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1. Viswanathan, M; Tsuchida, N; Shanmugam, G
   Selective deletion of p14(ARF) exon 1 beta of the INK4a locus in oral squamous cell carcinomas of Indians
   ORAL ONCOLOGY
   
   M. Viswanathan et al., "Selective deletion of p14(ARF) exon 1 beta of the INK4a locus in oral squamous cell carcinomas of Indians", ORAL ONCOL, 37(4), 2001, pp. 341-344
2. Mellick, GD; Buchanan, DD; Hattori, N; Brookes, AJ; Mizuno, Y; Le Couteur, DG; Silburn, PA
   The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls
   PARKINSONISM & RELATED DISORDERS
   
   G.D. Mellick et al., "The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls", PARKINS R D, 7(2), 2001, pp. 89-91
3. Bleichert, A; Fiedler, W; Claussen, U; Ernst, G; Loncarevic, IF; Heller, A; Liehr, T; Kunert, C; Von Eggeling, F
   A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients
   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
   
   A. Bleichert et al., "A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients", INT J MOL M, 7(6), 2001, pp. 591-595
4. Momoi, H; Okabe, H; Kamikawa, T; Satoh, S; Ikai, I; Yamamoto, M; Nakagawara, A; Shimahara, Y; Yamaoka, Y; Fukumoto, M
   Comprehensive allelotyping of human intrahepatic cholangiocarcinoma
   CLINICAL CANCER RESEARCH
   
   H. Momoi et al., "Comprehensive allelotyping of human intrahepatic cholangiocarcinoma", CLIN CANC R, 7(9), 2001, pp. 2648-2655
5. Gollin, SM
   Chromosomal alterations in squamous cell carcinomas of the head and neck: Window to the biology of disease
   HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
   
   S.M. Gollin, "Chromosomal alterations in squamous cell carcinomas of the head and neck: Window to the biology of disease", HEAD NECK, 23(3), 2001, pp. 238-253
6. Hedrich, K; Kann, M; Lanthaler, AJ; Dalski, A; Eskelson, C; Landt, F; Schwinger, E; Vieregge, P; Lang, AE; Breakefield, XO; Ozelius, LJ; Pramstaller, PP; Klein, C
   The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism
   HUMAN MOLECULAR GENETICS
   
   K. Hedrich et al., "The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism", HUM MOL GEN, 10(16), 2001, pp. 1649-1656
7. 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
   
   R. Dammann et al., "The CpG island of the novel tumor suppressor gene RASSF1A is intensely methylated in primary small cell lung carcinomas", ONCOGENE, 20(27), 2001, pp. 3563-3567
8. Omran, H; Haffner, KN; Burth, S; Ala-Mello, S; Antignac, C; Hildebrandt, F
   Evidence for further genetic heterogeneity in nephronophthisis
   NEPHROLOGY DIALYSIS TRANSPLANTATION
   
   H. Omran et al., "Evidence for further genetic heterogeneity in nephronophthisis", NEPH DIAL T, 16(4), 2001, pp. 755-758
9. Hildebrandt, F; Omram, H
   New insights: nephronophthisis-medullary cystic kidney disease
   PEDIATRIC NEPHROLOGY
   
   F. Hildebrandt e H. Omram, "New insights: nephronophthisis-medullary cystic kidney disease", PED NEPHROL, 16(2), 2001, pp. 168-176
10. Poi, MJ; Yen, T; Li, J; Song, HJ; Lang, JC; Schuller, DE; Pearl, DK; Casto, BC; Tsai, MD; Weghorst, CM
    Somatic INK4a-ARF locus mutations: A significant mechanism of gene inactivation in squamous cell carcinomas of the head and neck
    MOLECULAR CARCINOGENESIS
    
    M.J. Poi et al., "Somatic INK4a-ARF locus mutations: A significant mechanism of gene inactivation in squamous cell carcinomas of the head and neck", MOL CARCINO, 30(1), 2001, pp. 26-36
11. Sun, PC; Uppaluri, R; Schmidt, AP; Pashia, ME; Quant, EC; Sunwoo, JB; Gollin, SM; Scholnick, SB
    Transcript map of the 8p23 putative tumor suppressor region
    GENOMICS
    
