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    1. Romney, CA; Paulauskis, JD; Little, JB
      X-ray induction of microsatellite instability at autosomal loci in human lymphoblastoid WTK1 cells

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    2. Schurmann, M; Reichel, P; Muller-Myhsok, B; Schlaak, M; Muller-Quernheim, J; Schwinger, E
      Results from a genome-wide search for predisposing genes in sarcoidosis

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    3. Hodgson, G; Hager, JH; Volik, S; Hariono, S; Wernick, M; Moore, D; Albertson, DG; Pinkel, D; Collins, C; Hanahan, D; Gray, JW
      Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas

      NATURE GENETICS
    4. Phakdeekitcharoen, B; Watnick, TJ; Germino, GG
      Mutation analysis of the entire replicated portion of PKD1 using genomic DNA samples

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    5. Laczika, K; Mitterbauer, G; Mitterbauer, M; Knobl, P; Schwarzinger, I; Greinix, HT; Rabitsch, W; Fonatsch, C; Mannhalter, C; Lechner, K; Jaeger, U
      Prospective monitoring of minimal residual disease in acute myeloid leukemia with inversion(16) by CBF beta/MYH11 RT-PCR: Implications for a monitoring schedule and for treatment decisions

      LEUKEMIA & LYMPHOMA
    6. Horsley, SW; Daniels, RJ; Anguita, E; Raynham, HA; Peden, JF; Villegas, A; Vickers, MA; Green, S; Waye, JS; Chui, DHK; Ayyub, H; MacCarthy, AB; Buckle, VJ; Gibbons, RJ; Kearney, L; Higgs, DR
      Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects

      EUROPEAN JOURNAL OF HUMAN GENETICS
    7. Yakicier, MC; Legoix, P; Vaury, C; Gressin, L; Tubacher, E; Capron, F; Bayer, J; Degott, C; Balabaud, C; Zucman-rossi, J
      Identification of homozygous deletions at chromosome 16q23 in Aflatoxin B1exposed hepatocellular carcinoma

      ONCOGENE
    8. Yoon, DS; Li, L; Zhang, RD; Kram, A; Ro, JY; Johnston, D; Grossman, HB; Scherer, S; Czerniak, B
      Genetic mapping and DNA sequence-based analysis of deleted regions on chromosome 16 involved in progression of bladder cancer from occult preneoplastic conditions to invasive disease

      ONCOGENE
    9. Cai, L; Lumsden, A; Guenther, UP; Neldner, SA; Zach, S; Knoblauch, H; Ramesar, R; Hohl, D; Callen, DF; Neldner, KH; Lindpaintner, K; Richards, RI; Struk, B
      A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthomaelasticum

      JOURNAL OF MOLECULAR MEDICINE-JMM
    10. Tsuda, H; Takarabe, T; Akashi-Tanaka, S; Fukutomi, T; Hirohashi, S
      Pattern of chromosome 16q loss differs between an atypical proliferative lesion and an intraductal or invasive ductal carcinoma occurring subsequently in the same are of the breast

      MODERN PATHOLOGY
    11. Davisson, MT; Bechtel, LJ; Akeson, EC; Fortna, A; Slavov, D; Gardiner, K
      Evolutionary breakpoints on human chromosome 21

      GENOMICS
    12. Giorgi, D; Ferraz, C; Mattei, MG; Demaille, J; Rouquier, S
      The myosin light chain kinase gene is not duplicated in mouse: Partial structure and chromosomal localization of Mylk

      GENOMICS
    13. Marcucci, G; Caligiuri, MA; Dohner, H; Archer, KJ; Schlenk, RF; Dohner, K; Maghraby, EA; Bloomfield, CD
      Quantification of CBF beta/MYH11 fusion transcript by Real Time RT-PCR in patients with INV(16) acute myeloid leukemia

      LEUKEMIA
    14. Slywotzky, CM; Bosniak, MA
      Localized cystic disease of the kidney

      AMERICAN JOURNAL OF ROENTGENOLOGY
    15. Longa, L; Saluto, A; Brusco, A; Polidoro, S; Padovan, S; Allavena, A; Carbonara, C; Grosso, E; Migone, N
      TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the gene

      HUMAN GENETICS
    16. Brophy, S; Pavy, S; Lewis, P; Taylor, G; Bradbury, L; Robertson, D; Lovell, C; Calin, A
      Inflammatory eye, skin, and bowel disease in spondyloarthritis: Genetic, phenotypic, and environmental factors

