| scholarly article | Q13442814 |
| P50 | author | Thomas L Saunders | Q40082893 |
| P2093 | author name string | Jiaxue Wu | |
| Xiaochun Yu | |||
| Lin Ye | |||
| Lin-Yu Lu | |||
| Galina B Gavrilina | |||
| P2860 | cites work | Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 |
| N-Terminally extended human ubiquitin-conjugating enzymes (E2s) mediate the ubiquitination of RING-finger proteins, ARA54 and RNF8 | Q24291166 | ||
| Monoubiquitination of human histone H2B: the factors involved and their roles in HOX gene regulation | Q24297025 | ||
| Human USP3 is a chromatin modifier required for S phase progression and genome stability | Q24299488 | ||
| A critical role for the ubiquitin-conjugating enzyme Ubc13 in initiating homologous recombination | Q24299584 | ||
| RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins | Q24300411 | ||
| RNF8 transduces the DNA-damage signal via histone ubiquitylation and checkpoint protein assembly | Q24300428 | ||
| Roles of transition nuclear proteins in spermiogenesis | Q24301755 | ||
| Role of histone H2A ubiquitination in Polycomb silencing | Q24305090 | ||
| The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage | Q24309181 | ||
| RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins | Q24309287 | ||
| The histone H2B-specific ubiquitin ligase RNF20/hBRE1 acts as a putative tumor suppressor through selective regulation of gene expression | Q24318500 | ||
| Histone H2B monoubiquitination functions cooperatively with FACT to regulate elongation by RNA polymerase II | Q24337471 | ||
| Involvement of human MOF in ATM function | Q24529072 | ||
| hMOF histone acetyltransferase is required for histone H4 lysine 16 acetylation in mammalian cells | Q24529984 | ||
| A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16 | Q24534923 | ||
| DNA damage triggers nucleotide excision repair-dependent monoubiquitylation of histone H2A | Q24546161 | ||
| Orchestration of the DNA-damage response by the RNF8 ubiquitin ligase | Q24653776 | ||
| Acetylation-dependent chromatin reorganization by BRDT, a testis-specific bromodomain-containing protein | Q24681168 | ||
| The role of chromatin during transcription | Q27860995 | ||
| Histone crosstalk between H2B monoubiquitination and H3 methylation mediated by COMPASS. | Q27939071 | ||
| Histone ubiquitination: a tagging tail unfolds? | Q28218018 | ||
| Role of Bmi-1 and Ring1A in H2A ubiquitylation and Hox gene silencing | Q28287373 | ||
| Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation | Q28505166 | ||
| Histone ubiquitination associates with BRCA1-dependent DNA damage response | Q28506770 | ||
| Histone demethylase JHDM2A is critical for Tnp1 and Prm1 transcription and spermatogenesis | Q28509478 | ||
| Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis | Q28511362 | ||
| Monoubiquitinated H2B is associated with the transcribed region of highly expressed genes in human cells | Q40001798 | ||
| The RAD6 DNA repair pathway in Saccharomyces cerevisiae: what does it do, and how does it do it? | Q40671595 | ||
| Quantitative analysis of the digestion of yeast chromatin by staphylococcal nuclease | Q40749164 | ||
| Histone H4 isoforms acetylated at specific lysine residues define individual chromosomes and chromatin domains in Drosophila polytene nuclei | Q41116253 | ||
| Mass spectrometric quantification of acetylation at specific lysines within the amino-terminal tail of histone H4 | Q44403078 | ||
| H2B ubiquitylation plays a role in nucleosome dynamics during transcription elongation | Q46493188 | ||
| Chromatin structure; oligomers of the histones | Q47873595 | ||
| Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification. | Q48060228 | ||
| Intracytoplasmic sperm injection in the mouse | Q49058048 | ||
| Silencing of unsynapsed meiotic chromosomes in the mouse. | Q50668569 | ||
