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    1. McElreavey, K; Cortes, LS
      X-Y translocations and sex differentiation

      SEMINARS IN REPRODUCTIVE MEDICINE
    2. Skotheim, RI; Kraggerud, SM; Fossa, SD; Stenwig, AE; Gedde-Dahl, T; Danielsen, HE; Jakobsen, KS; Lothe, RA
      Familial/bilateral and sporadic testicular germ cell tumors show frequent genetic changes at loci with suggestive linkage evidence

      NEOPLASIA
    3. Olney, HJ; Le Beau, MM
      The cytogenetics of myelodysplastic syndromes

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    4. Kato, H; Komori, S; Nakata, Y; Sakata, K; Kanazawa, R; Kanda, M; Kobayashi, S; Koyama, K; Isojima, S
      Screening for deletions in interval D16-22 of the Y chromosome in azoospermic and oligozoospermic Japanese men

      JOURNAL OF HUMAN GENETICS
    5. Giver, CR; Wong, R; Moore, DH; Pallavicini, MG
      Persistence of aneuploid immature/primitive hemopoietic sub-populations inmice 8 months after benzene exposure in vivo

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    6. Trautner, MC; Sharief, N
      Pleural effusion in Noonan syndrome

      PRENATAL AND NEONATAL MEDICINE
    7. Imai, FL; Uzawa, K; Miyakawa, A; Shiiba, M; Tanzawa, H
      A detailed deletion map of chromosome 20 in human oral squamous cell carcinoma

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    8. Kawaguchi, TK; Skaletsky, H; Brown, LG; Minx, PJ; Cordum, HS; Waterston, RH; Wilson, RK; Silber, S; Oates, R; Rozen, S; Page, DC
      The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men

      NATURE GENETICS
    9. Zenklusen, JC; Conti, CJ; Green, ED
      Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31

      NATURE GENETICS
    10. Bor, P; Hindkjaer, J; Ingerslev, HJ; Kolvraa, S
      Multiplex PCR for screening of microdeletions on the Y chromosome

      JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
    11. Thiene, G; Basso, C
      Arrhythmogenic right ventricular cardiomyopathy: An update

      CARDIOVASCULAR PATHOLOGY
    12. Heidet, L; Arrondel, C; Forestier, L; Cohen-Solal, L; Mollet, G; Gutierrez, B; Stavrou, C; Gubler, MC; Antignac, C
      Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    13. Vieira, SAD; Deininger, MWN; Sorour, A; Sinclair, P; Foroni, L; Goldman, JM; Melo, JV
      Transcription factor BACH2 is transcriptionally regulated by the BCR/ABL oncogene

      GENES CHROMOSOMES & CANCER
    14. Goodarzi, G; Mashimo, T; Watabe, M; Cuthbert, AP; Newbold, RF; Pai, SK; Hirota, S; Hosobe, S; Miura, K; Bandyopadhyay, S; Gross, SC; Balaji, KC; Watabe, K
      Identification of tumor metastasis suppressor region on the short arm of human chromosome 20

      GENES CHROMOSOMES & CANCER
    15. Wu, MS; Chang, MC; Huang, SP; Tseng, CC; Sheu, JC; Lin, YW; Shun, CT; Lin, MT; Lin, JT
      Correlation of histologic subtypes and replication error phenotype with comparative genomic hybridization in gastric cancer

      GENES CHROMOSOMES & CANCER
    16. Lukusa, T; Willekens, D; Lukusa, N; De Cock, P; Fryns, JP
      Terminal 6q25.3 deletion and abnormal behaviour

      GENETIC COUNSELING
    17. Bartsch, C; Aslan, M; Kohler, J; Miny, P; Horst, J; Holzgreve, W; Rehder, H; Fritz, B
      Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): Further delineation of trisomies 1q

      FETAL DIAGNOSIS AND THERAPY
    18. Tiso, N; Stephan, DA; Nava, A; Bagattin, A; Devaney, JM; Stanchi, F; Larderet, G; Brahmbhatt, B; Brown, K; Bauce, B; Muriago, M; Basso, C; Thiene, G; Danieli, GA; Rampazzo, A
      Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

