Hiroyuki Sasaki | Academic Influence

Hiroyuki Sasaki's AcademicInfluence.com Rankings

Hiroyuki Sasaki

Biology

#7652

World Rank

#10605

Historical Rank

Genetics

#738

World Rank

#830

Historical Rank

Molecular Biology

#2388

World Rank

#2425

Historical Rank

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Biology

Hiroyuki Sasaki's Degrees

Bachelors Biology University of Tokyo
Masters Genetics University of Tokyo
PhD Genetics University of Tokyo

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Why Is Hiroyuki Sasaki Influential?

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According to Wikipedia, is a Japanese geneticist known for contributing to clarify epigenetic regulations during gametogenesis and embryogenesis through investigation of genomic imprinting as a model. He participates in the International Human Epigenome Consortium [IHEC].

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Hiroyuki Sasaki's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting (2004) (1316)
Endogenous siRNAs from naturally formed dsRNAs regulate transcripts in mouse oocytes (2008) (1138)
DNA methylation of retrotransposon genes is regulated by Piwi family members MILI and MIWI2 in murine fetal testes. (2008) (882)
Epigenetic events in mammalian germ-cell development: reprogramming and beyond (2008) (810)
Identification and characterization of two novel classes of small RNAs in the mouse germline: retrotransposon-derived siRNAs in oocytes and germline small RNAs in testes. (2006) (581)
Targets and dynamics of promoter DNA methylation during early mouse development (2010) (561)
Role of the Dnmt3 family in de novo methylation of imprinted and repetitive sequences during male germ cell development in the mouse. (2007) (505)
Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development. (2008) (448)
Parental-origin-specific epigenetic modification of the mouse H19 gene (1993) (437)
Derivation of Human Trophoblast Stem Cells. (2018) (417)
Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients. (2007) (395)
Role for piRNAs and Noncoding RNA in de Novo DNA Methylation of the Imprinted Mouse Rasgrf1 Locus (2011) (359)
Regulation of imprinted X-chromosome inactivation in mice by Tsix. (2001) (325)
Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. (1992) (290)
Genomic organization of the human-amyloid beta-protein precursor gene. (1990) (282)
The TDRD9-MIWI2 complex is essential for piRNA-mediated retrotransposon silencing in the mouse male germline. (2009) (280)
Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. (1997) (277)
Mouse Oocyte Methylomes at Base Resolution Reveal Genome-Wide Accumulation of Non-CpG Methylation and Role of DNA Methyltransferases (2013) (255)
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome. (1989) (254)
Genomic Imprinting and Physiological Processes in Mammals (2019) (250)
MITOPLD is a mitochondrial protein essential for nuage formation and piRNA biogenesis in the mouse germline. (2011) (250)
Tsix silences Xist through modification of chromatin structure. (2005) (245)
MVH in piRNA processing and gene silencing of retrotransposons. (2010) (237)
Synergistic Function of DNA Methyltransferases Dnmt3a and Dnmt3b in the Methylation of Oct4 and Nanog (2007) (236)
The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis development (2000) (229)
Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method (1994) (219)
Dynamic stage-specific changes in imprinted differentially methylated regions during early mammalian development and prevalence of non-CpG methylation in oocytes (2011) (217)
Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells (2014) (199)
Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS–M (1996) (197)
De novo DNA methylation drives 5hmC accumulation in mouse zygotes (2016) (181)
Generation of human oogonia from induced pluripotent stem cells in vitro (2018) (164)
Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos. (1995) (159)
Increased HTLV‐I proviral DNA in HTLV‐I–associated myelopathy: A quantitative polymerase chain reaction study (1991) (154)
