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The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesis

Nature communications, 2020-07, Vol.11 (1), p.1-14, Article 3571

2020

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Inherited Chromosomally Integrated Human Herpesvirus 6 Is a Risk Factor for Spontaneous Abortion

The Journal of infectious diseases, 2021-05, Vol.223 (10), p.1717-1723

2021

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Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events

Methods in molecular biology (Clifton, N.J.), 2018, Vol.1769, p.21

2018

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Experimental method for haplotype phasing across the entire length of chromosome 21 in trisomy 21 cells using a chromosome elimination technique

Journal of human genetics, 2022-10, Vol.67 (10), p.565-572

2022

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Age-related decrease of meiotic cohesins in human oocytes

PloS one, 2014-05, Vol.9 (5), p.e96710-e96710

2014

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CDH1 Is a Specific Marker for Undifferentiated Spermatogonia in Mouse Testes

Biology of reproduction, 2007-01, Vol.76 (1), p.130-141

2007

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Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes

Journal of human genetics, 2022-06, Vol.67 (6), p.363-368

2022

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A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia

Journal of human genetics, 2020-08, Vol.65 (8), p.705-709

2020

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Antisense oligonucleotide induced pseudoexon skipping and restoration of functional protein for Fukuyama muscular dystrophy caused by a deep-intronic variant

Human molecular genetics, 2023-04, Vol.32 (8), p.1301-1312

2023

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Incontinentia pigmenti inherited from a father with a low level atypical IKBKG deletion mosaicism: a case report

BMC pediatrics, 2022-06, Vol.22 (1), p.1-378, Article 378

2022

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An Analysis of Differentially Expressed Coding and Long Non-Coding RNAs in Multiple Models of Skeletal Muscle Atrophy

International journal of molecular sciences, 2021-03, Vol.22 (5), p.2558

2021

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Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like Diabetes

The Tohoku Journal of Experimental Medicine, 2022, Vol.256(1), pp.37-41

2022

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Chromosomal translocations and palindromic AT-rich repeats

Current opinion in genetics & development, 2012-06, Vol.22 (3), p.221-228

2012

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Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures

Journal of human genetics, 2019-05, Vol.64 (5), p.459-466

2019

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Chromosomally integrated human herpesvirus 6 in the Japanese population

Journal of medical virology, 2018-10, Vol.90 (10), p.1636-1642

2018

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Familial cardiac septal defect due to a novel nine‐base deletion in TBX20

Pediatrics international, 2022-01, Vol.64 (1), p.e14995-n/a

2022

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Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy

Nature (London), 2011-10, Vol.478 (7367), p.127-131

2011

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A case of early onset adenocarcinoma associated with colorectal polyposis with an unknown germline mutation

Surgical case reports, 2022-08, Vol.8 (1), p.160-160, Article 160

2022

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Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction

Reproductive biology and endocrinology, 2011-08, Vol.9 (1), p.107-107

2011

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Myoinositol to Total Choline Ratio in Glioblastomas as a Potential Prognostic Factor in Preoperative Magnetic Resonance Spectroscopy

Neurologia medico-chirurgica, 2021, Vol.61(8), pp.453-460

2021

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Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand

PloS one, 2015-11, Vol.10 (11), p.e0141739-e0141739

2015

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Analysis of the origin of inherited chromosomally integrated human herpesvirus 6 in the Japanese population

Journal of general virology, 2017-07, Vol.98 (7), p.1823-1830

2017

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An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 Deletion

The Tohoku Journal of Experimental Medicine, 2022, Vol.258(3), pp.183-193

2022

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An aggressive systemic mastocytosis preceded by ovarian dysgerminoma

BMC cancer, 2020-11, Vol.20 (1), p.1162-1162, Article 1162

2020

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Novel ARG1 variants identified in a patient with arginase 1 deficiency

Human genome variation, 2021-02, Vol.8 (1), p.8-8, Article 8

2021

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The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesis

Inherited Chromosomally Integrated Human Herpesvirus 6 Is a Risk Factor for Spontaneous Abortion

Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events

Experimental method for haplotype phasing across the entire length of chromosome 21 in trisomy 21 cells using a chromosome elimination technique

Age-related decrease of meiotic cohesins in human oocytes

CDH1 Is a Specific Marker for Undifferentiated Spermatogonia in Mouse Testes

Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes

A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia

Antisense oligonucleotide induced pseudoexon skipping and restoration of functional protein for Fukuyama muscular dystrophy caused by a deep-intronic variant

Incontinentia pigmenti inherited from a father with a low level atypical IKBKG deletion mosaicism: a case report

An Analysis of Differentially Expressed Coding and Long Non-Coding RNAs in Multiple Models of Skeletal Muscle Atrophy

Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like Diabetes

Chromosomal translocations and palindromic AT-rich repeats

Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures

Chromosomally integrated human herpesvirus 6 in the Japanese population

Familial cardiac septal defect due to a novel nine‐base deletion in TBX20

Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy

A case of early onset adenocarcinoma associated with colorectal polyposis with an unknown germline mutation

Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction

Myoinositol to Total Choline Ratio in Glioblastomas as a Potential Prognostic Factor in Preoperative Magnetic Resonance Spectroscopy

Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand

Analysis of the origin of inherited chromosomally integrated human herpesvirus 6 in the Japanese population

An Infant Case of Streptococcus Pneumoniae-Associated Thrombotic Microangiopathy with Heterozygous CFI Mutation and CFHR3-CFHR1 Deletion

An aggressive systemic mastocytosis preceded by ovarian dysgerminoma

Novel ARG1 variants identified in a patient with arginase 1 deficiency

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