K. Fujii

发表

Raf-1 promotes cell survival by antagonizing apoptosis signal-regulating kinase 1 through a MEK–ERK independent mechanism

Jing Chen, Katsunori Fujii, H. Fu, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Composition of Change in Phase Angle with Age in Japanese Children

K. Hayakawa, K. Fujii, 2020 .

Advantages of Phase Angle in Evaluating Physical Vitality Level

K. Fujii, Yuki Takeyama, 2020 .

Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays.

Toshiyuki Miyashita, Masao Yamada, Katsunori Fujii, 2005, Human molecular genetics.

Changes in Psoas Major and Quadriceps Cross Sectional Area in Elderly People after 12 Weeks of Exercise

S. Torii, K. Fujii, Toshiki Tachi, 2011 .

Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in PTCH1

T. Miyashita, M. Toyoda, K. Fujii, 2019, bioRxiv.

Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in PTCH1

T. Miyashita, M. Toyoda, K. Fujii, 2019, bioRxiv.

Homozygous female Becker muscular dystrophy

J. Takanashi, I. Nonaka, Y. Hayashi, 2009, American journal of medical genetics. Part A.

Negative control of apoptosis signal-regulating kinase 1 through phosphorylation of Ser-1034

H. Park, H. Fu, J. Chen, 2004, Oncogene.

Coexistence of neuroblastoma and ganglioneuroma in a girl with a hemizygous deletion of chromosome 11q14.1–23.3

K. Fujii, Y. Nakatani, H. Ohashi, 2016, American journal of medical genetics. Part A.

An Examination Regarding The PHV in Weight Growth of Male Students by Wavelet Interpolation Method

K. Fujii, Yutaka Yamamoto, 1995 .

Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly

N. Matsumoto, Y. Kohno, T. Nishizawa, 2010, Genesis.

Verification regarding changing construction in accumulation of fat for BMI based on change with age estimated from body composition balance.

K. Fujii, Nozomi Tanaka, T. Mishima, 2013, Journal of human ergology.

Relationship between body composition and BMI in preschool children

K. Fujii, S. Demura, Toshiro Sakai, 2012, Sport Sciences for Health.

K. Fujii, S. Demura, Toshiro Sakai, 2011, Journal of physiological anthropology.

Critical period for menarche derived by the wavelet interpolation method from changes in BMI with age in South Korean girls.

K. Fujii, Nozomi Tanaka, 2010, Journal of human ergology.

γ‐Irradiation Deregulates Cell Cycle Control and Apoptosis in Nevoid Basal Cell Carcinoma Syndrome‐derived Cells

J. Takanashi, T. Miyashita, Y. Kohno, 1999, Japanese journal of cancer research : Gann.

IL‐10 gene polymorphism, but not TGF‐β1 gene polymorphisms, is associated with food allergy in a Japanese population

A. Hata, Y. Kohno, K. Fujii, 2008, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Confirmation regarding critical period of onset menarche in estimated body fat mass

K. Fujii, K. Oguri, T. Ishigaki, 2006 .

Relationship between change in BMI with age and delayed menarche in female athletes.

K. Fujii, S. Demura, 2003, Journal of physiological anthropology and applied human science.

Atypical moyamoya syndrome with brain calcification and stenosis of abdominal aorta and renal arteries

K. Fujii, N. Shimojo, H. Uchikawa, 2017, Brain and Development.

MicroRNAs profiling in fibroblasts derived from patients with Gorlin syndrome

T. Miyashita, K. Fujii, N. Shimojo, 2019, Journal of Human Genetics.

PTCH1-null induced pluripotent stem cells exclusively differentiate into immature ectodermal cells with large areas of medulloblastoma-like tissue

T. Miyashita, K. Nagao, K. Fujii, 2022, Discover Oncology.

Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations

T. Miyashita, Kayoko Saito, K. Fujii, 2009, Journal of Human Genetics.

Periodical utilization of dental services is an effective breakthrough for declining masticatory performance: the Suita study

Y. Kokubo, K. Fujii, T. Ono, 2020, Odontology.

Detection of 14-3-3 protein in the cerebrospinal fluid in mitochondrial encephalopathy with lactic acidosis and stroke-like episodes

Y. Kohno, K. Fujii, H. Uchikawa, 2005, Journal of the Neurological Sciences.

Gorlin syndrome (nevoid basal cell carcinoma syndrome): Update and literature review