    P.C. Sun et al., "Transcript map of the 8p23 putative tumor suppressor region", GENOMICS, 75(1-3), 2001, pp. 17-25
12. Yanaihara, N; Kohno, T; Takakura, S; Takei, K; Otsuka, A; Sunaga, N; Takahashi, M; Yamazaki, M; Tashiro, H; Fukuzumi, Y; Fujimori, Y; Hagiwara, K; Tanaka, T; Yokota, J
    Physical and transcriptional map of a 311-kb segment of chromosome 18q21, a candidate lung tumor suppressor locus
    GENOMICS
    
    N. Yanaihara et al., "Physical and transcriptional map of a 311-kb segment of chromosome 18q21, a candidate lung tumor suppressor locus", GENOMICS, 72(2), 2001, pp. 169-179
13. Soenen, V; Lepelley, P; Gyan, E; Preudhomme, C; Lai, JL; Bauters, F; Fenaux, P; Quesnel, B
    Prognostic significance of p16(INK4a) immunocytochemistry in adult ALL with standard risk karyotype
    LEUKEMIA
    
    V. Soenen et al., "Prognostic significance of p16(INK4a) immunocytochemistry in adult ALL with standard risk karyotype", LEUKEMIA, 15(7), 2001, pp. 1054-1059
14. 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
    
    H. Cave et al., "Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia", LEUKEMIA, 15(3), 2001, pp. 371-376
15. Lu, CS; Wu, JC; Tsai, CH; Chen, RS; Chou, YHW; Hattori, N; Yoshino, H; Mizuno, Y
    Clinical and genetic studies on familial parkinsonism: The first report ona parkin gene mutation in a Taiwanese family
    MOVEMENT DISORDERS
    
    C.S. Lu et al., "Clinical and genetic studies on familial parkinsonism: The first report ona parkin gene mutation in a Taiwanese family", MOVEMENT D, 16(1), 2001, pp. 164-166
16. Corti, O; Brice, A
    Parkin and Parkinson's: More than homonymy?
    ANNALS OF NEUROLOGY
    
    O. Corti e A. Brice, "Parkin and Parkinson's: More than homonymy?", ANN NEUROL, 50(3), 2001, pp. 283-285
17. Richards, RI
    Fragile and unstable chromosomes in cancer: causes and consequences
    TRENDS IN GENETICS
    
    R.I. Richards, "Fragile and unstable chromosomes in cancer: causes and consequences", TRENDS GEN, 17(6), 2001, pp. 339-345
18. Gursky, S; Olopade, OI; Rowley, JD
    Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types
    CANCER GENETICS AND CYTOGENETICS
    
    S. Gursky et al., "Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types", CANC GENET, 129(2), 2001, pp. 93-101
19. Hildebrandt, F; Rensing, C; Betz, RC; Sommer, U; Birnbaum, S; Imm, A; Omran, H; Leipoldt, M; Otto, E
    Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis
    KIDNEY INTERNATIONAL
    
    F. Hildebrandt et al., "Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis", KIDNEY INT, 59(2), 2001, pp. 434-445
20. Lucking, CB; Bonifati, V; Periquet, M; Vanacore, N; Brice, A; Meco, G
    Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations
    NEUROLOGY
    
    C.B. Lucking et al., "Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations", NEUROLOGY, 57(5), 2001, pp. 924-927
21. Terreni, L; Calabrese, E; Calella, AM; Forloni, G; Mariani, C
    New mutation (RA2P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism
    NEUROLOGY
    
    L. Terreni et al., "New mutation (RA2P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism", NEUROLOGY, 56(4), 2001, pp. 463-466
22. Grady, B; Goharderakhshan, R; Chang, J; Ribeiro, LA; Perinchery, G; Franks, J; Presti, J; Carroll, P; Dahiya, R
    Frequently deleted loci on chromosome 9 may harbor several tumor suppressor genes in human renal cell carcinoma
    JOURNAL OF UROLOGY
    