      HUMAN MOLECULAR GENETICS
    19. Oriola, J; Halperin, I; Mallofre, C; Muntane, J; Angel, M; Rivera-Fillat, F
      Screening of selected genomic areas potentially involved in thyroid neoplasms

      EUROPEAN JOURNAL OF CANCER
    20. Acquati, F; Morelli, C; Cinquetti, R; Bianchi, MG; Porrini, D; Varesco, L; Gismondi, V; Rocchetti, R; Talevi, S; Possati, L; Magnanini, C; Tibiletti, MG; Bernasconi, B; Daidone, MG; Shridhar, V; Smith, DI; Negrini, M; Barbanti-Brodano, G; Taramelli, R
      Cloning and characterization of a senescence inducing and class II tumor suppressor gene in ovarian carcinoma at chromosome region 6q27

      ONCOGENE
    21. Liu, JM; Yuan, Y; Huan, J; Shen, ZY
      Inhibition of breast and brain cancer cell growth by BCCIP alpha, an evolutionarily conserved nuclear protein that interacts with BRCA2

      ONCOGENE
    22. Tobias, ES; Hurlstone, AFL; MacKenzie, E; McFarlane, R; Black, DM
      The TES gene at 7q31,1 is methylated in tumours and encodes a novel growth-suppressing LIM domain protein

      ONCOGENE
    23. Chalhoub, N; Benachenhou, N; Vacher, J
      Physical and transcriptional map of the mouse Chromosome 10 proximal region syntenic to human 6q16-q21

      MAMMALIAN GENOME
    24. Kong, G; Oga, A; Park, CK; Kawauchi, S; Furuya, T; Sasaki, K
      DNA sequence copy number aberrations associated with histological subtypesand DNA ploidy in gastric carcinoma

      JAPANESE JOURNAL OF CANCER RESEARCH
    25. Giver, CR; Wong, R; Moore, DH; Pallavicini, MG
      Dermal benzene and trichloroethylene induce aneuploidy in immature hematopoietic subpopulations in vivo

      ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
    26. Kratz, CP; Emerling, BM; Donovan, S; Laig-Webster, M; Taylor, BR; Thompson, P; Jensen, S; Banerjee, A; Bonifas, J; Makalowski, W; Green, ED; Le Beau, MM; Shannon, KM
      Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies

      GENOMICS
    27. Li, DX; Bachinski, LL; Roberts, R
      Genomic organization and isoform-specific tissue expression of human NAPOR(CUGBP2) as a candidate gene for familial arrhythmogenic right ventriculardysplasia

      GENOMICS
    28. Seiter, K; Feldman, EJ; Sreekantaiah, C; Pozzuoli, M; Weisberger, J; Liu, D; Papageorgio, C; Weiss, M; Kancherla, R; Ahmed, T
      Secondary acute myelogenous leukemia and myelodysplasia without abnormalities of chromosome 11q23 following treatment of acute leukemia with topoisomerase II-based chemotherapy

      LEUKEMIA
    29. McDonald, TA; Holland, NT; Skibola, C; Duramad, P; Smith, MT
      Hypothesis: Phenol and hydroquinone derived mainly from diet and gastrointestinal flora activity are causal factors in leukemia

      LEUKEMIA
    30. O'Sullivan, JM; Mihr, MJ; Santos, MAS; Tuite, MF
      Seryl-tRNA synthetase is not responsible for the evolution of CUG codon reassignment in Candida albicans

      YEAST
    31. Frohling, S; Nakabayashi, K; Scherer, SW; Dohner, H; Dohner, K
      Mutation analysis of the origin recognition complex subunit 5 (ORC5L) genein adult patients with myeloid leukemias exhibiting deletions of chromosome band 7q22

      HUMAN GENETICS
    32. Lin, HC; Morin, PJ
      A novel homozygous deletion at chromosomal band 6q27 in an ovarian cancer cell line delineates the position of a putative tumor suppressor gene