T. Miyashita, K. Fujii, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

Cortical liquefaction in severe human herpesvirus 6 encephalopathy

A. Barkovich, J. Takanashi, H. Tada, 2006, Neurology.

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome

T. Miyashita, K. Fujii, H. Ohashi, 2013, Familial Cancer.

Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome

T. Miyashita, K. Nagao, K. Fujii, 2012, Journal of Human Genetics.

Electrophysiological subtypes and prognosis of childhood Guillain–Barré syndrome in Japan

Y. Kohno, N. Yuki, K. Fujii, 2006, Muscle & nerve.

Acute motor axonal neuropathy during intensive immunosuppressive therapy for macrophage activation syndrome

Y. Kohno, K. Fujii, H. Uchikawa, 2008, Brain and Development.

Case report Acute motor axonal neuropathy during intensive immunosuppressive therapy for macrophage activation syndrome

Y. Kohno, K. Fujii, H. Uchikawa, 2008 .

Pelizaeus‐Merzbacher disease: Three novel mutations and implication for locus heterogeneity

I. Kanazawa, K. Fujii, S. Murayama, 1999, Annals of neurology.

Verification Regarding Secular Trend of Height Growth and The Maximum Peak Velocity during Adolescence

K. Fujii, 2009 .

A posterior fossa lipoma extending into the cervical spine and subcutaneous space via a cranium bifidum

Y. Kohno, K. Fujii, H. Arai, 2008, Brain and Development.

COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency

Y. Okada, Y. Goto, I. Nonaka, 2019, Annals of neurology.

Reversible white matter lesions during ketogenic diet therapy in glucose transporter 1 deficiency syndrome.

Y. Kohno, K. Fujii, T. Shiohama, 2013, Pediatric neurology.

Establishment of a Gorlin syndrome model from induced neural progenitor cells exhibiting constitutive GLI1 expression and high sensitivity to inhibition by smoothened (SMO)

T. Miyashita, K. Fujii, A. Umezawa, 2019, Laboratory Investigation.

Multiple cavitations in posterior reversible leukoencephalopathy syndrome associated with hemolytic-uremic syndrome

Y. Kohno, K. Fujii, H. Uchikawa, 2012, Brain and Development.

[Hedgehog signaling pathway and human disorders].

T. Miyashita, K. Fujii, 2009, No to hattatsu = Brain and development.

Cerebral hemorrhagic infarction following diffuse cerebral arteriopathy in a child with Takayasu's arteritis: A case report

K. Fujii, E. Kobayashi, Y. Higuchi, 2008 .

Acute disseminated encephalomyelitis following 2009 H1N1 influenza vaccine

Y. Kohno, K. Fujii, Koki Chiba, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Nationwide survey of childhood Guillain-Barré syndrome, Fisher syndrome, and Bickerstaff brainstem encephalitis in Japan

K. Fujii, S. Kuwabara, N. Shimojo, 2021, Brain and Development.

Anterior Commissure Involvement in Humanherpes Virus 6 Encephalitis

K. Fujii, K. Nagasawa, N. Shimojo, 2014, Child neurology open.

Intradural spinal meningioma in a 5-year-old female

K. Fujii, K. Sugita, N. Ishiwada, 1995, Brain and Development.

Catathrenia in Pitt–Hopkins syndrome associated with 18q interstitial deletion

K. Fujii, H. Ohashi, H. Arakawa, 2018, Pediatrics international : official journal of the Japan Pediatric Society.

Acute Disseminated Encephalomyelitis

K. Fujii, H. Arai, T. Motojima, 2014, Journal of child neurology.

Neuroradiologic findings in glutaric aciduria type II.

J. Takanashi, Y. Kohno, K. Fujii, 1999, Pediatric neurology.

An Acquired Form of Dandy-Walker Malformation with Enveloping Hemosiderin Deposits

K. Fujii, N. Shimojo, T. Shiohama, 2017, Case reports in pediatrics.

Activated microglia in acute encephalopathy with biphasic seizures and late reduced diffusion

J. Takanashi, K. Fujii, H. Sakuma, 2016, Journal of the Neurological Sciences.

High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome

S. Ishikawa, M. Shapero, D. Komura, 2007, Human Genetics.

A case of nevoid basal cell carcinoma syndrome with a splicing mutation in the PTCH1gene

T. Takato, K. Fujii, Y. Mori, 2013 .

[PTCH1 gene analysis in 25 Japanese patients with Gorlin syndrome].