      JOURNAL OF RHEUMATOLOGY
    17. Verlinsky, Y; Cieslak, J; Ivakhnenko, V; Evsikov, S; Wolf, G; White, M; Lifchez, A; Kaplan, B; Moise, J; Valle, J; Ginsberg, N; Strom, C; Kuliev, A
      Chromosomal abnormalities in the first and second polar body

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    18. Hengstschlager, M; Bettelheim, D; Drahonsky, R; Deutinger, J; Bernaschek, G
      Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16

      PRENATAL DIAGNOSIS
    19. Yamamoto, K; Nagata, K; Kida, A; Hamaguchi, H
      Deletion of 16q11 is a recurrent cytogenetic aberration in acute myeloblastic leukemia during disease progression

      CANCER GENETICS AND CYTOGENETICS
    20. Hampe, J; Cuthbert, A; Croucher, PJP; Mirza, MM; Mascheretti, S; Fisher, S; Frenzel, H; King, K; Hasselmeyer, A; MacPherson, AJS; Bridger, S; van Deventer, S; Forbes, A; Nikolaus, S; Lennard-Jones, JE; Foelsch, UR; Krawczak, M; Lewis, C; Schreiber, S; Mathew, CG
      Association between insertion mutation in NOD2 gene and Crohn's disease inGerman and British populations

      LANCET
    21. Haagerup, A; Bjerke, T; Schiotz, PO; Dahl, R; Binderup, HG; Kruse, TA
      No linkage and association of atopy to chromosome 16 including the interleukin-4 receptor gene

      ALLERGY
    22. Etzell, JE; Devries, S; Chew, K; Florendo, C; Molinaro, A; Ljung, BM; Waldman, FM
      Loss of chromosome 16q in lobular carcinoma in situ

      HUMAN PATHOLOGY
    23. Church, JM
      Molecular genetics and Crohn's disease

      SURGICAL CLINICS OF NORTH AMERICA
    24. Bisgaard, ML; Jager, AC; Dalgaard, P; Sondergaard, JO; Rehfeld, JF; Nielsen, FC
      Allelic loss of chromosome 2p21-16.3 is associated with reduced survival in sporadic colorectal cancer

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    25. Craggs, A; West, S; Curtis, A; Welfare, M; Hudson, M; Donaldson, P; Mansfield, J
      Absence of a genetic association between IL-1RN and IL-1B gene polymorphisms in ulcerative colitis and crohn disease in multiple populations from northeast England

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    26. Ogura, Y; Bonen, DK; Inohara, N; Nicolae, DL; Chen, FF; Ramos, R; Britton, H; Moran, T; Karaliuskas, R; Duerr, RH; Achkar, JP; Brant, SR; Bayless, TM; Kirschner, BS; Hanauer, SB; Nunez, G; Cho, JH
      A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

      NATURE
    27. Yin, XL; Pang, JC; Liu, YH; Chong, EY; Cheng, Y; Poon, WS; Ng, HK
      Analysis of loss of heterozygosity on chromosomes 10q, 11, and 16 in medulloblastomas

      JOURNAL OF NEUROSURGERY
    28. Guerrini, R
      Idiopathic epilepsy and paroxysmal dyskinesia

      EPILEPSIA
    29. Hyde, LA; Crnic, LS; Pollock, A; Bickford, PC
      Motor learning in Ts65Dn mice, a model for Down syndrome

      DEVELOPMENTAL PSYCHOBIOLOGY
    30. Yabuuchi, H; Shimizu, H; Takayanagi, S; Ishikawa, T
      Multiple splicing variants of two new human ATP-binding cassette transporters, ABCC11 and ABCC12

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    31. Akolkar, PN; Gulwani-Akolkar, B; Lin, XY; Zhou, ZF; Daly, M; Katz, S; Levine, J; Present, D; Gelb, B; Desnick, R; Mayer, L; Silver, J
      The IBD1 locus for susceptibility to Crohn's disease has a greater impact in Ashkenazi Jews with early onset disease

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    32. Pletcher, MT; Roe, BA; Chen, F; Do, T; Do, A; Malaj, E; Reeves, RH
      Chromosome evolution: The junction of mammalian chromosomes in the formation of mouse chromosome 10

