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La ricerca find articoli where soggetti phrase all words 'CHROMOSOME-11' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 821 riferimenti
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    1. Ricketts, SL; Garcia, NF; Betz, BL; Coleman, WB
      Identification of candidate liver tumor suppressor genes from human 11p11.2-p12

      GENES CHROMOSOMES & CANCER
    2. Clerici, T; Schmid, C; Komminoth, P; Lange, F; Spinas, GA; Brandle, M
      10 Swiss kindreds with multiple endocrine neoplasia type 1: assessment of screening methods

      SWISS MEDICAL WEEKLY
    3. Granerus, M; Johannisson, A; Ekblom, P; Engstrom, W
      Insulin-like growth factors I and II induce cell death in Wilms's tumour cells

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    4. Devon, RS; Anderson, S; Teague, PW; Muir, WJ; Murray, V; Pelosi, AJ; Blackwood, DHR; Porteous, DJ
      The genomic organisation of the metabotropic glutamate receptor subtype 5 gene, and its association with schizophrenia

      MOLECULAR PSYCHIATRY
    5. Millar, JK; Christie, S; Anderson, S; Lawson, D; Loh, DHW; Devon, RS; Arveiler, B; Muir, WJ; Blackwood, DHR; Porteous, DJ
      Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia

      MOLECULAR PSYCHIATRY
    6. Manne, U; Gary, BD; Oelschlager, DK; Weiss, HL; Frost, AR; Grizzle, WE
      Altered subcellular localization of suppressin, a novel inhibitor of cell-cycle entry, is an independent prognostic factor in colorectal adenocarcinomas

      CLINICAL CANCER RESEARCH
    7. Chan, WY; Chan, ABW; Liu, AGY; Chow, JHS; Ng, EKW; Chung, SSC
      Chromosome 11 copy number gains and Epstein-Barr virus-associated malignancies

      DIAGNOSTIC MOLECULAR PATHOLOGY
    8. Tsujimoto, H; Nishizuka, S; Redpath, LJ; Stanbridge, EJ
      Examination of the oncogenic potential of H19 gene in HeLa x normal human fibroblast hybrid cells

      INTERNATIONAL JOURNAL OF ONCOLOGY
    9. Frisk, T; Zedenius, J; Lundberg, J; Wallin, G; Kytola, S; Larsson, C
      CGH alterations in medullary thyroid carcinomas in relation to the RET M918T mutation and clinical outcome

      INTERNATIONAL JOURNAL OF ONCOLOGY
    10. Sanz, R; Lorda-Sanchez, I; Fernandez-Moya, JM; Cifuentes-Sulzberger, S; de Alba, MR; Gonzalez-Gonzalez, MC; Ibanez, MA; Robledo, M; Ayuso, C; Ramos, C
      Chromosomal mosaicism for isochromosome 11q confined to CVS direct preparations

      FETAL DIAGNOSIS AND THERAPY
    11. Papillon, E; Rolachon, A; Calender, A; Chabre, O; Barnoud, R; Fournet, J
      A malignant gastrointestinal stromal tumour in a patient with multiple endocrine neoplasia type 1

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    12. Juriloff, DM; Harris, MJ; Brown, CJ
      Unravelling the complex genetics of cleft lip in the mouse model

      MAMMALIAN GENOME
    13. Sato, M; Matsubara, S; Murao, K; Ishida, T; Takahara, J
      Multiple endocrine neoplasia type 1: Usefulness of genetic tests in atypical cases

      INTERNAL MEDICINE
    14. Lam, DH; Aplan, PD
      NUP98 gene fusions in hematologic malignancies

      LEUKEMIA
    15. Pal, T; Liede, A; Mitchell, M; Calender, A; Narod, SA
      Intestinal carcinoid tumours in a father and daughter

      CANADIAN JOURNAL OF GASTROENTEROLOGY
    16. Schofield, PN; Joyce, JA; Lam, WK; Grandjean, V; Ferguson-Smith, A; Reik, W; Maher, ER
      Genomic imprinting and cancer; new paradigms in the genetics of neoplasia

      TOXICOLOGY LETTERS
    17. Nishizuka, S; Winokur, ST; Simon, M; Martin, J; Tsujimoto, H; Stanbridge, EJ
      Oligonucleotide microarray expression analysis of genes whose expression is correlated with tumorigenic and non-tumorigenic phenotype of HeLa X humanfibroblast hybrid cells