Crucial role of antisense transcription across the Xist promoter in Tsix-mediated Xist chromatin modification (2007) (144)
Complementary DNA for the mouse homolog of the human amyloid beta protein precursor. (1987) (140)
Genome-wide profiling of promoter methylation in human (2006) (136)
Small RNA class transition from siRNA/piRNA to miRNA during pre-implantation mouse development (2010) (132)
Conditional knockdown of Nanog induces apoptotic cell death in mouse migrating primordial germ cells (2009) (132)
Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome (2015) (125)
Genomic imprinting in mammals: its life cycle, molecular mechanisms and reprogramming (2011) (124)
A proximal conserved repeat in the Xist gene is essential as a genomic element for X-inactivation in mouse (2009) (119)
Correlation between Shh expression and DNA methylation status of the limb-specific Shh enhancer region during limb regeneration in amphibians. (2007) (118)
An atomic model of Zfp57 recognition of CpG methylation within a specific DNA sequence. (2012) (115)
In Vitro Derivation and Propagation of Spermatogonial Stem Cell Activity from Mouse Pluripotent Stem Cells. (2016) (112)
Lysyl 5-Hydroxylation, a Novel Histone Modification, by Jumonji Domain Containing 6 (JMJD6)* (2013) (111)
De novo DNA methylation is dispensable for the initiation and propagation of X chromosome inactivation (2004) (111)
Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques. (1984) (108)
Three novel DNMT3B mutations in Japanese patients with ICF syndrome. (2002) (103)
Global Landscape and Regulatory Principles of DNA Methylation Reprogramming for Germ Cell Specification by Mouse Pluripotent Stem Cells. (2016) (103)
Meiotic and epigenetic aberrations in Dnmt3L‐deficient male germ cells (2006) (102)
Re-investigation and RNA sequencing-based identification of genes with placenta-specific imprinted expression. (2012) (102)
DNA methylation and gene expression dynamics during spermatogonial stem cell differentiation in the early postnatal mouse testis (2015) (101)
Microarray analysis of promoter methylation in lung cancers (2006) (99)
Loss of the maternal imprint in Dnmt3Lmat-/- mice leads to a differentiation defect in the extraembryonic tissue. (2006) (97)
Maternal high-fat diet induces insulin resistance and deterioration of pancreatic β-cell function in adult offspring with sex differences in mice. (2014) (93)
Genetic evidence for Dnmt3a‐dependent imprinting during oocyte growth obtained by conditional knockout with Zp3‐Cre and complete exclusion of Dnmt3b by chimera formation (2010) (93)
Bisulfite sequencing and dinucleotide content analysis of 15 imprinted mouse differentially methylated regions (DMRs): paternally methylated DMRs contain less CpGs than maternally methylated DMRs (2006) (93)
Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution (2007) (93)
Type I familial amyloid polyneuropathy. A pathological study of the peripheral nervous system. (1990) (92)
Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome (2016) (90)
Role of UHRF1 in de novo DNA methylation in oocytes and maintenance methylation in preimplantation embryos (2017) (86)
Unusually high conservation of untranslated sequences in cDNAs for Trimeresurus flavoviridis phospholipase A2 isozymes. (1992) (84)
Abnormal DNA Methyltransferase Expression in Mouse Germline Stem Cells Results in Spermatogenic Defects1 (2009) (79)
Accumulation and loss of asymmetric non-CpG methylation during male germ-cell development (2012) (79)
In vitro expansion of mouse primordial germ cell‐like cells recapitulates an epigenetic blank slate (2017) (77)
Polycomb Group Proteins Regulate Chromatin Architecture in Mouse Oocytes and Early Embryos. (2019) (77)
Evolution of the vertebrate DNMT3 gene family: a possible link between existence of DNMT3L and genomic imprinting (2006) (76)
Genomic imprinting and its relevance to congenital disease, infertility, molar pregnancy and induced pluripotent stem cell (2012) (76)
Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta. (2016) (75)
Stochastic imprinting in the progeny of Dnmt3L-/- females. (2006) (72)
Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP). (1991) (72)