    B. Grady et al., "Frequently deleted loci on chromosome 9 may harbor several tumor suppressor genes in human renal cell carcinoma", J UROL, 166(3), 2001, pp. 1088-1092
23. Gruttgen, A; Reichenzeller, M; Junger, M; Schlien, S; Affolter, A; Bosch, FX
    Detailed gene expression analysis but not microsatellite marker analysis of 9p21 reveals differential defects in the INK4a gene locus in the majorityof head and neck cancers
    JOURNAL OF PATHOLOGY
    
    A. Gruttgen et al., "Detailed gene expression analysis but not microsatellite marker analysis of 9p21 reveals differential defects in the INK4a gene locus in the majorityof head and neck cancers", J PATHOLOGY, 194(3), 2001, pp. 311-317
24. Bonifati, V; Lucking, CB; Fabrizio, E; Periquet, M; Meco, G; Brice, A
    Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    
    V. Bonifati et al., "Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism", J NE NE PSY, 71(4), 2001, pp. 531-534
25. Kubo, S; Kitami, T; Noda, S; Shimura, H; Uchiyama, Y; Asakawa, S; Minoshima, S; Shimizu, N; Mizuno, Y; Hattori, N
    Parkin is associated with cellular vesicles
    JOURNAL OF NEUROCHEMISTRY
    
    S. Kubo et al., "Parkin is associated with cellular vesicles", J NEUROCHEM, 78(1), 2001, pp. 42-54
26. Ausserlechner, MJ; Obexer, P; Wiegers, GJ; Hartmann, BL; Geley, S; Kofler, R
    The cell cycle inhibitor p16(INK4A) sensitizes lymphoblastic leukemia cells to apoptosis by physiologic glucocorticoid levels (vol 276, pg 10984, 2001)
    JOURNAL OF BIOLOGICAL CHEMISTRY
    
    M.J. Ausserlechner et al., "The cell cycle inhibitor p16(INK4A) sensitizes lymphoblastic leukemia cells to apoptosis by physiologic glucocorticoid levels (vol 276, pg 10984, 2001)", J BIOL CHEM, 276(24), 2001, pp. 21990
27. Ausserlechner, MJ; Obexer, P; Wiegers, GJ; Hartmann, BL; Geley, S; Kofler, R
    The cell cycle inhibitor p16(INK4A) sensitizes lymphoblastic leukemia cells to apoptosis by physiologic glucocorticoid levels
    JOURNAL OF BIOLOGICAL CHEMISTRY
    
    M.J. Ausserlechner et al., "The cell cycle inhibitor p16(INK4A) sensitizes lymphoblastic leukemia cells to apoptosis by physiologic glucocorticoid levels", J BIOL CHEM, 276(14), 2001, pp. 10984-10989
28. Klaes, R; Friedrich, T; Spitkovsky, D; Ridder, R; Rudy, W; Petry, U; Dallenbach-Hellweg, G; Schmidt, D; Doeberitz, MV
    Overexpression of p16(ink4a) as a specific marker for dysplastic and neoplastic epithelial cells of the cervix uteri
    INTERNATIONAL JOURNAL OF CANCER
    
    R. Klaes et al., "Overexpression of p16(ink4a) as a specific marker for dysplastic and neoplastic epithelial cells of the cervix uteri", INT J CANC, 92(2), 2001, pp. 276-284
29. Pollock, PM; Welch, J; Hayward, NK
    Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development
    CANCER RESEARCH
    
    P.M. Pollock et al., "Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development", CANCER RES, 61(3), 2001, pp. 1154-1161
30. Wong, DJ; Paulson, TG; Prevo, LJ; Galipeau, PC; Longton, G; Blount, PL; Reid, BJ
    p16(INK4a) lesions are common, early abnormalities that undergo clonal expansion in Barrett's metaplastic epithelium
    CANCER RESEARCH
    
