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La ricerca find articoli where soggetti phrase all words '18Q' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 122 riferimenti
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    1. Wuyts, W; Van Wesenbeeck, L; Morales-Piga, A; Ralston, S; Hocking, L; Vanhoenacker, F; Westhovens, R; Verbruggen, L; Anderson, D; Hughes, A; Van Hul, W
      Evaluation of the role of RANK and OPG genes in Paget's disease of bone

      BONE
    2. McNairn, JDK; Damron, TA; Landas, SK; Ambrose, JL; Shrimpton, AE
      Inheritance of osteosarcoma and Paget's disease of bone - A familial loss of heterozygosity study

      JOURNAL OF MOLECULAR DIAGNOSTICS
    3. Pande, KC; Ashford, RU; Dey, A; Kayan, K; McCloskey, EV; Kanis, JA
      Atypical familial Paget's disease of bone

      JOINT BONE SPINE
    4. Sarela, AI; Scott, N; Ramsdale, J; Markham, AF; Guillou, PJ
      Immunohistochemical detection of the anti-apoptosis protein, survivin, predicts survival after curative resection of stage II colorectal carcinomas

      ANNALS OF SURGICAL ONCOLOGY
    5. Inoue, H; Furukawa, T; Sunamura, M; Takeda, K; Matsuno, S; Horii, A
      Exclusion of SMAD4 mutation as an early genetic change in human pancreaticductal tumorigenesis

      GENES CHROMOSOMES & CANCER
    6. Ohtaki, N; Yamaguchi, A; Goi, T; Fukaya, T; Takeuchi, K; Katayama, K; Hirose, K; Urano, T
      Somatic alterations of the DPC4 and Madr2 genes in colorectal cancers and relationship to metastasis

      INTERNATIONAL JOURNAL OF ONCOLOGY
    7. Ranade, K; Wu, KD; Hwu, CM; Ting, CT; Pei, D; Pesich, R; Hebert, J; Chen, YDI; Pratt, R; Olshen, R; Masaki, K; Risch, N; Cox, DR; Botstein, D
      Genetic variation in the human urea transporter-2 is associated with variation in blood pressure

      HUMAN MOLECULAR GENETICS
    8. Yin, ZN; Babaian, RJ; Troncoso, P; Strom, SS; Spitz, MR; Caudell, JJ; Stein, JD; Kagan, J
      Limiting the location of putative human prostate cancer tumor suppressor genes on chromosome 18q

      ONCOGENE
    9. Hadjipavlou, AG; Gaitanis, IN; Katonis, PG; Lander, P
      Paget's Disease of the spine and its management

      EUROPEAN SPINE JOURNAL
    10. Lyles, KW; Siris, ES; Singer, FR; Meunier, PJ
      A clinical approach to diagnosis and management of Paget's disease of bone

      JOURNAL OF BONE AND MINERAL RESEARCH
    11. Atwood, LD; Samollow, PB; Hixson, JE; Stern, MP; MacCluer, JW
      Genome-wide linkage analysis of pulse pressure in Mexican Americans

      HYPERTENSION
    12. De Angelis, PM; Stokke, T; Beigi, M; Mjaland, O; Clausen, OPF
      Prognostic significance of recurrent chromosomal aberrations detected by comparative genomic hybridization in sporadic colorectal cancer

      INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
    13. Sparks, AB; Peterson, SN; Bell, C; Loftus, BJ; Hocking, L; Cahill, DP; Frassica, FJ; Streeten, EA; Levine, MA; Fraser, CM; Adams, MD; Broder, S; Venter, JC; Kinzler, KW; Vogelstein, B; Ralston, SH
      Mutation screening of the TNFRSF11A gene encoding receptor activator of NFkappa B (RANK) in familial and sporadic Paget's disease of bone and osteosarcoma

      CALCIFIED TISSUE INTERNATIONAL
    14. Stewart, H; Smith, PT; Gaunt, L; Moore, L; Tarpey, P; Andrew, S; Dady, I; Rifkin, R; Clayton-Smith, J
      De novo deletion of chromosome 18q in a baby with harlequin ichthyosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Sutcliffe, MJ; Mueller, OT; Kousseff, BG; Dumont, DP; McFarland, JA; Mawani, F; Conforto, D; Ranells, JD
      Three cell line mosaicism involving structural and numerical abnormalitiesof chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Watanabe, T; Wu, T; Catalano, PJ; Ueki, T; Satriano, R; Benson, AB; Hamilton, SR
      Molecular predictors of survival after adjuvant chemotherapy for colon cancer.

