| scholarly article | Q13442814 |
| P2093 | author name string | S P Goff | |
| H Scherthan | |||
| M Jerratsch | |||
| T K Pandita | |||
| S Dhar | |||
| Y A Wang | |||
| P2860 | cites work | The complete coding sequence of arg defines the Abelson subfamily of cytoplasmic tyrosine kinases | Q24292892 |
| Atm-dependent interactions of a mammalian chk1 homolog with meiotic chromosomes | Q24309630 | ||
| A single ataxia telangiectasia gene with a product similar to PI-3 kinase | Q24323579 | ||
| Interaction of human rad51 recombination protein with single-stranded DNA binding protein, RPA | Q24548334 | ||
| The Schizosaccharomyces pombe rad3 checkpoint gene | Q24561779 | ||
| Meiotic chromosomes: it takes two to tango | Q27930023 | ||
| Rad52 associates with RPA and functions with rad55 and rad57 to assemble meiotic recombination complexes | Q27931495 | ||
| Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein | Q27933995 | ||
| PIK-related kinases: DNA repair, recombination, and cell cycle checkpoints | Q27934828 | ||
| Saccharomyces cerevisiae checkpoint genes MEC1, RAD17 and RAD24 are required for normal meiotic recombination partner choice | Q27935546 | ||
| Saccharomyces cerevisiae recA homologues RAD51 and DMC1 have both distinct and overlapping roles in meiotic recombination | Q27936736 | ||
| Mammalian Chk2 is a downstream effector of the ATM-dependent DNA damage checkpoint pathway | Q28141324 | ||
| Radiation-induced assembly of Rad51 and Rad52 recombination complex requires ATM and c-Abl | Q28142095 | ||
| Recruitment of ATM protein to double strand DNA irradiated with ionizing radiation | Q28143124 | ||
| Interaction between ATM protein and c-Abl in response to DNA damage | Q28239339 | ||
| The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells | Q28262541 | ||
| Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma | Q28509780 | ||
| Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene | Q28512170 | ||
| Localization of SCP2 and SCP3 protein molecules within synaptonemal complexes of the rat | Q28571074 | ||
| Abnormal peripheral lymphocyte function in c-abl mutant mice | Q28588624 | ||
| Centromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairing | Q28609152 | ||
| Regulation of RAD53 by the ATM-like kinases MEC1 and TEL1 in yeast cell cycle checkpoint pathways | Q29615271 | ||
| Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity | Q29615388 | ||
| A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia | Q29615437 | ||
| Atm-deficient mice: a paradigm of ataxia telangiectasia | Q29619532 | ||
| Ataxia telangiectasia mutant protein activates c-Abl tyrosine kinase in response to ionizing radiation | Q29871427 | ||
| Histone H1 dephosphorylation is mediated through a radiation-induced signal transduction pathway dependent on ATM. | Q30304081 | ||
| The association of ATR protein with mouse meiotic chromosome cores | Q30724277 | ||
| Characterization of ATM expression, localization, and associated DNA-dependent protein kinase activity | Q32028114 | ||
| ATM and RPA in meiotic chromosome synapsis and recombination | Q32179137 | ||
| Nuclear compartments and gene regulation. | Q33632367 | ||
| Telomeres and telomerase: broad effects on cell growth | Q33632382 | ||
| RecA-like proteins are components of early meiotic nodules in lily | Q33922121 | ||
| Atm inactivation results in aberrant telomere clustering during meiotic prophase | Q33958817 | ||
| Altered telomere nuclear matrix interactions and nucleosomal periodicity in ataxia telangiectasia cells before and after ionizing radiation treatment | Q33959767 | ||
| Sequence organization and cytological localization of the minor satellite of mouse | Q34049249 | ||
| Localization of RecA-like recombination proteins on chromosomes of the lily at various meiotic stages | Q34312545 | ||
| Multiple ATM-dependent pathways: an explanation for pleiotropy | Q34388494 | ||
| The meiotic checkpoint monitoring synapsis eliminates spermatocytes via p53-independent apoptosis. | Q34460123 | ||
| Intermediate filaments in Sertoli cells | Q35323742 | ||
| A model for the structure of chromatin in mammalian sperm | Q36208902 | ||
| Meiosis in the foetal mouse ovary. I. An analysis at the light microscope level using surface-spreading | Q36590763 | ||
| The gene encoding a major component of the lateral elements of synaptonemal complexes of the rat is related to X-linked lymphocyte-regulated genes | Q36645944 | ||