    D.J. Wong et al., "p16(INK4a) lesions are common, early abnormalities that undergo clonal expansion in Barrett's metaplastic epithelium", CANCER RES, 61(22), 2001, pp. 8284-8289
31. Chim, CS; Tam, CYY; Liang, R; Kwong, YL
    Methylation of p15 and p16 genes in adult acute leukemia - Lack of prognostic significance
    CANCER
    
    C.S. Chim et al., "Methylation of p15 and p16 genes in adult acute leukemia - Lack of prognostic significance", CANCER, 91(12), 2001, pp. 2222-2229
32. Ramakers-van Woerden, NL; Pieters, R; Slater, RM; Loonen, AH; Beverloo, HB; van Drunen, E; Heyman, M; Moreno, TC; Rots, MG; van Wering, ER; Kamps, WA; Janka-Schaub, GE; Veerman, AJP
    In vitro drug resistance and prognostic impact of p16(INK4A)/p15(INK4B) deletions in childhood T-cell acute lymphoblastic leukaemia
    BRITISH JOURNAL OF HAEMATOLOGY
    
    N.L. Ramakers-van Woerden et al., "In vitro drug resistance and prognostic impact of p16(INK4A)/p15(INK4B) deletions in childhood T-cell acute lymphoblastic leukaemia", BR J HAEM, 112(3), 2001, pp. 680-690
33. Dai, CH; Krantz, SB
    Inn-eased expression of the INK4a/ARF locus in polycythemia vera
    BLOOD
    
    C.H. Dai e S.B. Krantz, "Inn-eased expression of the INK4a/ARF locus in polycythemia vera", BLOOD, 97(11), 2001, pp. 3424-3432
34. Lee, SH; Kim, WH; Kim, HK; Woo, KM; Nam, HS; Kim, HS; Kim, JG; Cho, MH
    Altered expression of the fragile histidine triad gene in primary gastric adenocarcinomas
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    
    S.H. Lee et al., "Altered expression of the fragile histidine triad gene in primary gastric adenocarcinomas", BIOC BIOP R, 284(3), 2001, pp. 850-855
35. Bostrom, J; Meyer-Puttlitz, B; Wolter, M; Blaschke, B; Weber, RG; Lichter, P; Ichimura, K; Collins, VP; Reifenberger, G
    Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas
    AMERICAN JOURNAL OF PATHOLOGY
    
    J. Bostrom et al., "Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas", AM J PATH, 159(2), 2001, pp. 661-669
36. Nakayama, T; Taback, B; Turner, R; Morton, DL; Hoon, DSB
    Molecular clonality of in-transit melanoma metastasis
    AMERICAN JOURNAL OF PATHOLOGY
    
    T. Nakayama et al., "Molecular clonality of in-transit melanoma metastasis", AM J PATH, 158(4), 2001, pp. 1371-1378
37. Schraml, P; Struckmann, K; Bednar, R; Fu, WT; Gasser, T; Wilber, K; Kononen, J; Sauter, G; Mihatsch, MJ; Moch, H
    CDKN2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas - Evidence for a second tumor suppressor gene proximal to CDKN2A
    AMERICAN JOURNAL OF PATHOLOGY
    
    P. Schraml et al., "CDKN2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas - Evidence for a second tumor suppressor gene proximal to CDKN2A", AM J PATH, 158(2), 2001, pp. 593-601
38. Periquet, M; Lucking, CB; Vaughan, JR; Bonifati, V; Durr, A; De Michele, G; Horstink, MW; Farrer, M; Illarioshkin, SN; Pollak, P; Borg, M; Brefel-Courbon, C; Denefle, P; Meco, G; Gasser, T; Breteler, MMB; Wood, NW; Agid, Y; Brice, A
    Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects
    AMERICAN JOURNAL OF HUMAN GENETICS
    