T. Miyashita, Y. Kohno, K. Fujii, 2009, No to hattatsu = Brain and development.

[Clinical manifestations in 25 Japanese patients with Gorlin syndrome].

T. Miyashita, Y. Kohno, K. Fujii, 2009, No to hattatsu = Brain and development.

Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients

T. Miyashita, Y. Kohno, K. Urabe, 2003, Human mutation.

Nationwide survey of nevoid basal cell carcinoma syndrome in Japan revealing the low frequency of basal cell carcinoma

T. Miyashita, Y. Kohno, Kayoko Saito, 2012, American journal of medical genetics. Part A.

Neurofibromatosis type 2 in an infant with multiple plexiform schwannomas as first symptom

Takashi Kobayashi, K. Fujii, Y. Nagai, 2007, The Journal of dermatology.

Drugs indicated for mitochondrial dysfunction as treatments for acute encephalopathy with onset of febrile convulsive status epileptics

J. Takanashi, K. Fujii, Yoshimi Watanabe, 2016, Journal of the Neurological Sciences.

Empty sella syndrome in nevoid basal cell carcinoma syndrome

J. Takanashi, Y. Kohno, K. Fujii, 2000, Brain and Development.

New mutation of the PTCH gene in nevoid basal-cell carcinoma syndrome with West syndrome.

T. Miyashita, K. Fujii, N. Tachi, 2007, Pediatric neurology.

Coronary ostium occlusion by coronary cusp displacement in Williams syndrome

N. Funabashi, K. Fujii, Y. Nakatani, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Oxidative stress-induced JNK1 phosphorylation inhibits hedgehog signalling and osteoblast differentiation

Y. Kohno, K. Fujii, T. Shiohama, 2014 .

Ellis–van Creveld syndrome associated with chronic intestinal pseudo‐obstruction

Y. Furutani, K. Fujii, T. Kishimoto, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Downregulation of microRNA-431 by human interferon-β inhibits viability of medulloblastoma and glioblastoma cells via upregulation of SOCS6.

T. Miyashita, A. Kaneda, O. Yokosuka, 2014, International journal of oncology.

Inhibition of cell viability by human IFN-β is mediated by microRNA-431.

O. Yokosuka, K. Kita, S. Sugaya, 2012, International journal of oncology.

Brain morphology in children with nevoid basal cell carcinoma syndrome

T. Miyashita, K. Fujii, N. Shimojo, 2017, American journal of medical genetics. Part A.

Somatic mosaicism containing double mutations in PTCH1 revealed by generation of induced pluripotent stem cells from nevoid basal cell carcinoma syndrome

T. Miyashita, K. Nagao, M. Toyoda, 2017, Journal of Medical Genetics.

Confirmation of physical growth pattern in children with a slim body type: analysis of longitudinal data in Korean youth

K. Fujii, S. Demura, Naomi Yasubayashi, 2012, Sport Sciences for Health.

Recurrent Meningitis Associated With a Petrous Apex Cephalocele

J. Takanashi, Y. Kohno, K. Fujii, 2005, Journal of child neurology.

Connection between Growth/Development and Mathematical Function

K. Fujii, 2006 .

Analysis of the velocity curve for height by the wavelet interpolation method in children classified by maturity rate

K. Fujii, Y. Matsuura, 1999, American journal of human biology : the official journal of the Human Biology Council.

Facial nerve palsy associated with atomoxetine-induced hypertension

K. Fujii, N. Shimojo, T. Shiohama, 2019, Brain and Development.

Acute myelitis associated with human herpesvirus 7 infection

K. Fujii, N. Shimojo, T. Shiohama, 2018, Pediatrics international : official journal of the Japan Pediatric Society.

U7 snRNA-mediated correction of aberrant splicing caused by activation of cryptic splice sites

T. Miyashita, Y. Kohno, K. Nagao, 2007, Journal of Human Genetics.

Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrome

T. Miyashita, R. Kosaki, K. Nagao, 2012, American journal of medical genetics. Part A.

Phrenic nerve palsy associated with birth trauma – Case reports and a literature review

Y. Kohno, T. Hishiki, K. Fujii, 2013, Brain and Development.

Case report Phrenic nerve palsy associated with birth trauma - Case reports and a literature review

Y. Kohno, T. Hishiki, K. Fujii, 2013 .

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.

Therapeutic regimen of l-arginine for MELAS: 9-year, prospective, multicenter, clinical research

Yasuhiro Suzuki, M. Kubota, E. Inoue, 2018, Journal of Neurology.