      NEW ENGLAND JOURNAL OF MEDICINE
    17. Bekiesinska-Figatowska, M; Walecki, J
      MRI of the hypophysis in a patient with the 18q-syndrome

      NEURORADIOLOGY
    18. Woodford-Richens, KL; Rowan, AJ; Gorman, P; Halford, S; Bicknell, DC; Wasan, HS; Roylance, RR; Bodmer, WF; Tomlinson, IPM
      SMAD4 mutations in colorectal cancer probably occur before chromosomal instability, but after divergence of the microsatellite instability pathway

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    19. Leach, RJ; Singer, FR; Roodman, GD
      Genetics of endocrine disease - The genetics of Paget's disease of the bone

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    20. Marco-Mingot, M; San-Millan, JL; Wuyts, W; Bachiller-Corral, J; Van Hul, W; Morales-Piga, AA
      Lack of mutations in the RANK gene in Spanish patients with Paget disease of bone

      CLINICAL GENETICS
    21. Merkel, S; Wein, A; Gunther, K; Papadopoulos, T; Hohenberger, W; Hermanek, P
      High-risk groups of patients with stage II colon carcinoma

      CANCER
    22. Luttges, J; Galehdari, H; Brocker, V; Schwarte-Waldhoff, I; Henne-Bruns, D; Kloppel, G; Schmiegel, W; Hahn, SA
      Allelic loss is often the first hit in the biallelic inactivation of the p53 and DPC4 genes during pancreatic carcinogenesis

      AMERICAN JOURNAL OF PATHOLOGY
    23. Hocking, LJ; Herbert, CA; Nicholls, RK; Williams, F; Bennett, ST; Cundy, T; Nicholson, GC; Wuyts, W; Van Hul, W; Ralston, SH
      Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35

      AMERICAN JOURNAL OF HUMAN GENETICS
    24. Laurin, N; Brown, JP; Lemainque, A; Duchesne, A; Huot, D; Lacourciere, Y; Drapeau, G; Verreault, J; Raymond, V; Morissette, J
      Paget disease of bone: Mapping of two loci at 5q35-qter and 5q31

      AMERICAN JOURNAL OF HUMAN GENETICS
    25. Hocking, L; Slee, F; Haslam, SI; Cundy, T; Nicholson, G; van Hul, W; Ralston, SH
      Familial Paget's disease of bone: Patterns of inheritance and frequency oflinkage to chromosome 18q

      BONE
    26. Karkera, JD; Ayache, S; Ransome, RJ; Jackson, MA; Elsayem, AF; Sridhar, R; Detera-Wadleigh, SD; Wadleigh, RG
      Refinement of regions with allelic loss on chromosome 18p11.2 and 18q12.2 in esophageal squamous cell carcinoma

      CLINICAL CANCER RESEARCH
    27. Hughes, AE; Ralston, SH; Marken, J; Bell, C; MacPherson, H; Wallace, RGH; van Hul, W; Whyte, MP; Nakatsuka, K; Hovy, L; Anderson, DM
      Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis

      NATURE GENETICS
    28. Jonson, T; Mahlamaki, EH; Karhu, R; Gorunova, L; Johansson, B; Hoglund, M
      Characterization of genomically amplified segments using PCR: Optimizing relative-PCR for reliable and simple gene expression and gene copy analyses

      GENES CHROMOSOMES & CANCER
    29. Kadota, M; Tamaki, Y; Sakita, I; Komoike, Y; Miyazaki, M; Ooka, M; Masuda, N; Fujiwara, Y; Ohnishi, T; Tomita, N; Sekimoto, M; Ohue, M; Ikeda, T; Kobayashi, T; Horii, A; Monden, M
      Identification of a 7-cM region of frequent allelic loss on chromosome band 16p13.3 that is specifically associated with anaplastic thyroid carcinoma

