geny2

geny2



28.

28.

29.

30.

31.

32.

33.

34.

35.

36.

37.

38.

39.

40.

41.

42.

43.

44.

45. 4'6.

47.

48.

49.

50.

51.

52.

53.

54.

55.

56.

57.


Warner E, et a!.: Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashke-nazi Jewish women with breast cancer. J Natl Cancerlnst 1999; 91:1241-1247.

Jakubowska A, et al.: BRCA2 gene mutation in families with aggregations ofbreastand stornach cancers.

BrJ Cancer 2002; 87: 888-891.

Jakubowska A, et al.: A high freąuency of BRCA2 gene mutations in Poiish families with ovarian and słomach cancer. Eur J Hum Genet 2003; 11: 955-958.    ,*a

Kwiatkowska E, et al.: BRCA2 germline mutations in małe breast cancer patients in the Poiish popula- ' §j! tion. Hum Mutat 2001; 17: 73.

Boyd J, et al.: Clinicopathologic features of BRCA-linked and sporadic ovarian cancer. JAMA 2000; 283; 2260-2265.

Malkin D, et al.: Germline p53 mutations in a familiar syndrome of breast cancer, sarcomas and other neoplasms. Science 1990; 250: 1233-1238.

Nelen MR, et al.: Loćalization of the gene forCowden disease to chromosome 10q22-23. Nat Genet 1996; 13:114-116.    '!■

Hanssen AM, Fryns JP: Cowden syndrome. J Med Genet 1995; 32: 117-119.

Risinger Jl, et al.: Molecular genetic evidence of the occurrence of breast cancer as on integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome. Cancer 1996; 77: 1836-1843. Spigelman AD, Murday V, Phillips RK: Cancer and Peutz-Jeghers syndrome. Gut 1989; 30: 1588-1590.    :'i

Cohen MM Jr: A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Adv Hum Genet 1989; 18: 181-303, 373-376.

Shiloh Y: Ataxia telangiectasia: closer to unraveling the mystery. Eur J Hum Genet 1995; 3: 116-138.

Lynch HT, Kapłan AR, Lynch JF: Klinefelter syndrome and cancer. A family study. JAMA 1974; 229: 809-811.

Wooster R, et al.: A germline mutation in the androgen receptor in two brothers with breast cancer and Reifenstein syndrome. Nat Genet 1992; 2: 132-134.

Lindblom A, et al.: Predisposition for breast cancer in carriers of constilutional translocation 1 lq;22q. Am J Hum Genet 1994; 54: 871 -876.

Naród SA, et al.: Orał contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinicai Study Group. N Engl J Med 1998; 339: 424-428.

McLaughlin JR, et al.: Hereditary Ovarian Cancer Clinicai Study Group. Reproductive risk factors for oyarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study. Lancet Oncol 2007; 8: 26-34.    ?

Naród SA, et a.: Orał contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carri-ers. J Nat! Cancer Inst 2002; 94: 1773-1779.

Grabrick DM, et al.; Risk of breast cancer with orał contraceplive use in women with a family history of breast cancer. JAMA 2000; 284: 1791-1798.

Armstrong K, et al.: Hormon replacement therapy and life expectancy after prophylactic oophorectomy in women with BRCAII2 mutations: a decision analysis. J Clin Oncol 2004; 22: 1045-1054.

Rebbeck TR, et al.: Effect of Short-Term Hormone Replacement Therapy on Breast Cancer Risk Reduc-tion After Bilateral Prophylactic Oophorectomy in BRCAI and BRCA2 Mutation Carriers: The PROSE Study Group. J Clin Oncol 2005; 23: 7804-7810.

Buchet-Poyau K, et al.: Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK1 IIP gene on chromosome 2. Cyto-genet Genome Res 2002; 97: 171-178.

Gronwald J, et al.: Influence of selected lifestyle factors on breast and ovarian cancer risk in BRCAI mutation carriers from Poland. Breast Cancer Res Treat 2006; 95: 105-109.

Naród SA: Hormonal prevention of hereditary breast cancer. Ann N Y Acad Sci 2001; 952: 36-43. Kotsopoulos J, et al.: Age at First birth and the risk of breast cancer in BRCAI and BRCA2 mutation carri-ers. Breast Cancer Res Treat 2007; 105:221-228.

Gronwald J, et al.: Hereditary Breast Cancer Clinicai Study Group. Tamoxifen and contralateral breast cancer in BRCAI and BRCA2 carriers: an update. Int J Cancer 2006; 118: 2281-2284.

Naród SA, et al.: Hereditary Breast Cancer Clinicai Study Group. Tamoxifen and risk of contralateral breast cancer in BRCAI and BRCA2 mutation carriers: a case-control study. Hereditary Breast Cancer Clinicai Study Group. Lancet 2000; 356: 1876-1881.