      CANCER LETTERS
    18. Drueke, TB
      Genetic aspects of secondary hyperparathyroidism in uremia

      AMERICAN JOURNAL OF KIDNEY DISEASES
    19. Gregory, RI; Randall, TE; Johnson, CA; Khosla, S; Hatada, I; O'Neill, LP; Turner, BM; Feil, R
      DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1

      MOLECULAR AND CELLULAR BIOLOGY
    20. Cummings, M; Brown, KW
      Low frequency of genetic lesions in Wilms tumors by representational difference analysis

      CANCER GENETICS AND CYTOGENETICS
    21. Udayakumar, AM; Sundareshan, TS; Goud, TM; Devi, MG; Biswas, S; Appaji, L; Arunakumari, BS; Rajan, KR; Prabhakaran, PS
      Cytogenetic characterization of Ewing tumors using fine needle aspiration samples: a 10-year experience and review of the literature

      CANCER GENETICS AND CYTOGENETICS
    22. Barr, CL; Best, L; Weksberg, R
      Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. Wu, CH; Hwu, WL; Wang, JK; Young, C; Peng, SSF; Kuo, MF
      Deletion of 11q24.2-qter with agenesis of unilateral internal carotid artery and total anomalous pulmonary venous return

      AMERICAN JOURNAL OF MEDICAL GENETICS
    24. Shaffer, LG
      Reply to the letter to the editor by Wuyts et al. - "Burning down DEFECT11"

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Robinson, D; Hasharoni, A; Oganesian, A; Sandell, LJ; Yayon, A; Nevo, Z
      Role of FGF9 and FGF receptor 3 in osteochondroma formation

      ORTHOPEDICS
    26. Seeliger, MW; Zrenner, E; Apfelstedt-Sylla, E; Jaissle, GB
      Identification of Usher syndrome subtypes by ERG implicit time

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    27. Maayan, C; Becker, Y; Gesundheit, B; Girgis, SI
      Calcitonin gene-related peptide in familial dysautonomia

      NEUROPEPTIDES
    28. Fegan, C
      Molecular abnormalities in B-cell chronic lymphocytic leukaemia

      CLINICAL AND LABORATORY HAEMATOLOGY
    29. Sakamoto, J; Takata, A; Fukuzawa, R; Kikuchi, H; Sugiyama, M; Kanamori, Y; Hashizume, K; Hata, J
      A novel WT1 gene mutation associated with Wilms' tumor and congenital malegenitourinary malformation

      PEDIATRIC RESEARCH
    30. Otterstedde, CR; Spandau, U; Blankenagel, A; Kimberling, WJ; Reisser, C
      A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I

      LARYNGOSCOPE
    31. 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
    32. Francannet, C; Cohen-Tanugi, A; Le Merrer, M; Munnich, A; Bonaventure, J; Legeai-Mallet, L
      Genotype-phenotype correlation in hereditary multiple exostoses

      JOURNAL OF MEDICAL GENETICS
    33. Mogensen, J; Andersen, PS; Steffensen, U; Christiansen, M; Egeblad, H; Gregersen, N; Borglum, AD
      Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy

      JOURNAL OF MEDICAL GENETICS
    34. Pannett, AAJ; Thakker, RV
      Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesis

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    35. Kitagawa, H; Egusa, N; Tamura, J; Kusche-Gullberg, M; Lindahl, U; Sugahara, K
      rib-2, a Caenorhabditis elegans homolog of the human tumor suppressor EXT genes encodes a novel alpha 1,4-N-acetylglucosaminyltransferase involved inthe biosynthetic initiation and elongation of heparan sulfate

      JOURNAL OF BIOLOGICAL CHEMISTRY
    36. Sotomaru, Y; Kawase, Y; Ueda, T; Obata, Y; Suzuki, H; Domeki, I; Hatada, I; Kono, T
      Disruption of imprinted expression of U2afbp-rs/U2af1-rs1 gene in mouse parthenogenetic fetuses

      JOURNAL OF BIOLOGICAL CHEMISTRY
    37. Matturri, L; Cazzullo, A; Turconi, P; Lavezzi, AM; Vandone, PL; Gabrielli, L; Alonso, GF; Grana, D; Milei, J
      Chromosomal alterations in atherosclerotic plaques