Regulation of DNA methylation activity through Dnmt3L promoter methylation by Dnmt3 enzymes in embryonic development. (2008) (71)
Structure and expression of the alternatively-spliced forms of mRNA for the mouse homolog of Alzheimer's disease amyloid beta protein precursor. (1989) (69)
Mechanism of chromosomal integration of transgenes in microinjected mouse eggs: sequence analysis of genome-transgene and transgene-transgene junctions at two loci. (1993) (66)
Positive and negative regulatory elements for the expression of the Alzheimer's disease amyloid precursor-encoding gene in mouse. (1992) (66)
Structure of the chromosomal gene for human serum prealbumin. (1985) (65)
Parental methylation patterns of a transgenic locus in adult somatic tissues are imprinted during gametogenesis. (1992) (64)
Inherited type of allelic methylation variations in a mouse chromosome region where an integrated transgene shows methylation imprinting. (1991) (61)
Activation of an imprinted Igf 2 gene in mouse somatic cell cultures (1993) (59)
Genomic imprinting: significance in development and diseases and the molecular mechanisms. (1996) (57)
Mutations in DNA methyltransferase DNMT3B in ICF syndrome affect its regulation by DNMT3L. (2006) (56)
Dynamic transition of Dnmt3b expression in mouse pre- and early post-implantation embryos. (2009) (54)
Unregulated Expression of the Imprinted Genes H19 andIgf2r in Mouse Uniparental Fetuses* (2002) (54)
Histone H3K9 Methyltransferase G9a in Oocytes Is Essential for Preimplantation Development but Dispensable for CG Methylation Protection. (2019) (52)
RNA sequencing-based identification of aberrant imprinting in cloned mice. (2014) (51)
Tsix defective in splicing is competent to establish Xist silencing (2006) (49)
CDCA7 and HELLS mutations undermine nonhomologous end joining in centromeric instability syndrome (2018) (49)
Locus- and domain-dependent control of DNA methylation at mouse B1 retrotransposons during male germ cell development. (2011) (48)
ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutation (2004) (47)
Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region. (2005) (46)
Creutzfeldt‐Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann‐Sträussler syndrome (1990) (45)
HSP90α plays an important role in piRNA biogenesis and retrotransposon repression in mouse (2014) (42)
Polycomb protein SCML2 facilitates H3K27me3 to establish bivalent domains in the male germline (2018) (42)
Roles of MIWI, MILI and PLD6 in small RNA regulation in mouse growing oocytes (2017) (42)
DNA methylation and genomic imprinting in mammals. (1993) (41)
DNMT3L promotes quiescence in postnatal spermatogonial progenitor cells (2014) (41)
An evolutionarily conserved putative insulator element near the 3' boundary of the imprinted Igf2/H19 domain. (2002) (41)
Isolation and sequencing of a cDNA clone encoding 107 kDa sialoglycoprotein in rat liver lysosomal membranes (1989) (40)
Most T790M mutations are present on the same EGFR allele as activating mutations in patients with non-small cell lung cancer. (2017) (39)
Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients (2013) (39)
Switching of dominant retrotransposon silencing strategies from posttranscriptional to transcriptional mechanisms during male germ-cell development in mice (2017) (39)
A methylation imprint mark in the mouse imprinted gene Grf1/Cdc25Mm locus shares a common feature with the U2afbp-rs gene: an association with a short tandem repeat and a hypermethylated region. (1998) (39)
Disruption of mesodermal enhancers for Igf2 in the minute mutant. (2002) (39)
Imprinting and looping: epigenetic marks control interactions between regulatory elements. (2005) (38)
A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip (2010) (38)
DBTSS/DBKERO for integrated analysis of transcriptional regulation (2017) (37)
Role of de novo DNA methyltransferases in initiation of genomic imprinting and X-chromosome inactivation. (2004) (36)
Effect of Tsix disruption on Xist expression in male ES cells (2003) (35)
Generation of transgenic mice producing a human transthyretin variant: a possible mouse model for familial amyloidotic polyneuropathy. (1986) (34)
