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La ricerca find articoli where soggetti phrase all words 'GERMLINE MUTATIONS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 808 riferimenti
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    1. Marsh, DJ; Theodosopoulos, G; Howell, V; Richardson, AL; Benn, DE; Proos, AL; Eng, C; Robinson, BG
      Rapid mutation scanning of genes associated with familial cancer syndromesusing denaturing high-performance liquid chromatography

      NEOPLASIA
    2. Thakker, RV
      Molecular genetics and patient management of multiple endocrine neoplasia type I

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    3. De Caestecker, M; Meyrick, B
      Bone morphogenetic proteins, genetics and the pathophysiology of primary pulmonary hypertension

      RESPIRATORY RESEARCH
    4. Virolle, T; Adamson, ED; Baron, V; Birle, D; Mercola, D; Mustelin, T; de Belle, I
      The Egr-1 transcription factor directly activates PTEN during irradiation-induced signalling

      NATURE CELL BIOLOGY
    5. Salahshor, S; Lei, HX; Huo, HG; Kristensen, VN; Loman, N; Sjoberg-Margolin, S; Borg, A; Borresen-Dale, AL; Vorechovsky, I; Lindblom, A
      Low frequency of E-cadherin alterations in familial breast cancer

      BREAST CANCER RESEARCH
    6. Boussioutas, A; Taupin, D
      Towards a molecular approach to gastric cancer management

      INTERNAL MEDICINE JOURNAL
    7. Arver, B; Borg, A; Lindblom, A
      First BRCA1 and BRCA2 gene testing implemented in the health care system of Stockholm

      GENETIC TESTING
    8. Rothberg, PG; Bradley, JF; Baker, DW; Huelsman, KM
      Is P25L a "Real" VHL mutation?

      MOLECULAR DIAGNOSIS
    9. Gatti, RA; Becker-Catania, S; Chun, HH; Sun, X; Mitui, M; Lai, CH; Khanlou, N; Babaei, M; Cheng, R; Clark, C; Huo, Y; Udar, NC; Iyer, RK
      The pathogenesis of ataxia-telangiectasia - Learning from a Rosetta Stone

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    10. Nathanson, KN; Wooster, R; Weber, BL
      Breast cancer genetics: What we know and what we need

      NATURE MEDICINE
    11. Minaguchi, T; Yoshikawa, H; Oda, K; Ishino, T; Yasugi, T; Onda, T; Nakagawa, S; Matsumoto, K; Kawana, K; Taketani, Y
      PTEN mutation located only outside exons 5, 6, and 7 is an independent predictor of favorable survival in endometrial carcinomas

      CLINICAL CANCER RESEARCH
    12. Vaziri, SAJ; Krumroy, LM; Elson, P; Budd, GT; Darlington, G; Myles, J; Tubbs, RR; Casey, G
      Breast tumor immunophenotype of BRCA1-mutation carriers is influenced by age at diagnosis

      CLINICAL CANCER RESEARCH
    13. Becker, TM; Rizos, H; Kefford, RF; Mann, GJ
      Functional impairment of melanoma-associated p16(INK4a) mutants in melanoma cells despite retention of cyclin-dependent kinase 4 binding

      CLINICAL CANCER RESEARCH
    14. Fuchs, S; Amiel, J; Claudel, S; Lyonnet, S; Corvol, P; Pinet, F
      Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: Evidence for selective lossof G(i) coupling

      MOLECULAR MEDICINE
    15. Suzuki, A; Yamaguchi, MT; Ohteki, T; Sasaki, T; Kaisho, T; Kimura, Y; Yoshida, R; Wakeham, A; Higuchi, T; Fukumoto, M; Tsubata, T; Ohashi, PS; Koyasu, S; Penninger, JM; Nakano, T; Mak, TW
      T cell-specific loss of Pten leads to defects in central and peripheral tolerance