      GENOME RESEARCH
    33. Forabosco, P; Collins, A; Latiano, A; Annese, V; Clementi, M; Andriulli, A; Fortina, P; Devoto, M; Morton, NE
      Combined segregation and linkage analysis of inflammatory bowel disease inthe IBD1 region using severity to characterise Crohn's disease and ulcerative colitis

      EUROPEAN JOURNAL OF HUMAN GENETICS
    34. Eliakim, R; Reif, S; Lavy, A; Keter, D; Odes, S; Halak, A; Broide, E; Niv, Y; Ron, Y; Paz, J; Fich, A; Villa, Y; Gilat, T
      Passive smoking in patients with inflammatory bowel disease: an Israeli multicentre case-control study

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    35. Tsuda, H; Takarabe, T; Fukutomi, T; Hirohashi, S
      Preferential occurrence of breast carcinomas with loss of chromosome 16q and der(16)t(1;16)/der(1;16) in middle-aged patients with hyperplasia of mammary glands

      JAPANESE JOURNAL OF CANCER RESEARCH
    36. Mancini, M; Cedrone, M; Diverio, D; Emanuel, B; Stul, M; Vranckx, H; Brama, M; De Cuia, MR; Nanni, M; Fazi, F; Mecucci, C; Alimena, G; Hagemeijer, A
      Use of dual-color interphase FISH for the detection of inv(16) in acute myeloid leukemia at diagnosis, relapse and during follow-up: a study of 23 patients

      LEUKEMIA
    37. Morschhauser, F; Cayuela, JM; Martini, S; Baruchel, A; Rousselot, P; Socie, G; Berthou, P; Jouet, JP; Straetmans, N; Sigaux, F; Fenaux, P; Preudhomme, C
      Evaluation of minimal residual disease using reverse-transcription polymerase chain reaction in t(8;21) acute myeloid leukemia: A multicenter study of 51 patients

      JOURNAL OF CLINICAL ONCOLOGY
    38. Martin, G; Barragan, E; Bolufer, P; Chillon, C; Garcia-Sanz, R; Gomez, T; Brunet, S; Gonzalez, M; Sanz, MA
      Relevance of presenting white blood cell count and kinetics of molecular remission in the prognosis of acute myeloid leukemia with CBF beta/MYH11 rearrangement

      HAEMATOLOGICA
    39. Hernandez, JM; Gonzalez, MB; Granada, I; Gutierrez, N; Chillon, C; Ramos, F; Ribera, JM; Gonzalez, M; Feliu, E; San Miguel, J
      Detection of inv(16) and t(16;16) by fluorescence in situ hybridization inacute myeloid leukemia M4Eo

      HAEMATOLOGICA
    40. Martinelli, G; Ottavlani, E; Testoni, N; Montefusco, V; Buonamici, S; Tura, S
      Long-term disease-free acute myeloblastic leukemia with inv(16) is associated with PCR undetectable CBF beta/MYH11 transcript

      HAEMATOLOGICA
    41. Ghosh, S
      Linking genotype with phenotype in inflammatory bowel disease - Will we ever have reagent standard patients?

      DISEASE MARKERS
    42. Cohen, Z; Weizman, Z; Kurtzbart, E; Newman, N; Kapuller, V; Maor, E; Mares, AJ
      Infantile colonic Crohn's disease: A report of four cases in one family

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    43. Krause, JR
      Morphology and classification of acute myeloid leukemias

      CLINICS IN LABORATORY MEDICINE
    44. Suarez, BK; Lin, J; Witte, JS; Conti, DV; Resnick, MI; Klein, EA; Burmester, JK; Vaske, DA; Banerjee, TK; Catalona, WJ
      Replication linkage study for prostate cancer susceptibility genes

      PROSTATE
    45. Sanz, R; Anabitarte, MA; Querejeta, ME; Lorda-Sanchez, I; Ibanez, MA; de Alba, MR; Ayuso, C; Ramos, C
      Rapid identification of a small dicentric supernumerary marker derived from chromosome 16 with a modified FISH technique on amniotic fluid

      PRENATAL DIAGNOSIS
    46. McGhee, EM; Cohen, NR; Wolf, JL; Ledesma, CT; Cotter, PD
      Monosomy 16 as the sole abnormality in myeloid malignancies

      CANCER GENETICS AND CYTOGENETICS
    47. Reddy, KS; Wang, S; Montgomery, P; Grove, W; Robertson, LE
      Fluorescence in situ hybridization identifies inversion 16 masked by t(10;16)(q24;q22), t(7;16)(q21;q22), and t(2;16)(q37;q22) in three cases of AML-M4Eo