      CANCER LETTERS
    33. Fox, MS; Pera, RAR
      Male infertility, genetic analysis of the DAZ genes on the human Y chromosome and genetic analysis of DNA repair

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    34. Maurer, B; Gromoll, J; Simoni, M; Nieschlag, E
      Prevalence of Y chromosome microdeletions in infertile men who consulted atertiary care medical centre: the Munster experience

      ANDROLOGIA
    35. Goto, A; Aoki, M; Ichihara, S; Kitagawa, Y
      alpha- beta- or gamma-chain -specific RNA interference of laminin assemblyin Drosophila Kc167 cells

      BIOCHEMICAL JOURNAL
    36. Courtens, W; Vroman, S; Vandenhove, J; Wiedemann, U; Schinzel, A
      Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7)

      PRENATAL DIAGNOSIS
    37. Brown, LY; Alonso, ML; Yu, J; Warburton, D; Brown, S
      Prenatal diagnosis of a familial Xq deletion in a female fetus: a case report

      PRENATAL DIAGNOSIS
    38. 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
    39. Scholz, I; Popp, S; Granzow, M; Schoell, B; Holtgreve-Grez, H; Takeuchi, S; Schrappe, M; Harbott, J; Teigler-Schlegel, A; Zimmermann, M; Fischer, C; Koeffler, HP; Bartram, CR; Jauch, A
      Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis

      CANCER GENETICS AND CYTOGENETICS
    40. Foresta, C; Moro, E; Ferlin, A
      Y chromosome microdeletions and alterations of spermatogenesis

      ENDOCRINE REVIEWS
    41. Keeling, SL; Lee-Jones, L; Thompson, P
      Brief clinical report - Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    42. Walsh, LE; Vance, GH; Weaver, DD
      Distal 13q deletion syndrome and the VACTERL association: Case report, literature review, and possible implications

      AMERICAN JOURNAL OF MEDICAL GENETICS
    43. Pallotta, R; Dalpra, L; Miozzo, M; Ehresmann, T; Fusilli, P
      A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Emberger, W; Petek, E; Kroisel, PM; Zierler, H; Wagner, K
      Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. Kato, R; Kishibayashi, J; Shimokawa, O; Harada, N; Niikawa, N; Matsumoto, N
      Congenital glaucoma and silver-russell phenotype associated with partial trisomy 7q and monosomy 15q

      AMERICAN JOURNAL OF MEDICAL GENETICS
    46. Rapley, EA; Hargrave, D; Persinguhe, N; Barfoot, R; Moore, I; Radford, M; Stratton, MR; Rahman, N; Pritchard-Jones, K
      Case of interstitial 12q deletion in association with Wilms tumor

      AMERICAN JOURNAL OF MEDICAL GENETICS
    47. 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
    48. Houdayer, C; Portnoi, MF; Vialard, F; Soupre, V; Crumiere, C; Taillemite, JL; Couderc, R; Vazquez, JP; Bahuau, M
      Pierre Robin sequence and interstitial deletion 2q32.3-q33.2

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. 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
    50. Martin, DM; Gencyuz, CF; Petty, EM
      Systemic lupus erythematosus in a man with Noonan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Stankiewicz, P; Brozek, I; Helias-Rodzewicz, Z; Wierzba, J; Pilch, J; Bocian, E; Balcerska, A; Wozniak, A; Kardas, I; Wirth, J; Mazurczak, T; Limon, J
      Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. Stankiewicz, P; Helias-Rodzewicz, Z; Jakubow-Durska, K; Bocian, E; Obersztyn, E; Rappold, GA; Mazurczak, T
      Cytogenetic and molecular characterization of two isodicentric Y chromosomes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    53. Tzschach, A; Thamm, B; Imthurn, B; Weber, W; Alexander, H; Glander, HJ; Froster, U
      Absence of Yq microdeletions in infertile men

      ARCHIVES OF ANDROLOGY
    54. Osterlund, C; Stabi, B; Bhasin, S; Kvist, U; Pousette, A; Arver, S
      Specific localization of RBM1a in the nuclei of all cell types except elongated spermatids within seminiferous tubules of the human