      IMMUNITY
    16. Franz, DN; Brody, A; Meyer, C; Leonard, J; Chuck, G; Dabora, S; Sethuraman, G; Colby, TV; Kwiatkowski, DJ; McCormack, FX
      Mutational and radiographic analysis of pulmonary disease consistent with lymphangioleiomyomatosis and micronodular pneumocyte hyperplasia in women with tuberous sclerosis

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    17. Strizheva, GD; Carsillo, T; Kruger, WD; Sullivan, EJ; Ryu, JH; Henske, EP
      The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosis

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    18. Chan, JKC; Wong, CSC
      Loss of E-cadherin is the fundamental defect in diffuse-type gastric carcinoma and infiltrating lobular carcinoma of the breast

      ADVANCES IN ANATOMIC PATHOLOGY
    19. Newman, LA; Kuerer, HM; Hunt, KK; Vlastos, G; Ames, FC; Ross, MI; Singletary, SE
      Educational review: Role of the surgeon in hereditary breast cancer

      ANNALS OF SURGICAL ONCOLOGY
    20. Backman, SA; Stambolic, V; Suzuki, A; Haight, J; Elia, A; Pretorius, J; Tsao, MS; Shannon, P; Bolon, B; Ivy, GO; Mak, TW
      Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease

      NATURE GENETICS
    21. Rickert, CH; Paulus, W
      Tumors of the choroid plexus

      MICROSCOPY RESEARCH AND TECHNIQUE
    22. Abed, AA; Gunther, K; Kraus, C; Hohenberger, W; Ballhausen, WG
      Mutation screening at the RNA level of the STK11/LKB-1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform(STK11 c.597 (boolean AND) 598insIVS4)

      HUMAN MUTATION
    23. Jakubowska, A; Gorski, B; Kurzawski, G; Debniak, T; Hadaczek, P; Cybulski, C; Kladny, J; Oszurek, O; Scott, RJ; Lubinski, J
      Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes

      HUMAN MUTATION
    24. Nagashima, T; Murakami, M; Onigata, K; Morimura, T; Nagashima, K; Mori, M; Morikawa, A
      Novel inactivating missense mutations in the thyrotropin receptor gene in Japanese children with resistance to thyrotropin

      THYROID
    25. Saito, J; Kohn, AD; Roth, RA; Noguchi, Y; Tatsumo, I; Hirai, A; Suzuki, K; Kohn, LD; Saji, M; Ringel, MD
      Regulation of FRTL-5 thyroid cell growth by phosphatidylinositol (OH) 3 kinase-dependent Akt-mediated signaling

      THYROID
    26. Harach, HR
      Familial nonmedullary thyroid neoplasia

      ENDOCRINE PATHOLOGY
    27. Pollock, PM; Stark, MS; Palmer, JM; Walters, MK; Aitken, JF; Martin, NG; Hayward, NK
      Mutation analysis of the CDKN2A promoter in Australian melanoma families

      GENES CHROMOSOMES & CANCER
    28. Borg, A
      Molecular and pathological characterization of inherited breast cancer

      SEMINARS IN CANCER BIOLOGY
    29. Yang, FC; Merlino, G; Chin, L
      Genetic dissection of melanoma pathways in the mouse

      SEMINARS IN CANCER BIOLOGY
    30. Einsiedel, HGV; Taube, T; Beyermann, B; Dragon, S; Moricke, A; Kebelmann-Betzig, C; Kochling, J; Henze, G; Seeger, K
      Absence of mutations in the CDKN2 binding site of CDK4 in childhood acute lymphoblastic leukemia

      LEUKEMIA & LYMPHOMA
    31. Halachmi, S; Gilchrest, BA
      Update on genetic events in the pathogenesis of melanoma

      CURRENT OPINION IN ONCOLOGY
    32. Papp, T; Schipper, H; Pemsel, H; Unverricht, M; Muller, KM; Wiethege, T; Schiffmann, D; Rahman, Q
      Mutational analysis of the PTEN/MMAC1 tumour suppressor gene in primary human malignant mesotheliomas