      ATHEROSCLEROSIS
    38. Gigante, M; Matera, MG; Seripa, D; Izzo, AM; Venanzi, R; Giannotti, A; Digilio, MC; Gravina, C; Lazzari, M; Monteleone, G; Monteleone, M; Dallapiccola, B; Fazio, VM
      Ext-mutation analysis in Italian sporadic and hereditary osteochondromas

      INTERNATIONAL JOURNAL OF CANCER
    39. Hall, CR; Wu, Y; Shaffer, LG; Hecht, JT
      Familial case of Potocki-Shaffer syndrome associated with microdeletion ofEXT2 and ALX4

      CLINICAL GENETICS
    40. Bullrich, F; Fujii, H; Calin, G; Mabuchi, H; Negrini, M; Pekarsky, Y; Rassenti, L; Alder, H; Reed, JC; Keating, MJ; Kipps, TJ; Croce, CM
      Characterization of the 13q14 tumor suppressor locus in CLL: Identification of ALT1, an alternative splice variant of the LEU2 gene

      CANCER RESEARCH
    41. Nishizuka, SS; Tsujimoto, HY; Stanbridge, EJ
      Detection of differentially expressed genes in HeLa x fibroblast hybrids using subtractive suppression hybridization

      CANCER RESEARCH
    42. Bhuiyan, MMR; Sato, M; Murao, K; Imachi, H; Namihira, H; Ishida, T; Takahara, J; Miyauchi, A
      Differential expression of menin in various adrenal tumors - The role of menin in adrenal tumors

      CANCER
    43. Luttikhuis, MEMO; Powell, JE; Rees, SA; Genus, T; Chughtai, S; Ramani, P; Mann, JR; McConville, CM
      Neuroblastomas with chromosome 11q loss and single copy MYCN comprise a biologically distinct group of tumours with adverse prognosis

      BRITISH JOURNAL OF CANCER
    44. Xia, CY; Wang, J; Zhang, SZ; Van Hul, W; Wuyts, W; Qiu, WM; Wu, H; Zhang, G
      A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis

      BRITISH JOURNAL OF CANCER
    45. Hulett, MD; Pagler, E; Hornby, JR; Hogarth, PM; Eyre, HJ; Baker, E; Crawford, J; Sutherland, GR; Ohms, SJ; Parish, CR
      Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and Fc epsilon RI-beta

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    46. DeAngelis, MM; McGee, TL; Keats, BJB; Slim, R; Berson, EL; Dryja, TP
      Two families from New England with Usher syndrome type IC with distinct haplotypes

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    47. Ahmed, ZM; Riazuddin, S; Bernstein, SL; Ahmed, Z; Khan, S; Griffith, AJ; Morell, RJ; Friedman, TB; Riazuddin, S; Wilcox, ER
      Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

      AMERICAN JOURNAL OF HUMAN GENETICS
    48. Ravenel, JD; Broman, KW; Perlman, EJ; Niemitz, EL; Jayawardena, TM; Bell, DW; Haber, DA; Uejima, H; Feinberg, AP
      Loss of imprinting of insulin-like growth factor-II (IGF2) gene in distinguishing specific biologic subtypes of Wilms tumor

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    49. Seki, N; Ueki, N; Yano, K; Saito, T; Masuho, Y; Muramatsu, M
      cDNA cloning of a novel human gene NAKAP95, neighbor of A-kinase anchoringprotein 95 (AKAP95) on chromosome 19p13.11-p13.12 region

      JOURNAL OF HUMAN GENETICS
    50. Llerena, JC; de Almeida, JCC; Bastos, E; Crolla, JA
      FISH studies in a girl with sporadic aniridia and an apparently balanced de novo t(11;13)(p13;q33) translocation detect a microdeletion involving theWAGR region

      GENETICS AND MOLECULAR BIOLOGY
    51. Tsukahara, K; Hirasawa, T; Makino, S
      Tss (Tail-short Shionogi), a new short tail mutation found in the BALB/cMsstrain, maps quite closely to the tail-short (Ts) locus on mouse chromosome 11

