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1 itochondrial partitioning into growing buds (mitochondrial inheritance).
2 ion of paternal mitochondria ensure maternal mitochondrial inheritance.
3 sociation is essential for Ypt11 function in mitochondrial inheritance.
4 features of Ypt11 function and regulation in mitochondrial inheritance.
5 ernal inheritance, a pattern consistent with mitochondrial inheritance.
6 r mutant (mmr1Delta gem1Delta) with impaired mitochondrial inheritance.
7 hat GEM1, MMR1, and YPT11 each contribute to mitochondrial inheritance.
8 e most consistent with a biparental model of mitochondrial inheritance.
9 e maternal lineage with a pattern indicating mitochondrial inheritance.
10 ty of Rsp5p is essential for its function in mitochondrial inheritance.
11 ugh the HOG pathway to control the timing of mitochondrial inheritance.
12 er generation" rule and three other rules of mitochondrial inheritance.
13 for rare early-onset forms with monogenic or mitochondrial inheritance.
14 role of mitochondrial dynamics in asymmetric mitochondrial inheritance.
15 , protecting embryo development and maternal mitochondrial inheritance.
16  agent-based stochastic model of dynamics of mitochondrial inheritance.
17 which are suppressed by artificially forcing mitochondrial inheritance.
18 iparental disomy, unusual characteristics of mitochondrial inheritance also have been found that defy
19 Ypt11, bind Myo2 and have been implicated in mitochondrial inheritance, although their specific roles
20 tion of a yeast mutant, mdm20, in which both mitochondrial inheritance and actin cables (bundles of a
21 cking MDM20 function display defects in both mitochondrial inheritance and actin organization, specif
22 usly implicated in endoplasmic reticulum and mitochondrial inheritance and for a COPI coatomer subuni
23 nfiltration of this mistake into concepts of mitochondrial inheritance and human evolution.
24 e first evidence of a role for prohibitin in mitochondrial inheritance and in the regulation of mitoc
25 ay temperature-sensitive growth and aberrant mitochondrial inheritance and morphology at the nonpermi
26       These results indicate that Mgm1p is a mitochondrial inheritance and morphology component that
27 ith an mgm1-null mutation displayed aberrant mitochondrial inheritance and morphology.
28 tin cables, mutations in these genes disrupt mitochondrial inheritance and nuclear segregation to dif
29  mitophagy determinants in the regulation of mitochondrial inheritance and provides a master list of
30 sses, including secretory vesicle transport, mitochondrial inheritance, and nuclear orientation.
31 mediated by Rsp5p plays an essential role in mitochondrial inheritance, and reveal a novel function f
32                               In the case of mitochondrial inheritance, anterograde movement drives t
33 mes and the assortment of chromosomes during mitochondrial inheritance appears to have contributed to
34                 Thus quantity and quality of mitochondrial inheritance are ensured by two opposing pr
35 tin-dependent force generators contribute to mitochondrial inheritance: Arp2/3 complex and the myosin
36  findings indicate that Mmr1p contributes to mitochondrial inheritance as a mediator of anchorage of
37 ission; Class II alleles displayed defective mitochondrial inheritance but had no effect on nuclear m
38 atase, has previously been shown to regulate mitochondrial inheritance by an unknown mechanism.
39 lta double mutants correlated with defective mitochondrial inheritance by large buds.
40 licative segregation, and threshold effects, mitochondrial inheritance can allow for the apparent spo
41  mitochondrial nucleoid, the genetic unit of mitochondrial inheritance, can contain a single copy of
42 showing no evidence of a proposed cell-cycle mitochondrial inheritance checkpoint.
43 hen combined with a mutation in any of three mitochondrial inheritance components of the mitochondria
44 cue temperature-sensitive growth defects and mitochondrial inheritance defects and partially restore
45 lament-binding protein tropomyosin, suppress mitochondrial inheritance defects and partially restore
46                                          The mitochondrial inheritance delay in the ptc1 mutant is no
47 lly controlled and provide new evidence that mitochondrial inheritance does not depend on a physical
48 olution fluorescence microscopy to visualize mitochondrial inheritance during meiosis by differential
49  restrictive temperature, cells defective in mitochondrial inheritance give rise to dead buds that go
50  As a result, much of what we know regarding mitochondrial inheritance has been uncovered using yeast
51 ant inactivation of Slt2p is also needed for mitochondrial inheritance; however, in this case, the re
52 conserved mechanism ensuring the uniparental mitochondrial inheritance in animals.
53 hibits cytokinesis in response to defects in mitochondrial inheritance in budding yeast.
54        Here we show that autophagy regulates mitochondrial inheritance in CD8(+) T cells.
55 have been identified as the genetic units of mitochondrial inheritance in yeast and man, little is kn
56 emonstrates that multiple pathways influence mitochondrial inheritance in yeast and that Miro GTPases
57 ese results provide compelling evidence that mitochondrial inheritance in yeast is an actin-mediated
58               Proteins reported to influence mitochondrial inheritance include the mitochondrial rho
59                                 Thus, active mitochondrial inheritance is an essential process and a
60                                              Mitochondrial inheritance is essential for cell division
61                                         When mitochondrial inheritance is inhibited, Num1 clusters ar
62                           We show that yeast mitochondrial inheritance is not required for inheritanc
63                                              Mitochondrial inheritance is tightly coupled with bud em
64 ence of sex chromosomes, obligate sexuality, mitochondrial inheritance linked to the mating type, and
65 tion causes temperature-dependent defects in mitochondrial inheritance, mitochondrial morphology, and
66 e develop a toolkit to screen for mutants in mitochondrial inheritance (mti), and use fine mapping to
67                           In wild-type yeast mitochondrial inheritance occurs early in the cell cycle
68  have a specific and severe defect in active mitochondrial inheritance, revealing mitochondrial trans
69 ausative role in governing the non-Mendelian mitochondrial inheritance, revolutionizing our knowledge
70 c pair was used to investigate three traits: mitochondrial inheritance, the effect of the MAT alleles
71                                              Mitochondrial inheritance, the transfer of mitochondria
72                                   Inhibiting mitochondrial inheritance to buds, by deletion of MMR1,
73 uggesting a role for both Num1p and Dnm1p in mitochondrial inheritance, we find that num1 dnm1 double