      ONCOLOGY REPORTS
    33. Takakura, S; Kohno, T; Manda, R; Okamoto, A; Tanaka, T; Yokota, J
      Genetic alterations and expression of the protein phosphatase 1 genes in human cancers

      INTERNATIONAL JOURNAL OF ONCOLOGY
    34. Sarantaus, L; Auranen, A; Nevanlinna, H
      BRCA1 and BRCA2 mutations among Finnish ovarian carcinoma families

      INTERNATIONAL JOURNAL OF ONCOLOGY
    35. Hildenbrand, C; Burgdorf, WHC; Lautenschlager, S
      Cowden syndrome - Diagnostic skin signs

      DERMATOLOGY
    36. Sarantaus, L; Vahteristo, P; Bloom, E; Tamminen, A; Unkila-Kallio, L; Butzow, R; Nevanlinna, H
      BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients

      EUROPEAN JOURNAL OF HUMAN GENETICS
    37. Denis, D; Maugey-Laulom, B; Carles, D; Pedespan, JM; Brun, M; Chateil, JF
      Prenatal diagnosis of schizencephaly by fetal magnetic resonance imaging

      FETAL DIAGNOSIS AND THERAPY
    38. Friedrich, CA
      Genotype-phenotype correlation in von Hippel-Lindau syndrome

      HUMAN MOLECULAR GENETICS
    39. Weng, LP; Brown, JL; Eng, C
      PTEN coordinates G(1) arrest by down-regulating cyclin D1 via its protein phosphatase activity and up-regulating p27 via its lipid phosphatase activity in a breast cancer model

      HUMAN MOLECULAR GENETICS
    40. Weng, LP; Brown, JL; Eng, C
      PTEN induces apoptosis and cell cycle arrest through phosphoinositol-3-kinase/Akt-dependent and -independent pathways

      HUMAN MOLECULAR GENETICS
    41. Weng, LP; Gimm, O; Kum, JB; Smith, WM; Zhou, XP; Wynford-Thomas, D; Leone, G; Eng, C
      Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death

      HUMAN MOLECULAR GENETICS
    42. Harland, M; Mistry, S; Bishop, DT; Bishop, JAN
      A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees

      HUMAN MOLECULAR GENETICS
    43. Ellison, AR; Lofing, J; Bitter, GA
      Functional analysis of human MLH1 and MSH2 missense variants and hybrid human-yeast MLH1 proteins in Saccharomyces cerevisiae

      HUMAN MOLECULAR GENETICS
    44. Cacheux, V; Dastot-Le Moal, F; Kaariainen, H; Bondurand, N; Rintala, R; Boissier, B; Wilson, M; Mowat, D; Goossens, M
      Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease

      HUMAN MOLECULAR GENETICS
    45. Hoffman, MA; Ohh, M; Yang, HF; Klco, JM; Ivan, M; Kaelin, WG
      von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF

      HUMAN MOLECULAR GENETICS
    46. Clifford, SC; Cockman, ME; Smallwood, AC; Mole, DR; Woodward, ER; Maxwell, PH; Ratcliffe, PJ; Maher, ER
      Contrasting effects on HIF-1 alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease

      HUMAN MOLECULAR GENETICS
    47. Pericay, C; Brunet, J; Diez, O; Sanz, J; Cortes, J; Baiget, M; Alonso, C
      Clinical and pathological findings of BRCA1/2 associated breast cancer

      BREAST
    48. Walker, G; Hayward, N
      No evidence of a role for activating CDK2 mutations in melanoma

      MELANOMA RESEARCH
    49. Hemminki, K; Lonnstedt, I; Vaittinen, P
      A population-based study of familial cutaneous melanoma

      MELANOMA RESEARCH
    50. Torres, J; Navarro, S; Rogla, I; Ripoll, F; Lluch, A; Garcia-Conde, J; Llombart-Bosch, A; Cervera, J; Pulido, R
      Heterogeneous lack of expression of the tumour suppressor PTEN protein in human neoplastic tissues

