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A robust xenotransplantation model for acute myeloid leukemia

Leukemia, 2009-11, Vol.23 (11), p.2109-2117

2009

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Primary Intracranial Atypical Teratoid/Rhabdoid Tumors of Infancy and Childhood: MRI Features and Patient Outcomes

American Journal of Neuroradiology, 2006-05, Vol.27 (5), p.962-971

2006

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Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1

Journal of medical genetics, 2009-01, Vol.46 (1), p.68-72

2009

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TrkC Expression Predicts Good Clinical Outcome in Primitive Neuroectodermal Brain Tumors

Journal of clinical oncology, 2000-03, Vol.18 (5), p.1027-1035

2000

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Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity

Journal of neurosurgery, 1996-07, Vol.85 (1), p.56-65

1996

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Frequent expression of a mutant epidermal growth factor receptor in multiple human tumors

Cancer research (Chicago, Ill.), 1995-12, Vol.55 (23), p.5536-5539

1995

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Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma

Cancer research (Chicago, Ill.), 1994-06, Vol.54 (11), p.2869-2872

1994

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In Vivo Amplification of the PAX3-FKHR and PAX7-FKHR Fusion Genes in Alveolar Rhabdomyosarcoma

Human molecular genetics, 1996-01, Vol.5 (1), p.15-21

1996

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Mutations of the INI1 Rhabdoid Tumor Suppressor Gene in Medulloblastomas and Primitive Neuroectodermal Tumors of the Central Nervous System

Clinical cancer research, 2000-07, Vol.6 (7), p.2759-2763

2000

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Congenital disseminated malignant rhabdoid tumor: a distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

The American journal of surgical pathology, 1999-03, Vol.23 (3), p.249-256

1999

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Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors

Cancer research (Chicago, Ill.), 1999-01, Vol.59 (1), p.74-79

1999

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A Region of Consistent Deletion in Neuroblastoma Maps within Human Chromosome 1p36.2-36.3

Proceedings of the National Academy of Sciences - PNAS, 1995-06, Vol.92 (12), p.5520-5524

1995

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Prognostic significance of chromosome 17p deletions in childhood primitive neuroectodermal tumors (medulloblastomas) of the central nervous system

Clinical cancer research, 1997-03, Vol.3 (3), p.473-478

1997

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Monosomy 22 in rhabdoid or atypical tumors of the brain

Journal of neurosurgery, 1990-11, Vol.73 (5), p.710-714

1990

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Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

Journal of medical genetics, 1993-10, Vol.30 (10), p.807-812

1993

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Cytogenetics and molecular genetics of childhood brain tumors

Neuro-oncology (Charlottesville, Va.), 1999-04, Vol.1 (2), p.139-151

Biegel, J A

1999

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Genetics of pediatric central nervous system tumors

Journal of pediatric hematology/oncology, 1997-11, Vol.19 (6), p.492-501

Biegel, J A

1997

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Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors

Cancer research (Chicago, Ill.), 1992-06, Vol.52 (12), p.3391-3395

1992

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Atypical teratoid/rhabdoid tumor of the central nervous system in an 18-year-old patient

Clinical neuropathology, 2009-01, Vol.28 (1), p.1-10

2009

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Molecular cytogenetic studies of pediatric ependymomas

Journal of neuro-oncology, 1998-03, Vol.37 (1), p.25-33

1998

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Lack of Germline Transmission of Vector Sequences Following Systemic Administration of Recombinant AAV-2 Vector in Males

Molecular therapy, 2001-12, Vol.4 (6), p.586-592

2001

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Distinctive multicystic hemispheric lesions suggesting a novel variant of infantile astrocytoma

Clinical neuropathology, 2011-09, Vol.30 (5), p.235-241

2011

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ECK, a human EPH-related gene, maps to 1p36.1, a common region of alteration in human cancers

Genomics (San Diego, Calif.), 1997-03, Vol.40 (2), p.371-374

1997

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Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2)

Genomics (San Diego, Calif.), 1995, Vol.25 (2), p.538-546

1995

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Exon scanning for mutations of the nf2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas

International journal of cancer, 1995-08, Vol.64 (4), p.243-247

1995

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A robust xenotransplantation model for acute myeloid leukemia

Primary Intracranial Atypical Teratoid/Rhabdoid Tumors of Infancy and Childhood: MRI Features and Patient Outcomes

Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1

TrkC Expression Predicts Good Clinical Outcome in Primitive Neuroectodermal Brain Tumors

Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity

Frequent expression of a mutant epidermal growth factor receptor in multiple human tumors

Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma

In Vivo Amplification of the PAX3-FKHR and PAX7-FKHR Fusion Genes in Alveolar Rhabdomyosarcoma

Mutations of the INI1 Rhabdoid Tumor Suppressor Gene in Medulloblastomas and Primitive Neuroectodermal Tumors of the Central Nervous System

Congenital disseminated malignant rhabdoid tumor: a distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11

Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors

A Region of Consistent Deletion in Neuroblastoma Maps within Human Chromosome 1p36.2-36.3

Prognostic significance of chromosome 17p deletions in childhood primitive neuroectodermal tumors (medulloblastomas) of the central nervous system

Monosomy 22 in rhabdoid or atypical tumors of the brain

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

Cytogenetics and molecular genetics of childhood brain tumors

Genetics of pediatric central nervous system tumors

Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors

Atypical teratoid/rhabdoid tumor of the central nervous system in an 18-year-old patient

Molecular cytogenetic studies of pediatric ependymomas

Lack of Germline Transmission of Vector Sequences Following Systemic Administration of Recombinant AAV-2 Vector in Males

Distinctive multicystic hemispheric lesions suggesting a novel variant of infantile astrocytoma

ECK, a human EPH-related gene, maps to 1p36.1, a common region of alteration in human cancers

Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2)

Exon scanning for mutations of the nf2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas

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