Kowalska E, et al.: Increased rates of chromosome breakage in BRCAI carriers are normalized by orał se-lenium supplementation. Cancer Epidemio! Biomarkers Prev 2005; 14: 1302-1306.

Mehkisz3k J, et al.: Attitudes toward preventive oophorectomy among BRCAI mutation carriers in Poland. Eur J Gyuaecol Oncol 2004; 25: 93-95.

Zeigler LD, Kroll SS: Primary breast cancer after prophylactic mastectomy. Am J Clin Oncol 1991; 14: 451-454.

Tempie WJ, et al.: Technical considerations for prophylactic mastectomy in patients at high risk for breast cancer. Am J Surg 1991; 161: 413-415.

Warner E, et al.: Compadson of breast magnetic resonance imaging, mammography, and ultrasound for surveillance of women at high risk for hereditary breast cancer. J Clin Oncol 2001; 19: 3524-3531.

Naród SA, et al.: Orał contraceptives and the risk of breast cancer in BRCAI and BRCA2 mutation carriers. J Nat! Cancer Inst 2002; 94: 1773-1779.

Byrski T, et al: Response to neo-adjuvant chemotherapy in women with f-positive breast cancers. Breast Cancer Res Treat 2008; 108: 289-296.

Lubiński J, et al.: Genetic contribution to all cancers: the fitst demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology. Breast Cancer Res Treat 2008 Apr 15.

Cybulski C, et al.: CHEK2-positive breast cancers in young Poiish women. Clin Cancer Res 2006; 12: 4832-4835.

Cybulski C, et al.: A deletion in CHEK2 of 5,395 bp predisposes lo breast cancer in Poland. Breast Cancer Res Treat 2007; 102:119-122.

Huzarski T, et al: Pathology of breast cancer in wometi with constitutional CHEK2 mutations. Breast Cancer Res Treat 2005; 90: 187-189.

Steffen J, et al: Germline mutations 657del5 of the NBS l gene contribute sigtiiftcantly to the incidence of breast cancer in Central Poland. tnt J Cancer 2006: 119: 472-475.

Górski B, et al.: Germline 657del5 mutation in the NBS i gene in breast cancer patients. Int J Cancer 2003; 106:379-381.

Huzarski T, et al: The 3020insC allele of NOD2 predisposes to eatly onset breast cancer. Breast Cancer Res Treat 2005; 89: 91-93. 69. Górski B, Naród SA, Lubiński J: A common missense variant in BRCA2 predisposes to early onset breast cancer. Breast Cancer Res 2005; 7: R1023-R1027.

Menkiszak J, et al.: Clinicai features of familial ovarian cancer lacking mutations in BRCAI or BRCA2. Eur J Gynaecol Oncol 2004; 25: 99-100.

Hart WR: Mucinous tumors of the ovary: A review. Int J Gyuecol Pathol 2005; 24: 4-25.

Shilr IeM, Kurman RJ: Ovarian tumorigenesis: a proposed model based on morphological and molecular genetic analysis. Am S Pathol 2004; 164: 1511-1518.

Szymańska A: Identyfikacja genów związanych z predyspozycji do gruczoiako-torbielaków oeluzowych jajnika. Doctofs thesis. Pomorska Akademia Medyczna, Szczecin 2006.

Szymańska-Pa5temak J: Identyfikacja genów związanych z predyspozycją do gruczoiako-torbielaków surowiczych jajnika. Doctofs thesis. Pomorska Akademia Medyczna, Szczecin 2007.

77


Wyszukiwarka

Podobne podstrony:
25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 mruczus.jedzenie =
31. 32. 33. 34. 35. 36. 37. 38. 39. 40. 41. 42. 43. 44. Rys. S2 Podać wzór na
.31 .32 .33 .34 .35 36 .37 .38 .39 .40 .41 .42 43 RADA KÓŁ NAUKOWYCH Koto Naukowe
Poznaj C++ w$ godziny0114 Więcej o klasach 101 32 33 34:    < 35 36 37 38 39 40 41
P7092597 %,■ L r 18 19 20 21 l 35 36 37 38 39 40 41 42 43 44 45 8 Nakrętka M 10 CSN 02 1802.29
s11 iei wutniaki tu. 26. 27. 28. 29. 30. 31. 32. 33. 34. 35. 36. 37. Reakcje substratowe
8111 161454 Kinm: 1 2 18 19 20 21 22 23 24 <25) 26 27 ?B 29 30 31 32 33 34 35 36 37 38 3 4
bez tytułu48 Inflacja 259 22*. N, 23*. P, 24. P. 25. N. 26. N, 27. N, 28. P, 29. N. 30*. P, 31. N, 3
W11 2 23 23 24 25 20 27 20 29 30 31 32 33 34 35 36 37 31 » Jeże* podczas ałsfclrolery
P8022920 60 X 129 31 32 33 34 35 36 37 38 39/    / 4141 42 43 44 Ol Plartel.ń Mliezpl

więcej podobnych podstron