      EUROPEAN JOURNAL OF CANCER
    51. Dussaulx-Garin, L; Blayau, M; Pagenault, M; Le Berre-Heresbach, N; Raoul, JL; Campion, JP; David, V; Bretagne, JF
      A new mutation of E-cadherin gene in familial gastric linitis plastica cancer with extra-digestive dissemination

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    52. Lore, F; Talidis, F; Di Cairano, G; Renieri, A
      Multiple endocrine neoplasia type 2 syndromes may be associated with renalmalformations

      JOURNAL OF INTERNAL MEDICINE
    53. Fan, SJ; Yuan, RQ; Ma, YX; Meng, QH; Goldberg, ID; Rosen, EM
      Mutant BRCA1 genes antagonize phenotype of wild-type BRCA1

      ONCOGENE
    54. Koul, D; Parthasarathy, R; Shen, RJ; Davies, MA; Jasser, SA; Chintala, SK; Rao, JS; Sun, Y; Benvenisite, EN; Liu, TJ; Yung, WKA
      Suppression of matrix metalloproteinase-2 gene expression and invasion in human glioma cells by MMAC/PTEN

      ONCOGENE
    55. Yu, WP; Pallen, CJ; Tay, A; Jirik, FR; Brenner, S; Tan, YH; Venkatesh, B
      Conserved synteny between the Fugu and human PTEN locus and the evolutionary conservation of vertebrate PTEN function

      ONCOGENE
    56. Birch, JM; Alston, RD; McNally, RJQ; Evans, DGR; Kelsey, AM; Harris, M; Eden, OB; Varley, JM
      Relative frequency and morphology of cancers in carriers of germline TP53 mutations

      ONCOGENE
    57. Malkin, D; Chilton-MacNeill, S; Meister, LA; Sexsmith, E; Diller, L; Garcea, RL
      Tissue-specific expression of SV40 in tumors associated with the Li-Fraumeni syndrome

      ONCOGENE
    58. Inoue, K; Shimotake, T; Tomiyama, H; Iwai, N
      Mutational analysis of the RET and GDNF gene in children with hypoganglionosis

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    59. Gill, P; Brenner, C; Brinkmann, B; Budowle, B; Carracedo, A; Jobling, MA; de Knijff, P; Kayser, M; Krawczak, M; Mayr, WR; Morling, N; Olaisen, B; Pascali, V; Prinz, M; Roewer, L; Schneider, PM; Sajantila, A; Tyler-Smith, C
      DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    60. Olopade, OI; Pichert, G
      Cancer genetics in oncology practice

      ANNALS OF ONCOLOGY
    61. Tomita, N; Moriguchi, A; Yamasaki, K; Taniyama, Y; Kotani, N; Hashiya, N; Yoshida, M; Yao, M; Higaki, J; Ogihara, T
      A family with Von Hippel-Lindau disease revealed by pheochromocytoma

      Hypertension research
    62. Tuder, RM; Yeager, ME; Geraci, M; Golpon, HA; Voelkel, NF
      Severe pulmonary hypertension after the discovery of the familial primary pulmonary hypertension gene

      EUROPEAN RESPIRATORY JOURNAL
    63. Lee, WR; Perantie, DC; Clark, KB; Guillot, DA; Wilson, VL
      Effect of mutagen-induced cell lethality on the dose response of germline mutations

      ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
    64. Ascano, JJ; Frierson, H; Moskaluk, CA; Harper, JC; Roviello, F; Jackson, CE; El-Rifai, W; Vindigni, C; Tosi, P; Powell, SM
      Inactivation of the E-cadherin gene in sporadic diffuse-type gastric cancer

      MODERN PATHOLOGY
    65. Guo, SS; Sawicki, MP
      Molecular and genetic mechanism of tumorigenesis in Multiple Endocrine Neoplasia type-1

