M. Kudo

Publication List Details

Period

1995 - 2008

Number

19

Co-Authors

Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning (2001)

Montgomery, GW, Duffy, DL, Hall, J, Kudo, M, Martin, NG, Hsueh, AJ

Concentrations of follicle-stimulating hormone (FSH) have an important role in multiple ovulation. An association has been reported between mutations in the FSH receptor (FSHR) in a family with...

Dizygotic twinning is not linked to variation at the alpha-inhibin locus on human chromosome 2 (2000)

Montgomery, GW, Duffy, DL, Hall, J, Haddon, BR, Kudo, M, McGee, EA, ...

Natural multiple pregnancy in women leading to dizygotic (DZ) twins is familial and varies across racial groups, suggesting a genetic predisposition. Mothers of DZ twins have a higher incidence of...

Construction of a Nonlinear Discrimination Function Based on the MDL Criterion (1998)

M. Sato, M. Kudo, J. Toyama, M. Shimbo

Although a nonlinear discrimination function may be superior to linear or quadratic classifiers, it is difficult to construct such a function. In this paper, we propose a method to construct a...

Feature Selection for a Nonlinear Classifier (1998)

M. Kudo, J. Toyama, M. Shimbo

. The nonlinear classifier is effective for many practical problems. We have already proposed a method for constructing a nonlinear classifier using Legendre polynomials and have obtained good...

Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty.

Laue, L, Chan, W Y, Hsueh, A J, Kudo, M, Hsu, S Y, Wu, S M, ...

Genomic DNA from 32 unrelated families with male-limited precocious puberty was examined for the previously described Asp-578-->Gly, Met-571-->Ile, and Thr-577-->Ile mutations in transmembrane helix...

Endothelin receptor is coupled to phospholipase C via a pertussis toxin-insensitive guanine nucleotide-binding regulatory protein in vascular smooth muscle cells.

Takuwa, Y, Kasuya, Y, Takuwa, N, Kudo, M, Yanagisawa, M, Goto, K, ...

The mechanisms of endothelin-1 (ET) actions were investigated in cultured rat aortic vascular smooth muscle A-10 cells. The A-10 cells have a single class of high affinity binding sites for ET with...

Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty.

Laue, L, Chan, W Y, Hsueh, A J, Kudo, M, Hsu, S Y, Wu, S M, ...

Genomic DNA from 32 unrelated families with male-limited precocious puberty was examined for the previously described Asp-578-->Gly, Met-571-->Ile, and Thr-577-->Ile mutations in transmembrane helix...

Endothelin receptor is coupled to phospholipase C via a pertussis toxin-insensitive guanine nucleotide-binding regulatory protein in vascular smooth muscle cells.

Takuwa, Y, Kasuya, Y, Takuwa, N, Kudo, M, Yanagisawa, M, Goto, K, ...

The mechanisms of endothelin-1 (ET) actions were investigated in cultured rat aortic vascular smooth muscle A-10 cells. The A-10 cells have a single class of high affinity binding sites for ET with...

High prevalence of anti-hepatitis B virus serological markers in patients with hepatitis C virus related chronic liver disease in Japan

Marusawa, H, Osaki, Y, Kimura, T, Ito, K, Yamashita, Y, Eguchi, T, ...

BACKGROUND/AIMS—Evidence is accumulating that hepatitis B virus (HBV) is present in patients who are hepatitis B surface antigen negative but have antibody to hepatitis B core antigen (anti-HBc)....

Dynamic imaging of pancreatic diseases by contrast enhanced coded phase inversion harmonic ultrasonography

Kitano, M, Kudo, M, Maekawa, K, Suetomi, Y, Sakamoto, H, Fukuta, N, ...

Background: Coded phase inversion harmonic ultrasonography, a newly available sonographic technique, enables visualisation of slow flow in minute vessels in a real time fashion with the use of a...

Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders

Wada, T, Takei, K, Kudo, M, Shimura, S, Kasahara, Y, Koizumi, S, ...

Omenn syndrome was recently found to be caused by missense mutations in RAG1 or RAG2 gene that result in partial V(D)J recombination activity. Although the clinical hallmarks of the disease are well...

CagA in Barrett’s oesophagus in Colombia, a country with a high prevalence of gastric cancer

Kudo, M, Gutierrez, O, Cardona, H, Nurgalieva, Z Z, Wu, J, ...

Background: In the USA, atrophic gastritis and gastric cancer are rare, whereas gastro-oesophageal reflux disease (GERD) is common. Infection with Helicobacter pylori, especially a CagA positive...