      ONCOLOGY REPORTS
    30. Gebert, J; Sun, M; Ridder, R; Hinz, U; Lehnert, T; Moller, P; Schackert, HK; Herfarth, C; Doeberitz, MV
      Molecular profiling of sporadic colorectal tumors by microsatellite analysis

      INTERNATIONAL JOURNAL OF ONCOLOGY
    31. Goossens, D; Villafuerte, S; Tissir, F; Van Gestel, S; Claes, S; Souery, D; Massat, I; Van den Bossche, D; Van Zand, K; Mendlewicz, J; Van Broeckhoven, C; Del-Favero, J
      No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder

      EUROPEAN JOURNAL OF HUMAN GENETICS
    32. Bal, M; Schrander-Stumpel, CTRM; Meers, LEC; Theunissen, PMVM; Hamers, AJH; Wennekes, MJ; Engelen, JJM
      De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphism

      GENETIC COUNSELING
    33. Tarafa, G; Villanueva, A; Farre, L; Rodriguez, J; Musulen, E; Reyes, G; Seminago, R; Olmedo, E; Paules, AB; Peinado, MA; Bachs, O; Capella, G
      DCC and SMAD4 alterations in human colorectal and pancreatic tumor dissemination

      ONCOGENE
    34. Barbera, VM; Martin, M; Marinoso, L; Munne, A; Carrato, A; Real, FX; Fabre, M
      The 18q21 region in colorectal and pancreatic cancer: independent loss of DCC and DPC4 expression

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    35. Ramelli, GP; Remonda, L; Lovblad, KO; Hirsiger, H; Moser, H
      Abnormal myelination in a patient with deletion 14q11.2q13.1

      PEDIATRIC NEUROLOGY
    36. Wise, CA; Barnes, R; Gillum, J; Herring, JA; Bowcock, AM; Lovett, M
      Localization of susceptibility to familial idiopathic scoliosis

      SPINE
    37. Leonard, NJ; Tomkins, DJ; Demianczuk, N
      Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat

      PRENATAL DIAGNOSIS
    38. Froster, UG; Horn, LC; Holland, H; Strenge, S; Faber, R
      Prenatal diagnosis of del(15)(q26.1) and del(18)(q21.3) due to an unbalanced de novo translocation: ultrasound, molecular cytogenetic and autopsy findings

      PRENATAL DIAGNOSIS
    39. Nakashima, T; Pak, SC; Silverman, GA; Spring, PM; Frederick, MJ; Clayman, GL
      Genomic cloning, mapping, structure and promoter analysis of HEADPIN, a serpin which is down-regulated in head and neck cancer cells

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    40. Nance, MA; Nuttall, FQ; Econs, MJ; Lyles, KW; Viles, KD; Vance, JM; Pericak-Vance, MA; Speer, MC
      Heterogeneity in Paget disease of the bone

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. Yokota, J
      Tumor progression and metastasis

      CARCINOGENESIS
    42. Sugai, T; Habano, W; Nakamura, S; Sato, H; Uesugi, N; Orii, S; Itoh, C; Katoh, R
      Allelic losses of 17p, 5q, and 18q loci in diploid and aneuploid populations of multiploid colorectal carcinomas

      HUMAN PATHOLOGY
    43. Schleger, C; Arens, N; Zentgraf, H; Bleyl, U; Verbeke, C
      Identification of frequent chromosomal aberrations in ductal adenocarcinoma of the pancreas by comparative genomic hybridization (CGH)

      JOURNAL OF PATHOLOGY
    44. Shahrier, M; Ahnen, DJ
      Colorectal cancer survival in Europe: the Will Rogers phenomenon revisited

      GUT
    45. Sarela, AI; Macadam, RCA; Farmery, SM; Markham, AF; Guillou, PJ
      Expression of the antiapoptosis gene, Survivin, predicts death from recurrent colorectal carcinoma