| Transmission of modified nucleosomes from the mouse male germline to the zygote and subsequent remodeling of paternal chromatin. | Q50745250 | ||
| Histones are first hyperacetylated and then lose contact with the activated PHO5 promoter. | Q51599592 | ||
| DNA damage response during chromatin remodeling in elongating spermatids of mice. | Q51971590 | ||
| The genes coding for the MYST family histone acetyltransferases, Tip60 and Mof, are expressed at high levels during sperm development. | Q51985292 | ||
| BRCA1, histone H2AX phosphorylation, and male meiotic sex chromosome inactivation. | Q52064286 | ||
| Histone ubiquitination and chromatin remodeling in mouse spermatogenesis. | Q52178915 | ||
| Post-transcriptional control of gene expression during spermatogenesis. | Q52182321 | ||
| Histone acetylation in insect chromosomes. | Q52502351 | ||
| Ubiquitination of histone H3 in elongating spermatids of rat testes. | Q52530661 | ||
| Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila. | Q52580421 | ||
| Highly acetylated H4 is associated with histone displacement in rat spermatids | Q54646685 | ||
| Basic nuclear proteins in testicular cells and ejaculated spermatozoa in man | Q67416234 | ||
| Postmeiotic sex chromatin in the male germline of mice | Q83041214 | ||
| Haploinsufficiency of protamine-1 or -2 causes infertility in mice | Q28512831 | ||
| Histone H4-K16 acetylation controls chromatin structure and protein interactions | Q29614521 | ||
| Ubiquitination of histone H2B regulates H3 methylation and gene silencing in yeast | Q29617217 | ||
| Multivalent engagement of chromatin modifications by linked binding modules | Q29617236 | ||
| Histone ubiquitination: triggering gene activity | Q29617523 | ||
| Rad6-dependent ubiquitination of histone H2B in yeast | Q29617525 | ||
| Functions of site-specific histone acetylation and deacetylation | Q29617894 | ||
| A drying-down technique for the spreading of mammalian meiocytes from the male and female germline | Q29618406 | ||
| Transition nuclear proteins are required for normal chromatin condensation and functional sperm development | Q29871104 | ||
| Abnormalities and reduced reproductive potential of sperm from Tnp1- and Tnp2-null double mutant mice | Q29871127 | ||
| Gene silencing: trans-histone regulatory pathway in chromatin | Q30309681 | ||
| mof, a putative acetyl transferase gene related to the Tip60 and MOZ human genes and to the SAS genes of yeast, is required for dosage compensation in Drosophila | Q33886451 | ||
| Spermiogenesis and exchange of basic nuclear proteins are impaired in male germ cells lacking Camk4. | Q33912824 | ||
| Genomic characterization reveals a simple histone H4 acetylation code. | Q33935027 | ||
| H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis | Q33965393 | ||
| Expression of hyperacetylated histone H4 during normal and impaired human spermatogenesis | Q34163376 | ||
| Splicing components are excluded from the transcriptionally inactive XY body in male meiotic nuclei | Q34446336 | ||
| Demethylation of H3K27 regulates polycomb recruitment and H2A ubiquitination | Q34673352 | ||
| Arginine methylation at histone H3R2 controls deposition of H3K4 trimethylation | Q34694111 | ||
| RNF8-dependent and RNF8-independent regulation of 53BP1 in response to DNA damage | Q34761198 | ||
| Histone 2B can be modified by the attachment of ubiquitin | Q35626907 | ||
| Pericentric heterochromatin reprogramming by new histone variants during mouse spermiogenesis. | Q36117733 | ||
| Complicated tails: histone modifications and the DNA damage response | Q36179927 | ||
| Cross-talking histones: implications for the regulation of gene expression and DNA repair | Q36226144 | ||
| The mammalian ortholog of Drosophila MOF that acetylates histone H4 lysine 16 is essential for embryogenesis and oncogenesis | Q36421093 | ||
