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1 re identified, exhibiting large effects when paternally inherited.
2       No effect is seen when the deletion is paternally inherited.
3 we show that the GRC has the potential to be paternally inherited.
4 ow-1/grow-1 TA is specifically inactive when paternally inherited.
5  c.1433G>A, predicting p.Arg478His, that was paternally inherited.
6 ities about which alleles are maternally vs. paternally inherited.
7 t, occurring only when the Gct4(J) allele is paternally inherited.
8 printing defect and perinatal lethality when paternally inherited.
9 inherited 1p, whereas 16 had deletion of the paternally inherited 1p (P = 0.58).
10                                            A paternally inherited activating mutation (N72S) in the A
11 t abnormal acquisition of methylation on the paternally inherited allele at intron 2.
12 enes that are expressed at later stages, the paternally inherited allele becomes active three to four
13 t is likely to affect pre-RNA splicing and a paternally inherited allele in which the TYR gene is com
14     The Peg3 gene is expressed only from the paternally inherited allele located on proximal mouse ch
15                                         This paternally inherited allele was also significantly assoc
16     Nap1l5 is a retrogene expressed from the paternally inherited allele, is situated within an intro
17 3A antisense transcript (UBE3A-ATS) from the paternally inherited allele, which silences the paternal
18  gene expression to either the maternally or paternally inherited allele.
19  gene that is exclusively expressed from the paternally inherited allele.
20  expressed either from the maternally or the paternally inherited allele.
21  the maternal allele, and Igf2 only from the paternally inherited allele.
22 y on an asymmetry between the maternally and paternally inherited alleles at a locus that favours the
23 there is no asymmetry between maternally and paternally inherited alleles in this model, other means
24                Here we show that none of the paternally inherited alleles of 20 loci that we tested i
25 late the growth of body weight by expressing paternally inherited alleles were identified.
26  (genomic imprinting) between maternally and paternally inherited alleles.
27 ic differential expression of maternally and paternally inherited alleles.
28 erentially expressed from the maternally and paternally inherited alleles.
29 s to differential behavior of maternally and paternally inherited alleles.
30  show that ROS1 prevents hypermethylation of paternally-inherited alleles in the endosperm at regions
31     Acceptance of the fetus, which expresses paternally inherited alloantigens, by the mother during
32 sms suppress the maternal immune response to paternally inherited alloantigens.
33      The H19 imprinted gene is silenced when paternally inherited and active only when inherited mate
34 en caused by deletions of the same region of paternally inherited and maternally inherited human chro
35 on females carrying embryos with overlapping paternally inherited antigens.
36 d thus traits or behaviors that are strictly paternally inherited are unlikely to be under strong cul
37 e are present in heterozygotes that harbor a paternally inherited, but not in those with a maternally
38 sociations occur when their HLA-C2 ligand is paternally inherited by a fetus.
39 y on the Z sex chromosome, which is strictly paternally inherited by daughters.
40 ) results in the inappropriate expression of paternally inherited Cdkn1c in the brains of embryonic a
41 requires centrosomes that are assembled from paternally inherited centrioles and maternally inherited
42 r data supports the idea that, in zebrafish, paternally inherited centrosomes are required for the fi
43 ted mitochondrial DNA polymorphisms than for paternally inherited chloroplast DNA, indicating that wi
44 s from the deletion of an imprinted locus on paternally inherited chromosome 15.
45 al chromosome 1 and on both the maternal and paternally inherited chromosome 4.
46 nes, Dlk1, Rtl1 and Dio3, expressed from the paternally inherited chromosome and several imprinted la
47 combination of alleles on the maternally and paternally inherited chromosome copies.
48 wn to be imprinted, being expressed from the paternally inherited chromosome homologue.
49 pn genomic region which, when deleted on the paternally inherited chromosome, resulted in the loss of
50  expressed from either the maternally or the paternally inherited chromosome.
51 er of imprinted genes, is expressed from the paternally inherited chromosome.
52  All six de novo deletions originated on the paternally inherited chromosome.
53 and DHS2 within intron 1, exclusively on the paternally inherited chromosome.
54                In PGE, males eliminate their paternally inherited chromosomes during meiosis, transmi
55 ocally imprinted genes on the maternally and paternally inherited chromosomes.
56 lk1 to be expressed from both maternally and paternally inherited chromosomes.
57 pression is reduced when the DMD deletion is paternally inherited; conversely, upon maternal transmis
58 as been associated with abnormalities of the paternally inherited copy of chromosome 6, including dup
59 ility, suggesting that the expression of the paternally inherited copy of Dot1l in the embryo is suff
60 ater for maternally inherited mtDNA than for paternally inherited cpDNA, though this difference was n
61  nuclear markers with a single maternally or paternally inherited cytoplasmic marker, or with two cyt
62 alized hypomethylation of maternally but not paternally inherited DNA, with certain small RNAs also d
63 ratio may reflect an epigenetic influence on paternally-inherited DNA.
64 ches has been established for aneuploidy and paternally inherited dominant traits.
65                                              Paternally inherited Dp/+ (patDp/+) mice showed expected
66 hylation differences between maternally- and paternally-inherited endosperm genomes after fertilizati
67 cohort of CD8+ T cells specific for a single paternally inherited fetal major histocompatibility comp
68 showed strong evidence for the effect of the paternally inherited G allele of rs10009104 on AAR (P =
69 cus is of considerable importance, since the paternally inherited gene product is exposed to the mate
70 s expressed in mothers and by maternally and paternally inherited genes expressed in offspring.