      GUT
    46. Sturm, K; Knake, S; Schomburg, U; Wakat, JP; Hamer, HM; Fritz, B; Oertel, WH; Rosenow, F
      Autonomic seizures versus syncope in 18q-deletion syndrome: A case report

      EPILEPSIA
    47. Takebayashi, S; Ogawa, T; Jung, KY; Muallem, A; Mineta, H; Fisher, SG; Grenman, R; Carey, TE
      Identification of new minimally lost regions on 18q in head and neck squamous cell carcinoma

      CANCER RESEARCH
    48. Lindforss, U; Fredholm, H; Papadogiannakis, N; Gad, A; Zetterquist, H; Olivecrona, H
      Allelic loss is heterogeneous throughout the tumor in colorectal carcinoma

      CANCER
    49. Vogels, A; Devriendt, K; Vermeesch, JR; Van Dael, R; Marynen, P; Dewaele, P; Hageman, J; Holvoet, M; Fryns, JP
      Cryptic translocation t(5;18) in familial mental retardation

      ANNALES DE GENETIQUE
    50. Naidoo, R; Tarin, M; Chetty, R
      A comparative microsatellite analysis of colorectal cancer in patients < 35 years and > 50 years of age

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    51. Mee, AP
      Paramyxoviruses and Paget's disease: The affirmative view

      BONE
    52. Van Hul, W
      Paget's disease from a genetic perspective

      BONE
    53. Wirfel, KL; Bruder, JM; Vardag, A; Roodman, GD
      Osteoclast function in healthy subjects and in patients with Paget's disease

      ENDOCRINOLOGIST
    54. Komoike, Y; Tamaki, Y; Sakita, I; Tomita, N; Ohue, M; Sekimoto, M; Miyazaki, M; Kadota, M; Masuda, N; Ooka, M; Ohnishi, T; Nakano, Y; Kozaki, T; Kobayashi, T; Matsuura, N; Ikeda, T; Horii, A; Monden, M
      Comparative genomic hybridization defines frequent loss on 16p in human anaplastic thyroid carcinoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    55. Velcich, A; Corner, G; Palumbo, L; Augenlicht, L
      Altered phenotype of HT29 colonic adenocarcinoma cells following expression of the DCC gene

      ONCOGENE
    56. Zhou, Y; Kato, H; Shan, D; Minami, R; Kitazawa, S; Matsuda, T; Arima, T; Barrett, JC; Wake, N
      Involvement of mutations in the DPC4 promoter in endometrial carcinoma development

      MOLECULAR CARCINOGENESIS
    57. Robey, PG; Biano, P
      The role of osteogenic cells in the pathophysiology of Paget's disease

      JOURNAL OF BONE AND MINERAL RESEARCH
    58. Leach, RJ; Singer, FR; Cody, JD; Roodman, GD
      Variable disease severity associated with a Paget's disease predispositiongene

      JOURNAL OF BONE AND MINERAL RESEARCH
    59. Beedles, KE; Sharpe, PT; Wagner, EF; Grigoriadis, AE
      A putative role for c-Fos in the pathophysiology of Paget's disease

      JOURNAL OF BONE AND MINERAL RESEARCH
    60. Hansen, MF; Nellissery, MJ; Bhatia, P
      Common mechanisms of osteosarcoma and Paget's disease

      JOURNAL OF BONE AND MINERAL RESEARCH
    61. Sun, XF; Rutten, S; Zhang, H; Nordenskjold, B
      Expression of the deleted in colorectal cancer gene is related to prognosis in DNA diploid and low proliferative colorectal adenocarcinoma

      JOURNAL OF CLINICAL ONCOLOGY
    62. Sanz-Ortega, J; Bryant, B; Sanz-Esponera, J; Asenjo, JA; Saez, MC; Torres, A; Balibrea, JL; Sobel, ME; Merino, MJ
      LOH at the APC/MCC gene (5Q21) is frequent in early stages of non-small cell lung cancer

      PATHOLOGY RESEARCH AND PRACTICE
    63. Wang, ZQ; Cody, JD; Leach, RJ; O'Connell, P
      Gene expression patterns in cell lines from patients with 18q-syndrome

