A genomic scanning method for higher organisms using restriction sites as landmarks.

I. Hatada, Yoshihide Hayashizaki, Shinji Hirotsune, +2

Proceedings of the National Academy of Sciences

Genomic Scanning MethodComparative GenomicsGeneticsDna AnalysisMolecular Biology +18

Peptide inhibitors for angiotensin I-converting enzyme from enzymatic hydrolysates of porcine skeletal muscle proteins

Keizo Arihara, Yoshiki Nakashima, T Mukai, +2

Meat Science

Protein ChemistryBiochemistryNatural SciencesMedicinePeptide Library +9

Tissue-specific expression of rat aldolase A mRNAs. Three molecular species differing only in the 5'-terminal sequences.

T Mukai, Keiichiro Joh, Yuji Arai, +2

Journal of Biological Chemistry

New approach for detection of amplification in cancer DNA using restriction landmark genomic scanning.

Shinji Hirotsune, Izuho Hatada, H. Komatsubara, +7

PubMed

Gene AmplificationGeneticsDna AnalysisMolecular BiologyPathology +16

Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation.

H Kishi, T Mukai, Akira Hirono, +3

Proceedings of the National Academy of Sciences

GeneticsMolecular BiologyIron DeficiencyAplastic AnemiaHemolytic Anemia +16

Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours

Y. Satoh, Hisaya Nakadate, Tetsuji Nakagawachi, +7

British Journal of Cancer

ChromatinWilms Tumour 1Somatic VariantCell DivisionEpigenetic Alterations +12

Imprinting disruption of the <i>CDKN1C</i>/<i>KCNQ1OT1</i> domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer

Ken Higashimoto, Hidenobu Soejima, Takeshi Saito, +2

Cytogenetic and Genome Research

CpG methylation of MGMT and hMLH1 promoter in hepatocellular carcinoma associated with hepatitis viral infection

Shiroh Matsukura, Hidenobu Soejima, Tetsuji Nakagawachi, +7

British Journal of Cancer

Epigenetic ChangeDna MethylationPathologyHmlh1 PromoterEpigenetics +18

Nucleotide sequence of rat liver aldolase B messenger RNA.

Ken‐ichi Tsutsumi, T Mukai, Reiko Tsutsumi, +6

Journal of Biological Chemistry

Autosomal recessive cystinuria caused by genome‐wide paternal uniparental isodisomy in a patient with Beckwith–Wiedemann syndrome

Yasufumi Ohtsuka, Ken Higashimoto, Kensaku Sasaki, +12

Clinical Genetics

GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification +15