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    1. Simsir, A; Palacios, D; Linehan, WM; Merino, MJ; Abati, A
      Detection of loss of heterozygosity at chromosome 3p25-26 in primary and metastatic ovarian clear-cell carcinoma: Utilization of microdissection and polymerase chain reaction in archival tissues

      DIAGNOSTIC CYTOPATHOLOGY
    2. Wada, T; Louhelainen, J; Hemminki, K; Adolfsson, J; Wijkstrom, H; Norming, U; Borgstrom, E; Hansson, J; Steineck, G
      The prevalence of loss of heterozygosity in chromosome 3, including FHIT, in bladder cancer, using the fluorescent multiplex polymerase chain reaction

      BJU INTERNATIONAL
    3. Clements, J; Hooper, J; Dong, Y; Harvey, T
      The expanded human kallikrein (KLK) gene family: Genomic organisation, tissue-specific expression and potential functions

      BIOLOGICAL CHEMISTRY
    4. Irwin, MS; Kaelin, WG
      Role of the newer p53 family proteins in malignancy

      APOPTOSIS
    5. Kirov, G; Lowry, CA; Stephens, M; Oldfield, S; O'Donovan, MC; Lightman, SL; Owen, MJ
      Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder

      MOLECULAR PSYCHIATRY
    6. Nover, L; Bharti, K; Doring, P; Mishra, SK; Ganguli, A; Scharf, KD
      Arabidopsis and the heat stress transcription factor world: how many heat stress transcription factors do we need?

      CELL STRESS & CHAPERONES
    7. Barlow, GM; Chen, XN; Shi, ZY; Lyons, GE; Kurnit, DM; Celle, L; Spinner, NB; Zackai, E; Pettenati, MJ; Van Riper, AJ; Vekemans, MJ; Mjaatvedt, CH; Korenberg, JR
      Down syndrome congenital heart disease: A narrowed region and a candidate gene

      GENETICS IN MEDICINE
    8. Pavelic, K; Krizanac, S; Cacev, T; Hadzija, MP; Radosevic, S; Crnic, I; Levanat, S; Kapitanovic, S
      Aberration of FHIT gene is associated with increased tumor proliferation and decreased apoptosis - Clinical evidence in lung and head and neck carcinomas

      MOLECULAR MEDICINE
    9. Dawkins, JL; Hulme, DJ; Brahmbhatt, SB; Auer-Grumbach, M; Nicholson, GA
      Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain basesubunit-1, cause hereditary sensory neuropathy type I

      NATURE GENETICS
    10. Wieser, R; Schreiner, U; Pirc-Danoewinata, H; Aytekin, M; Schmidt, HH; Rieder, H; Fonatsch, C
      Interphase fluorescence in situ hybridization assay for the detection of 3q21 rearrangements in myeloid malignancies

      GENES CHROMOSOMES & CANCER
    11. Steinhart, H; Bohlender, JE; Constantinidis, J; Urbschat, S; Fischer, U; Iro, H; Pahl, S; Meese, E
      Genetic imbalances in preinvasive tissue of hypopharynx provide evidence for cytogenetic heterogeneity

      ONCOLOGY REPORTS
    12. Alonso, ME; Bello, MJ; Lomas, J; Gonzalez-Gomez, P; Arjona, D; De Campos, JM; Gutierrez, M; Isla, A; Vaquero, J; Rey, JA
      Absence of mutation of the p73 gene in astrocytic neoplasms

      INTERNATIONAL JOURNAL OF ONCOLOGY
    13. Louhelainen, J; Wijstrom, H; Hemminki, K
      Multiple regions with allelic loss at chromosome 3 in superficial multifocal bladder tumors

      INTERNATIONAL JOURNAL OF ONCOLOGY
    14. Barajas-Barjas, LO; Velarde-Felix, S; Elizarraras-Rivas, J; Hernandez-Zaragoza, G; Vazquez-Herrera, JA
      De novo ring chromosome 3 in a girl with hypoplastic thumb and coloboma ofiris

      GENETIC COUNSELING
    15. Smeets, E; Vandenbossche, L; Fryns, JP
      Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic features

      GENETIC COUNSELING
    16. Bastepe, M; Pincus, JE; Sugimoto, T; Tojo, K; Kanatani, M; Azuma, Y; Kruse, K; Rosenbloom, AL; Koshiyama, H; Juppner, H
      Positional dissociation between the genetic mutation responsible for pseudohypoparathyroidism type Ib and the associated methylation defect at exon A/B: evidence for a long-range regulatory element within the imprinted GNAS1locus

