Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome.
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Maria Merino | W Marston Linehan | W. Linehan | L. Schmidt | M. Walther | M. Lerman | B. Zbar | M. Merino | P. Duray | M. Turner | M. Nickerson | J. Toro | V. Matrosova | C. Greenberg | D. Munroe | E. Maher | C. Pavlovich | Maria L Turner | Jorge R Toro | Laura S Schmidt | M. Warren | G. Glenn | N. Sharma | Berton Zbar | Christian P Pavlovich | Michael L Nickerson | Michelle B Warren | Vera Matrosova | Gladys Glenn | Paul Duray | Peter Choyke | Nirmala Sharma | McClellan Walther | David Munroe | Rob Hill | Eamonn Maher | Cheryl Greenberg | Michael I Lerman | Peter Choyke | Rob Hill | Laura S. Schmidt | R. Hill | Christian P. Pavlovich | P. Choyke | M. Merino
[1] R. Klausner,et al. Studying cancer families to identify kidney cancer genes. , 2003, Annual review of medicine.
[2] W. Linehan,et al. Renal Tumors in the Birt-Hogg-Dubé Syndrome , 2002, The American journal of surgical pathology.
[3] P. Choyke,et al. Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[4] A. Paetau,et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer , 2002, Nature Genetics.
[5] S. Bale,et al. Exclusion of PTEN, CTNNB1, and PTCH as candidate genes for Birt-Hogg-Dube syndrome , 2002, Journal of medical genetics.
[6] P. Patel,et al. Genomic organisation of the ∼1.5 Mb Smith-Magenis syndrome critical interval: Transcription map, genomic contig, and candidate gene analysis , 2001, European Journal of Human Genetics.
[7] O. Hino,et al. A Novel Renal Carcinoma Predisposing Gene of the Nihon Rat Maps on Chromosome 10 , 2001, Japanese journal of cancer research : Gann.
[8] W. Linehan,et al. Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2. , 2001, American journal of human genetics.
[9] B. Teh,et al. Birt-Hogg-Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2 , 2001, Oncogene.
[10] P. Oefner,et al. Denaturing high‐performance liquid chromatography: A review , 2001, Human mutation.
[11] W. Kaelin,et al. The von Hippel-Lindau tumor suppressor gene. , 2001, Experimental cell research.
[12] E. Ostrander,et al. Genetic mapping of a naturally occurring hereditary renal cancer syndrome in dogs. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[13] B. Zbar,et al. Birt-Hogg-Dubé syndrome: a novel marker of kidney neoplasia. , 1999, Archives of dermatology.
[14] W. Linehan,et al. Novel mutations of the MET proto-oncogene in papillary renal carcinomas , 1999, Oncogene.
[15] P. Choyke,et al. Familial renal oncocytoma: clinicopathological study of 5 families. , 1998, The Journal of urology.
[16] Michael Gribskov,et al. Combining evidence using p-values: application to sequence homology searches , 1998, Bioinform..
[17] L. Schmidt,et al. Activating mutations for the met tyrosine kinase receptor in human cancer. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[18] Holger Moch,et al. The Heidelberg classification of renal cell tumours , 1997, The Journal of pathology.
[19] Thomas L. Madden,et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. , 1997, Nucleic acids research.
[20] Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas , 1997, Nature Genetics.
[21] J. Jung,et al. Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the neurofibromatosis type 1 (NF1) tumour-suppressor gene. , 1997, Mutation research.
[22] Roudebush Vamc,et al. THE HEIDELBERG CLASSIFICATION OF RENAL CELL TUMOURS , 1997 .
[23] Gapped BLAST and PSI-BLAST: A new , 1997 .
[24] P. Ainsworth,et al. Heterogenous point mutations in the BRCA1 breast cancer susceptibility gene occur in high frequency at the site of homonucleotide tracts, short repeats and methylatable CpG/CpNpG motifs. , 1996, Oncogene.
[25] P. Choyke,et al. Original Articles: Kidney Cancer , 1995 .
[26] K. Kinzler,et al. Monoallelic mutation analysis (MAMA) for identifying germline mutations , 1995, Nature Genetics.
[27] M. Benson,et al. Bilateral renal cell carcinoma in the Birt-Hogg-Dubé syndrome. , 1993, Journal of the American Academy of Dermatology.
[28] J. Gnarra,et al. Identification of the von Hippel-Lindau disease tumor suppressor gene. , 1993, Science.
[29] E. Myers,et al. Basic local alignment search tool. , 1990, Journal of molecular biology.
[30] O. Binet,et al. Fibromes périfolliculaires polypose colique familiale pneumothorax spontanés familiaux , 1986 .
[31] W. J. Dubé,et al. Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons. , 1977, Archives of dermatology.
[32] M. Inouye,et al. Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday. , 1966, Cold Spring Harbor symposia on quantitative biology.