      INTERNATIONAL JOURNAL OF ANDROLOGY
    55. Friel, A; Houghton, JA; Maher, M; Smith, T; Noel, S; Nolan, A; Egan, D; Glennon, M
      Molecular detection of Y chromosome microdeletions: an Irish study

      INTERNATIONAL JOURNAL OF ANDROLOGY
    56. Maymon, BBS; Elliott, DJ; Kleiman, SE; Yogev, L; Hauser, R; Botchan, A; Schreiber, L; Cooke, HJ; Paz, G; Yavetz, H
      The contribution of RNA-binding motif (RBM) antibody to the histopathologic evaluation of testicular biopsies from infertile men

      HUMAN PATHOLOGY
    57. Perron, H; Jouvin-Marche, E; Michel, M; Ounanian-Paraz, A; Camelo, S; Dumon, A; Jolivet-Reynaud, C; Marcel, F; Souillet, Y; Borel, E; Gebuhrer, L; Santoro, L; Marcel, S; Seigneurin, JM; Marche, PN; Lafon, M
      Multiple sclerosis retrovirus particles and recombinant envelope trigger an abnormal immune response in vitro, by inducing polyclonal V beta 16 T-lymphocyte activation

      VIROLOGY
    58. del Palacio, MJF; Bernal, LJ; Bayon, A; Bernabe, A; de Oca, RM; Seva, J
      Arrhythmogenic right ventricular dysplasia/cardiomyopathy in a Siberian husky

      JOURNAL OF SMALL ANIMAL PRACTICE
    59. Tonnies, H; Schulze, I; Hennies, HC; Neumann, LM; Keitzer, R; Neitzel, H
      De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes

      JOURNAL OF MEDICAL GENETICS
    60. Brennan, P; Croaker, GD; Heath, M
      Congenital diaphragmatic hernia and interstitial deletion of chromosome 3

      JOURNAL OF MEDICAL GENETICS
    61. Baker, KL; Rees, MI; Thompson, PW; Howell, RT; Cole, TR; Hughes, HE; Upadhyaya, M; Ravine, D
      Chromosome 2 interstitial deletion (del(2) (q14.1q21)) associated with connective tissue laxity and an attention deficit disorder

      JOURNAL OF MEDICAL GENETICS
    62. Haberlandt, E; Loffler, J; Hirst-Stadlmann, A; Stockl, B; Judmaier, W; Fischer, H; Heinz-Erian, P; Muller, T; Utermann, G; Smith, RJH; Janecke, AR
      Split hand/split foot malformation associated with sensorineural deafness,inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3

      JOURNAL OF MEDICAL GENETICS
    63. De Vries, BBA; Knight, SJL; Homfray, T; Smithson, SF; Flint, J; Winter, RM
      Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?

      JOURNAL OF MEDICAL GENETICS
    64. McEntagart, M; Carey, A; Breen, C; McQuaid, S; Stallings, RL; Green, AJ; King, MD
      Molecular characterisation of a proximal chromosome 18q deletion

      JOURNAL OF MEDICAL GENETICS
    65. Jaruzelska, J; Korcz, A; Wojda, A; Jedrzejczak, P; Bierla, J; Surmacz, T; Pawelczyk, L; Page, DC; Kotecki, M
      Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion

      JOURNAL OF MEDICAL GENETICS
    66. Varrault, A; Bilanges, B; Mackay, DJG; Basyuk, E; Ahr, B; Fernandez, C; Robinson, DO; Bockaert, J; Journot, L
      Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitus

      JOURNAL OF BIOLOGICAL CHEMISTRY
    67. Sekiguchi, K; Miya, Y; Kaneko, Y; Kanda, T; Fukumura, Y; Kotajima, N; Tamura, J; Kobayashi, I
      Evaluation of signal-averaged electrocardiography for clinical diagnosis in arrhythmogenic right ventricular dysplasia

      JAPANESE HEART JOURNAL
    68. Neville, PJ; Thomas, N; Campbell, IG
      Loss of heterozygosity at 7q22 and mutation analysis of the CDP gene in human epithelial ovarian tumors

