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    1. Marsh, DJ; Theodosopoulos, G; Howell, V; Richardson, AL; Benn, DE; Proos, AL; Eng, C; Robinson, BG
      Rapid mutation scanning of genes associated with familial cancer syndromesusing denaturing high-performance liquid chromatography

      NEOPLASIA
    2. Constanzer, M; Chavez-Eng, C; Matuszewski, B
      Determination of a thermally labile metabolite of a novel growth hormone secretagogue in human and dog plasma by liquid chromatography with ion spraytandem mass spectrometric detection

      JOURNAL OF CHROMATOGRAPHY B
    3. Moore, L; Wiencke, J; Eng, C; Zheng, SC; Smith, A
      Evaluation of buccal cell collection protocols for genetic susceptibility studies

      BIOMARKERS
    4. Covinsky, KE; Eng, C; Lui, LY; Sands, LP; Sehgal, AR; Walter, LC; Wieland, D; Eleazer, GP; Yaffe, K
      Reduced employment in caregivers of frail elders: Impact of ethnicity, patient clinical characteristics, and caregiver characteristics

      JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES
    5. Eng, C
      To be or not to BMP

      NATURE GENETICS
    6. Weng, LP; Brown, JL; Eng, C
      PTEN coordinates G(1) arrest by down-regulating cyclin D1 via its protein phosphatase activity and up-regulating p27 via its lipid phosphatase activity in a breast cancer model

      HUMAN MOLECULAR GENETICS
    7. Weng, LP; Smith, WM; Brown, JL; Eng, C
      PTEN inhibits insulin-stimulated MEK/MAPK activation and cell growth by blocking IRS-1 phosphorylation and 1RS-1/Grb-2/Sos complex formation in a breast cancer model

      HUMAN MOLECULAR GENETICS
    8. Weng, LP; Brown, JL; Eng, C
      PTEN induces apoptosis and cell cycle arrest through phosphoinositol-3-kinase/Akt-dependent and -independent pathways

      HUMAN MOLECULAR GENETICS
    9. Weng, LP; Gimm, O; Kum, JB; Smith, WM; Zhou, XP; Wynford-Thomas, D; Leone, G; Eng, C
      Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death

      HUMAN MOLECULAR GENETICS
    10. Kurose, K; Hoshaw-Woodard, S; Adeyinka, A; Lemeshow, S; Watson, PH; Eng, C
      Genetic model of multi-step breast carcinogenesis involving the epitheliumand stroma: clues to tumour-microenvironment interactions

      HUMAN MOLECULAR GENETICS
    11. Smiraglia, DJ; Rush, LJ; Fruhwald, MC; Dai, ZY; Held, WA; Costello, JF; Lang, JC; Eng, C; Li, B; Wright, FA; Caligiuri, MA; Plass, C
      Excessive CpG island hypermethylation in cancer cell lines versus primary human malignancies

      HUMAN MOLECULAR GENETICS
    12. 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
    13. Gimm, O; Dziema, H; Brown, J; Cuong, HV; Hinze, R; Dralle, H; Mulligan, LM; Eng, C
      Over-representation of a germline variant in the gene encoding RET co-receptor GFR alpha-1 but not GFR alpha-2 or GFR alpha-3 in cases with sporadic medullary thyroid carcinoma

      ONCOGENE
    14. Murphy, AM; Gilliland, A; Eng Wong, C; West, J; Singh, DP; Carr, JP
      Signal transduction in resistance to plant viruses

      EUROPEAN JOURNAL OF PLANT PATHOLOGY
    15. Walter, LC; Eng, C; Covinsky, KE
      Screening mammography for frail older women - What are the burdens?

