H. Morisaki

发表

Estimation of haplotype frequencies, linkage-disequilibrium measures, and combination of haplotype copies in each pool by use of pooled DNA data.

Toshikazu Ito, S. Chiku, E. Inoue, 2003, American journal of human genetics.

Molecular basis of AMP deaminase deficiency in skeletal muscle.

T. Morisaki, H. Morisaki, D. Pongratz, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Hereditary hemorrhagic telangiectasia in Japanese patients

T. Morisaki, H. Morisaki, M. Komiyama, 2013, Journal of Human Genetics.

AMPD1: a novel therapeutic target for reversing insulin resistance

Jidong Cheng, T. Morisaki, H. Morisaki, 2014, BMC Endocrine Disorders.

Silent myocardial ischemia in asymptomatic patients with type 2 diabetes mellitus without previous histories of cardiovascular disease.

H. Morisaki, T. Inoguchi, Y. Kawano, 2016, International journal of cardiology.

Phenotypic heterogeneity of Marfan-like connective tissue disorders associated with mutations in the transforming growth factor-beta receptor genes.

T. Morisaki, H. Morisaki, N. Yokoyama, 2007, Circulation journal : official journal of the Japanese Circulation Society.

Histologic differences between the ascending and descending aortas in young adults with fibrillin-1 mutations.

T. Morisaki, H. Morisaki, H. Ishibashi-Ueda, 2020, The Journal of thoracic and cardiovascular surgery.

Neuroradiological Manifestations of Hereditary Hemorrhagic Telangiectasia in 139 Japanese Patients

H. Morisaki, H. Nakajima, M. Komiyama, 2015, Neurologia medico-chirurgica.

Functional analysis of the p57KIP2 gene mutation in Beckwith-Wiedemann syndrome

T. Mukai, T. Morisaki, H. Morisaki, 1999, Human Genetics.

New p57KIP2 mutations in Beckwith-Wiedemann syndrome

Y. Fukushima, N. Niikawa, T. Mukai, 1997, Human Genetics.

Genetics of hereditary large vessel diseases

T. Morisaki, H. Morisaki, 2015, Journal of Human Genetics.

BMPR2 mutations found in Japanese patients with familial and sporadic primary pulmonary hypertension

T. Morisaki, H. Morisaki, H. Tomoike, 2004, Human mutation.

Clinical outcomes of aortic repair in young adult patients with ACTA2 mutations

T. Morisaki, H. Morisaki, Hiroshi Tanaka, 2017, General Thoracic and Cardiovascular Surgery.

Pulmonary arterial hypertension associated with hereditary hemorrhagic telangiectasia successfully treated with sildenafil.

T. Fujino, H. Morisaki, K. Abe, 2016, International journal of cardiology.

Genetic analysis of young adult patients with aortic disease not fulfilling the diagnostic criteria for Marfan syndrome.

T. Morisaki, H. Morisaki, H. Ogino, 2010, Circulation journal : official journal of the Japanese Circulation Society.

Impact of connective tissue disease on the surgical outcomes of aortic dissection in patients with cystic medial necrosis

T. Morisaki, H. Morisaki, H. Ogino, 2017, Journal of Cardiothoracic Surgery.

Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection.

A. F. Scott, D. Milewicz, H. Dietz, 2018, Journal of the American College of Cardiology.

Reversible cerebral vasoconstriction syndrome and posterior reversible encephalopathy syndrome in a boy with Loeys‐Dietz syndrome

T. Morisaki, H. Morisaki, K. Kosaki, 2015, American journal of medical genetics. Part A.

Familial thoracic aortic aneurysm and dissection associated with Marfan-related gene mutations: case report of a family with two gene mutations.

T. Morisaki, H. Morisaki, K. Sadamatsu, 2009, Internal medicine.

The differences in surgical long-term outcomes between Marfan syndrome and Loeys-Dietz syndrome.

T. Morisaki, H. Morisaki, J. Kobayashi, 2020, The Journal of thoracic and cardiovascular surgery.

Surgical experience with aggressive aortic pathologic process in Loeys-Dietz syndrome.