| Pleiotropic defects in ataxia-telangiectasia protein-deficient mice | Q36687853 | ||
| The ATM homologue MEC1 is required for phosphorylation of replication protein A in yeast | Q36840988 | ||
| The cytogenetics of ataxia telangiectasia | Q36847861 | ||
| Haploid expression of a unique c-abl transcript in the mouse male germ line | Q36903930 | ||
| The initiation of meiotic chromosome pairing: the cytological view | Q37791630 | ||
| Bouquet formation in budding yeast: initiation of recombination is not required for meiotic telomere clustering | Q38500975 | ||
| DNA repair at the level of the gene | Q39577782 | ||
| Cell interactions during the seminiferous epithelial cycle. | Q39743681 | ||
| Ataxia-telangiectasia: closer to unraveling the mystery | Q40409276 | ||
| Telomere-mediated chromosome pairing during meiosis in budding yeast | Q40445528 | ||
| The nature of ataxia-telangiectasia: problems and perspectives | Q40580160 | ||
| Mammalian spermatogenesis in vivo and in vitro: a partnership of spermatogenic and somatic cell lineages | Q40739751 | ||
| Ataxia-telangiectasia and cellular responses to DNA damage. | Q40922688 | ||
| Targeting double-strand breaks to replicating DNA identifies a subpathway of DSB repair that is defective in ataxia-telangiectasia cells. | Q40939072 | ||
| Chromosome end-to-end associations and telomerase activity during cancer progression in human cells after treatment with alpha-particles simulating radon progeny | Q41159819 | ||
| The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes. | Q41164271 | ||
| Differential expression of the c-abl proto-oncogene and the homeo box-containing gene Hox 1.4 during mouse spermatogenesis | Q41341916 | ||
| Chromosome end associations, telomeres and telomerase activity in ataxia telangiectasia cells | Q41400791 | ||
| Cell-cycle signaling: Atm displays its many talents | Q41651111 | ||
| Alterations of cell cycle kinetics and vimentin expression in TPA-treated, asynchronous MPC-11 mouse plasmacytoma cells | Q41719448 | ||
| Structure, subnuclear distribution, and nuclear matrix association of the mammalian telomeric complex | Q41774217 | ||
| Co-expression of cytokeratin and vimentin filaments in rete testis and epididymis. An immunohistochemical study | Q42466326 | ||
| RAD51 and DMC1 form mixed complexes associated with mouse meiotic chromosome cores and synaptonemal complexes | Q42918693 | ||
| A cytological and cytoskeletal comparison of Sertoli cells without germ cell and those with germ cells using the W/WV mutant mouse | Q43413761 | ||
| Meiotic chromosome metabolism: one view | Q45213180 | ||
| TEL1, a gene involved in controlling telomere length in S. cerevisiae, is homologous to the human ataxia telangiectasia gene | Q48070727 | ||
| Arrangement of centromeres in mouse cells | Q48875582 | ||
| Atm deficiency results in severe meiotic disruption as early as leptonema of prophase I. | Q48932881 | ||
| Requirements for p53 and the ATM gene product in the regulation of G1/S and S phase checkpoints. | Q50754744 | ||
| Patterns of keratins 8, 18 and 19 during gonadal differentiation in the mouse: sex- and time-dependent expression of keratin 19. | Q50857993 | ||
| Interphase chromosome arrangement in Sertoli cells of adult mice. | Q51021141 | ||
| Dual roles of ATM in the cellular response to radiation and in cell growth control. | Q52521591 | ||
| Partial rescue of the prophase I defects of Atm-deficient mice by p53 and p21 null alleles. | Q52528386 | ||
| DNA nicks and increased sensitivity of DNA to fluorescence in situ end labeling during functional spermiogenesis. | Q52992946 | ||
| THE LEPTOTENE-ZYGOTENE TRANSITION OF MEIOSIS | Q56136641 | ||
| Ending up with the right partner | Q56969720 | ||
| A meiotic recombination checkpoint controlled by mitotic checkpoint genes | Q59098626 | ||
| Eighth International Workshop on Ataxia-Telangiectasia (ATW8) | Q64388828 | ||
| Nucleolar transcriptional activity in mouse Sertoli cells is dependent on centromere arrangement | Q68581755 | ||
| Transient coexpression of cytokeratin and vimentin in differentiating rat Sertoli cells | Q68971015 | ||
| Histones H1 and H4 of surface-spread meiotic chromosomes | Q70806570 | ||
| A reassessment of Y chromosomal behaviour in germ cells and Sertoli cells of the mouse as revealed by in situ hybridisation | Q70910301 | ||
| The distribution pattern of cytokeratin and vimentin immunoreactivity in testicular biopsies of infertile men | Q71681239 | ||