      CANCER GENETICS AND CYTOGENETICS
    48. Gramantieri, L; Trere, D; Pession, A; Piscaglia, F; Masi, L; Gaiani, S; Mazziotti, A; Bolondi, L
      Allelic imbalance on 16q in small, unifocal hepatocellular carcinoma - Correlation with HBV and HCV infections and cellular proliferation rate

      DIGESTIVE DISEASES AND SCIENCES
    49. Kerbeshian, J; Severud, R; Burd, L; Larson, L
      Peek-a-boo fragile site at 16D associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. Faivre, L; Prieur, AM; Le Merrer, M; Hayem, F; Penet, C; Woo, P; Hofer, M; Dagoneau, N; Sermet, I; Munnich, A; Cormier-Daire, V
      Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Petrij, F; Dorsman, JC; Dauwerse, HG; Giles, RH; Peeters, T; Hennekam, RCM; Breuning, MH; Peters, DJM
      Rubinstein-Taybi syndrome caused by a de novo reciprocal translocation t(2;16)(q38.3;p13.3)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. Kohlhase, J; Janssen, P; Weidenauer, K; Harms, K; Bartels, I
      First confirmed case with paternal uniparental disomy of chromosome 16

      AMERICAN JOURNAL OF MEDICAL GENETICS
    53. Yamamoto, K; Nagata, K; Tsurukubo, Y; Morishita, K; Hamaguchi, H
      A novel translocation t(3;22)(q21;q11) involving 3q21 in myelodysplastic syndrome-derived overt leukemia with thrombocytosis

      LEUKEMIA RESEARCH
    54. Weiss, MJ; Guo, C; Shusterman, S; Hii, G; Mirensky, TL; White, PS; Hogarty, MD; Rebbeck, TR; Teare, D; Urbanek, M; Brodeur, GM; Maris, JM
      Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13

      MEDICAL AND PEDIATRIC ONCOLOGY
    55. Olavesen, MG; Hampe, J; Mirza, MM; Saiz, R; Lewis, CM; Bridger, S; Teare, D; Easton, DF; Herrmann, T; Scott, G; Hirst, J; Sanderson, J; Hodgson, SV; Lee, J; MacPherson, A; Schreiber, S; Lennard-Jones, JE; Curran, ME; Mathew, CG
      Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease

      IMMUNOGENETICS
    56. Phakdeekitcharoen, B; Watnick, TJ; Ahn, C; Whang, DY; Burkhart, B; Germino, GG
      Thirteen novel mutations of the replicated region of PKD1 in an Asian population

      KIDNEY INTERNATIONAL
    57. Bennett, LB; Roach, ES; Bowcock, AM
      A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16

      NEUROLOGY
    58. Mason, JE; Goodfellow, PJ; Grundy, PE; Skinner, MA
      16q loss of heterozygosity and microsatellite instability in Wilms' tumor

      JOURNAL OF PEDIATRIC SURGERY
    59. Knoblauch, H; Thiel, G; Tinschert, S; Korner, H; Tennstedt, C; Chaoui, R; Kohlhase, J; Dixkens, C; Blanck, C
      Clinical and molecular cytogenetic studies of a large de novo interstitialdeletion 16q11.2-16q21 including the putative transcription factor gene SALL1

      JOURNAL OF MEDICAL GENETICS
    60. Aho, S; Buisson, M; Pajunen, T; Ryoo, YW; Giot, JF; Gruffat, H; Sergeant, A; Uitto, J
      Ubinuclein, a novel nuclear protein interacting with cellular and viral transcription factors

      JOURNAL OF CELL BIOLOGY
    61. Schreiber, S
      Genetics of inflammatory bowel disease: a puzzle with contradictions?

