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Items: 1 to 20 of 30

1.

BLAT--the BLAST-like alignment tool.

Kent WJ.

Genome Res. 2002 Apr;12(4):656-64.

2.

Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome.

Zbar B, Alvord WG, Glenn G, Turner M, Pavlovich CP, Schmidt L, Walther M, Choyke P, Weirich G, Hewitt SM, Duray P, Gabril F, Greenberg C, Merino MJ, Toro J, Linehan WM.

Cancer Epidemiol Biomarkers Prev. 2002 Apr;11(4):393-400.

3.

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.

Tomlinson IP, Alam NA, Rowan AJ, Barclay E, Jaeger EE, Kelsell D, Leigh I, Gorman P, Lamlum H, Rahman S, Roylance RR, Olpin S, Bevan S, Barker K, Hearle N, Houlston RS, Kiuru M, Lehtonen R, Karhu A, Vilkki S, Laiho P, Eklund C, Vierimaa O, Aittomäki K, Hietala M, Sistonen P, Paetau A, Salovaara R, Herva R, Launonen V, Aaltonen LA; Multiple Leiomyoma Consortium..

Nat Genet. 2002 Apr;30(4):406-10. Epub 2002 Feb 25.

PMID:
11865300
4.

Hysterectomy rates in the United States 1990-1997.

Farquhar CM, Steiner CA.

Obstet Gynecol. 2002 Feb;99(2):229-34.

PMID:
11814502
5.

Mitochondrial and cytosolic isoforms of yeast fumarase are derivatives of a single translation product and have identical amino termini.

Sass E, Blachinsky E, Karniely S, Pines O.

J Biol Chem. 2001 Dec 7;276(49):46111-7. Epub 2001 Oct 3.

6.

Multiple leiomyomas of the esophagus, lung, and uterus in multiple endocrine neoplasia type 1.

McKeeby JL, Li X, Zhuang Z, Vortmeyer AO, Huang S, Pirner M, Skarulis MC, James-Newton L, Marx SJ, Lubensky IA.

Am J Pathol. 2001 Sep;159(3):1121-7.

7.

Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology.

Kiuru M, Launonen V, Hietala M, Aittomäki K, Vierimaa O, Salovaara R, Arola J, Pukkala E, Sistonen P, Herva R, Aaltonen LA.

Am J Pathol. 2001 Sep;159(3):825-9.

8.

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.

Schmidt LS, Warren MB, Nickerson ML, Weirich G, Matrosova V, Toro JR, Turner ML, Duray P, Merino M, Hewitt S, Pavlovich CP, Glenn G, Greenberg CR, Linehan WM, Zbar B.

Am J Hum Genet. 2001 Oct;69(4):876-82. Epub 2001 Aug 30.

9.

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

Alam NA, Bevan S, Churchman M, Barclay E, Barker K, Jaeger EE, Nelson HM, Healy E, Pembroke AC, Friedmann PS, Dalziel K, Calonje E, Anderson J, August PJ, Davies MG, Felix R, Munro CS, Murdoch M, Rendall J, Kennedy S, Leigh IM, Kelsell DP, Tomlinson IP, Houlston RS.

Am J Hum Genet. 2001 May;68(5):1264-9. Epub 2001 Mar 14.

10.

Inherited susceptibility to uterine leiomyomas and renal cell cancer.

Launonen V, Vierimaa O, Kiuru M, Isola J, Roth S, Pukkala E, Sistonen P, Herva R, Aaltonen LA.

Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3387-92. Epub 2001 Feb 27.

11.

Uterine fibroids.

Stewart EA.

Lancet. 2001 Jan 27;357(9252):293-8. Review.

PMID:
11214143
12.

Prevalence of microscopic tumors in normal appearing renal parenchyma of patients with hereditary papillary renal cancer.

Ornstein DK, Lubensky IA, Venzon D, Zbar B, Linehan WM, Walther MM.

J Urol. 2000 Feb;163(2):431-3.

PMID:
10647647
13.

BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences.

Tatusova TA, Madden TL.

FEMS Microbiol Lett. 1999 May 15;174(2):247-50. Erratum in: FEMS Microbiol Lett 1999 Aug 1;177(1):187-8.

14.

Molecular analysis and prenatal diagnosis of human fumarase deficiency.

Coughlin EM, Christensen E, Kunz PL, Krishnamoorthy KS, Walker V, Dennis NR, Chalmers RA, Elpeleg ON, Whelan D, Pollitt RJ, Ramesh V, Mandell R, Shih VE.

Mol Genet Metab. 1998 Apr;63(4):254-62.

PMID:
9635293
15.

Variation in the incidence of uterine leiomyoma among premenopausal women by age and race.

Marshall LM, Spiegelman D, Barbieri RL, Goldman MB, Manson JE, Colditz GA, Willett WC, Hunter DJ.

Obstet Gynecol. 1997 Dec;90(6):967-73.

PMID:
9397113
16.

The Heidelberg classification of renal cell tumours.

Kovacs G, Akhtar M, Beckwith BJ, Bugert P, Cooper CS, Delahunt B, Eble JN, Fleming S, Ljungberg B, Medeiros LJ, Moch H, Reuter VE, Ritz E, Roos G, Schmidt D, Srigley JR, Störkel S, van den Berg E, Zbar B.

J Pathol. 1997 Oct;183(2):131-3. Review.

PMID:
9390023
17.

Imaging features of hereditary papillary renal cancers.

Choyke PL, Walther MM, Glenn GM, Wagner JR, Venzon DJ, Lubensky IA, Zbar B, Linehan WM.

J Comput Assist Tomogr. 1997 Sep-Oct;21(5):737-41.

PMID:
9294565
18.

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas.

Schmidt L, Duh FM, Chen F, Kishida T, Glenn G, Choyke P, Scherer SW, Zhuang Z, Lubensky I, Dean M, Allikmets R, Chidambaram A, Bergerheim UR, Feltis JT, Casadevall C, Zamarron A, Bernues M, Richard S, Lips CJ, Walther MM, Tsui LC, Geil L, Orcutt ML, Stackhouse T, Lipan J, Slife L, Brauch H, Decker J, Niehans G, Hughson MD, Moch H, Storkel S, Lerman MI, Linehan WM, Zbar B.

Nat Genet. 1997 May;16(1):68-73.

PMID:
9140397
19.

Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites.

Nielsen H, Engelbrecht J, Brunak S, von Heijne G.

Protein Eng. 1997 Jan;10(1):1-6.

PMID:
9051728
20.

High-density mapping of chromosomal arm 1q in renal collecting duct carcinoma: region of minimal deletion at 1q32.1-32.2.

Steiner G, Cairns P, Polascik TJ, Marshall FF, Epstein JI, Sidransky D, Schoenberg M.

Cancer Res. 1996 Nov 1;56(21):5044-6.

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