    M. Periquet et al., "Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects", AM J HU GEN, 68(3), 2001, pp. 617-626
39. Pateromichelakis, S; Lee, G; Langdon, JD; Partridge, M
    The FHIT gene in oral squamous cell carcinoma: allelic imbalance is frequent but cDNA aberrations are uncommon
    ORAL ONCOLOGY
    
    S. Pateromichelakis et al., "The FHIT gene in oral squamous cell carcinoma: allelic imbalance is frequent but cDNA aberrations are uncommon", ORAL ONCOL, 36(2), 2000, pp. 180-188
40. Chung, MY; Wu, JC; Chau, GY; Lui, WY; Tsay, SH; Chiang, H
    Preferentially deleted chromosome region 9p21 in large hepatocellular carcinomas
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    
    M.Y. Chung et al., "Preferentially deleted chromosome region 9p21 in large hepatocellular carcinomas", INT J MOL M, 5(5), 2000, pp. 521-524
41. Cachia, AR; Indsto, JO; McLaren, KM; Mann, GJ; Arends, MJ
    CDKN2A mutation and deletion status in thin and thick primary melanoma
    CLINICAL CANCER RESEARCH
    
    A.R. Cachia et al., "CDKN2A mutation and deletion status in thin and thick primary melanoma", CLIN CANC R, 6(9), 2000, pp. 3511-3515
42. Hui, R; Macmillan, RD; Kenny, FS; Musgrove, EA; Blamey, RW; Nicholson, RI; Robertson, JFR; Sutherland, RL
    INK4a gene expression and methylation in primary breast cancer: Overexpression of p16(INK4a) messenger RNA is a marker of poor prognosis
    CLINICAL CANCER RESEARCH
    
    R. Hui et al., "INK4a gene expression and methylation in primary breast cancer: Overexpression of p16(INK4a) messenger RNA is a marker of poor prognosis", CLIN CANC R, 6(7), 2000, pp. 2777-2787
43. Omura-Minamisawa, M; Diccianni, MB; Batova, A; Chang, RC; Bridgeman, LJ; Yu, J; Pullen, J; Bowman, WP; Yu, AL
    Universal inactivation of both p16 and p15 but not downstream components is an essential event in the pathogenesis of T-cell acute lymphoblastic leukemia
    CLINICAL CANCER RESEARCH
    
    M. Omura-Minamisawa et al., "Universal inactivation of both p16 and p15 but not downstream components is an essential event in the pathogenesis of T-cell acute lymphoblastic leukemia", CLIN CANC R, 6(4), 2000, pp. 1219-1228
44. Baffa, R; Santoro, R; Bullrich, F; Mandes, B; Ishii, H; Croce, CM
    Definition and refinement of chromosome 8p regions of loss of heterozygosity in gastric cancer
    CLINICAL CANCER RESEARCH
    
    R. Baffa et al., "Definition and refinement of chromosome 8p regions of loss of heterozygosity in gastric cancer", CLIN CANC R, 6(4), 2000, pp. 1372-1377
45. Seelan, RS; Qian, CP; Yokomizo, A; Bostwick, DG; Smith, DI; Liu, WG
    Human acid ceramidase is overexpressed but not mutated in prostate cancer
    GENES CHROMOSOMES & CANCER
    
    R.S. Seelan et al., "Human acid ceramidase is overexpressed but not mutated in prostate cancer", GENE CHROM, 29(2), 2000, pp. 137-146
46. Arcellana-Panlilio, MY; Egeler, AM; Ujack, E; Pinto, A; Demetrick, DJ; Robbins, SM; Coppes, MJ
    Decreased expression of the INK4 family of cyclin-dependent kinase inhibitors in Wilms tumor
    GENES CHROMOSOMES & CANCER
    
    M.Y. Arcellana-Panlilio et al., "Decreased expression of the INK4 family of cyclin-dependent kinase inhibitors in Wilms tumor", GENE CHROM, 29(1), 2000, pp. 63-69
47. Hilgers, W; Koerkamp, BG; Geradts, J; Tang, DJ; Yeo, CJ; Hruban, RH; Kern, SE
    Genomic FHIT analysis in RER+ and RER- adenocarcinomas of the pancreas
    GENES CHROMOSOMES & CANCER
    