      GUT
    62. Brant, SR; Panhuysen, CIM; Bailey-Wilson, JE; Rohal, PM; Lee, S; Mann, J; Ravenhill, G; Kirschner, BS; Hanauer, SB; Cho, JH; Bayless, TM
      Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity

      GASTROENTEROLOGY
    63. Plaat, BEC; Molenaar, WM; Sagrudny, J; Bohle, RM; Mastik, MF; Hoekstra, HJ; Van der Graaf, WTA; Hollema, H; van den Berg, E
      The 16p11 breakpoint in myxoid liposarcomas might affect the expression ofthe LRP gene on 16p11.2 encoding the multidrug resistance associated majorvault protein

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    64. Valente, EM; Spacey, SD; Wali, GM; Bhatia, KP; Dixon, PH; Wood, NW; Davis, MB
      A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

      BRAIN
    65. van der Kolk, DM; Vellenga, E; van der Veen, AY; Noordhoek, L; Timmer-Bosscha, H; Ossenkoppele, GJ; Raymakers, RA; Muller, M; van den Berg, E; de Vries, EGE
      Deletion of the multidrug resistance protein MRP1 gene in acute myeloid leukemia: the impact on MRP activity

      BLOOD
    66. Hunt, LE; Eichenberger, MR; Petras, R; Galandiuk, S
      Use of a microsatellite marker in predicting dysplasia in ulcerative colitis

      ARCHIVES OF SURGERY
    67. Kokalj-Vokac, N; Medica, I; Zagorac, A; Zagradisnik, B; Erjavec, A; Gregoric, A
      A case of insertional translocation resulting in partial trisomy 16p

      ANNALES DE GENETIQUE
    68. Parkes, M; Barmada, MM; Satsangi, J; Weeks, DE; Jewell, DP; Duerr, RH
      The IBD2 locus shows linkage heterogeneity between ulcerative colitis and Crohn disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    69. Rioux, JD; Silverberg, MS; Daly, MJ; Steinhart, AH; McLeod, RS; Griffiths, AM; Green, T; Brettin, TS; Stone, V; Bull, SB; Bitton, A; Williams, CN; Greenberg, GR; Cohen, Z; Lander, ES; Hudson, TJ; Siminovitch, KA
      Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci

      AMERICAN JOURNAL OF HUMAN GENETICS
    70. Gaffney, PM; Ortmann, WA; Selby, SA; Shark, KB; Ockenden, TC; Rohlf, KE; Walgrave, NL; Boyum, WP; Malmgren, ML; Miller, ME; Kearns, GM; Messner, RP; King, RA; Rich, SS; Behrens, TW
      Genome screening in human systemic lupus erythematosus: Results from a second Minnesota cohort and combined analyses of 187 sib-pair families

      AMERICAN JOURNAL OF HUMAN GENETICS
    71. Holinski-Feder, E; Reyniers, E; Uhrig, S; Golla, A; Wauters, J; Kroisel, P; Bossuyt, P; Rost, I; Jedele, K; Zierler, H; Schwab, S; Wildenauer, D; Speicher, MR; Willems, PJ; Meitinger, T; Kooy, RF
      Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)

      AMERICAN JOURNAL OF HUMAN GENETICS
    72. Reif, S; Lavy, A; Keter, D; Fich, A; Eliakim, R; Halak, A; Broide, E; Niv, Y; Ron, Y; Patz, J; Odes, S; Villa, Y; Gilat, T
      Lack of association between smoking and Crohn's disease but the usual association with ulcerative colitis in Jewish patients in Israel: A multicenterstudy

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    73. Mitterbauer, M; Laczika, K; Novak, M; Mitterbauer, G; Hilgarth, B; Pirc-Danoewinata, H; Schwarzinger, I; Haas, OA; Fonatsch, C; Lechner, K; Jaeger, U
      High concordance of karyotype analysis and RT-PCR for CBF beta/MYH11 in unselected patients with acute myeloid leukemia - A single center study

      AJCP. American journal of clinical pathology
    74. Majeed, HA; Rawashdeh, M; El-Shanti, H; Qubain, H; Khuribulos, N; Shahin, HM
      Familial Mediterranean fever in children: the expanded clinical profile

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    75. Koch, C; Bednarek, N; Motte, J
      Benign epileptic seizures in infancy followed by paroxysmal choreo-athetosis during adolescence

      EPILEPTIC DISORDERS
    76. Rybicki, BA; Maliarik, MJ; Bock, CH; Elston, RC; Baughman, RP; Kimani, AP; Sheffer, RG; Chen, KM; Major, M; Popovich, J; Iannuzzi, MC
      The Blau syndrome gene is not a major risk factor for sarcoidosis

      SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES
    77. Ma, YH; Ohmen, JD; Li, ZM; Bentley, L; McElree, C; Pressman, S; Targan, SR; Fischel-Ghodsian, N; Rotter, JI; Yang, HY
      A genome-wide search identifies potential new susceptibility loci for Crohn's disease

      INFLAMMATORY BOWEL DISEASES
    78. Bain, BJ
      The relationship between the myelodysplastic syndromes and the myeloproliferative disorders

