Nature Search

A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene

K. Fukino
A. Teramoto
M. Emi
Research01 Jan 2000
Journal of Human Genetics

Volume: 45, P: 47-51
Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21

M Tavassoli
H Steingrimsdottir
IG Campbell
Research01 Jul 1996
British Journal of Cancer

Volume: 74, P: 115-119
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

Here, Imamuraet al. conduct meta-analysis of genome-wide association studies to identify novel susceptibility loci for type 2 diabetes (T2D) in the Japanese population. By doing so, this study shows that both ethnicity-specific and ethnically-shared genetic loci can contribute to T2D risk.

Minako Imamura
Atsushi Takahashi
Takashi Kadowaki
ResearchOpen Access28 Jan 2016
Nature Communications

Volume: 7, P: 1-12
Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p

I Petersen
H Langreck
M Dietel
Research01 Jan 1997
British Journal of Cancer

Volume: 75, P: 79-86
Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinoma

H. Kayahara
H. Yamagata
H. Hamakawa
Research01 May 2001
Journal of Human Genetics

Volume: 46, P: 335-341
The FHIT gene is alternatively spliced in normal kidney and renal cell carcinoma

Xudong Luan
Guangping Shi
Linda A Cannizzaro
Research03 Jul 1997
Oncogene

Volume: 15, P: 79-86
A phase II study of cisplatin, vindesine and continuously infused 5-fluorouracil in the treatment of advanced non-small-cell lung cancer

T Nakano
H Ikegami
K Higashino
Research01 May 1996
British Journal of Cancer

Volume: 73, P: 1096-1100
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population

Genome-wide association analyses identify 28 new susceptibility loci for type 2 diabetes in the Japanese population. Transethnic comparisons highlight the key role of beta cell dysfunction in type 2 diabetes across different ancestry groups.

Ken Suzuki
Masato Akiyama
Takashi Kadowaki
Research04 Feb 2019
Nature Genetics

Volume: 51, P: 379-386
Spinal subarachnoid hematoma compressing the conus medullaris and associated with neurofibromatosis type 2

T Inoue
K Miyamoto
K Shimizu
Research21 Oct 2003
Spinal Cord

Volume: 41, P: 649-652
Gemcitabine and vinorelbine followed by docetaxel in patients with advanced non-small-cell lung cancer: a multi-institutional phase II trial of nonplatinum sequential triplet combination chemotherapy (JMTO LC00-02)

S Hosoe
K Komuta
M Kawahara
ResearchOpen Access10 Feb 2003
British Journal of Cancer

Volume: 88, P: 342-347
Intramedullary teratoma of the spine: report of two adult cases

Y Nonomura
K Miyamoto
K Shimizu
Research30 Jan 2002
Spinal Cord

Volume: 40, P: 40-43
Clinical outcomes of multilevel anterior corpectomy and fusion as a revision surgery of the cervical spine: report of seven cases

K Fushimi
K Miyamoto
K Shimizu
Research29 Nov 2005
Spinal Cord

Volume: 44, P: 449-456
Foramen magnum decompression for the treatment of Arnold Chiari malformation type I with associated syringomyelia in an elderly patient

I Takigami
K Miyamoto
K Shimizu
Research02 Nov 2004
Spinal Cord

Volume: 43, P: 249-251
Sudden onset of paraparesis caused by hypertrophy of the thoracic posterior longitudinal ligament

S Nozawa
K Shimizu
H Hosoe
Research18 Dec 2002
Spinal Cord

Volume: 41, P: 53-55
Transoral anterior approach for extensive anterior decompression at the C3 vertebra level in a patient with severe atlantoaxial vertical subluxation and rheumatoid arthritis

T Sasaki
K Miyamoto
K Shimizu
Research28 Jun 2005
Spinal Cord

Volume: 44, P: 52-55
Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome)

K Miyamoto
Y Sakaguchi
K Shimizu
Research07 Dec 2004
Spinal Cord

Volume: 43, P: 190-194

Search

A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL gene

Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p

Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinoma

The FHIT gene is alternatively spliced in normal kidney and renal cell carcinoma

A phase II study of cisplatin, vindesine and continuously infused 5-fluorouracil in the treatment of advanced non-small-cell lung cancer

Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population

Spinal subarachnoid hematoma compressing the conus medullaris and associated with neurofibromatosis type 2

Gemcitabine and vinorelbine followed by docetaxel in patients with advanced non-small-cell lung cancer: a multi-institutional phase II trial of nonplatinum sequential triplet combination chemotherapy (JMTO LC00-02)

Intramedullary teratoma of the spine: report of two adult cases

Clinical outcomes of multilevel anterior corpectomy and fusion as a revision surgery of the cervical spine: report of seven cases

Foramen magnum decompression for the treatment of Arnold Chiari malformation type I with associated syringomyelia in an elderly patient

Sudden onset of paraparesis caused by hypertrophy of the thoracic posterior longitudinal ligament

Transoral anterior approach for extensive anterior decompression at the C3 vertebra level in a patient with severe atlantoaxial vertical subluxation and rheumatoid arthritis

Tetraparesis due to exostotic osteochondroma at upper cervical cord in a patient with multiple exostoses–mental retardation syndrome (Langer–Giedion syndrome)

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