| Protamines and male infertility. | Q36438262 | ||
| Ubc13/Rnf8 ubiquitin ligases control foci formation of the Rap80/Abraxas/Brca1/Brcc36 complex in response to DNA damage | Q36696336 | ||
| Meiotic sex chromosome inactivation | Q36747812 | ||
| Acetylation in the globular core of histone H3 on lysine-56 promotes chromatin disassembly during transcriptional activation. | Q36752456 | ||
| Mechanisms of epigenetic inheritance | Q36805020 | ||
| Mof (MYST1 or KAT8) is essential for progression of embryonic development past the blastocyst stage and required for normal chromatin architecture. | Q36845983 | ||
| Nuclear regulator Pygo2 controls spermiogenesis and histone H3 acetylation | Q36908690 | ||
| Polo-like kinase 1 is essential for early embryonic development and tumor suppression | Q36949896 | ||
| Covalent modifications of histones during development and disease pathogenesis | Q36994153 | ||
| Chemically ubiquitylated histone H2B stimulates hDot1L-mediated intranucleosomal methylation | Q37175650 | ||
| Dynamic histone modifications mark sex chromosome inactivation and reactivation during mammalian spermatogenesis | Q37692429 | ||
| Vertebrate protamine genes and the histone-to-protamine replacement reaction | Q37716790 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | spermatogenesis | Q36961 |
| Ring finger protein 8 | Q21988000 | ||
| P1104 | number of pages | 14 | |
| P304 | page(s) | 371-384 | |
| P577 | publication date | 2010-02-11 | |
| P1433 | published in | Developmental Cell | Q1524277 |
| P1476 | title | RNF8-dependent histone modifications regulate nucleosome removal during spermatogenesis | |
| P478 | volume | 18 |
| Q55025212 | A Decade of Exploring the Mammalian Sperm Epigenome: Paternal Epigenetic and Transgenerational Inheritance. |
| Q38289619 | A mutation study of sperm head shape and motility in the mouse: lessons for the clinic |
| Q35098176 | A-MYB (MYBL1) transcription factor is a master regulator of male meiosis |
| Q36283879 | ATDC (Ataxia Telangiectasia Group D Complementing) Promotes Radioresistance through an Interaction with the RNF8 Ubiquitin Ligase |
| Q27933881 | Acetylation-mediated proteasomal degradation of core histones during DNA repair and spermatogenesis |
| Q42361116 | Arrested spermatogenesis and evidence for DNA damage in PTIP mutant testes |
| Q33731257 | BRCA1 establishes DNA damage signaling and pericentric heterochromatin of the X chromosome in male meiosis |
| Q36780664 | CHFR is important for the survival of male premeiotic germ cells |
| Q35854193 | Changing the ubiquitin landscape during viral manipulation of the DNA damage response |
| Q34117192 | Chd5 orchestrates chromatin remodelling during sperm development |
| Q35089499 | Chfr and RNF8 synergistically regulate ATM activation |
| Q26744843 | Choreographing the Double Strand Break Response: Ubiquitin and SUMO Control of Nuclear Architecture |
| Q51035830 | Chromatin regulators: weaving epigenetic nets. |
| Q24606850 | Chromatin remodelling initiation during human spermiogenesis |
| Q34360500 | DNA double-strand break signaling and human disorders |
| Q89121896 | Defects in meiotic recombination delay progression through pachytene in Tex19.1-/- mouse spermatocytes |
| Q35803418 | Dgcr8 and Dicer are essential for sex chromosome integrity during meiosis in males. |
| Q33678749 | Does the APC/C Mark MIWI and piRNAs for a final farewell? |
| Q26830517 | Double-strand break repair on sex chromosomes: challenges during male meiotic prophase |
| Q50432975 | EPC1/TIP60-Mediated Histone Acetylation Facilitates Spermiogenesis in Mice |
| Q46252011 | Early Histone H4 Acetylation during Chromatin Remodeling in Equine Spermatogenesis. |
| Q28077132 | Epigenetic Remodeling in Male Germline Development |
| Q41593402 | Epigenetic dynamics and interplay during spermatogenesis and embryogenesis: implications for male fertility and offspring health |
