| scholarly article | Q13442814 |
| P356 | DOI | 10.1006/GENO.1997.4857 |
| P698 | PubMed publication ID | 9299235 |
| P2093 | author name string | R Paul | |
| C Turc-Carel | |||
| C Desnuelle | |||
| V Paquis-Flucklinger | |||
| A Saunières | |||
| S Santucci-Darmanin | |||
| P2860 | cites work | Targeted gene disruption of Hsp70-2 results in failed meiosis, germ cell apoptosis, and male infertility | Q24308728 |
| A comprehensive set of sequence analysis programs for the VAX | Q26778432 | ||
| Molecular cloning of a putative novel human bZIP transcription factor on chromosome 17q22 | Q28243353 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
| Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| Mammalian meiotic recombination: a reexamination | Q40648901 | ||
| The mismatch repair system contributes to meiotic sterility in an interspecific yeast hybrid. | Q41064501 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction | Q48076989 | ||
| MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | MutS homolog 4 | Q21107253 |
| P304 | page(s) | 188-94 | |
| P577 | publication date | 1997-09-01 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene | |
| P478 | volume | 44 |
| Q27934895 | 'Saccharomyces cerevisiae MSH2/6 complex interacts with Holliday junctions and facilitates their cleavage by phage resolution enzymes |
| Q50982253 | A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency. |
| Q24548238 | A phylogenomic study of the MutS family of proteins |
| Q38320783 | Biochemical characterization of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 complex and mispaired bases in DNA. |
| Q53633045 | Chromosomal abnormality and Y chromosome microdeletion in Chinese patients with azoospermia or severe oligozoospermia. |
| Q37656154 | Control of Meiotic Crossovers: From Double-Strand Break Formation to Designation. |
| Q33878802 | Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast |
| Q24295128 | Cytoskeletal scaffolding proteins interact with Lynch-Syndrome associated mismatch repair protein MLH1 |
| Q37291391 | DNA damage induced MutS homologue hMSH4 acetylation |
| Q41723122 | DNA methylator and mismatch repair phenotypes are not mutually exclusive in colorectal cancer cell lines |
| Q27939116 | Eukaryotic DNA mismatch repair |
| Q38492090 | Family of SRY/Sox proteins is involved in the regulation of the mouse Msh4 (MutS Homolog 4) gene expression |
| Q28513158 | FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice |
| Q36016232 | Genetic screening for chromosomal abnormalities and Y chromosome microdeletions in Chinese infertile men |
| Q44068446 | HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions |
| Q73794909 | Human DNA repair genes |
| Q48269909 | Human infertility: meiotic genes as potential candidates |
| Q38322903 | Identification of the protein components of mismatch binding complexes in human cells using a gel-shift assay |
| Q36246487 | Lynch syndrome genes |
| Q34000404 | MBD4 cooperates with DNMT1 to mediate methyl-DNA repression and protects mammalian cells from oxidative stress |
| Q33751700 | Mammalian BLM helicase is critical for integrating multiple pathways of meiotic recombination |
| Q34282241 | Mechanisms of resistance to cisplatin |
| Q28593875 | Meiotic arrest and aneuploidy in MLH3-deficient mice |
| Q40980050 | Meiotic defects and decreased expression of genes located around the chromosomal breakpoint in the testis of a patient with a novel 46,X,t(Y;1)(p11.3;p31) translocation |
| Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
| Q52374566 | Mitotic and Meiotic Functions for the SUMOylation Pathway in the Caenorhabditis elegans Germline. |
| Q28214396 | Mouse models for human DNA mismatch-repair gene defects |
| Q64388676 | Multiple pathways of recombination define cellular responses to cisplatin |
| Q36798895 | MutS Homologues hMSH4 and hMSH5: Genetic Variations, Functions, and Implications in Human Diseases |
| Q24606421 | MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice |
| Q24294253 | MutS homologue hMSH4: interaction with eIF3f and a role in NHEJ-mediated DSB repair |
| Q34984353 | MutS homologue hMSH5: recombinational DSB repair and non-synonymous polymorphic variants |
| Q39207030 | Prioritization of cancer-related genomic variants by SNP association network |
| Q54710517 | RACE using only a gene-specific primer: application of a template-switching model. |
| Q36900915 | Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis. |
| Q52929756 | Repair bias of large loop mismatches during recombination in mammalian cells depends on loop length and structure. |
| Q77172147 | Role of MutS ATPase activity in MutS,L-dependent block of in vitro strand transfer |
| Q37628993 | The Arabidopsis MutS homolog AtMSH4 functions at an early step in recombination: evidence for two classes of recombination in Arabidopsis. |
| Q27931846 | The budding yeast Msh4 protein functions in chromosome synapsis and the regulation of crossover distribution |
| Q24596494 | The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2 |
| Q24298905 | Thymosin beta 4 expression and nuclear transport are regulated by hMLH1 |
| Q37327487 | VBP1 facilitates proteasome and autophagy-mediated degradation of MutS homologue hMSH4. |
| Q33922440 | hMSH5 is a nucleocytoplasmic shuttling protein whose stability depends on its subcellular localization |
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