      HUMAN MOLECULAR GENETICS
    17. Cho, YR; Walbot, V
      Computational methods for gene annotation: the Arabidopsis genome

      CURRENT OPINION IN BIOTECHNOLOGY
    18. Astuti, D; Agathanggelou, A; Honorio, S; Dallol, A; Martinsson, T; Kogner, P; Cummins, C; Neumann, HPH; Voutilainen, R; Dahia, P; Eng, C; Maher, ER; Latif, F
      RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours

      ONCOGENE
    19. Kondo, M; Ji, L; Kamibayashi, C; Tomizawa, Y; Randle, D; Sekido, Y; Yokota, J; Kashuba, V; Zabarovsky, E; Kuzmin, I; Lerman, M; Roth, J; Minna, JD
      Overexpression of candidate tumor suppressor gene FUS1 isolated from the 3p21.3 homozygous deletion region leads to G1 arrest and growth inhibition of lung cancer cells

      ONCOGENE
    20. Shigemitsu, K; Sekido, Y; Usami, N; Mori, S; Sato, M; Horio, Y; Hasegawa, Y; Bader, SA; Gazdar, AF; Minna, JD; Hida, T; Yoshioka, H; Imaizumi, M; Ueda, Y; Takahashi, M; Shimokata, K
      Genetic alteration of the beta-catenin gene (CTNNB1) in human lung cancer and malignant mesothelioma and identification of a new 3p21.3 homozygous deletion

      ONCOGENE
    21. Dammann, R; Takahashi, T; Pfeifer, GP
      The CpG island of the novel tumor suppressor gene RASSF1A is intensely methylated in primary small cell lung carcinomas

      ONCOGENE
    22. Sutherland, LC; Lerman, M; Williams, GT; Miller, BA
      LUCA-15 suppresses CD95-mediated apoptosis in Jurkat T cells

      ONCOGENE
    23. Michael, D; Rajewsky, MF
      Induction of the common fragile site FRA3B does not affect FHIT expression

      ONCOGENE
    24. Agathanggelou, A; Honorio, S; Macartney, DP; Martinez, A; Dallol, A; Radar, J; Fullwood, P; Chauhan, A; Walker, R; Shaw, JA; Hosoe, S; Lerman, MI; Minna, JD; Maher, ER; Latif, F
      Methylation associated inactivation of RASSF1A from region 3p21.3 in lung,breast and ovarian tumours

      ONCOGENE
    25. Ross, SR
      Commentary: phenotypic screening of radiation hybrid panels

      MAMMALIAN GENOME
    26. Li, T; Underhill, J; Liu, XH; Sham, PC; Donaldson, P; Murray, RM; Wright, P; Collier, DA
      Transmission disequilibrium analysis of HLA class II DRB1, DQA1, DQB1 and DPB1 polymorphisms in schizophrenia using family trios from a Han Chinese population

      SCHIZOPHRENIA RESEARCH
    27. Wright, P; Nimgaonkar, VL; Donaldson, PT; Murray, RM
      Schizophrenia and HLA: a review

      SCHIZOPHRENIA RESEARCH
    28. Fukunaga, K; Asano, K; Mao, XQ; Gao, PS; Roberts, MH; Oguma, T; Shiomi, T; Kanazawa, M; Adra, CN; Shirakawa, T; Hopkin, JM; Yamaguchi, K
      Genetic polymorphisms of CC chemokine receptor 3 in Japanese and British asthmatics

      EUROPEAN RESPIRATORY JOURNAL
    29. Lavabre-Bertrand, T; Bourquard, P; Chiesa, J; Bertheas, MF; Lefort, G; Taib, J; Lavabre-Bertrand, C; Navarro, M; Bureau, JP
      Diabetes insipidus revealing acute myelogenous leukaemia with a high platelet count, monosomy 7 and abnormalities of chromosome 3: a new entity?

