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Genetics of neuroendocrine and carcinoid tumours

Endocrine-related cancer, 2003-12, Vol.10 (4), p.437-450

2003

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The telomere profile distinguishes two classes of genetically distinct cutaneous squamous cell carcinomas

Oncogene, 2014-07, Vol.33 (27), p.3506-3518

2014

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DNA Ligase IV-Dependent NHEJ of Deprotected Mammalian Telomeres in G1 and G2

Current biology, 2002-10, Vol.12 (19), p.1635-1644

2002

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Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22‐q31

Journal of bone and mineral research, 1999-02, Vol.14 (2), p.230-239

1999

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Localization of the human FSH receptor to chromosome 2 p21 using a genomic probe comprising exon 10

Journal of molecular endocrinology, 1994-06, Vol.12 (3), p.265-271

1994

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Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2

International journal of cancer, 2003-02, Vol.103 (4), p.489-495

2003

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Erratum: Topoisomerase I suppresses genomic instability by preventing interference between replication and transcription

Nature cell biology, 2010-11, Vol.12 (11), p.1122-1122

2010

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Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and aneuploid carcinomas

Cancer research (Chicago, Ill.), 1995-11, Vol.55 (22), p.5415-5423

1995

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Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization

Cancer research (Chicago, Ill.), 1994-04, Vol.54 (7), p.1801-1806

1994

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MULTICOLOR KARYOTYPE ANALYSES OF MOUSE EMBRYONIC STEM CELLS

In vitro cellular & developmental biology. Animal, 2005-09, Vol.41 (8), p.278-283

2005

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Genetic Characterization of a Human Skin Carcinoma Progression Model: from Primary Tumor to Metastasis

Journal of investigative dermatology, 2000-12, Vol.115 (6), p.1095-1103

2000

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Comparison of dna gains and losses in primary renal clear cell carcinomas and metastatic sites : Importance of 1q and 3p copy number changes in metastatic events

Cancer research (Chicago, Ill.), 1997-02, Vol.57 (3), p.481-487

1997

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Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification

Human molecular genetics, 1993-11, Vol.2 (11), p.1907-1914

1993

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Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay

Human genetics, 2002-07, Vol.111 (1), p.31-39

2002

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Separate and variably shaped chromosome arm domains are disclosed by chromosome arm painting in human cell nuclei

Chromosome research, 1998, Vol.6 (1), p.25-33

1998

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Possible role for salivary gland protein in taste reception indicated by homology to lipophilic-ligand carrier proteins

Nature (London), 1990-01, Vol.343 (6256), p.366-369

1990

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Chromosomal abnormalities in renal cell neoplasms associated with acquired renal cystic disease. A series studied by comparative genomic hybridization and fluorescence in situ hybridization

The Journal of pathology, 1999-02, Vol.187 (3), p.308-312

1999

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Molecular evidence for derivation of metastatic cells from minor subclones of primary clear renal cell carcinomas

Cancer detection and prevention, 1999-01, Vol.23 (6), p.479-484

1999

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Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals

Human genetics, 2000-07, Vol.107 (1), p.51-57

2000

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The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia

Neurogenetics, 1998-08, Vol.1 (4), p.259-265

1998

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Assignment of the gene encoding the 5-HT1E serotonin receptor (S31) (locus HTR1E) to human chromosome 6q14-q15

Genomics (San Diego, Calif.), 1994-08, Vol.22 (3), p.637-640

1994

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Impact of altered protein structures on the intracellular traffic of a mutated vasopressin precursor from Brattleboro rats

European journal of biochemistry, 1989-07, Vol.182 (3), p.621-627

1989

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Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics

Cancer genetics and cytogenetics, 2001-10, Vol.130 (1), p.79-83

2001

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Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis

Cancer genetics and cytogenetics, 2001-01, Vol.124 (2), p.89-97

2001

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Assignment of the gene encoding the 5-HT sub(1E) serotonin receptor (S31) (locus HTR1E) to human chromosome 6q14-q15

Genomics (San Diego, Calif.), 1994-01, Vol.27 (3), p.637-640

1994

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Genetics of neuroendocrine and carcinoid tumours

The telomere profile distinguishes two classes of genetically distinct cutaneous squamous cell carcinomas

DNA Ligase IV-Dependent NHEJ of Deprotected Mammalian Telomeres in G1 and G2

Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22‐q31

Localization of the human FSH receptor to chromosome 2 p21 using a genomic probe comprising exon 10

Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2

Erratum: Topoisomerase I suppresses genomic instability by preventing interference between replication and transcription

Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and aneuploid carcinomas

Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization

MULTICOLOR KARYOTYPE ANALYSES OF MOUSE EMBRYONIC STEM CELLS

Genetic Characterization of a Human Skin Carcinoma Progression Model: from Primary Tumor to Metastasis

Comparison of dna gains and losses in primary renal clear cell carcinomas and metastatic sites : Importance of 1q and 3p copy number changes in metastatic events

Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification

Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay

Separate and variably shaped chromosome arm domains are disclosed by chromosome arm painting in human cell nuclei

Possible role for salivary gland protein in taste reception indicated by homology to lipophilic-ligand carrier proteins

Chromosomal abnormalities in renal cell neoplasms associated with acquired renal cystic disease. A series studied by comparative genomic hybridization and fluorescence in situ hybridization

Molecular evidence for derivation of metastatic cells from minor subclones of primary clear renal cell carcinomas

Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals

The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia

Assignment of the gene encoding the 5-HT1E serotonin receptor (S31) (locus HTR1E) to human chromosome 6q14-q15

Impact of altered protein structures on the intracellular traffic of a mutated vasopressin precursor from Brattleboro rats

Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics

Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis

Assignment of the gene encoding the 5-HT sub(1E) serotonin receptor (S31) (locus HTR1E) to human chromosome 6q14-q15

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