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Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions

Carcinogenesis (New York), 2004-11, Vol.25 (11), p.2053-2059

2004

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Chromosomal imbalances in human lung cancer: Lung cancer

Oncogene, 2002-10, Vol.21 (45), p.6877-6883

2002

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Characterization of MOAT-C and MOAT-D, new members of the MRP/cMOAT subfamily of transporter proteins

JNCI : Journal of the National Cancer Institute, 1998-11, Vol.90 (22), p.1735-1741

1998

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Comparative genomic hybridization analysis detects frequent, often high-level, overrepresentation of DNA sequences at 3q, 5p, 7p, and 8q in human non-small cell lung carcinomas

Cancer research (Chicago, Ill.), 1997-06, Vol.57 (11), p.2116-2120

1997

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Neurofibromatosis 2 and malignant mesothelioma

Neurology, 2002-07, Vol.59 (2), p.290-291

2002

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Detection of chromosomal aberrations by comparative genomic hybridization during transformation of human breast epithelial cells in vitro

International journal of oncology, 2006-10, Vol.29 (4), p.877-881

2006

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Comparative genomic hybridization and loss of heterozygosity analyses identify a common region of deletion at 15q11.1-15 in human malignant mesothelioma

Cancer research (Chicago, Ill.), 1999-01, Vol.59 (2), p.450-454

1999

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893P Clinico-genetic profiling of HRAS mutant head and neck squamous cell carcinoma (HNSCC)

Annals of oncology, 2021-09, Vol.32, p.S799-S800

2021

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Genomic imbalances in human lung adenocarcinomas and squamous cell carcinomas

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.282-287

2001

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LBA47 A phase II study evaluating tipifarnib in mHRAS, recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) (AIM-HN study)

Annals of oncology, 2023-10, Vol.34, p.S1286-S1287

2023

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Novel Human and Mouse Annexin A10 Are Linked to the Genome Duplications during Early Chordate Evolution

Genomics (San Diego, Calif.), 1999-08, Vol.60 (1), p.40-49

1999

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Functional roles of chromosomes 11 and 17 in the transformation of human breast epithelial cells in vitro

International journal of oncology, 1999-10, Vol.15 (4), p.629

1999

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Human hepatocellular carcinoma is characterized by a highly consistent pattern of genomic imbalances, including frequent loss of 16q23.1-24.1

Genes chromosomes & cancer, 2001-03, Vol.30 (3), p.245-253

2001

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Cloning and Chromosomal Localization of a Gene Encoding a Novel Serine/Threonine Kinase Belonging to the Subfamily of Testis-Specific Kinases

Genomics (San Diego, Calif.), 2001-10, Vol.77 (3), p.163-170

2001

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Loss of heterozygosity analysis defines a 3-cM region of 15q commonly deleted in human malignant mesothelioma

Oncogene, 2001-09, Vol.20 (43), p.6245-6249

2001

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Recurrent Lymphangiomyomatosis after Transplantation: Genetic Analyses Reveal a Metastatic Mechanism

American journal of respiratory and critical care medicine, 2003-04, Vol.167 (7), p.976-982

2003

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Comparative genomic hybridization of human breast epithelial cells transformed by estrogen and its metabolites

International journal of oncology, 2005-03, Vol.26 (3), p.691

2005

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Loss of Methylthioadenosine Phosphorylase and Elevated Ornithine Decarboxylase Is Common in Pancreatic Cancer

Clinical cancer research, 2004-11, Vol.10 (21), p.7290-7296

2004

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Cytogenetic studies on a patient with prepubertal breast cancer : a case report

Breast cancer research and treatment, 1996-01, Vol.39 (3), p.343-347

1996

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Characterization of Unconventional MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell's Waltzer Mice

Human molecular genetics, 1997-08, Vol.6 (8), p.1225-1231

1997

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Identification and Structural Analysis of Human RBM8A and RBM8B: Two Highly Conserved RNA-Binding Motif Proteins That Interact with OVCA1, a Candidate Tumor Suppressor

Genomics (San Diego, Calif.), 2000-10, Vol.69 (1), p.54-62

2000

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DNA analysis of breast cancer by flow cytometry & correlation with other prognostic parameters

Indian journal of medical research (New Delhi, India : 1994), 1992-08, Vol.96, p.223

1992

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Loss of heterozygosity analysis defines a critical region in chromosome 1p22 commonly deleted in human malignant mesothelioma

Cancer research (Chicago, Ill.), 1996-10, Vol.56 (19), p.4297-4301

1996

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T‐lymphoid blast crisis in chronic myeloid leukemia

American journal of hematology, 1991-02, Vol.36 (2), p.86-92

1991

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Multicentric clinical trials for safety and efficacy evaluation of alpha;beta arteether in complicated P. falciparum malaria

Journal of the Association of Physicians of India, 2001-12, Vol.49, p.1155

2001

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Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions

Chromosomal imbalances in human lung cancer: Lung cancer

Characterization of MOAT-C and MOAT-D, new members of the MRP/cMOAT subfamily of transporter proteins

Comparative genomic hybridization analysis detects frequent, often high-level, overrepresentation of DNA sequences at 3q, 5p, 7p, and 8q in human non-small cell lung carcinomas

Neurofibromatosis 2 and malignant mesothelioma

Detection of chromosomal aberrations by comparative genomic hybridization during transformation of human breast epithelial cells in vitro

Comparative genomic hybridization and loss of heterozygosity analyses identify a common region of deletion at 15q11.1-15 in human malignant mesothelioma

893P Clinico-genetic profiling of HRAS mutant head and neck squamous cell carcinoma (HNSCC)

Genomic imbalances in human lung adenocarcinomas and squamous cell carcinomas

LBA47 A phase II study evaluating tipifarnib in mHRAS, recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) (AIM-HN study)

Novel Human and Mouse Annexin A10 Are Linked to the Genome Duplications during Early Chordate Evolution

Functional roles of chromosomes 11 and 17 in the transformation of human breast epithelial cells in vitro

Human hepatocellular carcinoma is characterized by a highly consistent pattern of genomic imbalances, including frequent loss of 16q23.1-24.1

Cloning and Chromosomal Localization of a Gene Encoding a Novel Serine/Threonine Kinase Belonging to the Subfamily of Testis-Specific Kinases

Loss of heterozygosity analysis defines a 3-cM region of 15q commonly deleted in human malignant mesothelioma

Recurrent Lymphangiomyomatosis after Transplantation: Genetic Analyses Reveal a Metastatic Mechanism

Comparative genomic hybridization of human breast epithelial cells transformed by estrogen and its metabolites

Loss of Methylthioadenosine Phosphorylase and Elevated Ornithine Decarboxylase Is Common in Pancreatic Cancer

Cytogenetic studies on a patient with prepubertal breast cancer : a case report

Characterization of Unconventional MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell's Waltzer Mice

Identification and Structural Analysis of Human RBM8A and RBM8B: Two Highly Conserved RNA-Binding Motif Proteins That Interact with OVCA1, a Candidate Tumor Suppressor

DNA analysis of breast cancer by flow cytometry & correlation with other prognostic parameters

Loss of heterozygosity analysis defines a critical region in chromosome 1p22 commonly deleted in human malignant mesothelioma

T‐lymphoid blast crisis in chronic myeloid leukemia

Multicentric clinical trials for safety and efficacy evaluation of alpha;beta arteether in complicated P. falciparum malaria

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