      INTERNATIONAL JOURNAL OF CANCER
    69. Kleiman, SE; Lagziel, A; Yogev, L; Botchan, A; Paz, G; Yavetz, H
      Expression of CDY1 may identify complete spermatogenesis

      FERTILITY AND STERILITY
    70. Back, E; Toder, R; Fuchshuber, A
      De novo inverted duplication of chromosome 7(q21.3 -> q35): cytogenetic diagnosis confirmed by FISH analysis

      CLINICAL GENETICS
    71. Wenger, SL; Cutenese, C; Hummel, M
      Three-way unbalanced translocation in a mildly dysmorphic mentally retarded child

      CLINICAL GENETICS
    72. Tackels-Horne, D; Toburen, A; Sangiorgi, E; Gurrieri, F; de Mollerat, X; Fischetto, R; Causio, F; Clarkson, K; Stevenson, RE; Schwartz, CE
      Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21

      CLINICAL GENETICS
    73. Corrado, D; Basso, C; Thiene, G
      Sudden cardiac death in young people with apparently normal heart

      CARDIOVASCULAR RESEARCH
    74. Cleton-Jansen, AM; Callen, DF; Seshadri, R; Goldup, S; McCallum, B; Crawford, J; Powell, JA; Settasatian, C; van Beerendonk, H; Moerland, EW; Smit, VTBHM; Harris, WH; Millis, R; Morgan, NV; Barnes, D; Mathew, CG; Cornelisse, CJ
      Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions

      CANCER RESEARCH
    75. Satge, D; Monteil, P; Sasco, AJ; Vital, A; Ohgaki, H; Geneix, A; Malet, P; Vekemans, M; Rethore, MO
      Aspects of intracranial and spinal tumors in patients with Down syndrome and report of a rapidly progressing Grade 2 astrocytoma

      CANCER
    76. Todd, R; Bia, B; Johnson, E; Jones, C; Cotter, F
      Molecular characterization of a myelodysplasia-associated chromosome 7 inversion

      BRITISH JOURNAL OF HAEMATOLOGY
    77. Yamamoto, N; Uzawa, K; Yakushiji, T; Shibahara, T; Noma, H; Tanzawa, H
      Analysis of the ANA gene as a candidate for the chromosome 21q oval cancersusceptibility locus

      BRITISH JOURNAL OF CANCER
    78. Wiktor, A; Feldman, GL; Bawle, EV; Czarnecki, P; Conard, JV; Van Dyke, DL
      Deletion of 2q37 and duplication of 10q24: Two cases in the same family and review of the literature

      ANNALES DE GENETIQUE
    79. Birnbacher, R; Chudoba, I; Pirc-Danoewinata, H; Konig, M; Kohlhauser, C; Schnedl, W; Haas, OA
      Microdissection and reverse painting reveals a microdeletion 6(q26qter) ina de novo r(6) chromosome

      ANNALES DE GENETIQUE
    80. Kai, WC; Diatchenko, L; Agoulnik, A; Scharff, KM; Schober, H; Arlt, K; Zhumabayeva, B; Siebert, PD; Dietel, M; Schafer, R; Sers, C
      Caveolin-1 is down-regulated in human ovarian carcinoma and acts as a candidate tumor suppressor gene

      AMERICAN JOURNAL OF PATHOLOGY
    81. Kim, YH; Kim, NG; Lim, JG; Park, C; Kim, H
      Chromosomal alterations in paired gastric adenomas and carcinomas

      AMERICAN JOURNAL OF PATHOLOGY
    82. Raedle, JC; Friedl, W; Engels, H; Koenig, R; Trojan, J; Zeuzem, S
      A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardation

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    83. Volleth, M; Stumm, M; Mohnike, K; Kalscheuer, VM; Jakubiczka, S; Wieacker, P
      Preferential inactivation of a dupX(q23 -> q27-28) chromosome in a girl with mental retardation and dysmorphy