Haplotype analysis of familial amyloidotic polyneuropathy (1989) (34)
Tsix-deficient X chromosome does not undergo inactivation in the embryonic lineage in males: implications for Tsix-independent silencing of Xist (2006) (33)
Sequence-specific microscopic visualization of DNA methylation status at satellite repeats in individual cell nuclei and chromosomes (2013) (33)
Aging of spermatogonial stem cells by Jnk-mediated glycolysis activation (2019) (33)
Targeted gene silencing in mouse germ cells by insertion of a homologous DNA into a piRNA generating locus (2013) (32)
De novo DNA methylation independent establishment of maternal imprint on X chromosome in mouse oocytes (2008) (32)
Large-scale identification and mapping of nuclear matrix-attachment regions in the distal imprinted domain of mouse chromosome 7. (2004) (32)
Allele‐specific detection of nascent transcripts by fluorescence in situ hybridization reveals temporal and culture‐induced changes in Igf2 imprinting during pre‐implantation mouse development (2001) (31)
X‐inactivation is stably maintained in mouse embryos deficient for histone methyl transferase G9a (2004) (30)
Human transthyretin (prealbumin) gene and molecular genetics of familial amyloidotic polyneuropathy. (1989) (29)
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster. (2000) (28)
Genomic organization and promoter analysis of the Dnmt3b gene. (2003) (28)
Accurate estimation of 5-methylcytosine in mammalian mitochondrial DNA (2018) (28)
Cloning and sequence analysis of cDNA for Trimeresurus flavoviridis phospholipase A2, and consequent revision of the amino acid sequence. (1990) (27)
The inheritance of germline-specific epigenetic modifications during development. (1993) (27)
The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster (2005) (26)
Assignment of the prealbumin (PALB) gene (familial amyloidotic polyneuropathy) to human chromosome region 18q11.2–q12.1 (1987) (26)
Reprogramming of the histone H3.3 landscape in the early mouse embryo (2020) (25)
Regional DNA methylation differences between humans and chimpanzees are associated with genetic changes, transcriptional divergence and disease genes (2013) (25)
Haplotype analysis of familial amyloidotic polyneuropathy. Evidence for multiple origins of the Val----Met mutation most common to the disease. (1989) (25)
Production of functional oocytes requires maternally expressed PIWI genes and piRNAs in golden hamsters (2021) (24)
Zfp281 Shapes the Transcriptome of Trophoblast Stem Cells and Is Essential for Placental Development. (2019) (24)
Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy. (1986) (24)
Software updates in the Illumina HiSeq platform affect whole-genome bisulfite sequencing (2017) (23)
Germline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology (2014) (23)
Clinical and Immunological Characterization of ICF Syndrome in Japan (2018) (22)
Broad Heterochromatic Domains Open in Gonocyte Development Prior to De Novo DNA Methylation. (2019) (22)
Incomplete X-inactivation initiated by a hypomorphic Xist allele in the mouse (2011) (21)
Defects in dosage compensation impact global gene regulation in the mouse trophoblast (2017) (21)
Structure and expression of the mouse L23mrp gene downstream of the imprinted H19 gene: biallelic expression and lack of interaction with the H19 enhancers. (1997) (20)
Active role of small non-coding RNAs derived from SINE/B1 retrotransposon during early mouse development (2012) (20)
PRESYMPTOMATIC DIAGNOSIS OF HETEROZYGOSITY FOR FAMILIAL AMYLOIDOTIC POLYNEUROPATHY BY RECOMBINANT DNA TECHNIQUES (1985) (19)
A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip (2010) (19)
Imprinted genes are up-regulated by growth arrest in embryonic fibroblasts. (1997) (18)
Nucleotide sequence of a 28-kb mouse genomic region comprising the imprinted Igf2 gene. (1996) (18)
Amyloid beta-protein gene duplication is not common in Alzheimer's disease: analysis by polymorphic restriction fragments. (1988) (18)
Isolation and sequencing of a cDNA clone encoding 96 kDa sialoglycoprotein in rat liver lysosomal membranes. (1989) (18)