    W. Hilgers et al., "Genomic FHIT analysis in RER+ and RER- adenocarcinomas of the pancreas", GENE CHROM, 27(3), 2000, pp. 239-243
48. Yoshinouchi, M; Hongo, A; Takamoto, N; Ono, Y; Nagao, S; Miyagi, Y; Kudo, T; Kodama, J
    Alteration of the CDKN2/p16 gene is not required for HPV-positive uterine cervical cancer cell lines
    INTERNATIONAL JOURNAL OF ONCOLOGY
    
    M. Yoshinouchi et al., "Alteration of the CDKN2/p16 gene is not required for HPV-positive uterine cervical cancer cell lines", INT J ONCOL, 16(3), 2000, pp. 537-541
49. Kahle, PJ; Leimer, U; Haass, C
    Does failure of parkin-mediated ubiquitination cause juvenile parkinsonism?
    TRENDS IN BIOCHEMICAL SCIENCES
    
    P.J. Kahle et al., "Does failure of parkin-mediated ubiquitination cause juvenile parkinsonism?", TRENDS BIOC, 25(11), 2000, pp. 524-527
50. Puig, S; Castro, J; Ventura, PJ; Ruiz, A; Ascaso, C; Melvehy, J; Estivill, X; Mascaro, JM; Lecha, M; Castel, T
    Large deletions of chromosome 9p in cutaneous malignant melanoma identify patients with a high risk of developing metastases
    MELANOMA RESEARCH
    
    S. Puig et al., "Large deletions of chromosome 9p in cutaneous malignant melanoma identify patients with a high risk of developing metastases", MELANOMA RE, 10(3), 2000, pp. 231-236
51. Louhelainen, J; Wijkstrom, H; Hemminki, K
    Initiation-development modelling of allelic losses on chromosome 9 in multifocal bladder cancer
    EUROPEAN JOURNAL OF CANCER
    
    J. Louhelainen et al., "Initiation-development modelling of allelic losses on chromosome 9 in multifocal bladder cancer", EUR J CANC, 36(11), 2000, pp. 1441-1451
52. D'Agata, V; Grimaldi, M; Pascale, A; Cavallaro, S
    Regional and cellular expression of the parkin gene in the rat cerebral cortex
    EUROPEAN JOURNAL OF NEUROSCIENCE
    
    V. D'Agata et al., "Regional and cellular expression of the parkin gene in the rat cerebral cortex", EUR J NEURO, 12(10), 2000, pp. 3583-3588
53. Schmid, M; Sen, M; Rosenbach, MD; Carrera, CJ; Friedman, H; Carson, DA
    A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer
    ONCOGENE
    
    M. Schmid et al., "A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer", ONCOGENE, 19(50), 2000, pp. 5747-5754
54. Steiner, MS; Wang, Y; Zhang, Y; Zhang, XW; Lu, Y
    p16/MTS1/INK4A suppresses prostate cancer by both pRb dependent and independent pathways
    ONCOGENE
    
    M.S. Steiner et al., "p16/MTS1/INK4A suppresses prostate cancer by both pRb dependent and independent pathways", ONCOGENE, 19(10), 2000, pp. 1297-1306
55. Steiner, MS; Zhang, Y; Farooq, F; Lerner, J; Wang, Y; Lu, Y
    Adenoviral vector containing wild-type p16 suppresses prostate cancer growth and prolongs survival by inducing cell senescence
    CANCER GENE THERAPY
    
    M.S. Steiner et al., "Adenoviral vector containing wild-type p16 suppresses prostate cancer growth and prolongs survival by inducing cell senescence", CANC GENE T, 7(3), 2000, pp. 360-372
56. Wada, M; Okamura, T; Okada, M; Teramura, M; Masuda, M; Motoji, T; Mizoguchi, H
    Delineation of the frequently deleted region on chromosome arm 13q in B-cell non-Hodgkin's lymphoma
    INTERNATIONAL JOURNAL OF HEMATOLOGY
    