      EXPERIMENTAL ANIMALS
    52. Roijers, JFM; Apel, T; Neumann, HPH; Arnim, UV; Lips, CJM; Hoppener, JWM
      Internally shortened menin protein as a consequence of alternative RNA splicing due to a germline deletion in the multiple endocrine neoplasia type 1gene

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    53. Yang, XH; Wei, L; Tang, C; Slack, R; Montgomery, E; Lippman, M
      KAI1 protein is down-regulated during the progression of human breast cancer

      CLINICAL CANCER RESEARCH
    54. Clayton, RN; Pfeifer, M; Atkinson, AB; Belchetz, P; Wass, JAH; Kyrodimou, E; Vanderpump, M; Simpson, D; Bicknell, J; Farrell, WE
      Different patterns of allelic loss (loss of heterozygosity) in recurrent human pituitary tumors provide evidence for multiclonal origins

      CLINICAL CANCER RESEARCH
    55. Eng, C; Herman, JG; Baylin, SB
      A bird's eye view of global methylation

      NATURE GENETICS
    56. White, K; Marquardt, A; Weber, BHF
      VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies

      HUMAN MUTATION
    57. Chao, LY; Huff, V; Strong, LC; Saunders, GF
      Mutation in the PAX6 gene in twenty patients with aniridia

      HUMAN MUTATION
    58. Wuyts, W; Van Hul, W
      Molecular basis of multiple exostoses: Mutations in the EXT1 and EXT2 genes

      HUMAN MUTATION
    59. Stickens, D; Brown, D; Evans, GA
      EXT genes are differentially expressed in bone and cartilage during mouse embryogenesis

      DEVELOPMENTAL DYNAMICS
    60. Tucker, KE; Massello, LK; Gao, LM; Barber, TJ; Hebert, MD; Chan, EKL; Matera, AG
      Structure and characterization of the murine p80 coilin gene, Coil

      JOURNAL OF STRUCTURAL BIOLOGY
    61. Lin, SF; Lin, PM; Liu, TC; Chang, JG; Sue, YC; Chen, TP
      Clinical implications of aberrant TSG101 transcripts in acute myeloblasticleukemia

      LEUKEMIA & LYMPHOMA
    62. Adelaide, J; Chaffanet, M; Mozziconacci, MJ; Popovici, C; Conte, N; Fernandez, F; Sobol, H; Jacquemier, J; Pebusque, MJ; Ron, D; Lafage-Pochitaloff, M; Birnbaum, D
      Translocation and coamplification of loci from chromosome arms 8p and 11q in the MDA-MB-175 mammary carcinoma cell line

      INTERNATIONAL JOURNAL OF ONCOLOGY
    63. Dobson-Stone, C; Cox, RD; Lonie, L; Southam, L; Fraser, M; Wise, C; Bernier, F; Hodgson, S; Porter, DE; Simpson, AHRW; Monaco, AP
      Comparison of fluorescent single-strand conformation polymorphism analysisand denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses

      EUROPEAN JOURNAL OF HUMAN GENETICS
    64. Millar, JK; Wilson-Annan, JC; Anderson, S; Christie, S; Taylor, MS; Semple, CAM; Devon, RS; St Clair, DM; Muir, WJ; Blackwood, DHR; Porteous, DJ
      Disruption of two novel genes by a translocation co-segregating with schizophrenia

      HUMAN MOLECULAR GENETICS
    65. Blagitko, N; Mergenthaler, S; Schulz, U; Wollmann, HA; Craigen, W; Eggermann, T; Ropers, HH; Kalscheuer, VM
      Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion

      HUMAN MOLECULAR GENETICS
    66. Salih, MAM; Maisonobe, T; Kabiraj, M; Al Rayess, M; Al-Turaiki, MHS; Akbar, M; Tahan, A; Urtizberea, JA; Grid, D; Hamadouche, T; Guilbot, A; Brice, A; Leguern, E
      Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

      NEUROMUSCULAR DISORDERS
    67. Fonseca, F; Nunes, JFM; Soares, J
      Expression of CD44 isoforms in normal salivary gland tissue: an immunohistochemical and ultrastructural study

      HISTOCHEMISTRY AND CELL BIOLOGY
    68. Meyer, MF; Gerresheim, F; Pfeiffer, A; Epplen, JT; Schatz, H
      Association of polycystic ovary syndrome with an interstitial deletion of the long arm of chromosome 11 [del(11)(q21q23.1)]