T. Morisaki, H. Morisaki, H. Ogino, 2012, The Annals of thoracic surgery.

High prevalence of vertebral artery tortuosity of Loeys-Dietz syndrome in comparison with Marfan syndrome

A. Kono, K. Sugimura, T. Morisaki, 2010, Japanese Journal of Radiology.

Prevalence of Dural Ectasia in Loeys-Dietz Syndrome: Comparison with Marfan Syndrome and Normal Controls

A. Kono, K. Sugimura, T. Morisaki, 2013, PloS one.

Characteristics in phenotypic manifestations of genetically proved Marfan syndrome in a Japanese population.

T. Morisaki, H. Morisaki, H. Ogino, 2009, The American journal of cardiology.

Heterozygous TGFBR2 mutations in Marfan syndrome

Yusuke Nakamura, Naomichi Matsumoto, Mathilde Varret, 2004, Nature Genetics.

Endovascular treatment of a dural arteriovenous fistula in a patient with Loeys-Dietz syndrome: A case report

M. Matsumae, H. Morisaki, T. Sorimachi, 2017, Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences.

Prenatal complex congenital heart disease with Loeys–Dietz syndrome

H. Morisaki, N. Okamoto, F. Kayatani, 2011, Cardiology in the Young.

Progressive aortic root and pulmonary artery aneurysms in a neonate with Loeys–Dietz syndrome type 1B

Y. Fukushima, T. Morisaki, H. Morisaki, 2010, American journal of medical genetics. Part A.

Eight novel mutations of the FBN1 gene found in Japanese patients with Marfan syndrome

Y. Okita, T. Mukai, T. Morisaki, 2001, Human mutation.

Aortic dissection during pregnancy and puerperium: A Japanese nationwide survey

T. Ikeda, H. Morisaki, I. Ishiwata, 2021, The journal of obstetrics and gynaecology research.

Acute aortic dissection (Stanford type B) during pregnancy

T. Ikeda, T. Morisaki, H. Morisaki, 2013, Journal of Perinatology.

A Nonsense SMAD3 Mutation in a Girl with Familial Thoracic Aortic Aneurysm and Dissection without Joint Abnormality

T. Morio, H. Morisaki, K. Kashimada, 2019, Cardiology.

Ultrastructural appearance of iris flocculi associated with a thoracic aortic aneurysm and dissections

Y. Tano, T. Morisaki, H. Morisaki, 2009, British Journal of Ophthalmology.

Association study of 11beta-hydroxysteroid dehydrogenase type 1 gene polymorphisms and metabolic syndrome in urban Japanese cohort.

K. Nakao, Y. Kokubo, I. Yamanaka, 2009, Diabetes research and clinical practice.

CDH13 gene coding t‐cadherin influences variations in plasma adiponectin levels in the Japanese population

Y. Kokubo, I. Yamanaka, T. Morisaki, 2012, Human mutation.

Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient

T. Morisaki, H. Morisaki, M. Osame, 2000, Neuromuscular Disorders.

Genetic association analysis of 269 rare diseases reveals novel aetiologies

I. Yamanaka, S. Riazuddin, S. Mansour, 2022, medRxiv.

Characteristics of the clinical background and coronary artery lesions in patients with type 2 diabetes mellitus without a previous history of cardiovascular disease

H. Morisaki, Y. Maeda, K. Tamaya, 2018 .

Role of AMPD2 in impaired glucose tolerance induced by high fructose diet

Jidong Cheng, T. Morisaki, H. Morisaki, 2017, Molecular genetics and metabolism reports.

Resistin gene variations are associated with the metabolic syndrome in Japanese men.

Y. Kokubo, I. Yamanaka, T. Morisaki, 2009, Obesity research & clinical practice.

Impairment of ubiquitin-proteasome system by E334K cMyBPC modifies channel proteins, leading to electrophysiological dysfunction.

S. Matsuoka, A. Takeuchi, I. Hisatome, 2011, Journal of molecular biology.

Case Report: Spontaneous Postpartum Quadruple Cervicocephalic Arterial Dissection With a Heterozygous COL5A1 Variant of Unknown Significance

Katsutoshi Takahashi, H. Morisaki, G. Yoshikawa, 2022, Frontiers in Neurology.

A novel gene, ITM, located between p57KIP2 and IPL, is imprinted in mice.

