The COL4A5 gene in Japanese Alport syndrome patients: Spectrum of mutations of all exons

Shinichiro Kawai, Shinsuke Nomura, T. Harano, +4

Kidney International

Mendelian DisorderGenetic DisorderGeneticsPathologyCol4a5 Gene +6

Abnormal arrangements in the alpha- and gamma-globin gene clusters in a relatively large group of Japanese newborns.

Kōji Shimizu, T. Harano, K. Harano, +5

PubMed

High Incidence of 3-Thalassemia, Hemoglobin E, and Glucose-6-Phosphate Dehydrogenase Deficiency in Populations of Malaria-Endemic Southern Shan State, Myanmar

Aung Myint Than, T. Harano, K. Harano, +3

International Journal of Hematology

Glucose-6-phosphate Dehydrogenase DeficiencyGlobal HealthMalariaHematologyHemoglobin E +1

Hemoglobin Okayama [β‐2 (NA 2) His → Gln]: A new ‘silent’ hemoglobin variant with substituted amino acid residue at the 2,3‐diphosphoglycerate binding site

T. Harano, K. Harano, Susumu Shibata, +3

FEBS Letters

Molecular BiologyWhole BloodHeme TraffickingNew 'SilentBioanalysis +14

Hb Okazaki [β93(F8) Cys → Arg], a new hemoglobin variant with increased oxygen affinity and instability

K. Harano, T. Harano, Susumu Shibata, +3

FEBS Letters

Japanese ManBiochemistryNatural SciencesHeme DegradationPhysiology +12

γ‐Globin gene triplication and quadruplication in Japanese newborns

K. Harano, T. Harano, F. Kutlar, +1

FEBS Letters

A splicing mutation in the α5(IV) collagen gene of a family with Alport's syndrome

Shinsuke Nomura, Gengo Osawa, Tetsujun SAI, +2

Kidney International

Mendelian DisorderConnective Tissue DiseaseGenetic DisorderGeneticsPathology +5

A wider molecular spectrum of β‐thalassaemia in Myanmar

Ne‐Win, T. Harano, K. Harano, +5

British Journal of Haematology

Hb Fukuoka [β2(NA2)HISTYR]: A New Nutation at the 2,3-Diphosphoglycerate Binding Site

T. Harano, K. Harano, Shuichi Ueda, +4

Hemoglobin

GlycobiologyMolecular BiologyHb A1Chemical BiologyHeme Trafficking +15

Hemoglobin Kawachi [α44 (CE2) Pro → Arg] : A new Hemoglobin Variant of High Oxygen Affinity with Amino Acid Substitution at α₁β₂Contact

T. Harano, K. Harano, Shuichi Ueda, +7

Hemoglobin

BiochemistryNatural SciencesHematologyAmino Acid SubstitutionMolecular Biology +5