      JOURNAL OF GENERAL INTERNAL MEDICINE
    16. Dolgilevich, SM; Siri, FM; Atlas, SA; Eng, C
      Changes in collagenase and collagen gene expression after induction of aortocaval fistula in rats

      AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
    17. Smith, WM; Zhou, XP; Kurose, K; Gao, X; Latif, F; Kroll, T; Sugano, K; Cannistra, SA; Clinton, SK; Maher, ER; Prior, TW; Eng, C
      Opposite association of two PPARG variants with cancer: overrepresentationof H449H in endometrial carcinoma cases and underrepresentation of P12A inrenal cell carcinoma cases

      HUMAN GENETICS
    18. Vanhorne, JB; Gimm, O; Myers, SM; Kaushik, A; von Deimling, A; Eng, C; Mulligan, LM
      Cloning and characterization of the human GFRA2 locus and investigation ofthe gene in Hirschsprung disease

      HUMAN GENETICS
    19. Dahia, PLM; Eng, C
      Hereditary endocrine neoplasias: Fundamental insights and the practice of clinical cancer genetics

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    20. Ruiz, A; Antinolo, G; Fernandez, RM; Eng, C; Marcos, I; Borrego, S
      Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population

      CLINICAL ENDOCRINOLOGY
    21. Master, RJ; Eng, C
      Integrating acute and long-term care for high-cost populations

      HEALTH AFFAIRS
    22. Eng, C; Thiele, H; Zhou, XP; Gorlin, RJ; Hennekam, RCM; Winter, RM
      PTEN mutations and Proteus syndrome - Reply

      LANCET
    23. Zhou, XP; Hampel, H; Thiele, H; Gorlin, RJ; Hennekam, RCM; Parisi, M; Winter, RM; Eng, C
      Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes

      LANCET
    24. Astuti, D; Douglas, F; Lennard, TWJ; Aligianis, IA; Woodward, ER; Evans, DGR; Eng, C; Latif, F; Maher, ER
      Germline SDHD mutation in familial phaeochromocytoma

      LANCET
    25. Eng, C; Hampel, H; de la Chapelle, A
      Genetic testing for cancer predisposition

      ANNUAL REVIEW OF MEDICINE
    26. Waldman, FM; Hwang, ES; Etzell, J; Eng, C; DeVries, S; Bennington, J; Thor, A
      Genomic alterations in tubular breast carcinomas

      HUMAN PATHOLOGY
    27. Neumann, HPH; Reincke, M; Eng, C
      Case 13-2001: Genetic testing in pheochromocytoma.

      NEW ENGLAND JOURNAL OF MEDICINE
    28. Bender, BU; Eng, C; Olschewski, M; Berger, DP; Laubenberger, J; Altehofer, C; Kirste, G; Orszagh, M; van Velthoven, V; Miosczka, H; Schmidt, D; Neumann, HPH
      VHL c.505 T > C mutation confers a high age related penetrance but no increased overall mortality

      JOURNAL OF MEDICAL GENETICS
    29. Fackenthal, JD; Marsh, DJ; Richardson, AL; Cummings, SA; Eng, C; Robinson, BG; Olopade, OI
      Male breast cancer in Cowden syndrome patients with germline PTEN mutations

      JOURNAL OF MEDICAL GENETICS
    30. Parisi, MA; Dinulos, MB; Leppig, KA; Sybert, VP; Eng, C; Hudgins, L
      The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome

      JOURNAL OF MEDICAL GENETICS
    31. Duchateau, PN; Pullinger, CR; Cho, MH; Eng, C; Kane, JP
      Apolipoprotein L gene family: tissue-specific expression, splicing, promoter regions; discovery of a new gene

      JOURNAL OF LIPID RESEARCH
    32. Mills, RP; Wang, ZG; Abel, EW; Phil, M; Eng, C
      In vitro study of a multi-layer piezoelectric crystal attic hearing implant

      JOURNAL OF LARYNGOLOGY AND OTOLOGY
    33. Gimm, O; Chi, HB; Dahia, PLM; Perren, A; Hinze, R; Komminoth, P; Dralle, H; Reynolds, PR; Eng, C
      Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    34. Gimm, O; Dziema, H; Brown, J; De la Puente, A; Hoang-Vu, C; Dralle, H; Plass, C; Eng, C
      Mutation analysis of NTRK2 and NTRK3, encoding 2 tyrosine kinase receptors, in sporadic human medullary thyroid carcinoma reveals novel sequence variants

      INTERNATIONAL JOURNAL OF CANCER
    35. Gath, R; Goessling, A; Keller, KM; Koletzko, S; Coerdt, W; Muntefering, H; Wirth, S; Hofstra, RMW; Mulligan, L; Eng, C; von Deimling, A
      Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease

      GUT
    36. Baker, DI; Gottschalk, M; Eng, C; Weber, S; Tinetti, ME
      The design and implementation of a restorative care model for home care