71 pring extends to an offspring's genes, where paternally inherited genes favor demanding more from the
72     According to this "coadaptation theory," paternally inherited genes might be inactivated because
73 ay a unique pattern of imprinting at crucial paternally inherited genes that promotes their quiescenc
74 and spatial heterogeneity for maternally and paternally inherited genes were derived for populations
75                       Our data indicate that paternally inherited HLA-associated odors influence odor
76 n uterine natural killer (NK) cells, and the paternally inherited HLA-C*0501, expressed on fetal trop
77  by maternal alloantibodies directed against paternally inherited human platelet alloantigens (HPAs)
78   Understanding properties of maternally and paternally inherited imprints provides insight into the
79                                              Paternally inherited inactivating GNAS1 mutations cause
80 ives (p.Tyr2819Ter; frequency=0.00003) and a paternally-inherited intronic variant altering a canonic
81  dependent on whether they are maternally or paternally inherited, is restricted to mammals and angio
82 strated that Ashkenazi Levites, members of a paternally inherited Jewish priestly caste, display a di
83 sequence of somatic uniparental disomy for a paternally inherited K(ATP) channel mutation with enlarg
84 f a pathogenetic role for loss of the active paternally inherited locus.
85 eas males are heteroplasmic for this and the paternally inherited M mitotype.
86  interact synergistically with products from paternally inherited M' P elements.
87 igen-specific maternal T and B cells through paternally inherited major histocompatibility complex an
88                                              Paternally inherited MEA alleles are transcriptionally s
89 escue mea seeds by functionally reactivating paternally inherited MEA alleles during seed development
90 nherited unmethylated chromosome but not the paternally inherited methylated allele.
91                                    We show a paternally inherited miR-873-5p variant with altered bin
92 both parents but preferentially transmit the paternally inherited mtDNA to their sons.
93 hermore, an insulator was established on the paternally inherited mutated allele in vivo, reducing Ig
94                                          The paternally inherited mutation was present at 90% in lymp
95  2 fifth-degree relatives with HLHS shared a paternally-inherited MYO5A missense variant (p.Arg801Trp
96                              Mice carrying a paternally inherited Ndn deletion allele demonstrated ea
97 aternally derived allele, E326K+L444P, and a paternally inherited nonsense mutation, E233X.
98 s the maternal chromosome to behave like the paternally inherited one.
99 y relevant and deleterious alleles that were paternally inherited or had arisen as de novo germline m
100 Such significant disequilibria involving the paternally inherited organelle indicate that not only ar
101                                              Paternally inherited P element transposons thus escape s
102 ween a woman's maternally inherited (MI) and paternally inherited (PI) genes, over the trade-off betw
103 he maternally inherited mtDNA genome and the paternally inherited portion of the nonrecombining Y chr
104 lly inherited pathogenic CTLA4 variant and a paternally inherited rare LoF missense variant in CLEC7A
105 ave obtained robust evidence at rs941576 for paternally inherited risk of type 1 diabetes (T1D; ratio
106                                              Paternally inherited Sgce heterozygous knock-out (KO) mi
107 ll lines specifically lacking the expressed, paternally inherited, SNORD115 or SNORD116 cluster.
108 ion of FREM1's full-length transcripts and a paternally-inherited splice site mutation that causes ac
109 es, motor deficits or myoclonus, we produced paternally inherited striatum-specific Sgce conditional
110 y, we find that the Drosophila acrosome is a paternally inherited structure.
111 e manifests itself only if the transposon is paternally inherited, suggesting maternal transmission o
112 I allele does not predispose to disease when paternally inherited, suggestive of polymorphic imprinti
113 crosses are characterized by derepression of paternally inherited TE families that are rare or absent
114 metimes suffer from germline derepression of paternally inherited TE families, caused by a failure of
115 despread derepression of both maternally and paternally inherited TE families.
116 n control mice approximately half the litter paternally inherited the disrupted H19(Delta13), so the
117 e rejected only in mating combinations where paternally inherited tissue antigens elicited potent mat
118 ntly produced in the zygote, presumably from paternally inherited transcripts.
119                              In neurons, the paternally inherited UBE3A allele is silenced in cis by
120 ome analysis of offspring from maternally or paternally inherited Ube3a deletions revealed the expect
121 e therapy vector can restore the function of paternally inherited UBE3A throughout life, providing a
122 omeostasis, we generated fetuses harboring a paternally-inherited ubiquitous knock-in of the HAMP-res
123  and four offspring from two families have a paternally inherited variant.
124 printed form of XCI (iXCI) that silences the paternally inherited X chromosome (Xp) is initiated at t
125 embryogenesis, imprinted XCI inactivates the paternally inherited X chromosome (Xp) within the extra-
126  which undergo imprinted inactivation of the paternally inherited X chromosome.
127 ation resulting in silencing of genes on the paternally inherited X-chromosome.
128                 Results from mice carrying a paternally inherited X-linked green fluorescent protein
129                  However, an XO mouse with a paternally inherited Xist mutation was healthy and appea
130               In sharp contrast to this, the paternally inherited Y chromosome shows diversity simila
131  model has not been examined using data from paternally inherited Y chromosomes.
132                             In contrast, for paternally inherited Y-chromosome variation each caste i

 
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