T. Mukai, T. Morisaki, H. Morisaki, 1998, DNA research : an international journal for rapid publication of reports on genes and genomes.

Guidelines for diagnosis and treatment of aortic aneurysm and aortic dissection (JCS 2011): digest version.

M. Jinzaki, S. Kuribayashi, Y. Okita, 2013, Circulation journal : official journal of the Japanese Circulation Society.

Moyamoya disease and artery tortuosity as rare phenotypes in a patient with an elastin mutation

T. Morisaki, H. Morisaki, S. Sakao, 2016, American journal of medical genetics. Part A.

Surgical Outcome and Histological Differences between Individuals with TGFBR1 and TGFBR2 Mutations in Loeys-Dietz Syndrome

T. Morisaki, H. Morisaki, H. Ogino, 2021, Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia.

Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease

T. Morisaki, H. Morisaki, I. Shiraishi, 2015, Journal of Human Genetics.

A novel Thr56Met mutation of the autosomal recessive hypercholesterolemia gene associated with hypercholesterolemia.

Y. Kokubo, I. Yamanaka, T. Morisaki, 2010, Journal of atherosclerosis and thrombosis.

The Efficacy of a Genetic Analysis of the BMPR2 Gene in a Patient with Severe Pulmonary Arterial Hypertension and an Atrial Septal Defect Treated with Bilateral Lung Transplantation

H. Morisaki, H. Shimokawa, R. Saito, 2017, Internal medicine.

Haplotype analysis of human AMPD1 gene: origin of common mutant allele

T. Morisaki, H. Morisaki, N. Kamatani, 2004, Journal of Medical Genetics.

Proteinuria in AMPD2‐deficient mice

Jidong Cheng, M. Ikawa, M. Okabe, 2012, Genes to cells : devoted to molecular & cellular mechanisms.

Evaluation of the clinical performance of noninvasive prenatal testing at a Japanese laboratory

T. Sasagawa, T. Taketani, H. Morisaki, 2021, The journal of obstetrics and gynaecology research.

Japanese case of hereditary hemorrhagic telangiectasia type 2 with a novel mutation, c.154A>C (p.Thr52Pro), in the ALK1/ACVRL1 gene

H. Morisaki, N. Suzuki, Y. Nishimoto, 2014 .

AMP deaminase 3 plays a critical role in remote reperfusion lung injury.

I. Hisatome, T. Morisaki, H. Morisaki, 2013, Biochemical and biophysical research communications.

AMPD3‐deficient mice exhibit increased erythrocyte ATP levels but anemia not improved due to PK deficiency

Jidong Cheng, M. Ikawa, M. Okabe, 2012, Genes to cells : devoted to molecular & cellular mechanisms.

Remote reperfusion lung injury is associated with AMP deaminase 3 activation and attenuated by inosine monophosphate.

Jidong Cheng, I. Hisatome, T. Morisaki, 2007, Circulation journal : official journal of the Japanese Circulation Society.

Genomic organization of Ampd3, heart-type AMPD gene, located in mouse Chromosome 7

T. Mukai, Y. Matsuda, T. Morisaki, 1997, Mammalian Genome.

Cloning and expression of cDNA encoding heart-type isoform of AMP deaminase.

T. Mukai, T. Morisaki, H. Morisaki, 1997, Gene.

A Case of Spontaneously Improved Heritable Pulmonary Arterial Hypertension Diagnosed as Severe Primary Pulmonary Hypertension in Childhood

T. Morisaki, H. Morisaki, I. Shiraishi, 2020 .

Aortic aneurysm/dissection and osteogenesis imperfecta: Four new families and review of the literature.

G. Mortier, H. Morisaki, B. Loeys, 2019, Bone.

Clinical History and Management Recommendations of the Smooth Muscle Dysfunction Syndrome Due to ACTA2 Arginine 179 Alterations

M. Tekin, B. Lorenz, D. Milewicz, 2018, Genetics in Medicine.

Block of sodium channels by divalent mercury: role of specific cysteinyl residues in the P-loop region.