      LEUKEMIA & LYMPHOMA
    79. Wang, X; Gleich, L; Pavelic, ZP; Li, YQ; Gale, N; Hunt, S; Gluckman, JL; Stambrook, PJ
      Cervical metastases of head and neck squamous cell carcinoma correlate with loss of heterozygosity on chromosome 16q

      INTERNATIONAL JOURNAL OF ONCOLOGY
    80. Annese, V; Latiano, A; Bovio, P; Forabosco, P; Piepoli, A; Lombardi, G; Andreoli, A; Astegiano, M; Gionchetti, P; Riegler, G; Sturniolo, GC; Clementi, M; Rappaport, E; Fortina, P; Devoto, M; Gasparini, P; Andriulli, A
      Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus - A GISC study

      EUROPEAN JOURNAL OF HUMAN GENETICS
    81. Hocking, T; Feichtinger, W; Schmid, M; Haan, EA; Baker, E; Sutherland, GR
      Homozygotes for FRA16B are normal

      CHROMOSOME RESEARCH
    82. Coleman, J; Baird, DM; Royle, NJ
      The plasticity of human telomeres demonstrated by a hypervariable telomererepeat array that is located on some copies of 16p and 16q

      HUMAN MOLECULAR GENETICS
    83. Noguchi, E; Shibasaki, M; Arinami, T; Takeda, K; Yokouchi, Y; Kobayashi, K; Imoto, N; Nakahara, S; Matsui, A; Hamaguchi, H
      Lack of association of atopy/asthma and the interleukin-4 receptor alpha gene in Japanese

      CLINICAL AND EXPERIMENTAL ALLERGY
    84. Okano, H; Saito, Y; Miyazawa, T; Shinbo, T; Chou, DZ; Kosugi, S; Takahashi, Y; Odani, S; Niwa, O; Kominami, R
      Homozygous deletions and point mutations of the Ikaros gene in gamma-ray-induced mouse thymic lymphomas

      ONCOGENE
    85. van der Reijden, BA; Dauwerse, HG; Giles, RH; Jagmohan-Changur, S; Wijmenga, C; Liu, PP; Smit, B; Wessels, HW; Beverstock, GC; Jotterand-Bellomo, M; Martinet, D; Muhlematter, D; Lafage-Pochitaloff, M; Gabert, J; Reiffers, J; Bilhou-Nabera, C; van Ommen, GJB; Hagemeijer, A; Breuning, MH
      Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

      ONCOGENE
    86. Moore, CS; Lee, JS; Birren, B; Stetten, G; Baxter, LL; Reeves, RH
      Integration of cytogenetic with recombinational and physical maps of mousechromosome 16

      GENOMICS
    87. Dunphy, CH
      Comprehensive review of adult acute myelogenous leukemia: Cytomorphological, enzyme cytochemical, flow cytometric immunophenotypic, and cytogenetic findings

      JOURNAL OF CLINICAL LABORATORY ANALYSIS
    88. Barber, JCK; Reed, CJ; Dahoun, SP; Joyce, CA
      Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level

      HUMAN GENETICS
    89. Kessler, BH; So, HB; Becker, JM
      Crohn's disease mimicking enterocolitis in a patient with an endorectal pull-through for Hirschsprung's disease

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    90. Hammond, C; Jeffers, L; Carr, BI; Simon, D
      Multiple genetic alterations, 4q28, a new suppressor region, and potentialgender differences in human hepatocellular carcinoma

      HEPATOLOGY
    91. Martinelli, G; Ottaviani, E; Testoni, N; Visani, G; Terragna, C; Amabile, M; Trabacchi, E; Montefusco, V; Tura, S
      Molecular remission in PCR-positive acute myeloid leukemia patients with inv(16): role of bone marrow transplantation procedures

      BONE MARROW TRANSPLANTATION
    92. Caruso, ML; Valentini, AM
      Overexpression of p53 in a large series of patients with hepatocellular carcinoma: A clinicopathological correlation

      ANTICANCER RESEARCH
    93. Chen, CP; Chern, SR; Lee, CC; Town, DD; Chen, WL; Wang, WS
      Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3 : 1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)

      PRENATAL DIAGNOSIS
    94. Hugot, JP; Zouali, H; Lesage, S; Thomas, G
      Etiology of the inflammatory bowel diseases

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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/06/20 alle ore 00:18:35