Bilateral spinal anterior horn lesions in acute motor axonal neuropathy

K. Fujii, S. Kuwabara, N. Shimojo, 2018, Brain and Development.

A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features

M. Kogo, T. Yamashiro, T. Miyashita, 2019, Human Genome Variation.

Patched1 haploinsufficiency increases adult bone mass and modulates Gli3 repressor activity.

Kozo Nakamura, T. Miyashita, T. Takato, 2008, Developmental cell.

Complex IV subunit isoform COX6A2 protects fast‐spiking interneurons from oxidative stress and supports their function

J. Perrier, K. Hougaard, K. Fujii, 2020, The EMBO journal.

Consideration of the canalisation effect based on physical factors of mothers and their children

K. Fujii, Toshiro Sakai, 2009, Sport Sciences for Health.

A unique origin and multistep process for the generation of expanded DRPLA triplet repeats.

I. Kanazawa, T. Miyashita, Koichiro Nakamura, 1996, Human molecular genetics.

Alice in Wonderland syndrome associated with mycoplasma infection

K. Fujii, N. Shimojo, H. Kuroki, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

14-3-3 Proteins, particularly of the epsilon isoform, are detectable in cerebrospinal fluids of cerebellar diseases in children

I. Nonaka, Y. Kohno, K. Fujii, 2013, Brain and Development.

14-3-3 Protein Detection in the Cerebrospinal Fluid of Patients With Influenza-Associated Encephalopathy

J. Takanashi, Y. Kohno, K. Fujii, 2006, Journal of Child Neurology.

Postnatal development of Blake’s pouch cyst: a case report and new insight for its pathogenesis

K. Fujii, N. Saeki, S. Hirono, 2014, Child's Nervous System.

l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report

K. Fujii, H. Ohashi, Mitsuhiro Kato, 2017, Brain and Development.

Reversible cerebral vasoconstriction syndrome associated with brain parenchymal hemorrhage

Y. Kohno, K. Fujii, H. Oba, 2012, Brain and Development.

Ovarian teratoma development after anti-NMDA receptor encephalitis treatment

K. Fujii, Yoshimi Watanabe, N. Shimojo, 2017, Brain and Development.

Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations: a case report.

T. Miyashita, Kayoko Saito, K. Fujii, 2010, Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.

Gorlin syndrome with ulcerative colitis in a Japanese girl

J. Takanashi, T. Miyashita, Y. Kohno, 2003, American journal of medical genetics. Part A.

Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes

T. Miyashita, K. Nagao, M. Yamada, 2004, Journal of Human Genetics.

Molecular pathogenesis of keratocystic odontogenic tumors developing in nevoid basal cell carcinoma syndrome.

T. Miyashita, K. Nagao, Kayoko Saito, 2013, Oral surgery, oral medicine, oral pathology and oral radiology.

Hedgehog signaling is synergistically enhanced by nutritional deprivation and ligand stimulation in human fibroblasts of Gorlin syndrome.

K. Fujii, N. Shimojo, T. Shiohama, 2015, Biochemical and biophysical research communications.

Confirmation regarding Relational Construction of Body Composition and BMI in Preschool Children.

K. Fujii, S. Demura, 2012 .

Focal Coxsackie virus B5 encephalitis with synchronous seizure cluster and eruption: Infantile case

K. Fujii, N. Shimojo, K. Kodama, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Magnetic resonance neurography in diagnosing childhood chronic inflammatory demyelinating polyradiculoneuropathy

K. Fujii, S. Kuwabara, H. Yokota, 2020, Brain and Development.

Decreased head circumference at birth associated with maternal tobacco smoke exposure during pregnancy on the Japanese prospective birth cohort study

M. Shima, H. Iso, K. Hashimoto, 2021, Scientific Reports.

Significance of rostral brain lesions of Leigh syndrome associated with the mitochondrial DNA 8993T>G mutation

K. Fujii, Y. Iida, 2016, Journal of the Neurological Sciences.

A new diagnostic indication device of a biomarker growth differentiation factor 15 for mitochondrial diseases: From laboratory to automated inspection

E. Inoue, Y. Fukumoto, K. Fujii, 2020, Journal of inherited metabolic disease.

Angiogenesis in vitro: vascular tube formation from the differentiation of neural stem cells.