      MOLECULAR ENDOCRINOLOGY
    66. Teng, DHF; Chen, Y; Lian, LB; Ha, PC; Tavtigian, SV; Wong, AKC
      Mutation analyses of 268 candidate genes in human tumor cell lines

      GENOMICS
    67. Zhou, B; Bae, SK; Malone, AC; Levinson, BB; Kuo, YM; Cilio, MR; Bertini, E; Hayflick, SJ; Gitschier, JM
      hGFR alpha-4: A new member of the GDNF receptor family and a candidate forNBIA

      PEDIATRIC NEUROLOGY
    68. Humbert, M; Soubrier, F; Simonneau, G
      A gene for primary pulmonary hypertension

      REVUE DES MALADIES RESPIRATOIRES
    69. Salabe, GB
      Pathogenesis of thyroid nodules: histological classification?

      BIOMEDICINE & PHARMACOTHERAPY
    70. Ball, S; Arolker, M; Purushotham, AD
      Breast cancer, Cowden disease and PTEN-MATCHS syndrome

      EUROPEAN JOURNAL OF SURGICAL ONCOLOGY
    71. Ramus, SJ; Fishman, A; Pharoah, PDP; Yarkoni, S; Altaras, M; Ponder, BAJ
      Ovarian cancer survival in Ashkenazi Jewish patients with BRCA1 and BRCA2 mutations

      EUROPEAN JOURNAL OF SURGICAL ONCOLOGY
    72. Bittorf, B; Kessler, H; Merkel, S; Bruckl, W; Wein, A; Ballhausen, WG; Hohenberger, W; Gunther, K
      Multiple primary malignancies: An epidemiological and pedigree analysis of57 patients with at least three tumours

      EUROPEAN JOURNAL OF SURGICAL ONCOLOGY
    73. Brekelmans, CTM; Seynaeve, C; Bartels, CCM; Tilanus-Linthorst, MMA; Meijers-Heijboer, EJ; Crepin, CMG; van Geel, AN; Menke, M; Verhoog, LC; van den Ouweland, A; Obdeijn, IM; Klijn, JGM
      Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk

      JOURNAL OF CLINICAL ONCOLOGY
    74. McDonnell, SK; Schaid, DJ; Myers, JL; Grant, CS; Donohue, JH; Woods, JE; Frost, MH; Johnson, JL; Sitta, DL; Slezak, JM; Crotty, TB; Jenkins, RB; Sellers, TA; Hartmann, LC
      Efficacy of contralateral prophylactic mastectomy in women with a personaland family history of breast cancer

      JOURNAL OF CLINICAL ONCOLOGY
    75. Percesepe, A; Borghi, F; Menigatti, M; Losi, L; Foroni, M; Di Gregorio, C; Rossi, G; Pedroni, M; Sala, E; Vaccina, F; Roncucci, L; Benatti, P; Viel, A; Genuardi, M; Marra, G; Kristo, P; Peltomaki, P; de Leon, MP
      Molecular screening for hereditary nonpolyposis colorectal cancer: A prospective, population-based study

      JOURNAL OF CLINICAL ONCOLOGY
    76. Stratakis, CA
      Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    77. Hoff-Olsen, P; Jacobsen, S; Mevag, B; Olaisen, B
      Microsatellite stability in human post-mortem tissues

      FORENSIC SCIENCE INTERNATIONAL
    78. Kayser, M; Sajantila, A
      Mutations at Y-STR loci: implications for paternity testing and forensic analysis

      FORENSIC SCIENCE INTERNATIONAL
    79. Vanhorne, JB; Gimm, O; Myers, SM; Kaushik, A; von Deimling, A; Eng, C; Mulligan, LM
      Cloning and characterization of the human GFRA2 locus and investigation ofthe gene in Hirschsprung disease

      HUMAN GENETICS
    80. Cao, X; Eu, KW; Seow-Choen, F; Zhao, Y; Cheah, PY
      Topoisomerase-I- and Alu-mediated genomic deletions of the APC gene in familial adenomatous polyposis