      HUMAN GENETICS
    64. Hampl, M; Hampl, JA; Schwarz, P; Frank, S; Hahn, M; Schackert, G; Saeger, HD; Schackert, HK
      Accumulation of genetic alterations in brain metastases of sporadic breastcarcinomas is associated with reduced survival after metastasis

      INVASION & METASTASIS
    65. Arosarena, OA; Baranwal, S; Strome, S; Wolf, GT; Krauss, JC; Bradford, CR; Carey, TE
      Expression of major histocompatibility complex antigens in squamous cell carcinomas of the head and neck: Effects of interferon gene transfer

      OTOLARYNGOLOGY-HEAD AND NECK SURGERY
    66. Kujawski, M; Aalto, Y; Jaskula-Sztul, R; Szyfter, W; Szmeja, Z; Szyfter, K; Knuutila, S
      DNA copy number losses are more frequent in primary larynx tumors with lymph node metastases than in tumors without metastases

      CANCER GENETICS AND CYTOGENETICS
    67. van den Berg, C; Pijpers, L; Halley, DJJ; Van Opstal, D; Los, FJ
      Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    68. Cody, JD; Ghidoni, PD; DuPont, BR; Hale, DE; Hilsenbeck, SG; Stratton, RF; Hoffman, DS; Muller, S; Schaub, RL; Leach, RJ; Kaye, CI
      Congenital anomalies and anthropometry of 42 individuals with deletions ofchromosome 18q

      AMERICAN JOURNAL OF MEDICAL GENETICS
    69. Gustavsson, P; Kimber, E; Wahlstrom, J; Anneren, G
      Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    70. Rashid, A; Zahurak, M; Goodman, SN; Hamilton, SR
      Genetic epidemiology of mutated K-ras proto-oncogene, altered suppressor genes, and microsatellite instability in colorectal adenomas

      GUT
    71. Jernvall, P; Makinen, MJ; Karttunen, TJ; Makela, J; Vihko, P
      Loss of heterozygosity at 18q21 is indicative of recurrence and therefore poor prognosis in a subset of colorectal cancers

      BRITISH JOURNAL OF CANCER
    72. Halling, KC; French, AJ; McDonnell, SK; Burgart, LJ; Schaid, DJ; Peterson, BJ; Moon-Tasson, L; Mahoney, MR; Sargent, DJ; O'Connell, MJ; Witzig, TE; Farr, GH; Goldberg, RM; Thibodeau, SN
      Microsatellite instability and 8p allelic imbalance in stage B2 and C colorectal cancers

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    73. Cho, M; Konishi, N; Yamamoto, K; Inui, T; Kitahori, Y; Nakagawa, Y; Uemura, H; Hirao, Y; Hiasa, Y
      Genomic aberrations in renal cell carcinomas detected by restriction landmark genomic scanning

      EUROPEAN JOURNAL OF CANCER
    74. UEDA K; NISHIJIMA M; INUI H; WATATANI M; YAYOI E; OKAMURA J; YASUTOMI M; NAKAMURA Y; MIYOSHI Y
      INFREQUENT MUTATIONS IN THE PTEN MMAC1 GENE AMONG PRIMARY BREAST CANCERS/

      Japanese journal of cancer research
    75. HUIPING C; EIRIKSDOTTIR G; SIGURDSSON A; SIGURGEIRSDOTTIR JR; BARKARDOTTIR RB; EGILSSON V; INGVARSSON S
      HIGH-FREQUENCY OF LOH AT CHROMOSOME 18Q IN HUMAN BREAST-CANCER - ASSOCIATION WITH HIGH S-PHASE FRACTION AND LOW PROGESTERONE-RECEPTOR CONTENT

      Anticancer research
    76. CHEN CP; CHERN SR; LEE CC; TOWN DD
      ISOCHROMOSOME 18Q IN A FETUS WITH CONGENITAL MEGACYSTIS, INTRAUTERINEGROWTH-RETARDATION AND CLOACAL DYSGENESIS SEQUENCE