A 210-kb segment of tandem repeats and retroelements located between imprinted subdomains of mouse distal chromosome 7. (2004) (17)
Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human. (2000) (17)
Analysis of small RNA profiles during development. (2007) (16)
Tetramer formation of a variant type human transthyretin (prealbumin) produced by Escherichia coli expression system. (1989) (16)
Expression of Alzheimer amyloid beta-protein precursor gene in neuronal cells. (1991) (16)
Whole-Mount MeFISH: A Novel Technique for Simultaneous Visualization of Specific DNA Methylation and Protein/RNA Expression (2014) (15)
Evolution of the sperm methylome of primates is associated with retrotransposon insertions and genome instability (2017) (14)
Sequence of a 42-kb mouse region containing the imprinted H19 locus: identification of a novel muscle-specific transcription unit showing biallelic expression (1998) (14)
Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs. (1987) (13)
CDCA7 and HELLS suppress DNA:RNA hybrid-associated DNA damage at pericentromeric repeats (2020) (12)
Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy (1987) (12)
Role of SmcHD1 in establishment of epigenetic states required for the maintenance of the X-inactivated state in mice (2018) (12)
Locus-specific hypomethylation of the mouse IAP retrotransposon is associated with transcription factor-binding sites (2017) (11)
Genetic and clinical studies of Japanese patients with familial amyloid polyneuropathy. (1989) (10)
De novo DNA methylation independent establishment of maternal imprint on X chromosome in mouse oocytes. (2008) (10)
Activity of a metallothionein-transthyretin fusion gene in transgenic mice. Possible effect of plasmid sequences on tissue-specific expression. (1989) (9)
Differential chromatin packaging of genomic imprinted regions between expressed and non-expressed alleles. (2000) (8)
The 5′ region of Xist RNA has the potential to associate with chromatin through the A-repeat (2017) (7)
Stochastic imprinting in the progeny of Dnmt3L 2 / 2 females (2006) (7)
A histone H3.3K36M mutation in mice causes an imbalance of histone modifications and defects in chondrocyte differentiation (2020) (7)
The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes (2021) (7)
Maternal DNMT3A-dependent de novo methylation of the paternal genome inhibits gene expression in the early embryo (2020) (7)
Genetic analysis of familial amyloidotic polyneuropathy, an autosomal dominant disease. (1989) (6)
TFB2M and POLRMT are essential for mammalian mitochondrial DNA replication. (2021) (6)
Identification of SLC38A7 as a Prognostic Marker and Potential Therapeutic Target of Lung Squamous Cell Carcinoma (2021) (5)
A new Xist allele driven by a constitutively active promoter is dominated by Xist locus environment and exhibits the parent-of-origin effects (2015) (5)
Enhancer-dependent, locus-wide regulation of the imprinted mouse insulin-like growth factor II gene. (1998) (5)
Genomic organization of the human amyloid beta-protein precursor gene. (1990) (5)
Non-transmissible MV Vector with Segmented RNA Genome Establishes Different Types of iPSCs from Hematopoietic Cells. (2020) (5)
Poorly controlled diabetes during pregnancy and lactation activates the Foxo1 pathway and causes glucose intolerance in adult offspring (2019) (4)
Clinical features and diagnosis by recombinant DNA techniques of familial amyloid polyneuropathy in Japan. (1989) (3)
Localization of mouse imprinted gene U2af1-rs1 to A3.2-4 band of chromosome 11 by FISH. (1994) (3)
[Familial amyloid polyneuropathy (FAP), in an inborn habitat of Hiroshima Prefecture, Japan]. (1986) (3)
A HindIII polymorphism detected by the cDNA encoding amyloid beta protein of Alzheimer's disease. (1987) (3)
Germ line-specific programming of parental genomes for development (1993) (2)
Assessement of Structure and Binding Capacities of Secreted Mutant Transthyretins by an E. Coli System (1991) (2)
Structural and functional analysis of a 0 . 5-Mb chicken region orthologous to the imprinted mammalian Ascl 2 / Mash 2 – Igf 2 – H 19 region (2004) (2)
Histone H3K36me2 and H3K36me3 form a chromatin platform essential for DNMT3A-dependent DNA methylation in mouse oocytes (2022) (2)
Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegia (2021) (2)
Neuraminidase Amino Acid Sequences of Influenza A/H3N2 and B Viruses Isolated from Influenza Patients in the 2014/15 Japanese Influenza Season. (2016) (2)
Identification of ZBTB24 protein domains and motifs for heterochromatin localization and transcriptional activation (2019) (2)
[Analysis of the Neuraminidase Amino Acid Sequences of Influenza A/H1N1pdm09, A/H3N2, and B Viruses Isolated from Influenza Patients in the 2013/14 Japanese Influenza Season]. (2015) (2)
“Sporadic” prealbumin-related amyloid polyneuropathy: report of two cases (2004) (2)
Maternal DNMT3A-dependent de novo methylation of the zygotic paternal genome inhibits gene expression in the early embryo (2020) (1)
The UHRF protein family in epigenetics, development, and carcinogenesis (2022) (1)
Structure and expression of Alzheimer's amyloid β-protein precursor gene (1990) (1)
Characterization of genetic‐origin‐dependent monoallelic expression in mouse embryonic stem cells (2019) (1)
Diagnosis of Familial Amyloid Polyneuropathy by Recombinant DNA Techniques in Relation with Clinical Features (1988) (1)
[Establishment of genomic imprints in the mammalian germline and their maintenance in preimplantation embryos]. (2007) (1)
Sequences in the H19 ICR that are transcribed as small RNA in oocytes are dispensable for methylation imprinting in YAC transgenic mice. (2012) (1)
[DNA diagnosis of familial amyloidotic polyneuropathy]. (1985) (1)
Parental imprinting and epigenetic programming of the mouse genome: long lasting consequences for development and phenotype (1993) (1)
Biochemical and Genetic Characterization of a Variant Transthyretin Causing Familial Amyloidotic Polyneuropathy (1986) (1)
DNA methylation and gene expression dynamics during spermatogonial stem cell differentiation in the early postnatal mouse testis (2015) (1)
Identification of Genomic Alterations Acquired During Treatment With EGFR-TKIs in Non-small Cell Lung Cancer (2019) (1)
Localization of mouse imprinted gene U2af1-rs1 to A3.2-4 band of Chromosome 11 by FISH (2004) (1)
Supplemental Information In Vitro Derivation and Propagation of Spermatogonial Stem Cell Activity from Mouse Pluripotent Stem Cells (2016) (0)
Molecular Cloning and Structural Analysis of the Human Amyloid ß Protein Precursor Gene (1990) (0)
DNA Methylation-Dependent and -Independent Regulation of Monoallelic Expression by Zfp57 in Ground-State Embryonic Stem Cells (2016) (0)
Locus-specific hypomethylation of the mouse IAP retrotransposon is associated with transcription factor-binding sites (2017) (0)
DNA Polymorphisms Analysis in Families with Familial Amyloidotic Polyneuropathy (FAP) from Different Ethnic Origins (1988) (0)
Supplemental Information Derivation of Human Trophoblast Stem Cells (2017) (0)
Functional analysis of the PWWP domain (a H3K36me3 reader) of Dnmt3a in DNA methylation establishment in mouse oocytes and somatic cells (2017) (0)
Role for SmcHD1 in the establishment of the proper epigenetic states of the inactive X chromosome (2017) (0)
Promoter Methylation Patterns in Human Genome: Implication for Clinical Epigenomic Studies (2008) (0)
Role of H3K9 methyltransferase G9a during oogenesis and early embryo development (2016) (0)
Active role of small non-coding RNAs derived from SINE/B1 retrotransposon during early mouse development (2011) (0)
Reprogramming of the histone H3.3 landscape in the early mouse embryo (2020) (0)
Title Roles of MIWI , MILI and PLD 6 in small RNA regulation inmouse growing oocytes (2017) (0)
Long-term influence of maternal diabetes on the phenotype and gene expression of the offspring in adulthood (2016) (0)
DNA methylation in epigenetics, development, and imprinting (2005) (0)
A search for genomic regions associated with neurodevelopmental differences between Rett syndrome monozygotic twins by genomic and epigenomic comparative assays (2009) (0)
Identification of ZBTB24 protein domains and motifs essential for heterochromatin localization and transcriptional gene activation (2019) (0)