      EUROPEAN JOURNAL OF HAEMATOLOGY
    30. Bae, Y; Kim, H; Namgoong, H; Baek, M; Lee, J; Hwang, D; Hwang, Y; Ahn, C; Kang, S
      Characterization of microsatellite markers adjacent to AP-4 on chromosome 16p13.3

      MOLECULAR AND CELLULAR PROBES
    31. Yousef, GM; Diamandis, M; Jung, K; Diamandis, EP
      Molecular cloning of a novel human acid phosphatase gene (ACPT) that is highly expressed in the testis

      GENOMICS
    32. Cave, H; Avet-Loiseau, H; Devaux, I; Rondeau, G; Boutard, P; Lebrun, E; Mechinaud, F; Vilmer, E; Grandchamp, B
      Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia

      LEUKEMIA
    33. Sole, F; Salido, M; Espinet, B; Garcia, JL; Climent, JAM; Granada, I; Hernandez, JM; Benet, I; Piris, MA; Mollejo, M; Martinez, P; Vallespi , T; Domingo, A; Serrano, S; Woessner, S; Florensa, L
      Splenic marginal zone B-cell lymphomas: two cytogenetic subtypes, one withgain of 3q and the other with loss of 7q

      HAEMATOLOGICA
    34. Kashuba, VI; Kvasha, SM; Protopopov, AI; Gizatullin, RZ; Rynditch, AV; Wahlestedt, C; Wasserman, WW; Zabarovsky, ER
      Initial isolation and analysis of the human Kv1.7 (KCNA7) gene, a member of the voltage-gated potassium channel gene family

      GENE
    35. Dolney, DEA; Szalai, G; Duester, G; Felder, MR
      Molecular analysis of genetic differences among inbred mouse strains controlling tissue expression pattern of alcohol dehydrogenase 4

      GENE
    36. Wattenhofer, M; Shibuya, K; Kudoh, J; Lyle, R; Michaud, J; Rossier, C; Kawasaki, K; Asakawa, S; Minoshima, S; Berry, A; Bonne-Tamir, B; Shimizu, N; Antonarakis, SE; Scott, HS
      Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

      HUMAN GENETICS
    37. Goureau, A; Garrigues, A; Tosser-Klopp, G; Lahbib-Mansais, Y; Chardon, P; Yerle, M
      Conserved synteny and gene order difference between human chromosome 12 and pig chromosome 5

      CYTOGENETICS AND CELL GENETICS
    38. Reutzel, D; Mende, M; Naumann, S; Storkel, S; Brenner, W; Zabel, B; Decker, J
      Genomic imbalances in 61 renal cancers from the proximal tubulus detected by comparative genomic hybridization

      CYTOGENETICS AND CELL GENETICS
    39. Van Poucke, M; Yerle, M; Tuggle, C; Piumi, F; Genet, C; Van Zeveren, A; Peelman, LJ
      Integration of porcine chromosome 13 maps

      CYTOGENETICS AND CELL GENETICS
    40. Liu, L; Cui, X; Sakaguchi, T; Sasaki, M; Suda, T; Hatakeyama, K
      Expression of p73 in colorectal carcinoma: Clinicopathological relevance

      JOURNAL OF INTERNATIONAL MEDICAL RESEARCH
    41. Gaiddon, C; Lokshin, M; Ahn, J; Zhang, T; Prives, C
      A subset of tumor-derived mutant forms of p53 down-regulate p63 and p73 through a direct interaction with the p53 core domain

      MOLECULAR AND CELLULAR BIOLOGY
    42. Shi, XW; Fitzsimmons, CJ; Genet, C; Prather, R; Whitworth, K; Green, JA; Tuggle, CK
      Radiation hybrid comparative mapping between human chromosome 17 and porcine chromosome 12 demonstrates conservation of gene order

      ANIMAL GENETICS
    43. Hayashi, M; Tokuchi, Y; Hashimoto, T; Hayashi, SI; Nishida, K; Ishikawa, Y; Nakagawa, K; Tsuchiya, S; Okumura, S; Tsuchiya, E
      Reduced HIC-1 gene expression in non-small cell lung cancer and its clinical significance

      ANTICANCER RESEARCH
    44. Dominguez, G; Silva, JM; Silva, J; Garcia, JM; Sanchez, A; Navarro, A; Gallego, I; Provencio, M; Espana, P; Bonilla, F
      Wild type p73 overexpression and high-grade malignancy in breast cancer

      BREAST CANCER RESEARCH AND TREATMENT
    45. Sprenger, SHE; Gijtenbeek, JMM; Wesseling, P; Sciot, R; Van Calenbergh, F; Lammens, M; Jeuken, JWM
      Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization

      JOURNAL OF NEURO-ONCOLOGY
    46. Malkin, D
      The role of p53 in human cancer