      GERONTOLOGIST
    37. Lee, YJ; Eng, C; Grey, GP
      Li-6 magic angle spinning NMR study of the cathode material LiNixMn2-xO4 -The effect of Ni doping on the local structure during charging

      JOURNAL OF THE ELECTROCHEMICAL SOCIETY
    38. Mutter, GL; Ince, TA; Baak, JPA; Kust, GA; Zhou, XP; Eng, C
      Molecular identification of latent precancers in histologically normal endometrium

      CANCER RESEARCH
    39. Kulke, MH; Thakore, KS; Thomas, G; Wang, H; Loda, M; Eng, C; Odze, RD
      Microsatellite instability and hMLH1/hMSH2 expression in Barrett esophagus-associated adenocarcinoma

      CANCER
    40. Kulke, MH; Odze, RD; Thakore, KS; Thomas, G; Wang, H; Loda, M; Eng, C
      Allelic loss of 10q23, the PTEN tumour suppressor gene locus, in Barrett'soesophagus-associated adenocarcinoma

      BRITISH JOURNAL OF CANCER
    41. Kurose, K; Zhou, XP; Araki, T; Cannistra, SA; Maher, ER; Eng, C
      Frequent loss of PTEN expression is linked to elevated phosphorylated Akt levels, but not associated with p27 and cyclin D1 expression, in primary epithelial ovarian carcinomas

      AMERICAN JOURNAL OF PATHOLOGY
    42. Zhou, XP; Woodford-Richens, K; Lehtonen, R; Kurose, K; Aldred, M; Hampel, H; Launonen, V; Virta, S; Pilarski, R; Salovaara, R; Bodmer, WF; Conrad, BA; Dunlop, M; Hodgson, SV; Iwama, T; Jarvinen, H; Kellokumpu, I; Kim, JC; Leggett, B; Markie, D; Mecklin, JP; Neale, K; Phillips, R; Piris, J; Rozen, P; Houlston, RS; Aaltonen, LA; Tomlinson, IPM; Eng, C
      Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

      AMERICAN JOURNAL OF HUMAN GENETICS
    43. Astuti, D; Latif, F; Dallol, A; Dahia, PLM; Douglas, F; George, E; Skoldberg, F; Husebye, ES; Eng, C; Maher, ER
      Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

      AMERICAN JOURNAL OF HUMAN GENETICS
    44. Klapholz, M; Thomas, I; Eng, C; Iteld, BJ; Ponce, GA; Niederman, AL; Bilsker, M; Heywood, JT; Synhorst, D
      Effects of omapatrilat on hemodynamics and safety in patients with heart failure

      AMERICAN JOURNAL OF CARDIOLOGY
    45. Grady, WM; Willis, J; Guilford, PJ; Dunbier, AK; Toro, TT; Lynch, H; Wiesner, G; Ferguson, K; Eng, C; Park, JG; Kim, SJ; Markowitz, S
      Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer

      NATURE GENETICS
    46. Eng, C; Herman, JG; Baylin, SB
      A bird's eye view of global methylation

      NATURE GENETICS
    47. Kurose, K; Zhou, XP; Araki, T; Eng, C
      Biallelic inactivating mutations and an occult germline mutation of PTEN in primary cervical carcinomas

      GENES CHROMOSOMES & CANCER
    48. Zhou, XP; Marsh, DJ; Hampel, H; Mulliken, JB; Gimm, O; Eng, C
      Germline and germline mosaic PTEN mutations associated with a Proteus-likesyndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

      HUMAN MOLECULAR GENETICS
    49. Gimm, O; Attie-Bitach, T; Lees, JA; Vekemans, M; Eng, C
      Expression of the PTEN tumour suppressor protein during human development

      HUMAN MOLECULAR GENETICS
    50. Yeh, JJ; Lunetta, KL; van Orsouw, NJ; Moore, FD; Mutter, GL; Vijg, J; Dahia, PLM; Eng, C
      Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours

      ONCOGENE
    51. Moore, L; Godfrey, T; Eng, C; Smith, A; Ho, R; Waldman, FM
      Validation of fluorescent SSCP analysis for sensitive detection of p53 mutations

