D. Louis

发表

Up-regulation of specific NF 1 gene transcripts in sporadic pilocytic astrocytomas.

D. Louis, D. Gutmann, C. Dirven, 1996, The American journal of pathology.

Frequent disruption of the RB1 pathway in diffuse large B cell lymphoma: prognostic significance of E2F-1 and p16INK4A

D. Louis, Y. Ino, M. Møller, 2000, Leukemia.

Aberrations of the p53 pathway components p53, MDM2 and CDKN2A appear independent in diffuse large B cell lymphoma

D. Louis, D. Louis, Y. Ino, 1999, Leukemia.

CDKN2A gene deletions and loss of p16 expression occur in osteosarcomas that lack RB alterations.

D. Louis, G. Nielsen, D. Louis, 1998, The American journal of pathology.

Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas.

D. Louis, J. Gusella, A. von Deimling, 1994, Cancer research.

Association of loss of heterozygosity on chromosome 17p with high platelet-derived growth factor alpha receptor expression in human malignant gliomas.

D. Louis, D. Maintz, C. Heldin, 1996, Cancer research.

Malignant transformation of neurofibromas in neurofibromatosis 1 is associated with CDKN2A/p16 inactivation.

D. Louis, A. Stemmer-Rachamimov, G. Nielsen, 1999, The American journal of pathology.

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).

J. W. Thomas, M. Boguski, L. Morrison, 1999, Human molecular genetics.

Retrovirus-mediated gene therapy of experimental brain neoplasms using the herpes simplex virus-thymidine kinase/ganciclovir paradigm.

G. Harsh, D. Louis, C. Kramm, 1996, Cancer gene therapy.

Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions.

A. Stemmer-Rachamimov, D. Kwiatkowski, D. Louis, 2001, American journal of human genetics.

Malignant solitary fibrous tumour of the meninges with marked amianthoid fibre deposition

D. Louis, G. Nielsen, M. Lawlor, 2008, Neuropathology and applied neurobiology.

Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.

D. Lenartz, R. Wellenreuther, J. Gusella, 1995, The American journal of pathology.

Deletion mapping of chromosome 19 in human gliomas

D. Lenartz, J. Schramm, A. von Deimling, 1994, International journal of cancer.

Immunohistochemical survey of p16INK4A expression in normal human adult and infant tissues.

A. Stemmer-Rachamimov, G. Nielsen, D. Louis, 1999, Laboratory investigation; a journal of technical methods and pathology.

Mutational analysis of patients with neurofibromatosis 2.

D. Louis, M. Short, V. Ramesh, 1994, American journal of human genetics.

Regional expression and subcellular localization of the tyrosine-specific phosphatase SH-PTP2 in the adult human nervous system

M. DiFiglia, D. Louis, K. Ueki, 1996, Neuroscience.

Pre-existing herpes simplex virus 1 (HSV-1) immunity decreases, but does not abolish, gene transfer to experimental brain tumors by a HSV-1 vector

D. Finkelstein, D. Louis, E. Chiocca, 1998, Gene Therapy.

NF2 gene analysis distinguishes hemangiopericytoma from meningioma.

J. Bruner, J. Gusella, D. Louis, 1995, The American journal of pathology.

A clinical study of patients with multiple isolated neurofibromas

D. Louis, M. Short, M. Maccollin, 2001, Journal of medical genetics.

Universal absence of merlin, but not other ERM family members, in schwannomas.

D. Louis, J. Gusella, A. Stemmer-Rachamimov, 1997, The American journal of pathology.

A locus for cerebral cavernous malformations maps to chromosome 7q in two families.

L. Morrison, B. Hart, B. Kosofsky, 1995, Genomics.

Exon scanning for mutation of the NF2 gene in schwannomas.

J. Gusella, B. Seizinger, N. Kley, 1994, Human molecular genetics.

Familial schwannomatosis

D. Louis, D. Louis, J. Acierno, 2003, Neurology.

Molecular analysis of astrocytomas presenting after age 10 in individuals with NF1

C. James, D. Louis, D. Gutmann, 2003, Neurology.

A novel pancreatic endocrine tumor suppressor gene locus on chromosome 3p with clinical prognostic implications.

D. Chung, D. Louis, A. Arnold, 1997, The Journal of clinical investigation.

Familial occurrence of adiposis dolorosa.

D. Louis, M. Maccollin, M. Hirano, 2001, Journal of the American Academy of Dermatology.

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.

J. Weber, J. Weissenbach, L. Morrison, 1995, Genome research.

The NF2 gene and merlin protein in human osteosarcomas

J. Gusella, A. Stemmer-Rachamimov, G. Nielsen, 1998, Neurogenetics.

Loss of the NF2 gene and merlin occur by the tumorlet stage of schwannoma development in neurofibromatosis 2.

J. Gusella, A. Stemmer-Rachamimov, D. Louis, 1998, Journal of neuropathology and experimental neurology.

Expression of NF2-encoded merlin and related ERM family proteins in the human central nervous system.

A. Stemmer-Rachamimov, D. Louis, R. Beauchamp, 1997, Journal of neuropathology and experimental neurology.

A novel splice site associated polymorphism in the tuberous sclerosis 2 (TSC2) gene may predispose to the development of sporadic gangliogliomas.

M. Nöthen, D. Louis, I. Blümcke, 1997, Journal of neuropathology and experimental neurology.

Molecular genetic analysis of giant cell glioblastomas.

G. Reifenberger, D. Louis, A. von Deimling, 1997, The American journal of pathology.

NHE-RF, a merlin-interacting protein, is primarily expressed in luminal epithelia, proliferative endometrium, and estrogen receptor-positive breast carcinomas.

A. Stemmer-Rachamimov, M. James, D. Louis, 2001, The American journal of pathology.

Vaccination for experimental gliomas using GM-CSF-transduced glioma cells.

G. Dranoff, D. Finkelstein, G. Reznikoff, 1997, Cancer gene therapy.

Multiple polymorphisms, but no mutations, in the WAF1/CIP1 gene in human brain tumours.

D. Maintz, J. Schramm, A. von Deimling, 1995, British Journal of Cancer.

General method for PCR amplification and direct sequencing of mRNA differential display products.

D. Louis, S. A. Reeves, M. P. Rubio, 1995, BioTechniques.