      HUMAN GENETICS
    81. Frenzel, S; Apel, TW; Heidemann, PH; Zerres, K; Neumann, HPH; Dorr, HG
      Phaeochromocytoma associated with a de novo VHL mutation as form fruste ofvon Hippel-Lindau disease

      EUROPEAN JOURNAL OF PEDIATRICS
    82. Nicoletto, MO; Donach, M; De Nicolo, A; Artioli, G; Banna, G; Monfardini, S
      BRCA-1 and BRCA-2 mutations as prognostic factors in clinical practice andgenetic counselling

      CANCER TREATMENT REVIEWS
    83. Neumann, HPH; Riegler, P; Huber, W; Corradini, R; Sessa, A; Fontana, D; Wetterauer, U; Janetschek, G
      The challenge of kidney lesions in von Hippel-Lindau disease

      RARE KIDNEY DISEASES
    84. Murgia, A; Martella, M; Polli, R; Piermarocchi, S; Lo Giudice, G; Opocher, G
      Molecular diagnosis of von Hippel-Lindau disease

      RARE KIDNEY DISEASES
    85. Dahia, PLM
      Genetic disorders of endocrine neoplasia - Introduction

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    86. Mulligan, LM
      Multiple endocrine neoplasia type 2: Molecular aspects

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    87. Zweemer, RP; Verheijen, RHM; Coebergh, JWW; Jacobs, IJ; van Diest, PJ; Gille, JJP; Skates, S; Menko, FH; Ten Kate, LP; Kenemans, P
      Survival analysis in familial ovarian cancer, a case control study

      EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
    88. Marneros, AG; Mehenni, H; Reichenberger, E; Antonarakis, SE; Krieg, T; Olsen, BR
      Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome

      CYTOGENETICS AND CELL GENETICS
    89. Neumann, HPH; Schulenburg, S; Apel, TW
      Familial renal tumors in adults

      NIEREN-UND HOCHDRUCKKRANKHEITEN
    90. Hes, FJ; Lips, CJM; van der Luijt, RB
      Molecular genetic aspects of Von Hippel-Lindau (VHL) disease and criteria for DNA analysis in subjects at risk

      NETHERLANDS JOURNAL OF MEDICINE
    91. Barbera, JA
      Good news about pulmonary hypertension.

      ARCHIVOS DE BRONCONEUMOLOGIA
    92. Chew, SL
      Paraganglioma genes

      CLINICAL ENDOCRINOLOGY
    93. Meyrick, B
      The pathology of pulmonary artery hypertension

      CLINICS IN CHEST MEDICINE
    94. Thomas, AQ; Gaddipati, R; Newman, JH; Loyd, FE
      Genetics of primary pulmonary hypertension

      CLINICS IN CHEST MEDICINE
    95. Sotillo, R; Dubus, P; Martin, J; de la Cueva, E; Ortega, S; Malumbres, M; Barbacid, M
      Wide spectrum of tumors in knock-in mice carrying a Cdk4 protein insensitive to INK4 inhibitors

      EMBO JOURNAL
    96. Wanner, M; Celebi, JT; Peacocke, M
      Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome

      JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
    97. Bremer, M; Steinmann, D; Dork, T; Borger, J; Rades, D; Karstens, JH
      Bilateral breast cancer and local relapse: A hospital-based study of the prevalence of BRCA 1 and BRCA 2 gene mutations

      STRAHLENTHERAPIE UND ONKOLOGIE
    98. Werner, M; Becker, KF; Keller, G; Hofler, H
      Gastric adenocarcinoma: pathomorphology and molecular pathology

      JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
    99. Unnithan, J; Macklis, RM
      Contralateral breast cancer risk

      RADIOTHERAPY AND ONCOLOGY
    100. Malkin, D
      The role of p53 in human cancer

      JOURNAL OF NEURO-ONCOLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 17:20:54