H. Inaba

发表

Spectrum of mutations in CRM-positive and CRM-reduced hemophilia A.

S. Antonarakis, H. Kazazian, M. Mcginniss, 1993, Genomics.

Genotypic and phenotypic features of Japanese patients with mild to moderate hemophilia A

K. Amano, K. Fukutake, H. Inaba, 2013, International journal of hematology.

Genetic Counseling by Analysis of Intron 22 Inversions of the Factor VIII Gene

H. Mohri, E. Yamazaki, H. Inaba, 1998 .

Influence of Insertion in Human Immunodeficiency Virus Type 1 (HIV-1) Reverse Transcriptase on Clinical Course

K. Fukutake, H. Inaba, K. Moriya, 2001 .

Coagulation assay discrepancies in Japanese patients with non-severe hemophilia A

S. Nishikawa, S. Nishikawa, K. Amano, 2021, International Journal of Hematology.

Mild hemophilia A resulting from Arg-to-Leu substitution in exon 26 of the factor VIII gene

S. Antonarakis, H. Kazazian, H. Inaba, 1989, Human Genetics.

Identification of Two Point Mutations in Japanese Patients with Congenital Coagulation Factor XIII A Subunit Deficiencies

S. Yoshida, M. Shima, K. Fukutake, 1998 .

Cross-reacting Material-positive Hemophilia A Diagnosed in a Patient with a Spontaneous Thigh Hemorrhage

K. Nogami, K. Fukutake, T. Koyama, 2017, Internal medicine.

Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine).

S. Antonarakis, M. Higuchi, H. Kazazian, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Identification and characterization of an adenine to guanine transition within intron 10 of the factor VIII gene as a causative mutation in a patient with mild haemophilia A

K. Amano, K. Fukutake, H. Inaba, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of Missense Mutations in the FVII Gene of Three FVII Deficiencies

K. Amano, K. Fukutake, H. Inaba, 2001 .

Molecular characterization of 3 factor V mutations, R2174L, V1813M, and a 5-bp deletion, that cause factor V deficiency

K. Amano, K. Fukutake, H. Inaba, 2007 .

Pharmacokinetic and Pharmacodynamic Profiles of CS‐518, A Selective, Long‐Lasting Thromboxane Synthase Inhibitor, After Single and Multiple Oral Administration to Healthy Volunteers

M. Nakashima, K. Kosuge, H. Inaba, 1994, Journal of clinical pharmacology.

IgG antibodies against polyethylene glycol (PEG) in patient with hemophilia A

K. Amano, H. Inaba, E. Kinai, 2021, Japanese Journal of Thrombosis and Hemostasis.

Inversion in the Factor VIII Gene

H. Inaba, 1994 .

Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis.

S. Antonarakis, H. Kazazian, J. Oldenburg, 1991, Proceedings of the National Academy of Sciences of the United States of America.

MspI polymorphic site in intron 22 of the factor VIII gene in the Japanese population

S. Antonarakis, H. Kazazian, H. Inaba, 2004, Human Genetics.

Factor VIII gene inversions in severe hemophilia A: results of an international consortium study.

F E Preston, P G Mori, S S Sommer, 1995, Blood.

Prolonged α-thrombin-related activation and delayed active protein C-associated degradation confer mild phenotype in a patient with severe hemophilia A with F8 p.H118R

K. Amano, H. Inaba, E. Kinai, 2022, International Journal of Hematology.

In vitro validation of chromogenic substrate assay for evaluation of surrogate FVIII-activity of emicizumab.

S. Nagatoishi, K. Amano, H. Inaba, 2023, Thrombosis research.

Partial correction of a severe molecular defect in hemophilia A, because of errors during expression of the factor VIII gene.

S. Antonarakis, H. Kazazian, M. Higuchi, 1997, American journal of human genetics.

Genetic analysis of carrier status in female members of Japanese hemophilia families

K. Amano, K. Fukutake, H. Inaba, 2021, Journal of thrombosis and haemostasis : JTH.

Inversion in Japanese Patients with Hemophilia A

K. Fukutake, H. Inaba, T. Nagao, 1995, Thrombosis and Haemostasis.

Two double heterozygous mutations in the F7 gene show different manifestations

K. Amano, K. Fukutake, Y. Hatta, 2002, British journal of haematology.

Polymerase chain reaction (PCR)

H. Inaba, 1989 .

A Novel Mutation Glyl672→Arg in Type 2A and a Homozygous Mutation in Type 2B von Willebrand Disease

S. Yoshida, K. Fukutake, H. Inaba, 1996, Thrombosis and Haemostasis.

Epidemiology of clonorchiasis in Ninh Binh Province, Vietnam.