      BIOTECHNIQUES
    52. Lehrer, S; McCurdy, LD; Stock, RG; Kornreich, R; Stone, NN; Eng, C
      Body mass, age, and the APC I1307K allele in Ashkenazi Jewish prostate cancer patients

      CANCER GENETICS AND CYTOGENETICS
    53. Iliopoulos, O; Eng, C
      Genetic and clinical aspects of familial renal neoplasms

      SEMINARS IN ONCOLOGY
    54. Vyas, KP; Halpin, RA; Geer, LA; Ellis, JD; Liu, LD; Cheng, HY; Chavez-Eng, C; Matuszewski, BK; Varga, SL; Guiblin, AR; Rogers, JD
      Disposition and pharmacokinetics of the antimigraine drug, rizatriptan, inhumans

      DRUG METABOLISM AND DISPOSITION
    55. Tobias, DH; Eng, C; McCurdy, LD; Kalir, T; Mandelli, J; Dottino, PR; Cohen, CJ
      Founder BRCA 1 and 2 mutations among a consecutive series of Ashkenazi Jewish ovarian cancer patients

      GYNECOLOGIC ONCOLOGY
    56. Mueller, E; Smith, M; Sarraf, P; Kroll, T; Aiyer, A; Kaufman, DS; Oh, W; Demetri, G; Figg, WD; Zhou, XP; Eng, C; Spiegelman, BM; Kantoff, PW
      Effects of ligand activation of peroxisome proliferator-activated receptorgamma in human prostate cancer

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    57. Thia-Eng, C; Gorre, IRL; Ross, SA; Bernad, SR; Gervacio, B; Ebarvia, MC
      The Malacca Straits

      MARINE POLLUTION BULLETIN
    58. Syngal, S; Fox, EA; Eng, C; Kolodner, RD; Garber, JE
      Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1

      JOURNAL OF MEDICAL GENETICS
    59. Dahia, PM; Gimm, O; Chi, HB; Marsh, DJ; Reynolds, PR; Eng, C
      Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations

      JOURNAL OF MEDICAL GENETICS
    60. Borrego, S; Ruiz, A; Saez, ME; Gimm, O; Gao, X; Lopez-Alonso, M; Hernandez, A; Wright, FA; Antinolo, G; Eng, C
      RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease

      JOURNAL OF MEDICAL GENETICS
    61. Zhou, XP; Smith, WM; Gimm, O; Mueller, E; Gao, X; Sarraf, P; Prior, TW; Plass, C; von Deimling, A; Black, PM; Yates, AJ; Eng, C
      Over-representation of PPAR gamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population

      JOURNAL OF MEDICAL GENETICS
    62. Eng, C
      Will the real Cowden syndrome please stand up: revised diagnostic criteria

      JOURNAL OF MEDICAL GENETICS
    63. Mutter, GL; Lin, MC; Fitzgerald, JT; Kum, JB; Eng, C
      Changes in endometrial PTEN expression throughout the human menstrual cycle

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    64. Eng, C
      Editorial: Familial papillary thyroid cancer - Many syndromes, too many genes?

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    65. Bender, BU; Gutsche, M; Glasker, S; Muller, B; Kirste, G; Eng, C; Neumann, HPH
      Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    66. Woodford-Richens, K; Bevan, S; Churchman, M; Dowling, B; Jones, D; Norbury, CG; Hodgson, SV; Desai, D; Neale, K; Phillips, RKS; Young, J; Leggett, B; Dunlop, M; Rozen, P; Eng, C; Markie, D; Rodriguez-Bigas, MA; Sheridan, E; Iwama, T; Eccles, D; Smith, GT; Kim, JC; Kim, KM; Sampson, JR; Evans, G; Tejpar, S; Bodmer, WF; Tomlinson, IPM; Houlston, RS
      Analysis of genetic and phenotypic heterogeneity in juvenile polyposis

      GUT
    67. Kukin, ML; Kalman, J; Charney, RH; Levy, DK; Buchholz-Varley, C; Ocampo, ON; Eng, C
      Are all beta-blockers for heart failure the same? - Response

      CIRCULATION
    68. Matuszewski, BK; Chavez-Eng, C; Constanzer, ML
      Determination of unlabeled and C-14-radiolabeled drug candidates in biological fluids using LC-MS-MS - Issues and challenges