Mutations in PLD6 and MILI in mouse oocytes reveal sex-dependent differences in piRNA regulation (2016) (0)
A Recombinants System for Production of Variant Type Human Transthyretin(TTR) (1991) (0)
Toward Establishment of an Animal Model for Familial Amyloidotic Polyneuropathy: Generation and Characterization of Transgenic Mice (1988) (0)
Accurate estimation of 5-methylcytosine in mammalian mitochondrial DNA (2018) (0)
Software updates in the Illumina HiSeq platform affect whole-genome bisulfite sequencing (2017) (0)
Essential role of Uhrf1 during oocyte growth and preimplantation development (2016) (0)
Genomic imprinting : single topic volume ; 33 tables (2006) (0)
Defect of DNA repair pathway is involved in pathogenesis of ICF syndrome (2017) (0)
The mouse l23mrp gene located downstream of the imprinted ins2/igf2/h19 region is biallelically expressed and not influenced by the h19 enhancer (1997) (0)
Additional file 2: Table S1. of Locus-specific hypomethylation of the mouse IAP retrotransposon is associated with transcription factor-binding sites (2017) (0)
Haplotype Analisis of Familial Amyloidotic Polyneuropathy: an Evidence for Multiple Origins of the Val→met Mutation (1988) (0)
Genomic Imprinting: Mechanisms, Significance and Evolution (2003) (0)
Structure and Expression of mRNA for the Mouse Homolog of Alzheimer Amyloid Beta Protein Precursor (1990) (0)
Quantitative dynamics of epigenome remodeling in the primordial germ cell formation (2017) (0)
H3K9 methyltransferase G9a regulates oogenesis and early embryo development (2017) (0)
Incomplete reprogramming of germline DNA methylation in the human placenta (2016) (0)
Low Input Genome-Wide DNA Methylation Analysis with Minimal Library Amplification. (2022) (0)
Transcriptional Regulation of Monoallelically Expressed Genes in Ground-state Embryonic Stem Cells (2017) (0)
2011/12及び2012/13年インフルエンザ流行期に患者より分離されたA/H3N2型ウイルス96株のNA遺伝子配列と薬剤感受性との関連についての検討 (2015) (0)
2014/15年流行期に患者より分離されたインフルエンザA/H3N2，Bウイルスのノイラミニダーゼ遺伝子と薬剤感受性との関連についての検討 (2016) (0)
Elucidation of the role of ADD domain of Dnmt3a for DNA methylation establishment in mouse oocytes (2017) (0)
A convolutional neural network-based regression model to infer the epigenetic crosstalk responsible for CG methylation patterns (2021) (0)
CMIC: predicting DNA methylation inheritance of CpG islands with embedding vectors of variable-length k-mers (2022) (0)
The ADD domain of Dnmt3a is important for DNA methylation establishment in mouse oocytes (2019) (0)
SCML2 establishes germline epigenome during spermatogenesis (2016) (0)
CMIC: predicting DNA methylation inheritance of CpG islands with embedding vectors of variable-length k-mers (2022) (0)
Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with distinctive genome-wide DNA hypomethylation. (2022) (0)
Forward genetic screen using haploid embryonic stem cells identifies a regulator for extraembryonic development (2017) (0)
Poorly controlled diabetes during pregnancy and lactation activates the Foxo1 pathway and causes glucose intolerance in adult offspring (2019) (0)
A convolutional neural network-based regression model to infer the epigenetic crosstalk responsible for CG methylation patterns (2021) (0)
[Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan]. (2015) (0)
3D chromosome relaxation with TE-rich heterochromatin opening during de novo DNA methylation in gonocyte (2018) (0)
O-16. Comparative chromosome study between chicken and Guinea fowl by FISH(Abstracts of the 52nd Annual Meeting of the Society of Chromosome Research) (2001) (0)
New function of cytoplasmic Uhrf1 during oogenesis and early embryogenesis (2017) (0)
[Parental imprinting of mammalian genomes]. (1992) (0)
O13. Genomic imprinting and small RNAs in mammalian germ cells (2010) (0)
Dissection of Structure-Function Relationship of ZBTB24 and Molecular Pathology of ICF Syndrome (2017) (0)
Does mtDNA epigenetics exist? 〜 an investigation of DNA methylation in mammalian mitochondria (2016) (0)

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Other Resources About Hiroyuki Sasaki

en.wikipedia.org

What Schools Are Affiliated With Hiroyuki Sasaki?

Hiroyuki Sasaki is affiliated with the following schools: