| scholarly article | Q13442814 |
| P50 | author | Leonor Kremer | Q56154048 |
| P2093 | author name string | C Martínez-A | |
| C Valero | |||
| I Prieto | |||
| J L Barbero | |||
| L A Pérez Jurado | |||
| CARLOS MARTÍNEZ-A | |||
| CARMEN VALERO | |||
| IGNACIO PRIETO | |||
| J Del Mazo | |||
| JESÚS DEL MAZO | |||
| JOSÉ L. BARBERO | |||
| LUIS A. PÉREZ JURADO | |||
| N Pezzi | |||
| NIEVES PEZZI | |||
| P2860 | cites work | Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome | Q52223418 |
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| A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease | Q24561483 | ||
| Yeast cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication | Q24608777 | ||
| A comprehensive set of sequence analysis programs for the VAX | Q26778432 | ||
| Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis | Q27934770 | ||
| The meiosis-specific Hop2 protein of S. cerevisiae ensures synapsis between homologous chromosomes | Q27937163 | ||
| Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene | Q28115542 | ||
| A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK | Q28262012 | ||
| Identification of Xenopus SMC protein complexes required for sister chromatid cohesion | Q28275242 | ||
| Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis | Q28279936 | ||
| Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | Q28295022 | ||
| The human autosomal gene DAZLA: testis specificity and a candidate for male infertility | Q28299662 | ||
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| Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse | Q28513262 | ||
| 2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans | Q29547793 | ||
| Molecular cloning and expression of stromalin protein from Drosophila melanogaster: homologous to mammalian stromalin family of nuclear proteins | Q32028000 | ||
| Williams syndrome | Q33673673 | ||
| Distribution of the Rad51 recombinase in human and mouse spermatocytes | Q33887354 | ||
| Analysis of the 5' region of PMS2 reveals heterogeneous transcripts and a novel overlapping gene | Q34385102 | ||
| Natural history of Williams syndrome: physical characteristics | Q34406298 | ||
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| 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 | ||
| Case-control study of whether subfertility in men is familial | Q36887822 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. | Q38342141 | ||
| A new essential gene located on Saccharomyces cerevisiae chromosome IX. | Q42672484 | ||
| Microtubule-associated proteins during mouse spermatogenesis: localization of a protein immunologically related to brain MAP1B protein in the synaptonemal complex. | Q42824163 | ||
| Preparation of spermatogonia, spermatocytes, and round spermatids for analysis of gene expression using fluorescence-activated cell sorting | Q46864916 | ||
| Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin | Q47937221 | ||
| Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion | Q48064124 | ||
| Heterogeneity in the phosphorylation of microtubule-associated protein MAP1B during rat brain development | Q48230369 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Williams-Beuren syndrome | Q558077 |
| synaptonemal complex assembly | Q21097439 | ||
| Stromal antigen 3 | Q21126474 | ||
| Stromal antigen 3 | Q21991488 | ||
| P304 | page(s) | 581-592 | |
| 581-92 | |||
| P577 | publication date | 2000-03-01 | |
| P1433 | published in | FASEB Journal | Q520194 |
| P1476 | title | STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion | |
| P478 | volume | 14 |
| Q33930829 | A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. |
| Q37273052 | A conserved E2F6-binding element in murine meiosis-specific gene promoters |
| Q30328454 | A meiotic chromosomal core consisting of cohesin complex proteins recruits DNA recombination proteins and promotes synapsis in the absence of an axial element in mammalian meiotic cells. |
| Q34956023 | Activation of meiosis-specific genes is associated with depolyploidization of human tumor cells following radiation-induced mitotic catastrophe. |
| Q39454205 | Age-Related Loss of Cohesion: Causes and Effects |
| Q37535351 | Biochemical reconstitution of topological DNA binding by the cohesin ring |
| Q36139047 | Caenorhabditis elegans EVL-14/PDS-5 and SCC-3 Are Essential for Sister Chromatid Cohesion in Meiosis and Mitosis |
| Q83423039 | Can corruption of chromosome cohesion create a conduit to cancer? |
| Q34854141 | Characterization of the interaction between the cohesin subunits Rad21 and SA1/2. |
| Q24290512 | Characterization of vertebrate cohesin complexes and their regulation in prophase |
| Q34430835 | Chromosome cohesion and segregation in mitosis and meiosis |
| Q53275335 | Cohesin proteins load sequentially during prophase I in tomato primary microsporocytes. |
| Q50656356 | Cohesion proteins are present in centromere protein bodies associated with avian lampbrush chromosomes. |
| Q34126314 | Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer |
| Q33570597 | Comparative expression profiling of testis-enriched genes regulated during the development of spermatogonial cells. |
| Q37741019 | Copy number variants at Williams-Beuren syndrome 7q11.23 region. |
| Q33370539 | Corona is required for higher-order assembly of transverse filaments into full-length synaptonemal complex in Drosophila oocytes |
| Q37564432 | Deregulation of polycomb repressor complex 1 modifier AUTS2 in T-cell leukemia |
| Q24337562 | Differential association of SMC1alpha and SMC3 proteins with meiotic chromosomes in wild-type and SPO11-deficient male mice |
| Q21146371 | Dissociation of cohesin from chromosome arms and loss of arm cohesion during early mitosis depends on phosphorylation of SA2. |
| Q45023626 | Dynamics of cohesin subunits in grasshopper meiotic divisions. |
| Q88393395 | Effects of Heyan Kuntai Capsule () on Follicular Development and Oocyte Cohesin Levels in Aged Mice |
| Q28769508 | Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23 |
| Q31088185 | Female-specific features of recombinational double-stranded DNA repair in relation to synapsis and telomere dynamics in human oocytes. |
| Q35035094 | Gain of chromosome band 7q11 in papillary thyroid carcinomas of young patients is associated with exposure to low-dose irradiation |
| Q37612775 | High density of REC8 constrains sister chromatid axes and prevents illegitimate synaptonemal complex formation |
| Q31041388 | How to characterize meiotic functions in plants? |
| Q24685911 | Identification and characterization of SA/Scc3p subunits in the Xenopus and human cohesin complexes |
| Q30841621 | Loss of Centromere Cohesion in Aneuploid Human Oocytes Correlates with Decreased Kinetochore Localization of the Sac Proteins Bub1 and Bubr1 |
| Q34085734 | Mammalian STAG3 is a cohesin specific to sister chromatid arms in meiosis I. |
| Q37263648 | Mechanisms of sister chromatid pairing |
| Q33433256 | Meiosis genes in Daphnia pulex and the role of parthenogenesis in genome evolution |
| Q28573938 | Meiotic cohesin REC8 marks the axial elements of rat synaptonemal complexes before cohesins SMC1beta and SMC3 |
| Q34343224 | Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion |
| Q42914420 | Meiotic telomere clustering requires actin for its formation and cohesin for its resolution |
| Q48313866 | Merotelic kinetochore attachment in oocyte meiosis II causes sister chromatids segregation errors in aged mice. |
| Q36226840 | Molecular aspects of meiotic chromosome synapsis and recombination |
| Q29399144 | Mutant Cohesin in Premature Ovarian Failure |
| Q24548311 | Novel meiosis-specific isoform of mammalian SMC1 |
| Q35998496 | Nuclear localization of PRDM9 and its role in meiotic chromatin modifications and homologous synapsis |
| Q33846320 | Prevalence of scoliosis in Williams-Beuren syndrome patients treated at a regional reference center |
| Q39155608 | Prophase I: Preparing Chromosomes for Segregation in the Developing Oocyte |
| Q37333026 | Regulation of the meiotic prophase I to metaphase I transition in mouse spermatocytes |
| Q24522626 | STAG2 and Rad21 mammalian mitotic cohesins are implicated in meiosis. |
| Q28587843 | STAG3-mediated stabilization of REC8 cohesin complexes promotes chromosome synapsis during meiosis |
| Q27315020 | Sequential loading of cohesin subunits during the first meiotic prophase of grasshoppers |
| Q36729097 | Similarity of the domain structure of proteins as a basis for the conservation of meiosis |
| Q48097563 | Sororin is enriched at the central region of synapsed meiotic chromosomes |
| Q37686589 | Sororin loads to the synaptonemal complex central region independently of meiotic cohesin complexes. |
| Q41155792 | Synthetic lethality between the cohesin subunits STAG1 and STAG2 in diverse cancer contexts |
| Q35802860 | Telomere attachment, meiotic chromosome condensation, pairing, and bouquet stage duration are modified in spermatocytes lacking axial elements |
| Q36323282 | Telomere-independent homologue pairing and checkpoint escape of accessory ring chromosomes in male mouse meiosis |
| Q61455359 | The Caenorhabditis elegans SCC-3 homologue is required for meiotic synapsis and for proper chromosome disjunction in mitosis and meiosis |
| Q92207245 | The association of stromal antigen 3 (STAG3) sequence variations with spermatogenic impairment in the male Korean population |
| Q24796686 | The cohesin complex: sequence homologies, interaction networks and shared motifs |
| Q38215586 | The meiosis-specific modification of mammalian telomeres. |
| Q35831519 | The roles of cohesins in mitosis, meiosis, and human health and disease |
| Q92439389 | The structural basis for cohesin-CTCF-anchored loops |
| Q24291165 | The structural maintenance of chromosomes (SMC) family of proteins in mammals |
| Q34452313 | Tissue-specific disallowance of housekeeping genes: the other face of cell differentiation. |
| Q31808627 | Together until separin do us part |
| Q28585430 | Wapl is an essential regulator of chromatin structure and chromosome segregation |
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