      Prenatal diagnosis
    77. LOEVNER LA; OVERHAUSER J; KAMHOLZ J
      18Q-SYNDROME AND WHITE-MATTER ALTERATIONS - REPLY

      American journal of neuroradiology
    78. BATANIAN JR; ESWARA MS
      DE-NOVO APPARENTLY BALANCED COMPLEX CHROMOSOME REARRANGEMENT (CCR) INVOLVING CHROMOSOME-4, CHROMOSOME-18, AND CHROMOSOME-21 IN A GIRL WITH MENTAL-RETARDATION - REPORT AND REVIEW

      American journal of medical genetics
    79. KEPPLERNOREUIL KM; CARROLL AJ; FINLEY SC; DESCARTES M; CODY JD; DUPONT BR; GAY CT; LEACH RJ
      CHROMOSOME 18Q PARACENTRIC INVERSION IN A FAMILY WITH MENTAL-RETARDATION AND HEARING-LOSS

      American journal of medical genetics
    80. SUZUKI K; OGURA T; YOKOSE T; NAGAI K; MUKAI K; KODAMA T; NISHIWAKI Y; ESUMI H
      LOSS OF HETEROZYGOSITY IN THE TUBEROUS SCLEROSIS GENE ASSOCIATED REGIONS IN ADENOCARCINOMA OF THE LUNG ACCOMPANIED BY MULTIPLE ATYPICAL ADENOMATOUS HYPERPLASIA

      International journal of cancer
    81. FRIZELL ER; SUTPHEN R; DIAMOND FB; SHERWOOD M; OVERHAUSER J
      T(1-18)(Q32.1-Q22.1) ASSOCIATED WITH GENITOURINARY MALFORMATIONS

      Clinical genetics
    82. TAKANISHI DM; KIM SY; KELEMEN PR; YAREMKO ML; KIM AH; RAMESAR JE; HORRIGAN SK; MONTAG A; MICHELASSI F; WESTBROOK CA
      CHROMOSOME-8 LOSSES IN COLORECTAL-CARCINOMA - LOCALIZATION AND CORRELATION WITH INVASIVE DISEASE

      Molecular diagnosis
    83. MEYERHARDT JA; LOOK AT; BIGNER SH; FEARON ER
      IDENTIFICATION AND CHARACTERIZATION OF NEOGENIN, A DCC-RELATED GENE

      Oncogene
    84. KATO R; MATSUMOTO N; FUJIMOTO M; NAKANO M; NAKAMURA Y; NIIKAWA N
      FISH MAPPING OF A TRANSLOCATION BREAKPOINT AT 6Q21 (OR Q22) IN A PATIENT WITH HETEROTAXIA

      Japanese journal of human genetics
    85. NISHIZUKA S; TAMURA G; MAESAWA C; SAKATA K; SUZUKI Y; IWAYA T; TERASHIMA M; SAITO K; SATODATE R
      ANALYSIS OF THE DPC4 GENE IN GASTRIC-CARCINOMA

      Japanese journal of cancer research
    86. YOKOTA T; MATSUMOTO S; YOSHIMOTO M; KASUMI F; AKIYAMA F; SAKAMOTO G; NAKAMURA Y; EMI M
      MAPPING OF A BREAST-CANCER TUMOR-SUPPRESSOR GENE LOCUS TO A 4-CM INTERVAL ON CHROMOSOME 18Q21

      Japanese journal of cancer research
    87. LAURENTPUIG P; OLSCHWANG S
      COLON-CANCER - FROM MOLECULAR DIAGNOSIS TO CLINICAL-DIAGNOSIS AND THERAPY

      La Revue de medecine interne
    88. CHEN CP; CHERN SR; LIU FF; JAN SW; LEE CC; CHUNG YC; YUE CT
      PRENATAL-DIAGNOSIS OF A DELETION OF 18Q IN A FETUS ASSOCIATED WITH MULTIPLE-MARKER SCREEN POSITIVE RESULTS

      Prenatal diagnosis
    89. SUGIO K; MOLBERG K; ALBORESSAAVEDRA J; VIRMANI AK; KISHIMOTO Y; GAZDAR AF
      K-RAS MUTATIONS AND ALLELIC LOSS AT 5Q AND 18Q IN THE DEVELOPMENT OF HUMAN PANCREATIC CANCERS