| Expression of the mouse testicular histone gene H1t during spermatogenesis | Q71698419 | ||
| The product of the ATM gene is a 370-kDa nuclear phosphoprotein | Q71903513 | ||
| Sensing of ionizing radiation-induced DNA damage by ATM through interaction with histone deacetylase | Q73107002 | ||
| atm and p53 cooperate in apoptosis and suppression of tumorigenesis, but not in resistance to acute radiation toxicity | Q73552961 | ||
| Influence of ATM function on telomere metabolism | Q73945587 | ||
| Changes in protein composition of meiotic nodules during mammalian meiosis | Q74095093 | ||
| P433 | issue | 20 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 7773-7783 | |
| P577 | publication date | 2000-10-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Meiotic telomere distribution and Sertoli cell nuclear architecture are altered in Atm- and Atm-p53-deficient mice | |
| P478 | volume | 20 |
| Q39788913 | "Bouquet arrest", monopolar chromosomes segregation, and correction of the abnormal spindle |
| Q34085740 | A bouquet makes ends meet |
| Q34535665 | ATM function and telomere stability |
| Q28201456 | ATM: genome stability, neuronal development, and cancer cross paths |
| Q74069730 | Asynchronous chromosome pairing in male meiosis of the rat (Rattus norvegicus) |
| Q61852020 | Caracterización citogenética molecular de las células germinales masculinas en la azoospermia secretora: parada de la maduración |
| Q37128128 | Chromatin remodeling finds its place in the DNA double-strand break response |
| Q30597286 | Contrasting behavior of heterochromatic and euchromatic chromosome portions and pericentric genome separation in pre-bouquet spermatocytes of hybrid mice |
| Q34524647 | DNA repair kinetics in SCID mice Sertoli cells and DNA-PKcs-deficient mouse embryonic fibroblasts |
| Q24557469 | Distinct DNA-damage-dependent and -independent responses drive the loss of oocytes in recombination-defective mouse mutants |
| Q36434484 | From early homologue recognition to synaptonemal complex formation |
| Q28506379 | Genomic instability and enhanced radiosensitivity in Hsp70.1- and Hsp70.3-deficient mice |
| Q36324386 | H2AX regulates meiotic telomere clustering |
| Q37089006 | Homologous recombination-dependent repair of telomeric DSBs in proliferating human cells |
| Q38375354 | Imaging of Chromosome Dynamics in Mouse Testis Tissue by Immuno-FISH. |
| Q37012010 | Ku70 and non-homologous end joining protect testicular cells from DNA damage |
| Q33963853 | MOF and histone H4 acetylation at lysine 16 are critical for DNA damage response and double-strand break repair |
| Q41813386 | Mammalian Rad9 plays a role in telomere stability, S- and G2-phase-specific cell survival, and homologous recombinational repair |
| Q24646919 | Meiotic double-strand breaks at the interface of chromosome movement, chromosome remodeling, and reductional division |
| Q36226840 | Molecular aspects of meiotic chromosome synapsis and recombination |
| Q28506028 | Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages |
| Q35079512 | Nuclear reorganization and homologous chromosome pairing during meiotic prophase require C. elegans chk-2. |
| Q37131507 | Pluripotent Stem Cells and DNA Damage Response to Ionizing Radiations |
| Q49977627 | Pold3 is required for genomic stability and telomere integrity in embryonic stem cells and meiosis. |
| Q35075511 | Poly(ADP-ribose) polymerase-2 contributes to the fidelity of male meiosis I and spermiogenesis |
| Q35094244 | Rap1-independent telomere attachment and bouquet formation in mammalian meiosis |
| Q41851639 | Role of ATM in the telomere response to the G-quadruplex ligand 360A. |
| Q47915348 | Spontaneous testicular atrophy occurs despite normal spermatogonial proliferation in a Tp53 knockout rat. |
| Q35802860 | Telomere attachment, meiotic chromosome condensation, pairing, and bouquet stage duration are modified in spermatocytes lacking axial elements |
| Q34801165 | Telomeres in mammalian male germline cells |
| Q37384129 | Telomeres, histone code, and DNA damage response |
| Q36574666 | The cellular control of DNA double-strand breaks |
| Q36421093 | The mammalian ortholog of Drosophila MOF that acetylates histone H4 lysine 16 is essential for embryogenesis and oncogenesis |
| Q36036084 | β2-spectrin depletion impairs DNA damage repair |
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