I. Hisatome, H. Morisaki, N. Makita, 2000, Biophysical journal.

Nonsurgical treatment of cerebral ischemia associated with ACTA2 cerebral arteriopathy: a case report and literature review

H. Morisaki, Y. Nakai, S. Ihara, 2021, Child's Nervous System.

Recombinant HBsAg inhibits LPS-induced COX-2 expression and IL-18 production by interfering with the NFkappaB pathway in a human monocytic cell line, THP-1.

Jidong Cheng, T. Morisaki, H. Morisaki, 2005, Journal of hepatology.

Co-existence of mutations in the FBN1 gene and the ABCC6 gene in a patient with Marfan syndrome associated with pseudoxanthoma elasticum.

A. Utani, T. Morisaki, H. Morisaki, 2013, Journal of dermatological science.

Positive and negative elements mediate control of alternative splicing in the AMPD1 gene.

T. Morisaki, H. Morisaki, K. Karikó, 2000, Gene.

Genetics of Marfan Syndrome, Related Disorders, and Bicuspid Aortic Valve

T. Morisaki, H. Morisaki, 2017 .

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.

T. Mukai, H. Morisaki, H. Soejima, 2002, Genome research.

Leptin Gene and Leptin Receptor Gene Polymorphisms Are Associated with Sweet Preference and Obesity

Y. Kokubo, I. Yamanaka, T. Morisaki, 2008, Hypertension Research.

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.

T. Mukai, H. Morisaki, H. Soejima, 2004, Genome research.

Aortic Disease Presentation and Outcome Associated With ACTA2 Mutations

J. Coselli, S. Lemaire, D. Milewicz, 2015, Circulation. Cardiovascular genetics.

Control of AMP deaminase 1 binding to myosin heavy chain.

I. Hisatome, T. Morisaki, H. Morisaki, 1998, American journal of physiology. Cell physiology.

Control of AMP deaminase 1 binding to myosin heavy chain.

I. Hisatome, T. Morisaki, H. Morisaki, 1998, The American journal of physiology.

An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

Y. Fukushima, N. Niikawa, T. Mukai, 1996, Nature Genetics.

gene.U2af1-rs1 is a neomorphic imprinted

M. Oshimura, T. Mukai, H. Morisaki, 2013 .

Mouse U2af1-rs1 is a neomorphic imprinted gene

M. Oshimura, T. Mukai, H. Morisaki, 1997, Molecular and cellular biology.

Identification of functional domains in AMPD1 by mutational analysis.

T. Morisaki, H. Morisaki, E. Holmes, 1994, Biochemical and biophysical research communications.

Alternative splicing: a mechanism for phenotypic rescue of a common inherited defect.

Seymour, L. Newby, T. Morisaki, 1993, The Journal of clinical investigation.

AMPD2 Regulates GTP Synthesis and Is Mutated in a Potentially Treatable Neurodegenerative Brainstem Disorder

S. Gabriel, E. Nickerson, R. Naviaux, 2013, Cell.

A Novel Bipartite Intronic Splicing Enhancer Promotes the Inclusion of a Mini-exon in the AMP Deaminase 1 Gene*

T. Morisaki, H. Morisaki, E. Holmes, 2001, The Journal of Biological Chemistry.

Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections

M. Goumans, K. Devriendt, J. Timmermans, 2015, Journal of the American College of Cardiology.

Mutations in a TGF- b Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections

J. Timmermans, B. Beverloo, L. Pardo, 2015 .

Genetic Link Between Obesity and MMP14-Dependent Adipogenic Collagen Turnover

S. Weiss, I. Yamanaka, H. Morisaki, 2010, Diabetes.

A Genetic Link between Obesity and MMP14-Dependent Adipogenic Collagen Turnover Running title: MMP14 Links ECM Remodeling and Obesity

Tae Hwa Chun, Mayumi Inoue, Hiroko Morisaki, 2010 .

Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD)

I. Yamanaka, T. Morisaki, H. Morisaki, 2009, Human mutation.

A new ENG mutation in a Japanese family with hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations

H. Morisaki, A. Watanabe, H. Chiba, 2018, Respiratory medicine case reports.

Artery tortuosity syndrome exhibiting early‐onset emphysema with novel compound heterozygous SLC2A10 mutations

Y. Kohno, T. Morisaki, H. Morisaki, 2013, American journal of medical genetics. Part A.

Genotypic analysis using a Y‐chromosome‐specific probe following bone marrow transplantation

S. Asano, T. Morisaki, H. Morisaki, 1988, American journal of hematology.

A mutation update on the LDS‐associated genes TGFB2/3 and SMAD2/3

S. Mehta, J. Roos‐Hesselink, M. Kempers, 2018, Human mutation.

Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function

O. Ohara, T. Morisaki, H. Morisaki, 2015, European Journal of Human Genetics.

Establishment and Analysis of SLC22A12 (URAT1) Knockout Mouse

M. Ikawa, M. Okabe, T. Morisaki, 2010, Nucleosides, nucleotides & nucleic acids.

Serine-arginine-rich nuclear protein Luc7l regulates myogenesis in mice.

K. Hidaka, K. Yamamura, T. Morisaki, 2004, Gene.

Single-nucleotide polymorphism g.1548G > A (E469K) in human ICAM-1 gene affects mRNA splicing pattern and TPA-induced apoptosis.

T. Morisaki, H. Morisaki, Mutsumi Iwao, 2004, Biochemical and biophysical research communications.

Ascending Aortic Aneurysm in a Child With Fibulin-4 Deficiency.

T. Tsuzuki, H. Morisaki, A. Usui, 2018, The Annals of thoracic surgery.

Mutations of the TGF‐β type II receptor BMPR2 in pulmonary arterial hypertension

J. Carlquist, M. Humbert, W. Seeger, 2006, Human mutation.

Cellular and Molecular Cardiology: Novel Insights from Clinical Experience

T. Morio, H. Morisaki, K. Kashimada, 2019 .

Genetic association analysis of 77,539 genomes reveals rare disease etiologies

B. Gelb, I. Yamanaka, S. Riazuddin, 2023, Nature Medicine.

Association between hypertension and the alpha-adducin, beta1-adrenoreceptor, and G-protein beta3 subunit genes in the Japanese population; the Suita study.

Y. Kokubo, H. Morisaki, N. Iwai, 2004, Hypertension research : official journal of the Japanese Society of Hypertension.

Association of protein tyrosine phosphatase 1B gene polymorphism with the effects of weight reduction therapy on bodyweight and glycolipid profiles in obese patients

T. Morisaki, H. Morisaki, H. Yamakage, 2021, Journal of diabetes investigation.

Ubiquitin-proteasome system impairment caused by a missense cardiac myosin-binding protein C mutation and associated with cardiac dysfunction in hypertrophic cardiomyopathy.

I. Hisatome, T. Morisaki, H. Morisaki, 2008, Journal of molecular biology.

BMPR2 gene mutation in pulmonary arteriovenous malformation and pulmonary hypertension: a case report.

M. Mishima, T. Morisaki, H. Morisaki, 2014, Respiratory investigation.

Pulmonary arterial hypertension as the first manifestation in a patient with hereditary hemorrhagic telangiectasia.

H. Morisaki, S. Sakao, N. Tanabe, 2014, Internal medicine.

Pulmonary Hypertension and Hereditary Hemorrhagic Telangiectasia Related to an ACVRL1 Mutation

Y. Takeishi, H. Morisaki, Koichi Sugimoto, 2019, Internal medicine.

Determination of probability distribution of diplotype configuration (diplotype distribution) for each subject from genotypic data using the EM algorithm

T. Morisaki, H. Morisaki, N. Kamatani, 2002 .

Chapter 2 . 3 Mutations in a TGFß ligand , TGFB 3 , cause syndromic aortic aneurysms and dissections Mutations in TGFB 3 cause syndromic aortic aneurysms and dissections

M. Goumans, K. Devriendt, J. Timmermans, 2019 .

Loeys-Dietz Syndrome Presented with Giant Bullae and Asthma.

S. Muro, H. Morisaki, H. Matsumoto, 2020, The journal of allergy and clinical immunology. In practice.

Molecular analysis of mouse Ampd3 gene encoding heart-type isoform of AMP deaminase.

T. Mukai, Y. Matsuda, T. Morisaki, 1997, Advances in experimental medicine and biology.

Association between hypertension and the alpha-adducin, beta1-adrenoreceptor, and G-protein beta3 subunit genes in the Japanese population; the Suita study.

