240 results on '"Reeve, Anthony E."'
Search Results
52. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X
53. Preferential loss of maternal 9p alleles in childhood acute lymphoblastic leukemia
54. Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-Beckwith syndrome
55. 3?BCR recombines withIGL locus inBCR-ABL-positive Philadelphia-negative chronic myeloid leukemia
56. A potential imprint control element: identification of a conserved 42 bp sequence upstream of H19
57. E-cadherin unlikely to be a common ?low penetrance? gene for colorectal cancer
58. Analysis ofIGF2 gene imprinting in breast and colorectal cancer by allele specific-PCR
59. E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer
60. Insulin-like growth factor 2 and overgrowth: molecular biology and clinical implications
61. The Japanese Journal of Urology
62. Epigenetic changes at the insulin-like growth factor II/ H19 locus in developing kidney is an early event in Wilms tumorigenesis
63. Role of genomic imprinting in Wilms' tumour and overgrowth disorders
64. Equivalent Parental Distribution of Frequently Lost Alleles and Biallelic Expression of theH19Gene in Human Testicular Germ Cell Tumors
65. Somatic overgrowth associated with overexpression of insulin–like growth factor II
66. Genetic mosaicism at the insulin locus in liver associated with childhood hepatoblastoma
67. Good Prognosis of Cellular Mesoblastic Nephroma with Hyperdiploidy and Relaxation of Imprinting of the Maternal IGF2 Gene
68. Mosaic and polymorphic imprinting of the WT1 gene in humans
69. Global demethylation in loss of imprinting subtype of wilms tumor.
70. Constitutional relaxation of insulin–like growth factor II gene imprinting associated with Wilms' tumour and gigantism
71. Human insulin-like growth factor type I and type II receptors are not imprinted
72. The insulin-like growth factor 1 receptor gene is normally biallelically expressed in human juvenile tissue and tumours
73. PAX3 Is Expressed in the Stromal Compartment of the Developing Kidney and in Wilms Tumors with Myogenic Phenotype.
74. Heterogeneous gene expression changes in colorectal cancer cells share the WNT pathway in response to growth suppression by APHSmediated COX-2 inhibition.
75. 3′ BCR recombines with IGL locus in BCR-ABL-positive Philadelphia-negative chronic myeloid leukemia.
76. Analysis of IGF2 gene imprinting in breast and colorectal cancer by allele specific-PCR.
77. Familial gastric cancer: clinicopathological characteristics, RER phenotype and germline p53 and E-cadherin mutations.
78. A catalogue of imprinted genes and parent-of-origin effects in humans and animals.
79. A method for the enzymatic synthesis and purification of [α- nucleoside triphosphates.
80. Equivalent Parental Distribution of Frequently Lost Alleles and Biallelic Expression of the H19 Gene in Human Testicular Germ Cell Tumors.
81. Human p57KIP2 defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour.
82. Myogenesis in Wilms Tumors Is Associated with Mutations of the WT1Gene and Activation of Bcl-2 and the Wnt Signaling Pathway
83. The Roles of Supernumerical X Chromosomes and XISTExpression in Testicular Germ Cell Tumors
84. Analysis of IGF2gene imprinting in breast and colorectal cancer by allele specific‐PCR
85. Methylation Sequencing Analysis Refines the Region ofH19Epimutation in Wilms Tumor*
86. Analysis of <TOGGLE>IGF2</TOGGLE> gene imprinting in breast and colorectal cancer by allele specific-PCR
87. Pancreatoblastoma is associated with chromosome 11p loss of heterozygosity and IGF2 overexpression.
88. Genomic diversity correlates with clinical variation in Ph′-negative chronic myeloid leukaemia.
89. Pancreatoblastoma is associated with chromosome 11p loss of heterozygosity and <TOGGLE>IGF2</TOGGLE> overexpression
90. Analysis of rna initiated in isolated mouse myeloma nuclei using purine nucleoside 5′[γ-S]triphosphates as affinity probes
91. Loss of a Harvey ras allele in sporadic Wilms' tumour
92. Philadelphia Chromosome Negative CGL
93. Transcription of bacteriophage λ DNA in vitro using purine nucleoside 5'-[γ-S]triphosphates as affinity probes for RNA chain initiation
94. Incorporation of purine nucleoside 5'-[γ-S]triphosphates as affinity probes for initiation of RNA synthesis in vitro
95. Synthesis and affinity purification of β-32P-labeled [γ-S]GTP
96. A method for the enzymatic synthesis and purification of [α-32nucleoside triphosphates
97. Expression of insulin-like growth factor-II transcripts in Wilms' tumour
98. E-cadherin unlikely to be a common low penetrance gene for colorectal cancer
99. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.
100. Heterogeneous gene expression changes in colorectal cancer cells share the WNT pathway in response to growth suppression by APHS-mediated COX-2 inhibition.
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