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    69. Namihira, H; Sato, M; Miyauchi, A; Ohye, H; Matsubara, S; Bhuiyan, MMR; Murao, K; Ameno, S; Ameno, K; Ijiri, I; Takahara, J
      Different phenotypes of multiple endocrine neoplasia type 1 (MEN1) in monozygotic twins found in a Japanese MEN1 family with MEN1 gene mutation

      ENDOCRINE JOURNAL
    70. Zhang, WX; Yang, SY
      Cloning and characterization of a new member of the T-box gene family

      GENOMICS
    71. Pershouse, M; Li, JW; Yang, C; Su, H; Brundage, E; Di, WM; Biggs, PJ; Bradley, A; Chinault, AC
      BAC contig from a 3-cM region of mouse chromosome 11 surrounding BRCA1

      GENOMICS
    72. Squire, JA; Li, M; Perlikowski, S; Fei, YL; Bayani, J; Zhang, ZM; Weksberg, R
      Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome

      GENOMICS
    73. Wagenaar, M; Schuknecht, H; Nadol, J; Benraad-van Rens, M; Pieke-Dahl, S; Kimberling, W; Cremers, C
      Histopathologic features of the temporal bone in Usher syndrome type I

      ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
    74. Morelli, A; Falchetti, A; Martineti, V; Becherini, L; Mark, W; Friedman, E; Brandi, ML
      MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    75. Honda, M; Tsukada, T; Tanaka, H; Maruyama, K; Yamaguchi, K; Obara, T; Yamaji, T; Ishibashi, M
      A novel mutation of the MEN1 gene in a Japanese kindred with familial isolated primary hyperparathyroidism

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    76. Capello, D; Gaidano, G
      Molecular pathophysiology of indolent lymphoma

      HAEMATOLOGICA
    77. Baba, Y; Tsukuda, M; Kagata, H; Kato, Y; Nakatani, Y; Ehara, M; Nagashima, Y; Taki, A; Aoki, I
      Nasal natural killer/T cell lymphoma: Case report with molecular biologic examination on Epstein-Barr virus and cell cycle regulatory p16, cyclin D1,Rb, and p53 genes

      JOURNAL OF OTOLARYNGOLOGY
    78. Krasner, A; Wallace, L; Thiagalingam, A; Jones, C; Lengauer, C; Minahan, L; Ma, YK; Kalikin, L; Feinberg, AP; Jabs, EW; Tunnacliffe, A; Baylin, SB; Ball, DW; Nelkin, BD
      Cloning and chromosomal localization of the human BARX2 homeobox protein gene

      GENE
    79. Mullen, AJ; Barton, PJR
      Structural characterization of the human fast skeletal muscle troponin I gene (TNNI2)

      GENE
    80. Soukharev, S; Berlin, W; Hanover, JA; Bethke, B; Sauer, B
      Organization of the mouse ASGR1 gene encoding the major subunit of the hepatic asialoglycoprotein receptor

      GENE
    81. Friederich, P; Putensen, C; Stuber, F
      Prothrombin gene G20210A mutation and elevated anticardiolipin antibodies in a patient with combined portal-mesenteric vein thrombosis

      INTENSIVE CARE MEDICINE
    82. Iida, A; Emi, M; Matsuoka, R; Hiratsuka, E; Okui, K; Ohashi, H; Inazawa, J; Fukushima, Y; Imai, T; Nakamura, Y
      Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient withleft-right axis malformation

      HUMAN GENETICS
    83. Juan, V; Crain, C; Wilson, C
      Evidence for evolutionarily conserved secondary structure in the H19 tumorsuppressor RNA

      NUCLEIC ACIDS RESEARCH
    84. Kivioja, A; Ervasti, H; Kinnunen, J; Kaitila, I; Wolf, M; Bohling, T
      Chondrosarcoma in a family with multiple hereditary exostoses

      JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME
    85. Chang, TJ; Lei, HH; Yeh, JI; Chiu, KC; Lee, KC; Chen, MC; Tai, TY; Chuang, LM
      Vitamin D receptor gene polymorphisms influence susceptibility to type 1 diabetes mellitus in the Taiwanese population