    M. Wada et al., "Delineation of the frequently deleted region on chromosome arm 13q in B-cell non-Hodgkin's lymphoma", INT J HEMAT, 71(2), 2000, pp. 159-166
57. M'soka, TJ; Nishioka, J; Taga, A; Kato, K; Kawasaki, H; Yamada, Y; Yu, A; Komada, Y; Nobori, T
    Detection of methylthioadenosine phosphorylase (MTAP) and p16 gene deletion in T cell acute lymphoblastic leukemia by real-time quantitative PCR assay
    LEUKEMIA
    
    T.J. M'soka et al., "Detection of methylthioadenosine phosphorylase (MTAP) and p16 gene deletion in T cell acute lymphoblastic leukemia by real-time quantitative PCR assay", LEUKEMIA, 14(5), 2000, pp. 935-940
58. Gonzalez, M; Mateos, MV; Garcia-Sanz, R; Balanzategui, A; Lopez-Perez, R; Chillon, MC; Gonzalez, D; Alaejos, I; San Miguel, JF
    De novo methylation of tumor suppressor gene p16/INK4a is a frequent finding in multiple myeloma patients at diagnosis
    LEUKEMIA
    
    M. Gonzalez et al., "De novo methylation of tumor suppressor gene p16/INK4a is a frequent finding in multiple myeloma patients at diagnosis", LEUKEMIA, 14(1), 2000, pp. 183-187
59. Durr, A; Lucking, C; Brice, A
    Parkin gene mutations and Parkinson's disease
    M S-MEDECINE SCIENCES
    
    A. Durr et al., "Parkin gene mutations and Parkinson's disease", M S-MED SCI, 16(10), 2000, pp. 1112-1115
60. Yamamura, Y; Hattori, N; Matsumine, H; Kuzuhara, S; Mizuno, Y
    Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification
    BRAIN & DEVELOPMENT
    
    Y. Yamamura et al., "Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification", BRAIN DEVEL, 2000, pp. S87-S91
61. Saito, M; Maruyama, M; Ikeuchi, K; Kondo, H; Ishikawa, A; Yuasa, T; Tsuji, S
    Autosomal recessive juvenile parkinsonism
    BRAIN & DEVELOPMENT
    
    M. Saito et al., "Autosomal recessive juvenile parkinsonism", BRAIN DEVEL, 2000, pp. S115-S117
62. Maruyama, M; Ikeuchi, T; Saito, M; Ishikawa, A; Yuasa, T; Tanaka, H; Hayashi, S; Wakabayashi, K; Takahashi, H; Tsuji, S
    Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism
    ANNALS OF NEUROLOGY
    
    M. Maruyama et al., "Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism", ANN NEUROL, 48(2), 2000, pp. 245-250
63. Riess, O; Kuhn, W; Kruger, R
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64. Tunca, B; Egeli, U; Zorluoglu, A; Yilmazlar, T; Yerci, O; Kizil, A
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65. Chen, TC; Hsieh, LL; Kuo, TT; Ng, KF; Chou, YHW; Jeng, LB; Chen, MF
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66. Brauers, A; Jakse, G
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67. D'Agata, V; Zhao, WQ; Cavallaro, S
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68. Leuraud, P; Marie, Y; Robin, E; Huguet, S; He, J; Mokhtari, K; Cornu, P; Khe, HX; Sanson, M
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69. Guo, SX; Taki, T; Ohnishi, H; Piao, HY; Tabuchi, K; Bessho, F; Hanada, R; Yanagisawa, M; Hayashi, Y
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70. Muscheck, M; Abol-Enein, H; Chew, K; Moore, D; Bhargava, V; Ghoneim, MA; Carroll, PR; Waldman, FM
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71. Viallet, F
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72. Lucking, CB; Durr, A; Bonifati, V; Vaughan, J; De Michele, G; Gasser, T; Harhangi, BS; Meco, G; Denefle, P; Wood, NW; Agid, Y; Brice, A
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73. He, J; Hoang-Xuan, K; Marie, Y; Leuraud, P; Mokhtari, K; Kujas, M; Delattre, JY; Sanson, M
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74. Schraml, P; Muller, D; Bednar, R; Gasser, T; Sauter, G; Mihatsch, MJ; Moch, H
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75. Gu, WJ; Abbas, N; Lagunes, MZ; Parent, A; Pradier, L; Bohme, GA; Agid, Y; Hirsch, EC; Raisman-Vozari, R; Brice, A
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76. Bortolotto, S; Chiado-Piat, L; Cavalla, P; Bosone, I; Chio, A; Mauro, A; Schiffer, D
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77. Hu, CJ; Sung, SM; Liu, HC; Lee, CC; Tsai, CH; Chang, JG
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    EUROPEAN NEUROLOGY
    