| Q26768549 | Epigenetic regulation of the histone-to-protamine transition during spermiogenesis |
| Q42265769 | Essential role for SUN5 in anchoring sperm head to the tail |
| Q35577991 | Flickin' the ubiquitin switch: the role of H2B ubiquitylation in development |
| Q47927250 | Function of RAD6B and RNF8 in spermatogenesis |
| Q91844289 | Genetic Factors Affecting Sperm Chromatin Structure |
| Q46871393 | Genetic association study of RNF8 and BRDT variants with non-obstructive azoospermia in the Chinese Han population. |
| Q33892356 | Genomic instability, defective spermatogenesis, immunodeficiency, and cancer in a mouse model of the RIDDLE syndrome |
| Q46453565 | H3K9ac involved in the decondensation of spermatozoal nuclei during spermatogenesis in Chinese mitten crab Eriocheir sinensis |
| Q47445113 | Heritable Sperm Chromatin Epigenetics: A Break to Remember |
| Q35571865 | Heteromorphic sex chromosomes: navigating meiosis without a homologous partner |
| Q53440183 | Histone H2B Monoubiquitination Mediated by HISTONE MONOUBIQUITINATION1 and HISTONE MONOUBIQUITINATION2 Is Involved in Anther Development by Regulating Tapetum Degradation-Related Genes in Rice. |
| Q89976206 | Histone Post-Translational Modifications and CircRNAs in Mouse and Human Spermatozoa: Potential Epigenetic Marks to Assess Human Sperm Quality |
| Q37968540 | Histone crotonylation specifically marks the haploid male germ cell gene expression program: post-meiotic male-specific gene expression |
| Q38181507 | Histone exchange and histone modifications during transcription and aging |
| Q37098139 | How mammals pack their sperm: a variant matter |
| Q54590270 | Human PIWI (HIWI) is an azoospermia factor. |
| Q27355584 | Human X-linked Intellectual Disability Factor CUL4B Is Required for Post-meiotic Sperm Development and Male Fertility |
| Q37741354 | Identification of a variant-specific phosphorylation of TH2A during spermiogenesis |
| Q28571851 | Insights into role of bromodomain, testis-specific (Brdt) in acetylated histone H4-dependent chromatin remodeling in mammalian spermiogenesis |
| Q36138616 | JMJD1C Exhibits Multiple Functions in Epigenetic Regulation during Spermatogenesis |
| Q91559640 | L3MBTL2 regulates chromatin remodeling during spermatogenesis |
| Q36548438 | Loss of the Ubiquitin-conjugating Enzyme UBE2W Results in Susceptibility to Early Postnatal Lethality and Defects in Skin, Immune, and Male Reproductive Systems |
| Q43463528 | MARCH7 E3 ubiquitin ligase is highly expressed in developing spermatids of rats and its possible involvement in head and tail formation. |
| Q34879712 | MDC1 directs chromosome-wide silencing of the sex chromosomes in male germ cells |
| Q28396945 | Mammalian sperm nuclear organization: resiliencies and vulnerabilities |
| Q92265781 | Meiosis I progression in spermatogenesis requires a type of testis-specific 20S core proteasome |
| Q35780453 | Mice lacking the USP2 deubiquitinating enzyme have severe male subfertility associated with defects in fertilization and sperm motility |
| Q27319535 | Mouse BAZ1A (ACF1) is dispensable for double-strand break repair but is essential for averting improper gene expression during spermatogenesis |
| Q38069874 | New insights to the ubiquitin-proteasome pathway (UPP) mechanism during spermatogenesis |
| Q34047444 | Nucleolin and nucleophosmin: nucleolar proteins with multiple functions in DNA repair |
| Q58786750 | PARP2 mediates branched poly ADP-ribosylation in response to DNA damage |
| Q34364654 | PTEN interacts with histone H1 and controls chromatin condensation |
| Q34764527 | Poly(ADP-ribose) metabolism is essential for proper nucleoprotein exchange during mouse spermiogenesis |
| Q28507685 | Polycomb protein SCML2 associates with USP7 and counteracts histone H2A ubiquitination in the XY chromatin during male meiosis |
