J. Takahashi

发表

A novel frameshift mutation in the McLeod syndrome gene in a Japanese family

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 1999, Journal of the Neurological Sciences.

RHC/c genotyping based on polymorphism in the promoter region of the RHCE gene.

F. Hirayama, N. Yamashita, Y. Tani, 2001, Legal medicine.

Analysis of Receptor for Vibrio choleraeEl Tor Hemolysin with a Monoclonal Antibody That Recognizes Glycophorin B of Human Erythrocyte Membrane

T. Honda, Y. Tani, J. Takahashi, 1999, Infection and Immunity.

Defining the Jr(a–) phenotype in the Japanese population

Y. Tani, J. Takahashi, H. Matsukura, 2013, Transfusion.

Evaluation of a blood group genotyping platform (BLOODchip® Reference) in Japanese samples

F. Hirayama, Y. Tani, J. Takahashi, 2014, Transfusion medicine.

The genomic organization of the partial D category DVa: the presence of a new partial D associated with the DVa phenotype.

T. Omi, Y. Tani, J. Takahashi, 1999, Biochemical and biophysical research communications.

[Osteoporosis associated with chronic liver disease].

J. Takahashi, H. Takada, H. Kuwayama, 2004, Nihon rinsho. Japanese journal of clinical medicine.

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

M. Gall, J. Deybach, H. Puy, 2012, Nature Genetics.

A novel c.790C>T mutation in RHAG gene encoding the Rhnull phenotype in Japanese

Y. Tani, J. Takahashi, M. Tanaka, 2016 .

Treatment of Mcleod Phenotype Chronic Granulomatous Disease with Reduced-Intensity Conditioning and Unrelated-Donor Umbilical Cord Blood Transplantation

H. Tsutsumi, N. Hatakeyama, Masaki Yamamoto, 2007, International journal of hematology.

Expression analysis of human Rhesus blood group antigens by gene transduction into erythroid and non-erythroid cells.

T. Omi, Y. Tani, J. Takahashi, 1998, International journal of hematology.

Highly Sensitive Glycan Profiling of Hepatitis B Viral Particles and a Simple Method for Dane Particle Enrichment.

A. Kuno, M. Mizokami, H. Narimatsu, 2018, Analytical chemistry.

A forward genetic screen identifies erythrocyte CD55 as essential for Plasmodium falciparum invasion

S. Gygi, D. Root, J. Doench, 2015, Science.

A new mutation detected in RhAG of a Japanese family with Rhmod syndrome may form a longer RhAG protein

Y. Tani, J. Takahashi, E. Kajii, 2002, Transfusion.

AUTOANTI-ENaFS PRODUCTION IN A PATIENT WITH SCID AFTER CORD BLOOD TRANSPLANTATION

F. Hirayama, N. Yamashita, Y. Tani, 2004 .

Muscle CT scan findings in McLeod syndrome and chorea‐acanthocytosis

N. Tachibana, S. Ikeda, K. Tabata, 2000, Muscle and Nerve.

McLeod Syndrome: A Perspective from Japanese Blood Centers

Y. Tani, J. Takahashi, M. Tanaka, 2008 .

Molecular characterization of weak D phenotypes by site‐directed mutagenesis and expression of mutant Rh–green fluorescence protein fusions in K562 cells

T. Omi, Y. Tani, J. Takahashi, 2001, Vox sanguinis.

Detection and quantitation of ABO RBC chimerism by a modified coil planet centrifuge method

F. Hirayama, Y. Tomiyama, N. Yamashita, 2002, Transfusion.

Reactivity of autoantibodies of autoimmune hemolytic anemia with recombinant rhesus blood group antigens or anion transporter band3

T. Omi, Y. Tani, J. Takahashi, 2001, American journal of hematology.

Genotyping of the ABCG2 gene using Matrix‐Associated Laser Desorption/Ionisation, Time‐of‐Flight Mass Spectrometry

Y. Tani, J. Takahashi, M. Tanaka, 2018, Transfusion medicine.

Defining and finding the rare donor

J. Takahashi, M. Tanaka, H. Matsukura, 2014 .

Erythrocytes lacking the Langereis blood group protein ABCB6 are resistant to the malaria parasite Plasmodium falciparum

S. Gygi, A. Srinivasan, M. Weekes, 2018, Communications Biology.

Isolation, characterization, and family study of DTI, a novel partial D phenotype affecting the fourth external loop of D polypeptides

F. Hirayama, T. Omi, Y. Tani, 2002, Transfusion.

Detection of Rh23 in the partial D phenotype associated with the DVa category

T. Omi, Y. Tani, J. Takahashi, 2000, Transfusion.

A novel mutation in the RHD gene in Japanese individuals with weak D, encoding an amino acid change in the 11th transmembranous domain of the RhD protein

F. Hirayama, T. Omi, Y. Tani, 2003, Vox sanguinis.

A CASE OF HARD-TO-DIAGNOSIS COLD AGGLUTININ DISEASE WITH AUTO ANTI-I DUE TO TRANSIENTLY UNDETECTABLE I-ANTIGEN ON THE PATIENT'S RED BLOOD CELLS

J. Takahashi, Tomohito Matsuo, H. Kato, 2021, Japanese Journal of Transfusion and Cell Therapy.

The STR polymorphisms in intron 8 may provide information about the molecular evolution of RH haplotypes

T. Omi, S. Araki, H. Minakami, 1999, Human Genetics.

Ophthalmologic involvement in Japanese siblings with chorea-acanthocytosis caused by a novel chorein mutation.

K. Sugioka, S. Kusunoki, K. Saigoh, 2013, Parkinsonism & related disorders.

Novel alleles of Lan− in Japanese populations

K. Tadokoro, M. Uchikawa, Y. Tani, 2014, Transfusion.

THE FIRST CASE OF A JAPANESE PATIENT WITH AN ACUTE HEMOLYTIC TRANSFUSION REACTION TO A HIGH-FREQUENCY ANTIGEN, Emm, BY ANTI-Emm

Y. Tani, J. Takahashi, Mitsunobu Tanaka, 2015 .

A forward genetic screen identifies erythrocyte CD55 as essential for Plasmodium falciparum invasion

John G Doench, S. Gygi, D. Root, 2015, Science.

Erythrocytes lacking the Langereis blood group protein ABCB6 are resistant to the malaria parasite Plasmodium falciparum

S. Gygi, A. Srinivasan, M. Weekes, 2018, Communications Biology.