L. Cong, H. Inaba, N. van De, 1998, The Southeast Asian journal of tropical medicine and public health.

Identification of a Novel Point Mutation (Ala94 to Val) in a Hereditary Type I Antithrombin III Deficiency

S. Yoshida, K. Fukutake, H. Inaba, 1996 .

Five Novel and four recurrent point mutations in the antithrombin gene causing venous thrombosis

K. Amano, K. Fukutake, H. Inaba, 2003, International journal of hematology.

Comparison in Quantification of Human Immunodeficiency Virus Type 1 RNA Measured by Standard Method (Amplicor HIV Monitor Test Ver.1.0) and Add-in Primer Mix Method

K. Amano, K. Fukutake, H. Inaba, 2000 .

A novel synonymous variant in the F8 gene, p.(Leu40=)/c.120C>A, likely causes mild haemophilia A

K. Amano, K. Fukutake, H. Inaba, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of deep intronic individual variants in patients with hemophilia A by next‐generation sequencing of the whole factor VIII gene

K. Amano, K. Fukutake, H. Inaba, 2017, Research and practice in thrombosis and haemostasis.

Fluctuations in Plasma Levels of Thrombomodulin in Patients with DIC

K. Amano, K. Fukutake, H. Inaba, 1992, Thrombosis and Haemostasis.

Features of factor VIII activity measurement in Arg531His mutant detected in patients with mild hemophilia A

Y. Yatomi, K. Amano, K. Fukutake, 2008 .

Clinical application of the next-generation sequencing in the field of thrombosis and hemostasis

H. Inaba, 2015 .

Phase 1 study of L-627, biapenem, a new parenteral carbapenem antibiotic.

M. Nakashima, K. Kosuge, H. Inaba, 1993, International journal of clinical pharmacology, therapy, and toxicology.

The use of fresh frozen plasma infusion in a patient with congenital factor V deficiency in a case of eye ball extraction

H. Inaba, Mitsuru Suzuki, O. Tatsuzawa, 1976 .

Factor X M402T: a homozygous missense mutation identified as the cause of cross-reacting material-reduced deficiency

K. Amano, K. Fukutake, H. Inaba, 2014, International Journal of Hematology.

Design of a suitable formulation of FK613, a novel antiallergic agent, based on its pharmacokinetic and pharmacodynamic properties in healthy subjects

M. Nakashima, H. Inaba, A. Sugiyama, 2004, European Journal of Clinical Pharmacology.

PAM-flexible Cas9-mediated base editing of a hemophilia B mutation in induced pluripotent stem cells

H. Nishimasu, O. Nureki, Hideki Uosaki, 2023, Communications medicine.

Factor VIII haplotypes of Japanese population show similarity to those of Caucasian populations

K. Amano, K. Fukutake, H. Inaba, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Phase I Study of E1077, a Novel Parenteral Cephem Antibiotic

M. Nakashima, H. Inaba, Y. Tomono, 1994, Journal of clinical pharmacology.

Characteristics of the principal neutralizing determinant of HIV-1 prevalent in Japan.

S. Matsushita, H. Inaba, T. Hattori, 1991, AIDS research and human retroviruses.

Two cases of acquired factor V inhibitor which were initially diagnosed with congenital deficiency by cross mixing tests

K. Amano, K. Fukutake, H. Inaba, 2018 .

Molecular characterization of 3 factor V mutations, R2174L, V1813M, and a 5-bp deletion, that cause factor V deficiency.

K. Amano, K. Fukutake, H. Inaba, 2007, International journal of hematology.

Variation of incubation time in an in vitro drug susceptibility test of Plasmodium falciparum isolates studied in the Solomon Islands.

S. Kano, H. Ohmae, H. Inaba, 2001, Parasitology international.

Application of a next-generation genetic analysis in the field of hemophilia

H. Inaba, 2017 .

ANALYSIS OF DISCREPANT ASSAY-DETERMINED ACTIVITY LEVELS OF FACTOR VIII ASSOCIATED WITH R531H MUTATION

Y. Yatomi, K. Amano, K. Fukutake, 2007 .