UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.353

Sortiert nach

Single Missense Mutation in the Tyrosine Kinase Catalytic Domain of the RET Protooncogene is Associated with Multiple Endocrine Neoplasia Type 2B

Proceedings of the National Academy of Sciences - PNAS, 1994-02, Vol.91 (4), p.1579-1583

1994

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC

Human molecular genetics, 1993-07, Vol.2 (7), p.851-856

1993

Link zum Volltext

Verfügbarkeit prüfen

Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entity

British journal of surgery, 1986-04, Vol.73 (4), p.278-281

1986

Link zum Volltext

Verfügbarkeit prüfen

A 1.5-Megabase Yeast Artificial Chromosome Contig from Human Chromosome 10q11.2 Connecting Three Genetic Loci (RET, D10S94, and D10S102) Closely Linked to the MEN2A Locus

Proceedings of the National Academy of Sciences - PNAS, 1993-01, Vol.90 (2), p.492-496

1993

Link zum Volltext

Verfügbarkeit prüfen

Loss of heterozygosity of markers on chromosome 11 in tumors from patients with multiple endocrine neoplasia syndrome type 1

Cancer research (Chicago, Ill.), 1990-10, Vol.50 (20), p.6529-6533

1990

Link zum Volltext

Verfügbarkeit prüfen

Germline mutations in the multiple endocrine neoplasia type 1 gene: Evidence for frequent splicing defects

Human mutation, 1999, Vol.13 (3), p.175-185

1999

Link zum Volltext

Verfügbarkeit prüfen

Guidelines for diagnosis and therapy of MEN type 1 and type 2

The journal of clinical endocrinology and metabolism, 2001-12, Vol.86 (12), p.5658-5671

2001

Link zum Volltext

Verfügbarkeit prüfen

A specific CpG methylation pattern of the MGMT promoter region associated with reduced MGMT expression in primary colorectal cancers

Molecular carcinogenesis, 1999-02, Vol.24 (2), p.90-98

1999

Link zum Volltext

Verfügbarkeit prüfen

Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma

Cancer research (Chicago, Ill.), 1989-08, Vol.49 (15), p.4114-4119

1989

Link zum Volltext

Verfügbarkeit prüfen

Human Parathyroid Antigen: Characterization and Localization with Monoclonal Antibodies

Proceedings of the National Academy of Sciences - PNAS, 1986-08, Vol.83 (16), p.6112-6116

1986

Link zum Volltext

Verfügbarkeit prüfen

Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTC

Oncogene, 1997-06, Vol.14 (25), p.3103-3106

1997

Link zum Volltext

Verfügbarkeit prüfen

Genetic testing for multiple endocrine neoplasia

British journal of surgery, 1993-09, Vol.80 (9), p.1092-1093

1993

Link zum Volltext

Verfügbarkeit prüfen

Reduced Survival in Patients With Ductal Pancreatic Adenocarcinoma Associated With CDKN2 Mutation

JNCI : Journal of the National Cancer Institute, 1996-05, Vol.88 (10), p.680-682

1996

Link zum Volltext

Verfügbarkeit prüfen

Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B

Human molecular genetics, 1995-10, Vol.4 (10), p.1987-1988

1995

Link zum Volltext

Verfügbarkeit prüfen

Lethality of Multiple Endocrine Neoplasia Type I

World journal of surgery, 1998-06, Vol.22 (6), p.581-587

1998

Link zum Volltext

Verfügbarkeit prüfen

Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A

Genomics (San Diego, Calif.), 1991, Vol.9 (1), p.181-192

1991

Link zum Volltext

Verfügbarkeit prüfen

Parathyroid autotransplantation during thyroidectomy. Results of long-term follow-up

Annals of surgery, 1996-05, Vol.223 (5), p.472-480

1996

Link zum Volltext

Verfügbarkeit prüfen

The surgical scientist

Annals of surgery, 1996-09, Vol.224 (3), p.239-254

Wells, Jr, S A

1996

Link zum Volltext

Verfügbarkeit prüfen

Medullary Carcinoma of the Thyroid Gland

World journal of surgery, 2000-08, Vol.24 (8), p.952-956

2000

Link zum Volltext

Verfügbarkeit prüfen

Relationship of tissue carcinoembryonic antigen and calcitonin to tumor virulence in medullary thyroid carcinoma. An immunohistochemical study in early, localized, and virulent disseminated stages of disease

Cancer, 1984, Vol.54 (4), p.657-662

1984

Link zum Volltext

Verfügbarkeit prüfen

Mxi1 tumor suppressor gene is not mutated in primary pancreatic adenocarcinoma

Cancer letters, 1996-04, Vol.102 (1), p.73-76

1996

Link zum Volltext

Verfügbarkeit prüfen

Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A

Annals of surgery, 1994-09, Vol.220 (3), p.237-250

1994

Link zum Volltext

Verfügbarkeit prüfen

Surgical therapy of patients with primary hyperparathyroidism: Long‐term benefits

Journal of bone and mineral research, 1991-10, Vol.6 (S2), p.S143-S149

Wells, Samuel A.

1991

Link zum Volltext

Verfügbarkeit prüfen

Infrequent CDKN2 mutation in human differentiated thyroid cancers

Molecular carcinogenesis, 1996-01, Vol.15 (1), p.5-10

1996

Link zum Volltext

Verfügbarkeit prüfen

Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs

American journal of human genetics, 1992-12, Vol.51 (6), p.1430-1442

1992

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 1.353

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.024)
Mit Volltextzugriff
(1.044)

Publikationsform

4 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(1.352)
Japanisch
(124)
Koreanisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Single Missense Mutation in the Tyrosine Kinase Catalytic Domain of the RET Protooncogene is Associated with Multiple Endocrine Neoplasia Type 2B

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC

Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entity

A 1.5-Megabase Yeast Artificial Chromosome Contig from Human Chromosome 10q11.2 Connecting Three Genetic Loci (RET, D10S94, and D10S102) Closely Linked to the MEN2A Locus

Loss of heterozygosity of markers on chromosome 11 in tumors from patients with multiple endocrine neoplasia syndrome type 1

Germline mutations in the multiple endocrine neoplasia type 1 gene: Evidence for frequent splicing defects

Guidelines for diagnosis and therapy of MEN type 1 and type 2

A specific CpG methylation pattern of the MGMT promoter region associated with reduced MGMT expression in primary colorectal cancers

Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma

Human Parathyroid Antigen: Characterization and Localization with Monoclonal Antibodies

Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTC

Genetic testing for multiple endocrine neoplasia

Reduced Survival in Patients With Ductal Pancreatic Adenocarcinoma Associated With CDKN2 Mutation

Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B

Lethality of Multiple Endocrine Neoplasia Type I

Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A

Parathyroid autotransplantation during thyroidectomy. Results of long-term follow-up

The surgical scientist

Medullary Carcinoma of the Thyroid Gland

Relationship of tissue carcinoembryonic antigen and calcitonin to tumor virulence in medullary thyroid carcinoma. An immunohistochemical study in early, localized, and virulent disseminated stages of disease

Mxi1 tumor suppressor gene is not mutated in primary pancreatic adenocarcinoma

Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A

Surgical therapy of patients with primary hyperparathyroidism: Long‐term benefits

Infrequent CDKN2 mutation in human differentiated thyroid cancers

Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs

Suchergebnisse filtern