| Q34364048 | Protein acetylation and spermatogenesis |
| Q36547794 | Putative molecular mechanism underlying sperm chromatin remodelling is regulated by reproductive hormones |
| Q36352398 | RAP80 is critical in maintaining genomic stability and suppressing tumor development |
| Q39167940 | RNAi silencing targeting RNF8 enhances radiosensitivity of a non-small cell lung cancer cell line A549. |
| Q36882870 | RNF168 forms a functional complex with RAD6 during the DNA damage response |
| Q50422500 | RNF8 and SCML2 cooperate to regulate ubiquitination and H3K27 acetylation for escape gene activation on the sex chromosomes. |
| Q36853491 | RNF8 deficiency results in neurodegeneration in mice |
| Q36969257 | RNF8 promotes epithelial-mesenchymal transition of breast cancer cells |
| Q36496577 | RNF8 regulates active epigenetic modifications and escape gene activation from inactive sex chromosomes in post-meiotic spermatids. |
| Q34829400 | RNF8-dependent histone ubiquitination during DNA damage response and spermatogenesis |
| Q46820597 | RNF8/UBC13 ubiquitin signaling suppresses synapse formation in the mammalian brain |
| Q38938428 | Rad18 and Rnf8 facilitate homologous recombination by two distinct mechanisms, promoting Rad51 focus formation and suppressing the toxic effect of nonhomologous end joining |
| Q37137813 | Regulation of the DNA damage response on male meiotic sex chromosomes |
| Q92652925 | Retained Acetylated Histone Four in Bull Sperm Associated With Fertility |
| Q35338785 | SCML2 establishes the male germline epigenome through regulation of histone H2A ubiquitination. |
| Q58596731 | SETDB1 Links the Meiotic DNA Damage Response to Sex Chromosome Silencing in Mice |
| Q37098468 | Sex chromosome inactivation in germ cells: emerging roles of DNA damage response pathways |
| Q97423736 | Sperm DNA Integrity and Male Fertility in Farm Animals: A Review |
| Q34326278 | Synergistic interaction of Rnf8 and p53 in the protection against genomic instability and tumorigenesis. |
| Q92773147 | The PSMA8 subunit of the spermatoproteasome is essential for proper meiotic exit and mouse fertility |
| Q46169682 | The effects of chemotherapy with bleomycin, etoposide, and cis-platinum (BEP) on rat sperm chromatin remodeling, fecundity and testicular gene expression in the progeny |
| Q37445199 | The great escape: Active genes on inactive sex chromosomes and their evolutionary implications |
| Q64994764 | The histone methyltransferase SETD2 is required for expression of acrosin-binding protein 1 and protamines and essential for spermiogenesis in mice. |
| Q33707078 | The role of E3 ligases in the ubiquitin-dependent regulation of spermatogenesis |
| Q33736010 | The role of histone ubiquitination during spermatogenesis. |
| Q37571931 | The role of the double bromodomain-containing BET genes during mammalian spermatogenesis |
| Q27313726 | The specification and global reprogramming of histone epigenetic marks during gamete formation and early embryo development in C. elegans |
| Q37711890 | The sperm nucleus: chromatin, RNA, and the nuclear matrix. |
| Q33600336 | The ubiquitin-conjugating enzyme HR6B is required for maintenance of X chromosome silencing in mouse spermatocytes and spermatids. |
| Q37807639 | The ubiquitous role of ubiquitin in the DNA damage response |
| Q34278026 | UBR2 of the N-end rule pathway is required for chromosome stability via histone ubiquitylation in spermatocytes and somatic cells |
| Q37679191 | Ubiquitination regulates the morphogenesis and function of sperm organelles |
| Q32874809 | Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis. |
| Q33733955 | X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance |
| Q64976615 | piRNA-independent PIWI function in spermatogenesis and male fertility. |
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