      CHROMATOGRAPHIA
    69. Gimm, O; Armanios, M; Dziema, H; Neumann, HPH; Eng, C
      Somatic and occult germ-line mutations in SDHD, a mitochondrial complex IIgene, in nonfamilial pheochromocytoma

      CANCER RESEARCH
    70. Pullinger, CR; Hakamata, H; Duchateau, PN; Eng, C; Aouizerat, BE; Cho, MH; Fielding, CJ; Kane, JP
      Analysis of hABC1 gene 5 ' end: Additional peptide sequence, promoter region, and four polymorphisms

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    71. Perren, A; Komminoth, P; Saremaslani, P; Matter, C; Feurer, S; Lees, JA; Heitz, PU; Eng, C
      Mutation and expression analyses reveal differential subcellular compartmentalization of PTEN in endocrine pancreatic tumors compared to normal isletcells

      AMERICAN JOURNAL OF PATHOLOGY
    72. Zhou, XP; Gimm, O; Hampel, H; Niemann, T; Walker, MJ; Eng, C
      Epigenetic PTEN silencing in malignant melanomas without PTEN mutation

      AMERICAN JOURNAL OF PATHOLOGY
    73. Gimm, O; Perren, A; Weng, LP; Marsh, DJ; Yeh, JJ; Ziebold, U; Gil, E; Hinze, R; Delbridge, L; Lees, JA; Mutter, GL; Robinson, BG; Komminoth, P; Dralle, H; Eng, C
      Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumors

      AMERICAN JOURNAL OF PATHOLOGY
    74. Mutter, GL; Lin, MC; Fitzgerald, JT; Kum, JB; Baak, JPA; Lees, JA; Weng, LP; Eng, C
      Altered PTEN expression as a diagnostic marker for the earliest endometrial precancers

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    75. Aaltonen, LA; Roth, S; Eng, C
      Direct sequencing for Cowden syndrome gene PTEN (MMAC1) mutations

      COLORECTAL CANCER: METHODS AND PROTOCOLS
    76. Sarraf, P; Mueller, E; Smith, WM; Wright, HM; Kum, JB; Aaltonen, LA; de la Chapelle, A; Spiegelman, BM; Eng, C
      Loss-of-function mutations in PPAR gamma associated with human colon cancer

      MOLECULAR CELL
    77. Yeh, JJ; Marsh, DJ; Zedenius, J; Dwight, T; Delbridge, L; Robinson, BG; Eng, C
      Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathways

      GENES CHROMOSOMES & CANCER
    78. Clifford, SC; Walsh, S; Hewson, K; Green, EK; Brinke, A; Green, PM; Gianelli, F; Eng, C; Maher, ER
      Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 andVBPI) mutation and loss in renal-cell carcinoma development

      GENES CHROMOSOMES & CANCER
    79. Marsh, DJ; Kum, JB; Lunetta, KL; Bennett, MJ; Gorlin, RJ; Ahmed, SF; Bodurtha, J; Crowe, C; Curtis, MA; Dasouki, M; Dunn, T; Feit, H; Geraghty, MT; Graham, JM; Hodgson, SV; Hunter, A; Korf, BR; Manchester, D; Miesfeldt, S; Murday, VA; Nathanson, KL; Parisi, M; Pober, B; Romano, C; Tolmie, JL; Trembath, R; Winter, RM; Zackai, EH; Zori, RT; Weng, LP; Dahia, PLM; Eng, C
      PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

      HUMAN MOLECULAR GENETICS
    80. Dahia, PLM; Aguiar, RCT; Alberta, J; Kum, JB; Caron, S; Sill, H; Marsh, DJ; Ritz, J; Freedman, A; Stiles, C; Eng, C
      PTEN is inversely correlated with the cell survival factor Akt/PKB and is inactivated via multiple mechanisms in haematological malignancies

      HUMAN MOLECULAR GENETICS
    81. Gimm, O; Neuberg, DS; Marsh, DJ; Dahia, PLM; Cuong, HV; Raue, F; Hinze, R; Dralle, H; Eng, C
      Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation

      ONCOGENE
    82. Eng, C
      RET proto-oncogene in the development of human cancer