      CLINICAL ENDOCRINOLOGY
    86. Segers, K; Vaiman, D; Berghmans, S; Shay, T; Meyers, S; Beever, J; Cockett, N; Georges, M; Charlier, C
      Construction and characterization of an ovine BAC contig spanning the callipyge locus

      ANIMAL GENETICS
    87. Leonard, AE; Kelder, B; Bobik, EG; Chuang, LT; Parker-Barnes, JM; Thurmond, JM; Kroeger, PE; Kopchick, JJ; Huang, YS; Mukerji, P
      CDNA cloning and characterization of human Delta(5)-desaturase involved inthe biosynthesis of arachidonic acid

      BIOCHEMICAL JOURNAL
    88. Bodey, B; Bodey, B; Siegel, SE; Kaiser, HE
      Immunocytochemical detection of the homeobox B3, B4, and C6 gene products in breast carcinomas

      ANTICANCER RESEARCH
    89. Fleishman, EV; Sokova, OI; Kirichenko, OP; Konstantinova, LN; Popa, AV; Volkova, MA
      Chromosome translocation t(10;11) in acute nonlymphoblastic leukemia.

      GEMATOLOGIYA I TRANSFUZIOLOGIYA
    90. Yoshikawa, T; Seki, N; Azuma, T; Masuho, Y; Muramatsu, M; Miyajima, N; Saito, T
      Isolation of a cDNA for a novel human RING finger protein gene, RNF18, by the virtual transcribed sequence (VTS) approach

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    91. Steinberg, R; Freud, E; Zer, M; Ziperman, I; Goshen, Y; Ash, S; Stein, J; Zaizov, R; Avigad, S
      High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumor

      CANCER GENETICS AND CYTOGENETICS
    92. Rissanen, J; Mykkanen, L; Markkanen, A; Kuusisto, J; Karkkainen, P; Karhapaa, P; Pihlajamaki, J; Niskanen, L; Kekalainen, P; Laakso, M
      Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin

      DIABETES CARE
    93. Rubin, BP; Pins, MR; Nielsen, GP; Rosen, S; Hsi, BL; Fletcher, JA; Renshaw, AA
      Isochromosome 7q in adult Wilms' tumors: Diagnostic and pathogenetic implications

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    94. Stern, MC; Benavides, F; Klingelberger, EA; Conti, CJ
      Allelotype analysis of chemically induced squamous cell carcinomas in F-1 hybrids of two inbred mouse strains with different susceptibility to tumor progression

      CARCINOGENESIS
    95. Buryanov, YI; Shevchuk, TV; Zakharchenko, NS; D'yachenko, OV; Marinich, DV; Vorob'ev, IA
      The lack of the CpNpG methylation at the 5 '-terminal region of the human calcitonin gene in norm and leukemias

      BIOORGANICHESKAYA KHIMIYA
    96. Bovee, JVMG; van Roggen, JFG; Cleton-Jansen, AM; Taminiau, AHM; van der Woude, HJ; Hogendoorn, PCW
      Malignant progression in multiple enchondromatosis (Ollier's disease): An autopsy-based molecular genetic study

      HUMAN PATHOLOGY
    97. Korobko, IV; Korobko, EV; Kiselev, SL
      The MAK-V protein kinase regulates endocytosis in mouse

      MOLECULAR AND GENERAL GENETICS
    98. Lucarelli, P; Gloria-Bottini, F; Antonacci, E; Borgiani, P; Palmarino, R; Bottini, E
      A study of human growth hormone and insulin gene regions in relation to metabolic control of non-insulin-dependent diabetes mellitus

      METABOLISM-CLINICAL AND EXPERIMENTAL
    99. Schulz, S; Becker, KF; Braungart, E; Reichmuth, C; Klamt, B; Becker, I; Atkinson, M; Gessler, M; Hofler, H
      Molecular analysis of E-cadherin and cadherin-II in Wilms' tumours

      JOURNAL OF PATHOLOGY
    100. Richard, P; Charron, P; Leclercq, C; Ledeuil, C; Carrier, L; Dubourg, O; Desnos, M; Bouhour, JB; Schwartz, K; Daubert, JC; Komajda, M; Hainque, B
      Homozygotes for a R869G mutation in the beta-myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy

      JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY


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Documento generato il 14/08/20 alle ore 11:02:16