      International journal of pancreatology
    90. GAY CT; HARDIES LJ; RAUCH RA; LANCASTER JL; PLAETKE R; DUPONT BR; CODY JD; CORNELL JE; HERNDON RC; GHIDONI PD; SCHIFF JM; KAYE CI; LEACH RJ; FOX PT
      MAGNETIC-RESONANCE-IMAGING DEMONSTRATES INCOMPLETE MYELINATION IN 18Q- SYNDROME - EVIDENCE FOR MYELIN BASIC-PROTEIN HAPLOINSUFFICIENCY

      American journal of medical genetics
    91. CODY JD; HALE DE; BRKANAC Z; KAYE CI; LEACH RJ
      GROWTH-HORMONE INSUFFICIENCY ASSOCIATED WITH HAPLOINSUFFICIENCY AT 18Q23

      American journal of medical genetics
    92. CODY JD; PIERCE JF; BRKANAC Z; PLAETKE R; GHIDONI PD; KAYE CI; LEACH RJ
      PREFERENTIAL LOSS OF THE PATERNAL ALLELES IN THE 18Q- SYNDROME

      American journal of medical genetics
    93. GHIDONI PD; HALE DE; CODY JD; GAY CT; THOMPSON NM; MCCLURE EB; DANNEY MM; LEACH RJ; KAYE CI
      GROWTH-HORMONE DEFICIENCY ASSOCIATED IN THE 18Q DELETION SYNDROME

      American journal of medical genetics
    94. BERTONI F; BOSSHARD G; ROGGERO E; CERESA E; CAVALLI F; ZUCCA E
      CLINICAL RELEVANCE OF BCL-2(MBR) J(H) REARRANGEMENT DETECTED BY POLYMERASE CHAIN-REACTION IN THE PERIPHERAL-BLOOD OF PATIENTS WITH FOLLICULAR LYMPHOMA/

      British Journal of Cancer
    95. CAREY TE; FRANK CJ; RAVAL JR; JONES JW; MCCLATCHEY KD; BEALS TF; WORSHAM MJ; VANDYKE DL
      IDENTIFYING GENETIC CHANGES ASSOCIATED WITH TUMOR PROGRESSION IN SQUAMOUS-CELL CARCINOMA

      Acta oto-laryngologica
    96. GRONERT BJ
      LARYNGEAL MASK AIRWAY FOR MANAGEMENT OF A DIFFICULT AIRWAY AND EXTRACORPOREAL SHOCK-WAVE LITHOTRIPSY

      Paediatric anaesthesia
    97. SCHENK M; LEIBMOSCH C; SCHENCK IU; JAENICKE M; INDRACCOLO S; SAEGER HD; DALLENBACHHELLWEG G; HEHLMANN R
      LOWER FREQUENCY OF ALLELE LOSS ON CHROMOSOME 18Q IN HUMAN BREAST-CANCER THAN IN COLORECTAL TUMORS

      Journal of molecular medicine
    98. FEARON ER
      DCC - IS THERE A CONNECTION BETWEEN TUMORIGENESIS AND CELL GUIDANCE MOLECULES

      Biochimica et biophysica acta, CR. Reviews on cancer
    99. LEVYMOZZICONACCI A; PIQUET C; SCHEINER C; ADRAI J; POTIER A; PELISSIER MC; PHILIP N
      I(18Q) IN AMNIOTIC AND FETAL CELLS WITH A NORMAL KARYOTYPE IN DIRECT CHORIONIC VILLUS SAMPLING - CYTOGENETICS AND PATHOLOGY

      Prenatal diagnosis
    100. ESMER MD; CARNEVALE A; GOMEZ L; DELCASTILLO V; FRIAS S
      FLUORESCENCE IN-SITU HYBRIDIZATION IN 6 P ATIENTS WITH CHROMOSOME-18 STRUCTURAL-ABERRATIONS AND IN 7 PATIENTS WITH MARKER CHROMOSOMES

      Revista de Investigacion Clinica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 01:58:20