      JOURNAL OF CLINICAL ONCOLOGY
    83. Otto, LR; Boriack, RL; Marsh, DJ; Kum, JB; Eng, C; Burlina, AB; Bennett, MJ
      Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (ERRS)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    84. Syngal, S; Fox, EA; Li, C; Dovidio, M; Eng, C; Kolodner, RD; Garber, JE
      Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer - Implications for clinical predisposition testing

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    85. Nilsson, O; Tisell, LE; Jansson, S; Ahlman, H; Gimm, O; Eng, C
      Adrenal and extra-adrenal pheochromocytomas in a family with germline RET V804L mutation

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    86. Thia-Eng, C
      Marine pollution prevention and management in the East Asian Seas: A paradigm shift in concept, approach and methodology

      MARINE POLLUTION BULLETIN
    87. Myers, SM; Salomon, R; Goessling, A; Pelet, A; Eng, C; von Deimling, A; Lyonnet, S; Mulligan, LM
      Investigation of germline GFR alpha-1 mutations in Hirschsprung disease

      JOURNAL OF MEDICAL GENETICS
    88. van Orsouw, NJ; Dhanda, RK; Elhaji, Y; Narod, SA; Li, FP; Eng, C; Vijg, J
      A highly accurate, low cost test for BRCA1 mutations

      JOURNAL OF MEDICAL GENETICS
    89. Borrego, S; Saez, ME; Ruiz, A; Gimm, O; Lopez-Alonso, M; Antinolo, G; Eng, C
      Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression

      JOURNAL OF MEDICAL GENETICS
    90. Duerr, EM; Gimm, O; Neuberg, DS; Kum, JB; Clifford, SC; Toledo, SPA; Maher, ER; Dahia, PLM; Eng, C
      Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    91. Gimm, O; Greco, A; Hoang-Vu, C; Dralle, H; Pierotti, MA; Eng, C
      Mutation analysis reveals novel sequence variants in NTRK1 in sporadic human medullary thyroid carcinoma

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    92. Ahmed, SF; Marsh, DJ; Weremowicz, S; Morton, CC; Williams, DM; Eng, C
      Balanced translocation of 10q and 13q, including the PTEN gene, in a boy with a human chorionic gonadotropin-secreting tumor and the Bannayan-Riley-Ruvalcaba syndrome

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    93. Lauge, A; Lefebvre, C; Laurent-Puig, P; Caux, V; Gad, S; Eng, C; Longy, M; Stoppa-Lyonnet, D
      No evidence for germline PTEN mutations in families with breast and brain tumours

      INTERNATIONAL JOURNAL OF CANCER
    94. Bevan, S; Woodford-Richens, K; Rozen, P; Eng, C; Young, J; Dunlop, M; Neale, K; Phillips, R; Markie, D; Rodriguez-Bigas, M; Leggett, B; Sheridan, E; Hodgson, S; Iwama, T; Eccles, D; Bodmer, W; Houlston, R; Tomlinson, I
      Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndrome

      GUT
    95. Smith, VV; Eng, C; Milla, PJ
      Intestinal ganglioneuromatosis and multiple endocrine neoplasia type 2B: implications for treatment

      GUT
    96. Svensson, PJ; Tapper-Persson, M; Anvret, M; Molander, ML; Eng, C; Nordenskjold, A
      Mutations in the endothelin-receptor B gene in Hirschsprung disease in Sweden

      CLINICAL GENETICS
    97. Kukin, ML; Kalman, J; Charney, RH; Levy, DK; Buchholz-Varley, C; Ocampo, ON; Eng, C
      Prospective, randomized comparison of effect of long-term treatment with metoprolol or carvedilol on symptoms, exercise, ejection fraction, and oxidative stress in heart failure

      CIRCULATION
    98. Weng, LP; Smith, WM; Dahia, PLM; Ziebold, U; Gil, E; Lees, JA; Eng, C
      PTEN suppresses breast cancer cell growth by phosphatase activity-dependent G(1) arrest followed by cell death

      CANCER RESEARCH
    99. Gimm, O; Gossling, A; Marsh, DJ; Dahia, PLM; Mulligan, LM; von Deimling, A; Eng, C
      Mutation and deletion analysis of GFR alpha-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumours

      BRITISH JOURNAL OF CANCER
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/10/20 alle ore 20:44:39