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Expansion processes of two emblematic Luehdorfia butterflies across the Japanese archipelago

Journal of biogeography, 2023-10, Vol.50 (10), p.1710-1723

2023

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De novo SOX11 mutations cause Coffin-Siris syndrome

Nature communications, 2014-06, Vol.5 (1), p.4011-4011, Article 4011

2014

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Retrospective study of the recurrence risk of preterm birth in Japan

The journal of maternal-fetal & neonatal medicine, 2022-02, Vol.35 (3), p.515-519

2022

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Precise detection of chromosomal translocation or inversion breakpoints by whole-genome sequencing

Journal of human genetics, 2014-12, Vol.59 (12), p.649-654

2014

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A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association

Scientific reports, 2023-06, Vol.13 (1), p.9789-9789, Article 9789

2023

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Multiple Placental Infarcts in a Pregnant Woman with Essential Thrombocythemia

Internal Medicine, 2018/12/15, Vol.57(24), pp.3647-3650

2018

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A homozygous NOP14 variant is likely to cause recurrent pregnancy loss

Journal of human genetics, 2018-04, Vol.63 (4), p.425-430

2018

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Distal 2q duplication in a patient with intellectual disability

Human genome variation, 2022-11, Vol.9 (1), p.39-39, Article 39

2022

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Whole exome sequencing of fetal structural anomalies detected by ultrasonography

Journal of human genetics, 2021-05, Vol.66 (5), p.499-507

2021

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Synthesis of both enantiomers of 1,2,3,4-tetrahydroisoquinoline derivative IPPAM-1 and enantio-dependency of its positive allosteric modulation of prostacyclin receptor

Bioorganic & medicinal chemistry letters, 2017-06, Vol.27 (11), p.2567-2570

2017

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Interferon therapy for pregnant patients with essential thrombocythemia in Japan

International journal of hematology, 2021, Vol.113 (1), p.106-111

2021

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Cervical Cerclage to Prevent Intrauterine Balloon Prolapse

Surgery journal (New York), 2023-01, Vol.9 (1), p.e36-e38

2023

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Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

Journal of human genetics, 2019-05, Vol.64 (5), p.487-492

2019

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Nonsense variants of STAG2 result in distinct congenital anomalies

Human genome variation, 2020-09, Vol.7 (1), p.26-26, Article 26

2020

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Retraction Note to: Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

Journal of human genetics, 2020-09, Vol.65 (9), p.811-811

2020

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A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders

Annals of clinical and translational neurology, 2020-07, Vol.7 (7), p.1117-1131

2020

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Laparoscopic Removal of Modified Vertical Uterine Compression Sutures due to Postoperative Focal Pain

Surgery journal (New York), 2020-04, Vol.6 (2), p.e67-e70

2020

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Design and fabrication of MEMS-based monolithic fuel cells

Sensors and actuators. A. Physical., 2008-07, Vol.145-146, p.354-362

2008

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TMEM67 mutations found in a case of Joubert syndrome with renal hypodysplasia

CEN case reports, 2016-11, Vol.5 (2), p.137-140

2016

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Structural development of 1,2,3,4-tetrahydroisoquinoline-type positive allosteric modulators of prostacyclin receptor (IPPAMs) to improve metabolic stability, and investigation of metabolic fate

Bioorganic & medicinal chemistry letters, 2017-08, Vol.27 (15), p.3572-3575

2017

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Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder

Cell reports (Cambridge), 2018-01, Vol.22 (3), p.734-747

2018

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2D magnetic nanoparticle imaging using magnetization response second harmonic

Journal of magnetism and magnetic materials, 2015-06, Vol.383, p.170-174

2015

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PRENATAL DIAGNOSIS OF JACOBSEN SYNDROME WITH CYSTIC HYGROMA

Indian journal of child health, 2020-01, Vol.7 (1), p.45-46

2020

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Imaging of Magnetic Nanoparticles Using Second-Harmonic Signals

IEEE transactions on magnetics, 2015-11, Vol.51 (11), p.1-4

2015

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Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia

Journal of the neurological sciences, 2017-05, Vol.376, p.7-12

2017

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Expansion processes of two emblematic Luehdorfia butterflies across the Japanese archipelago

De novo SOX11 mutations cause Coffin-Siris syndrome

Retrospective study of the recurrence risk of preterm birth in Japan

Precise detection of chromosomal translocation or inversion breakpoints by whole-genome sequencing

A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association

Multiple Placental Infarcts in a Pregnant Woman with Essential Thrombocythemia

A homozygous NOP14 variant is likely to cause recurrent pregnancy loss

Distal 2q duplication in a patient with intellectual disability

Whole exome sequencing of fetal structural anomalies detected by ultrasonography

Synthesis of both enantiomers of 1,2,3,4-tetrahydroisoquinoline derivative IPPAM-1 and enantio-dependency of its positive allosteric modulation of prostacyclin receptor

Interferon therapy for pregnant patients with essential thrombocythemia in Japan

Cervical Cerclage to Prevent Intrauterine Balloon Prolapse

Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

Nonsense variants of STAG2 result in distinct congenital anomalies

Retraction Note to: Nonsense variants in STAG2 result in distinct sex-dependent phenotypes

A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders

Laparoscopic Removal of Modified Vertical Uterine Compression Sutures due to Postoperative Focal Pain

Design and fabrication of MEMS-based monolithic fuel cells

TMEM67 mutations found in a case of Joubert syndrome with renal hypodysplasia

Structural development of 1,2,3,4-tetrahydroisoquinoline-type positive allosteric modulators of prostacyclin receptor (IPPAMs) to improve metabolic stability, and investigation of metabolic fate

Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder

2D magnetic nanoparticle imaging using magnetization response second harmonic

PRENATAL DIAGNOSIS OF JACOBSEN SYNDROME WITH CYSTIC HYGROMA

Imaging of Magnetic Nanoparticles Using Second-Harmonic Signals

Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia

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