(Q34480137)

2 August 2017

1 reference

title

Familial neurogenic tumor syndromes (English)

1 reference

2 August 2017

Kimmelman A

1

1 reference

2 August 2017

Liang BC

series ordinal

2

1 reference

2 August 2017

publication date

1 December 2001

1 reference

Hematology / Oncology Clinics of North America

2 August 2017

published in

1 reference

2 August 2017

volume

15

1 reference

2 August 2017

issue

6

1 reference

2 August 2017

page(s)

1073-1084

1 reference

Cowden syndrome and Lhermitte-Duclos disease

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Suppression of human colorectal carcinoma cell growth by wild-type p53

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Sequence homology shared by neurofibromatosis type-1 gene and IRA-1 and IRA-2 negative regulators of the RAS cyclic AMP pathway.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Neurofibromatosis type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Tuberous sclerosis: analysis of linkage to red cell and plasma protein markers

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

p53 functions as a cell cycle control protein in osteosarcomas

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Identification and characterization of the tuberous sclerosis gene on chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Location of gene for Gorlin syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Menin, the product of the MEN1 gene, is a nuclear protein

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Benign spinal nerve sheath tumors: their occurrence sporadically and in neurofibromatosis types 1 and 2

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

The molecular basis of Turcot's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

The tumour suppressor protein NF2/merlin: the puzzle continues.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Binding of the von Hippel-Lindau tumor suppressor protein to Elongin B and C

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

von Hippel-Lindau disease affecting 43 members of a single kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Identification of the von Hippel-Lindau disease tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

The 1993 Walter Hubert Lecture: the role of the p53 tumour-suppressor gene in tumorigenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Genomic organization of the neurofibromatosis 1 gene (NF1).

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Hereditary tumor syndromes of the nervous system: overview and rare syndromes.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

p53 is required for radiation-induced apoptosis in mouse thymocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Cytoskeleton--plasma membrane interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Association between meningioma and Cowden's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Von Hippel-Lindau disease: a genetic study

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

UV Irradiation Stimulates Levels of p53 Cellular Tumor Antigen in Nontransformed Mouse Cells

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Germline PTEN mutations in Cowden syndrome-like families.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Cellular localization and cell cycle regulation by a temperature-sensitive p53 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm (17p13)

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymoma

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Synthetic peptides define critical contacts between elongin C, elongin B, and the von Hippel-Lindau protein

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

The gene causing multiple endocrine neoplasia type 2 (MEN 2).

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

1 reference

7 January 2021

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

p53 germline mutations in Li-Fraumeni syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

On the mutation rate of neurofibromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Clinical, neuropathological and genetic aspects of the tuberous sclerosis complex.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Neurofibromatosis type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Cervical neuroblastoma and multiple endocrine neoplasia type 2a

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

The neurofibromatosis type 1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Neurofibromatosis type 1: pathology, clinical features and molecular genetics.

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

The neurofibromatosis type 1 gene encodes a protein related to GAP

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

Wild-type p53 induces apoptosis of myeloid leukaemic cells that is inhibited by interleukin-6

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8588%2805%2970268-9

7 January 2021

10.1016/S0889-8588(05)70268-9

Identifiers

DOI

1 reference

2 August 2017

1 reference