      JOURNAL OF NEURO-ONCOLOGY
    47. Rauch, A; Schellmoser, S; Kraus, C; Dorr, HG; Trautmann, U; Altherr, MR; Pfeiffer, RA; Reis, A
      First known microdeletion within the Wolf-Hirschhorn-syndrome critical region refines genotype-phenotype correlation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Riegel, M; Morava, E; Czako, M; Kosztolanyi, G; Schinzel, A
      Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. Hoang, MP; Hruban, RH; Albores-Saavedra, J
      Clear cell endocrine pancreatic tumor mimicking renal cell carcinoma - A distinctive neoplasm of von Hippel-Lindau disease

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    50. Beccari, T; Balducci, C; Aisa, MC; Della Fazia, MA; Servillo, G; Orlacchio, A
      Promoter characterization and expression of the gene coding for the human GM2 activator protein

      BIOSCIENCE REPORTS
    51. El-Naggar, AK; Lai, SL; Clayman, GL; Mims, B; Lippman, SM; Coombes, M; Luna, MA; Lozano, G
      p73 gene alterations and expression in primary oral and laryngeal squamouscarcinomas

      CARCINOGENESIS
    52. 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
    53. Rosenberg, N
      New transformation tricks from a barnyard retrovirus: Implications for human lung cancer

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    54. Rai, SK; Duh, FM; Vigdorovich, V; Danilkovitch-Miagkova, A; Lerman, MI; Miller, AD
      Candidate tumor suppressor HYAL2 is a glycosylphosphatidylinositol (GPI)-anchored cell-surface receptor for jaagsiekte sheep retrovirus, the envelopeprotein of which mediates oncogenic transformation

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    55. Yang, Y; Kost-Alimova, M; Ingvarsson, S; Qiu, QH; Kiss, H; Szeles, A; Kholodnyuk, I; Cuthbert, A; Klein, G; Imreh, S
      Similar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) mice

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    56. Tomizawa, Y; Sekido, Y; Kondo, M; Gao, BN; Yokota, J; Roche, J; Drabkin, H; Lerman, MI; Gazdar, AF; Minna, JD
      Inhibition of lung cancer cell growth and induction of apoptosis after reexpression of 3p21.3 candidate tumor suppressor gene SEMA3B

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    57. Bazov, IV; Kazubskaya, TP; Ermilova, VD; Gar'kavtseva, RF; Loginov, VI; Zabarovsky, ER; Braga, EA
      Allele deletion mapping of the short arm of human chromosome 3 in renal carcinoma

      MOLECULAR BIOLOGY
    58. Palmarini, M; Maeda, N; Murgia, C; De-Fraja, C; Hofacre, A; Fan, H
      A phosphatidylinositol 3-kinase docking site in the cytoplasmic tail of the Jaagsiekte sheep retrovirus transmembrane protein is essential for envelope-induced transformation of NIH 3T3 cells

      JOURNAL OF VIROLOGY
    59. Barghom, A; Komminoth, P; Bachmann, D; Rutimann, K; Saremaslani, P; Muletta-Feurer, S; Perren, A; Roth, J; Heitz, PU; Speel, EJM
      Deletion at 3p25.3-p23 is frequently encountered in endocrine pancreatic tumours and is associated with metastatic progression

      JOURNAL OF PATHOLOGY
    60. Liu, HX; Oei, PTSP; Mitchell, EA; McGaughran, JM
      Interstitial deletion of 3p22.2-p24.2: the first reported case

      JOURNAL OF MEDICAL GENETICS
    61. Nopola-Hemmi, J; Myllyluoma, B; Haltia, T; Taipale, M; Ollikainen, V; Ahonen, T; Voutilainen, A; Kere, J; Widen, E
      A dominant gene for developmental dyslexia on chromosome 3

      JOURNAL OF MEDICAL GENETICS
    62. Schmitz, G; Langmann, T; Heimerl, S
      Role of ABCG1 and other ABCG family members in lipid metabolism

      JOURNAL OF LIPID RESEARCH
    63. Bashirova, AA; Geijtenbeek, TBH; van Duijnhoven, GCF; van Vliet, SJ; Eilering, JBG; Martin, MP; Wu, L; Martin, TD; Viebig, N; Knolle, PA; KewalRamani, VN; van Kooyk, Y; Carrington, M
      A dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN)-related protein is highly expressed on human liver sinusoidal endothelial cells and promotes HIV-1 infection

      JOURNAL OF EXPERIMENTAL MEDICINE
    64. Guerardel, C; Deltour, S; Pinte, S; Monte, D; Begue, A; Godwin, AK; Leprince, D
      Identification in the human candidate tumor suppressor gene HIC-1 of a newmajor alternative TATA-less promoter positively regulated by p53