      HUMAN HEREDITY
    84. Irons, RD
      Molecular models of benzene leukemogenesis

      JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
    85. Smith, MT; Rothman, N
      Biomarkers in the molecular epidemiology of benzene-exposed workers

      JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
    86. Kent, M
      The Y chromosome and its role in testis differentiation and spermatogenesis

      SEMINARS IN REPRODUCTIVE MEDICINE
    87. Werner, H; Le Roith, D
      New concepts in regulation and function of the insulin-like growth factors: implications for understanding normal growth and neoplasia

      CELLULAR AND MOLECULAR LIFE SCIENCES
    88. Mendes-da-Silva, P; Moreira, A; Duro-da-Costa, J; Matias, D; Monteiro, C
      Frequent loss of heterozygosity on chromosome 5 in non-small cell lung carcinoma

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    89. Saut, N; Terriou, P; Navarro, A; Levy, N; Mitchell, MJ
      The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility

      MOLECULAR HUMAN REPRODUCTION
    90. Blagosklonova, O; Fellmann, F; Clavequin, MC; Roux, C; Bresson, JL
      AZFa deletions in Sertoli cell-only syndrome: a retrospective study

      MOLECULAR HUMAN REPRODUCTION
    91. Van Landuyt, L; Lissens, W; Stouffs, K; Tournaye, H; Liebaers, I; Van Steirteghem, A
      Validation of a simple Yq deletion screening programme in an ICSI candidate population

      MOLECULAR HUMAN REPRODUCTION
    92. Hauptschein, RS; Gaidano, G; Rao, PH; Scotto, L; Edwards, YH; Chaganti, RSK; Dalla-Favera, R
      An apparent interlocus gene conversion-like event at a putative tumor suppressor gene locus on human chromosome 6q27 in a Burkitt's lymphoma cell line

      DNA RESEARCH
    93. Woolley, PV; Gollin, SM; Riskalla, W; Finkelstein, S; Stefanik, DF; Riskalla, L; Swaney, WP; Weisenthal, L; McKenna, RJ
      Cytogenetics, immunostaining for fibroblast growth factors, p53 sequencing, and clinical features of two cases of cystosarcoma phyllodes

      MOLECULAR DIAGNOSIS
    94. Christiano, AP; Yoshida, BA; Dubauskas, Z; Sokoloff, M; Rinker-Schaeffer, CW
      Development of markers of prostate cancer metastasis - Review and perspective

      UROLOGIC ONCOLOGY
    95. Ghosh, S; Stack, MS
      Proteolytic modification of laminins: Functional consequences

      MICROSCOPY RESEARCH AND TECHNIQUE
    96. Koul, A; Malander, S; Loman, N; Pejovic, T; Heim, S; Willen, R; Johannson, O; Olsson, H; Ridderheim, M; Borg, A
      BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
    97. Corrado, D; Fontaine, G; Marcus, FI; McKenna, WJ; Nava, A; Thiene, G; Wichter, T
      Arrhythmogenic right ventricular dysplasia/cardiomyopathy: Need for an international registry (Reprinted from Circulation Online, March 21, pg E101, 2000)

      JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
    98. Srivatsan, ES; Bengtsson, U; Manickam, P; Benyamini, P; Chandrasekharappa, SC; Sun, C; Stanbridge, EJ; Redpath, JL
      Interstitial deletion of 11q13 sequences in HeLa cells

      GENES CHROMOSOMES & CANCER
    99. Mashimo, T; Goodarzi, G; Watabe, M; Cuthbert, AP; Newbold, RF; Pai, SK; Hirota, S; Hosobe, S; Miura, K; Bandyopadhyay, S; Gross, SC; Watabe, K
      Localization of a novel tumor metastasis suppressor region on the short arm of human chromosome 2

      GENES CHROMOSOMES & CANCER
    100. Gao, Q; Horwitz, M; Roulston, D; Hagos, F; Zhao, ND; Freireich, EJ; Golomb, HM; Olopade, OI
      Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q

      GENES CHROMOSOMES & CANCER


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/08/20 alle ore 15:08:54