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Circularly polarized plane terahertz waves radiated from a resonant tunneling diode integrated with a collimating metalens and quarter-wave plate

Applied physics express, 2024-08, Vol.17 (8), p.82001

2024

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Non-multiple lymphomatous polyposis form of mantle cell lymphoma in the gastrointestinal tract

Journal of gastroenterology, 2004-10, Vol.39 (10), p.995-1000

2004

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Gene structure of human cholecystokinin (CCK) type-A receptor: body fat content is related to CCK type-A receptor gene promoter polymorphism

FEBS letters, 2000-01, Vol.466 (2), p.264-266

2000

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A case of acute myeloblastic leukemia with a novel variant of t(8;21)(q22;q22)

International journal of hematology, 2008-01, Vol.87 (1), p.78-82

2008

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9q34.3 deletion syndrome in three unrelated children

American journal of medical genetics, 2004-04, Vol.126A (3), p.278-283

2004

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Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

Nature genetics, 2008-02, Vol.40 (2), p.237-242

2008

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Two cases of partial trisomy 21 (pter-q22.1) without the major features of Down syndrome

American journal of medical genetics. Part A, 2006-02, Vol.140A (3), p.227-232

2006

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Eosinophils derived from acute promyelocytic leukemia cells after arsenic trioxide treatment

International journal of hematology, 2007-06, Vol.85 (5), p.456-457

2007

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MLL/AF-1p fusion in therapy-related early pre-B acute lymphoblastic leukemia with t(1;11)(p32;q23) translocation developing in the relapse phase of acute promyelocytic leukemia

International journal of hematology, 2003-12, Vol.78 (5), p.439-442

2003

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Fluorescent in situ hybridization analysis of Philadelphia chromosome: Negative chronic myeloid leukemia with the bcr/abl fusion gene

International journal of hematology, 2004-08, Vol.80 (2), p.155-158

2004

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EWS‐FLI‐1 and EWS‐ERG chimeric mRNAs in Ewing's sarcoma and primitive neuroectodermal tumor

International journal of cancer, 1995-11, Vol.63 (4), p.500-504

1995

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Detection of HER‐2/neu (c‐erb B‐2) DNA amplification in primary breast carcinoma

Cancer, 2001-12, Vol.92 (12), p.2965-2974

2001

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Terahertz vortex metasurface for integration into compact terahertz continuous-wave sources

2024 49th International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz), 2024, p.1-2

2024

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Detection of HER-2/neu (c-erb B-2) DNA amplification in primary breast carcinoma: Interobserver reproducibility and correlation with immunohistochemical HER-2 overexpression

Cancer, 2001-12, Vol.92 (12), p.2965-2974

2001

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Correlation of clonal T cell expansion with disease activity in systemic lupus erythematosus

International immunology, 1997-04, Vol.9 (4), p.547-554

1997

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Primary central nervous system lymphomas. Immunophenotypic, virologic, and cytogenetic findings of three patients without immune defects

Cancer, 1994-01, Vol.73 (2), p.455-463

1994

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Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism

American journal of medical genetics. Part A, 2008-06, Vol.146A (11), p.1458-1461

2008

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Microdeletion in the SHOX 3′ region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri–Weill dyschondrosteosis in her 46,XX mother: Implication for the SHOX enhancer

American journal of medical genetics. Part A, 2005-08, Vol.137A (1), p.72-76

2005

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Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1)

American journal of medical genetics. Part A, 2006-08, Vol.140A (16), p.1773-1777

2006

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Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomy

American journal of medical genetics, 2004-07, Vol.128A (2), p.214-216

2004

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Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients

American journal of medical genetics, 2002-04, Vol.108 (4), p.285-289

2002

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Metabolic disposition of pantoprazole, a proton pump inhibitor, in relation to S‐mephenytoin 4′‐hydroxylation phenotype and genotype

Clinical pharmacology and therapeutics, 1997-12, Vol.62 (6), p.619-628

1997

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Detection of the CBFB / MYH11 fusion gene in de novo acute myeloid leukemia (AML): A single-institution study of 224 Japanese AML patients

Leukemia research, 2007-04, Vol.31 (4), p.471-476

2007

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Homozygous Deletions of p16/MTS1 Gene Are Frequent But Mutations Are Infrequent in Childhood T-Cell Acute Lymphoblastic Leukemia

Blood, 1995-08, Vol.86 (4), p.1269-1275

1995

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Vitamin D receptor genotypes and bone mineral density

The Lancet (British edition), 1995-05, Vol.345 (8959), p.1238-1239

1995

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Circularly polarized plane terahertz waves radiated from a resonant tunneling diode integrated with a collimating metalens and quarter-wave plate

Non-multiple lymphomatous polyposis form of mantle cell lymphoma in the gastrointestinal tract

Gene structure of human cholecystokinin (CCK) type-A receptor: body fat content is related to CCK type-A receptor gene promoter polymorphism

A case of acute myeloblastic leukemia with a novel variant of t(8;21)(q22;q22)

9q34.3 deletion syndrome in three unrelated children

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

Two cases of partial trisomy 21 (pter-q22.1) without the major features of Down syndrome

Eosinophils derived from acute promyelocytic leukemia cells after arsenic trioxide treatment

MLL/AF-1p fusion in therapy-related early pre-B acute lymphoblastic leukemia with t(1;11)(p32;q23) translocation developing in the relapse phase of acute promyelocytic leukemia

Fluorescent in situ hybridization analysis of Philadelphia chromosome: Negative chronic myeloid leukemia with the bcr/abl fusion gene

EWS‐FLI‐1 and EWS‐ERG chimeric mRNAs in Ewing's sarcoma and primitive neuroectodermal tumor

Detection of HER‐2/neu (c‐erb B‐2) DNA amplification in primary breast carcinoma

Terahertz vortex metasurface for integration into compact terahertz continuous-wave sources

Detection of HER-2/neu (c-erb B-2) DNA amplification in primary breast carcinoma: Interobserver reproducibility and correlation with immunohistochemical HER-2 overexpression

Correlation of clonal T cell expansion with disease activity in systemic lupus erythematosus

Primary central nervous system lymphomas. Immunophenotypic, virologic, and cytogenetic findings of three patients without immune defects

Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism

Microdeletion in the SHOX 3′ region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri–Weill dyschondrosteosis in her 46,XX mother: Implication for the SHOX enhancer

Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1)

Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomy

Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients

Metabolic disposition of pantoprazole, a proton pump inhibitor, in relation to S‐mephenytoin 4′‐hydroxylation phenotype and genotype

Detection of the CBFB / MYH11 fusion gene in de novo acute myeloid leukemia (AML): A single-institution study of 224 Japanese AML patients

Homozygous Deletions of p16/MTS1 Gene Are Frequent But Mutations Are Infrequent in Childhood T-Cell Acute Lymphoblastic Leukemia

Vitamin D receptor genotypes and bone mineral density

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