      JOURNAL OF BIOLOGICAL CHEMISTRY
    65. Roberson, MS; Meermann, S; Morasso, MI; Mulvaney-Musa, JM; Zhang, T
      A role for the homeobox protein distal-less 3 in the activation of the glycoprotein hormone alpha subunit gene in choriocarcinoma cells

      JOURNAL OF BIOLOGICAL CHEMISTRY
    66. Hampe, J; Lynch, NJ; Daniels, S; Bridger, S; Macpherson, AJS; Stokkers, P; Forbes, A; Lennard-Jones, JE; Mathew, CG; Curran, ME; Schreiber, S
      Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease

      GUT
    67. Matsui, H; Takahashi, T
      Mouse testicular Leydig cells express Klk21, a tissue kallikrein that cleaves fibronectin and IGF-binding protein-3

      ENDOCRINOLOGY
    68. Lyons, PA; Armitage, N; Lord, CJ; Phillips, MS; Todd, JA; Peterson, LB; Wicker, LS
      Mapping by genetic interaction - High-resolution congenic mapping of the type 1 diabetes loci Idd10 and Idd18 in the NOD mouse

      DIABETES
    69. Brodwolf, S; Boddeker, IR; Ziegler, A; Rausch, P; Kunz, J
      Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3

      CLINICAL GENETICS
    70. Morrissey, C; Martinez, A; Zatyka, M; Agathanggelou, A; Honorio, S; Astuti, D; Morgan, NV; Moch, H; Richards, FM; Kishida, T; Yao, M; Schraml, P; Latif, F; Maher, ER
      Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma

      CANCER RESEARCH
    71. Lo, KW; Kwong, J; Hui, ABY; Chan, SYY; To, KF; Chan, SC; Chow, LSN; Teo, PML; Johnson, PJ; Huang, DP
      High frequency of promoter hypermethylation of RASSF1A in nasopharyngeal carcinoma

      CANCER RESEARCH
    72. Patel, KA; Edmondson, ND; Talbot, F; Parsons, MA; Rennie, IG; Sisley, K
      Prediction of prognosis in patients with uveal melanoma using fluorescencein situ hybridisation

      BRITISH JOURNAL OF OPHTHALMOLOGY
    73. Alonso, ME; Bello, MJ; Gonzalez-Gomez, P; Lomas, J; Arjona, D; de Campos, JM; Kusak, ME; Sarasa, JL; Isla, A; Rey, JA
      Mutation analysis of the p73 gene in nonastrocytic brain tumours

      BRITISH JOURNAL OF CANCER
    74. Ford, AM; Fasching, K; Panzer-Grumayer, ER; Koenig, M; Haas, OA; Greaves, MF
      Origins of "late" relapse in childhood acute lymphoblastic leukemia with TEL-AML1 fusion genes

      BLOOD
    75. Maia, AT; Ford, AM; Jalali, GR; Harrison, CJ; Taylor, GM; Eden, OB; Greaves, MF
      Molecular tracking of leukemogenesis in a triplet pregnancy

      BLOOD
    76. Chen, CM; Behringer, RR
      Cloning, structure, and expression of the mouse Ovca1 gene

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    77. Kojima, T; Yoshikawa, Y; Takada, S; Sato, M; Nakamura, T; Takahashi, N; Copeland, NG; Gilbert, DJ; Jenkins, NA; Mori, N
      Genomic organization of the Shc-related phosphotyrosine adapters and characterization of the full-length Sck/ShcB: Specific association of p68-Sck/ShcB with pp135

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    78. Nicholson, GA; Dawkins, JL; Blair, IP; Auer-Grumbach, M; Brahmbhatt, SB; Hulme, DJ
      Hereditary sensory neuropathy type I: Haplotype analysis shows founders insouthern England and Europe

      AMERICAN JOURNAL OF HUMAN GENETICS
    79. Bonglia, MC; Giorda, R; Borgatti, R; Felisari, G; Gagliardi, C; Selicorni, A; Zuffardi, O
      Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    80. Burbee, DG; Forgacs, E; Zochbauer-Muller, S; Shivakumar, L; Fong, K; Gao, BN; Randle, D; Kondo, M; Virmani, A; Bader, S; Sekido, Y; Latif, F; Milchgrub, S; Toyooka, S; Gazdar, AF; Lerman, MI; Zabarovsky, E; White, M; Minna, JD
      Epigenetic inactivation of RASSF14 in lung and breast cancers and malignant phenotype suppression

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    81. Shay, JW; Wright, WE
      Implications of mapping the human telomerase gene (hTERT) as the most distal gene on chromosome 5p

      NEOPLASIA
    82. Seki, N; Yoshikawa, T; Hattori, A; Miyajima, N; Muramatsu, M; Saito, T
      cDNA cloning of a human RAB26-related gene encoding a Ras-like GTP-bindingprotein on chromosome 16p13.3 region

      JOURNAL OF HUMAN GENETICS
    83. Seki, N; Azuma, T; Yoshikawa, T; Masuho, Y; Muramatsu, M; Saito, T
      CDNA cloning of a new member of the Ras superfamily, RAB9-like, on the human chromosome Xq22.1-q22.3 region

      JOURNAL OF HUMAN GENETICS
    84. Fukino, K; Teramoto, A; Adachi, K; Takahashi, H; Emi, M
      A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene

      JOURNAL OF HUMAN GENETICS
    85. Vandenbergh, DJ; Thompson, MD; Cook, EH; Bendahhou, E; Nguyen, T; Krasowski, MD; Zarrabian, D; Comings, D; Sellers, EM; Tyndale, RF; George, SR; O'Dowd, BF; Uhl, GR
      Human dopamine transporter gene: coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivitydisorder populations

      MOLECULAR PSYCHIATRY
    86. Leventer, RJ; Pilz, DT; Matsumoto, N; Ledbetter, DH; Dobyns, WB
      Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis

      MOLECULAR MEDICINE TODAY
    87. Kaneko, T; Katoh, T; Sato, S; Nakamura, Y; Asamizu, E; Tabata, S
      Structural analysis of Arabidopsis thaliana chromosome 3. II. Sequence features of the 4,251,695 bp regions covered by 90 P1, TAC and BAC clones

      DNA RESEARCH
    88. Sato, S; Nakamura, Y; Kaneko, T; Katoh, T; Asamizu, E; Tabata, S
      Structural analysis of Arabidopsis thaliana chromosome 3. I. Sequence features of the regions of 4,504,864 bp covered by sixty P1 and TAC clones

      DNA RESEARCH
    89. Ichimiya, S; Nakagawara, A; Sakuma, Y; Kimura, S; Ikeda, T; Satoh, M; Takahashi, N; Sato, N; Mori, M
      p73: Structure and function

      PATHOLOGY INTERNATIONAL
    90. Chen, CL; Ip, SM; Cheng, D; Wong, LC; Ngan, HYS
      p73 gene expression in ovarian cancer tissues and cell lines

      CLINICAL CANCER RESEARCH
    91. Petrek, M; Drabek, J; Kolek, V; Zlamal, J; Welsh, KI; Bunce, M; Weigl, E; du Bois, RM
      CC chemokine receptor gene polymorphisms in Czech patients with pulmonary sarcoidosis

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    92. Shen, T; Zhuang, ZP; Gersell, DJ; Tavassoli, FA
      Allelic deletion of VHL gene detected in papillary tumors of the broad ligament, epididymis, and retroperitoneum in von Hippel-Lindau disease patients

      INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY
    93. Boardman, LA; Couch, FJ; Burgart, LJ; Schwartz, D; Berry, R; McDonnell, SK; Schaid, DJ; Hartmann, LC; Schroeder, JJ; Stratakis, CA; Thibodeau, SN
      Genetic heterogeneity in Peutz-Jeghers syndrome

      HUMAN MUTATION
    94. Angeloni, D; Danilkovitch-Miagkova, A; Ivanov, SV; Breathnach, R; Johnson, BE; Leonard, EJ; Lerman, MI
      Gene structure of the human receptor tyrosine kinase RON and mutation analysis in lung cancer samples

      GENES CHROMOSOMES & CANCER
    95. Podolin, PL; Wilusz, MB; Cubbon, RM; Pajvani, U; Lord, CJ; Todd, JA; Peterson, LB; Wicker, LS; Lyons, PA
      Differential glycosylation of interleukin 2, the molecular basis for the NOD Idd3 type 1 diabetes gene?

      CYTOKINE
    96. Kempski, HM; Sturt, NT
      The TEL-AML1 fusion accompanied by loss of the untranslocated TEL allele in B-precursor acute lymphoblastic leukaemia of childhood

      LEUKEMIA & LYMPHOMA
    97. Sulimova, GE; Kompaniytsev, AA; Kunizheva, SS; Klimov, EA; Rakhmanaliev, ER; Udina, IG
      Mapping EST and STS markers by the radiation hybrid panel in the human genome

      RUSSIAN JOURNAL OF GENETICS
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 14:31:34