Y. Kokubo, H. Morisaki, T. Mannami, 2004, Hypertension research : official journal of the Japanese Society of Hypertension.

Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia

N. Matsumoto, T. Morisaki, H. Morisaki, 2021, BMC medical genomics.

Relationship Between Mutations in ENG and ALK1 Genes and the Affected Organs in Hereditary Hemorrhagic Telangiectasia

T. Morisaki, H. Morisaki, I. Shiraishi, 2020, Molecular Mechanism of Congenital Heart Disease and Pulmonary Hypertension.

Effect of isolated AMP deaminase deficiency on skeletal muscle function☆

S. Matsuo, Jidong Cheng, I. Hisatome, 2014, Molecular genetics and metabolism reports.

First missense mutations (R388W and R425H) of AMPD1 accompanied with myopathy found in a Japanese patient

T. Morisaki, H. Morisaki, M. Osame, 2000, Human mutation.

AMPD1 regulates mTORC1-p70 S6 kinase axis in the control of insulin sensitivity in skeletal muscle

Jidong Cheng, T. Morisaki, H. Morisaki, 2015, BMC Endocrine Disorders.

Assessing the Accuracy of Variant Detection in Cost-Effective Gene Panel Testing by Next-Generation Sequencing.

Makoto Ikeda, Akiko Yoshida, Tomohiko Ichikawa, 2018, The Journal of molecular diagnostics : JMD.

Coordinate induction of AMP deaminase in human atrium with mitochondrial DNA deletion.

M. Shimoyama, I. Hisatome, T. Morisaki, 2003, Biochemical and Biophysical Research Communications - BBRC.

[AMPD genes and urate metabolism].

T. Morisaki, H. Morisaki, 2008, Nihon rinsho. Japanese journal of clinical medicine.

Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)

O. Migita, C. Tifft, W. Gahl, 2021, Journal of Medical Genetics.

Computational and Experimental Analyses for Pathogenicity Prediction of ACVRL1 Missense Variants in Hereditary Hemorrhagic Telangiectasia

Akihiro Urasaki, H. Morisaki, I. Shiraishi, 2023, Journal of clinical medicine.

Title BMPR2 gene mutation in pulmonary arteriovenous malformation and pulmonary hypertension: a case report

H. Morisaki, 2020 .

BMPR 2 gene mutation in pulmonary arteriovenous malformation and pulmonary hypertension : a case report

M. Mishima, T. Morisaki, H. Morisaki, 2017 .

AMPD2 plays important roles in regulating hepatic glucose and lipid metabolism

T. Morisaki, H. Morisaki, Haiyan Yang, 2023, Molecular and Cellular Endocrinology.

Determination of probability distribution of diplotype configuration (diplotype distribution) for each subject from genotypic data using the EM algorithm.

T. Morisaki, H. Morisaki, N. Kamatani, 2002, Annals of human genetics.

Mouse Mef2b gene: unique member of MEF2 gene family.

K. Hidaka, T. Mukai, Y. Matsuda, 1997, Journal of biochemistry.

Postoperative mitral leaflet rupture in an infant with Loeys–Dietz syndrome

H. Morisaki, M. Yamagishi, S. Yamazaki, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

Loeys-Dietz Cardiomyopathy? Long-Term Follow-Up After Onset of Acute Decompensated Heart Failure.

T. Morisaki, H. Morisaki, M. Naya, 2021, Canadian Journal of Cardiology.

Ascending Aortic Aneurysm in Gene sequencing of his parents showed that the mutation a Child With Fibulin-4 De fi ciency

T. Tsuzuki, H. Morisaki, A. Usui, 2022 .

Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections

M. Goumans, K. Devriendt, J. Timmermans, 2015, Journal of the American College of Cardiology.

Left main coronary artery compression by a dilated main pulmonary artery and left coronary sinus of Valsalva aneurysm in a patient with heritable pulmonary arterial hypertension and FLNA mutation

T. Morisaki, H. Morisaki, T. Murohara, 2017, Pulmonary circulation.

Progressive aortic root and pulmonary artery aneurysms in a neonate with Loeys–Dietz syndrome type 1B

Y. Fukushima, T. Morisaki, H. Morisaki, 2010, American Journal of Medical Genetics. Part A.