Med Pediatr Oncol. 1996. PMID: 8827077

4

Epigenetic lesions at the H19 locus in Wilms' tumour patients.

Moulton T, Crenshaw T, Hao Y, Moosikasuwan J, Lin N, Dembitzer F, Hensle T, Weiss L, McMorrow L, Loew T, Kraus W, Gerald W, Tycko B. Moulton T, et al. Nat Genet. 1994 Jul;7(3):440-7. doi: 10.1038/ng0794-440. Nat Genet. 1994. PMID: 7920666

5

Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting.

Dao D, Walsh CP, Yuan L, Gorelov D, Feng L, Hensle T, Nisen P, Yamashiro DJ, Bestor TH, Tycko B. Dao D, et al. Hum Mol Genet. 1999 Jul;8(7):1337-52. doi: 10.1093/hmg/8.7.1337. Hum Mol Genet. 1999. PMID: 10369881

6

Three pediatric patients with extension of prostatic embryonal rhabdomyosarcoma anterior to the bladder into the space of Retzius.

Levin T, Berdon WE, Ruzal-Shapiro C, Abramson S, Garvin J, Altman RP, Hensle T, Ablin DS. Levin T, et al. Pediatr Radiol. 1992;22(3):200-2. doi: 10.1007/BF02012495. Pediatr Radiol. 1992. PMID: 1508589

7

Further delineation of the Opitz G/BBB syndrome: report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature.

Jacobson Z, Glickstein J, Hensle T, Marion RW. Jacobson Z, et al. Am J Med Genet. 1998 Jul 7;78(3):294-9. doi: 10.1002/(sici)1096-8628(19980707)78:3<294::aid-ajmg18>3.0.co;2-a. Am J Med Genet. 1998. PMID: 9677070 Review.

8

EDITORIAL COMMENT.

Hensle TW. Hensle TW. Urology. 2019 Jan;123:219. doi: 10.1016/j.urology.2018.05.047. Urology. 2019. PMID: 30598214 No abstract available.

9

Surgery in disorders of sex development (DSD) with a gender issue: If (why), when, and how?

Mouriquand PD, Gorduza DB, Gay CL, Meyer-Bahlburg HF, Baker L, Baskin LS, Bouvattier C, Braga LH, Caldamone AC, Duranteau L, El Ghoneimi A, Hensle TW, Hoebeke P, Kaefer M, Kalfa N, Kolon TF, Manzoni G, Mure PY, Nordenskjöld A, Pippi Salle JL, Poppas DP, Ransley PG, Rink RC, Rodrigo R, Sann L, Schober J, Sibai H, Wisniewski A, Wolffenbuttel KP, Lee P. Mouriquand PD, et al. Among authors: hensle tw. J Pediatr Urol. 2016 Jun;12(3):139-49. doi: 10.1016/j.jpurol.2016.04.001. Epub 2016 Apr 9. J Pediatr Urol. 2016. PMID: 27132944 Review.

10

Enterocystoplasty: The long-term effects on bone mineral density.

Hensle TW, Reiley EA, Fam MM, Carpenter CP. Hensle TW, et al. J Pediatr Urol. 2016 Aug;12(4):245.e1-6. doi: 10.1016/j.jpurol.2016.02.017. Epub 2016 Mar 28. J Pediatr Urol. 2016. PMID: 27068701

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