K. Fujii, M. Uchida, K. Oishi, 2004, Journal of pharmacological sciences.

Brain- and heart-specific Patched-1 containing exon 12b is a dominant negative isoform and is expressed in medulloblastomas.

T. Miyashita, Y. Kohno, R. Nishikawa, 2006, Biochemical and biophysical research communications.

Contralateral rhinorrhea as a feature of infantile Horner’s syndrome

J. Takanashi, H. Tada, Y. Kohno, 2003, Neurology.

THE ANALYSIS OF THE GROWTH VELOCITY CURVE IN HEIGHT BASED UPON THE MATURITY RATE

K. Fujii, Yutaka Yamamoto, 1995 .

Time series analysis in height growth by Waelet analysis

K. Fujii, Y. Hasegawa, Yutaka Yamamoto, 1994 .

Exploration of Viewpoints in Identification of Gymnastic Talent with the Back Hip Circle

K. Fujii, Yuki Takeyama, Hikaru Tanaka, 2021, American Journal of Sports Science.

Longitudinal magnetic resonance imaging changes in Japanese encephalitis

K. Fujii, Tomoko Uchida, A. Honda, 2019, Brain and Development.

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome

T. Miyashita, K. Fujii, H. Ohashi, 2013, Familial Cancer.

Identification and characterization of multiple isoforms of a murine and human tumor suppressor, patched, having distinct first exons.

T. Miyashita, K. Nagao, M. Toyoda, 2005, Genomics.

Optimum onset period for training based on maximum peak velocity of height by wavelet interpolation method in Japanese high school athletes.

K. Fujii, S. Demura, J. Matsuzawa, 2005, Journal of physiological anthropology and applied human science.

Confirmation of delayed menarche based on regression evaluation of age at menarche for age at MPV of height in female ball game players

K. Fujii, S. Demura, 2005, Environmental health and preventive medicine.

Anterior cingulate cortex involvement in non-paraneoplastic limbic encephalitis

K. Fujii, M. Senda, A. Honda, 2019, Brain and Development.

Ocular myasthenia gravis patients following the administration of tacrolimus and steroids

K. Fujii, Yoshimi Watanabe, N. Shimojo, 2019, Journal of the Neurological Sciences.

Specific temperament in patients with nevoid basal cell carcinoma syndrome

T. Miyashita, K. Fujii, N. Shimojo, 2020, Pediatrics international : official journal of the Japan Pediatric Society.

A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible: A case report

J. Takanashi, Y. Kohno, K. Fujii, 2009, Brain and Development.

MicroRNAs profiling in fibroblasts derived from patients with Gorlin syndrome

T. Miyashita, K. Fujii, N. Shimojo, 2019, Journal of Human Genetics.

Rostral brain lesions of Leigh syndrome associated with the mitochondrial DNA 8993T>G mutation

K. Fujii, N. Shimojo, H. Uchikawa, 2016, Journal of the Neurological Sciences.

Verification of delayed menarche evaluation system based on morphological differences in Korean females

K. Fujii, un-hyo baek, Kwang-Soo Koo, 2009, Sport Sciences for Health.

Periodical utilization of dental services is an effective breakthrough for declining masticatory performance: the Suita study

Y. Kokubo, K. Fujii, T. Ono, 2020, Odontology.

Periventricular Haemosiderin Deposition in Patients with Congenital Hemiplegia

J. Takanashi, K. Fujii, K. Sugita, 1995, Developmental medicine and child neurology.

Patched1 haploinsufficiency increases adult bone mass and modulates Gli3 repressor activity.

Kozo Nakamura, T. Miyashita, T. Takato, 2008, Developmental cell.

An Investigation Regarding Sequence of Age at MPV in Physique Growth of Male Athletes

K. Fujii, 1998 .

Nationwide survey of childhood Guillain-Barré syndrome, Fisher syndrome, and Bickerstaff brainstem encephalitis in Japan

K. Fujii, S. Kuwabara, N. Shimojo, 2022, Brain and Development.

Construction of a delayed menarche evaluation system for South Korean female athletes by the wavelet interpolation model

K. Fujii, 2012, Sport Sciences for Health.

CONSTRUCTION OF DELAYED MENARCHE EVALUATION IN KOREAN FEMALE ATHLETES

K. Fujii, Yeju Hong, un-hyo baek, 2011 .

Medullary streaks: Dilated medullary vessels in chronic ischemia in children

A. Barkovich, J. Takanashi, Y. Kohno, 2003, Neurology.