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78. Eissa, S; Ali-Labib, R; Khalifa, A
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79. Kholodnyuk, ID; Szeles, A; Yang, Y; Klein, G; Imreh, S
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80. Tang, BQ; Li, YNN; Kruger, WD
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81. Sarkar, S; Julicher, KP; Burger, MS; Della Valle, V; Larsen, CJ; Yeager, TR; Grossman, TB; Nickells, RW; Protzel, C; Jarrard, DF; Reznikoff, CA
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82. Baek, MJ; Piao, Z; Park, C; Shin, EC; Park, JH; Jung, HJ; Kim, CG; Kim, H
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83. Palmieri, G; Cossu, A; Ascierto, PA; Botti, G; Strazzullo, M; Lissia, A; Colombino, M; Casula, M; Floris, C; Tanda, F; Pirastu, M; Castello, G
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84. Wong, IHN; Ng, MHL; Huang, DP; Lee, JCK
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85. Hung, KS; Hong, CY; Lee, JH; Lin, SK; Huang, SC; Wang, TM; Tse, V; Sliverberg, GD; Weng, SC; Hsiao, M
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86. Yatsuoka, T; Sunamura, M; Furukawa, T; Fukushige, S; Yokoyama, T; Inoue, H; Shibuya, K; Takeda, K; Matsuno, S; Horii, A
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87. Brice, A
    Genome and neurology - The example of Parkinson's disease
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88. Gruis, NA; van der Velden, PA; Bergman, W; Frants, RR
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89. Hallas, C; Albitar, M; Letofsky, J; Keating, MJ; Huebner, K; Croce, CM
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90. Faderl, S; Kantarjian, HM; Manshouri, T; Chan, CY; Pierce, S; Hays, KJ; Cortes, J; Thomas, D; Estrov, Z; Albitar, M
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91. Gramantieri, L; Chieco, P; Di Tomaso, M; Masi, L; Piscaglia, F; Brillanti, S; Gaiani, S; Valgimigli, M; Mazziotti, A; Bolondi, L
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92. Hilgers, W; Kern, SE
    Molecular genetic basis of pancreatic adenocarcinoma
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93. Sato, H; Hiyama, K; Ishioka, S; Maeda, H; Yamakido, M
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94. Junker, K; Werner, W; Mueller, C; Ebert, W; Schubert, J; Claussen, U
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95. Lee, WC; Testa, JR
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96. Kumar, R; Smeds, J; Rozell, BL; Hemminki, K
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97. Rizos, H; Darmanian, AP; Indsto, JO; Shannon, JA; Kefford, RF; Mann, GJ
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98. Satoh, J; Kuroda, Y
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    NEUROREPORT
    
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99. Liew, CT; Li, HM; Lo, KW; Leow, CK; Chan, JYH; Hin, LY; Lau, WY; Lai, PBS; Lim, BK; Huang, J; Leung, WT; Wu, S; Lee, JCK
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100. Fujimoto, A; Morita, R; Hatta, N; Takehara, K; Takata, M
     p16(INK4a) inactivation is not frequent in uncultured sporadic primary cutaneous melanoma
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