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1 otent stem cells in somatic tissues (somatic gametogenesis).
2 ant roles in developmental processes such as gametogenesis.
3  to activate DNA-methylated promoters during gametogenesis.
4 fect was caused primarily by exposure during gametogenesis.
5 or all of PGC specification, development, or gametogenesis.
6 e required for triggering cGMP/PKG dependent gametogenesis.
7  state from fetal stages through meiosis and gametogenesis.
8 espread methylation events that occur during gametogenesis.
9 late stages of sexual development, including gametogenesis.
10 entral to initiating the meiotic program and gametogenesis.
11 or meiotic drivers to shape the evolution of gametogenesis.
12 cifies meiotic recombination hotspots during gametogenesis.
13 evelopment and single nurse cells supporting gametogenesis.
14 e and female sterility because of defects in gametogenesis.
15  but also to protect genome integrity during gametogenesis.
16 ecialize meiotic kinetochores for successful gametogenesis.
17  meiosis, the key developmental programme of gametogenesis.
18 -mediated testosterone metabolism to disrupt gametogenesis.
19 ed fertility attributable to a hampered male gametogenesis.
20 trol of zygote formation, recombination, and gametogenesis.
21 narily conserved function for this enzyme in gametogenesis.
22 lays a significant role specifically in male gametogenesis.
23 catalyzes this modification, is required for gametogenesis.
24 ess diverse aspects of stem cell biology and gametogenesis.
25 g yeast resetting of life span occurs during gametogenesis.
26 eginning at the late pachytene stage of male gametogenesis.
27 on of PS+ vs. PS- genomes takes place during gametogenesis.
28 a screen to uncover genes that control mouse gametogenesis.
29 rst mitotic division in both male and female gametogenesis.
30 nd changes in developmental programs such as gametogenesis.
31 ne in the gametophyte at different stages of gametogenesis.
32 ed brood sizes and low penetrance defects in gametogenesis.
33 d and then specialized to function in animal gametogenesis.
34 uld not be generated due to a defect in male gametogenesis.
35 evelopment and are irreversibly committed to gametogenesis.
36 omeostasis, tumor suppression, immunity, and gametogenesis.
37 and differentiate prior to the initiation of gametogenesis.
38 ion of coding and non-coding RNAs needed for gametogenesis.
39 ike genes to serve paralog-specific roles in gametogenesis.
40 ing defect) but were sterile with defects in gametogenesis.
41 e PfGCbeta gene had no significant effect on gametogenesis.
42 have been driven by the specialized needs of gametogenesis.
43 led to a severely reduced ability to undergo gametogenesis.
44 d in the MT(+) locus, is operant during plus gametogenesis.
45 o regulate multiple steps in male and female gametogenesis.
46  sterility of Miwi mutants suggest a role in gametogenesis.
47 ons (ICRs) that are differentially marked in gametogenesis.
48 ar differentiation for germline cells during gametogenesis.
49 -specific RNA-binding proteins essential for gametogenesis.
50  for sex-specific de novo methylation during gametogenesis.
51 so infertile and exhibit a primary defect in gametogenesis.
52 a methylation imprint acquired during female gametogenesis.
53 elopment and reproduction, particularly male gametogenesis.
54 tant reduction in germline proliferation and gametogenesis.
55 rerequisites for cell fate determination and gametogenesis.
56 gonadal cells to promote steroidogenesis and gametogenesis.
57 ntestinal tract motility, melanogenesis, and gametogenesis.
58 wing examination of the function of BRCA2 in gametogenesis.
59 rmline epigenetic modification and mammalian gametogenesis.
60 ation specifically affects post-meiotic male gametogenesis.
61 elopment and male testis differentiation and gametogenesis.
62  parental chromosomes during male and female gametogenesis.
63 ol region (ICR) is differentially set during gametogenesis.
64 rom the surrounding somatic cells throughout gametogenesis.
65 ow parental imprinting is established during gametogenesis.
66 eiotic chromosome morphogenesis and complete gametogenesis.
67 ocated to the nucleus at a specific stage of gametogenesis.
68 and tissue-specific target genes during male gametogenesis.
69  (Nesp and Gnasxl) is not established during gametogenesis.
70 g limb development, hair growth, hearing and gametogenesis.
71 for normal haematopoiesis, melanogenesis and gametogenesis.
72 ctions in hemato- poiesis, melanogenesis and gametogenesis.
73 nterstitial cells during asexual budding and gametogenesis.
74 ion and terminal differentiation during male gametogenesis.
75 f primate germ cell development and in vitro gametogenesis.
76 TPL1) with PLA2 activity plays a key role in gametogenesis.
77 es within the same stage of embryogenesis or gametogenesis.
78 truction of a defined transcriptional map of gametogenesis.
79 fish genetic elements to genes essential for gametogenesis.
80 tify that GEP1 is required for XA-stimulated gametogenesis.
81 F1B are expressed throughout female and male gametogenesis.
82 cts in both male and female sporogenesis and gametogenesis.
83 t of secondary sex characteristics (SSC) and gametogenesis.
84 re mother cells, which were able to initiate gametogenesis.
85 key cell-cycle transitions during Plasmodium gametogenesis.
86 ction in genes regulating pollen development/gametogenesis.
87 ected to high and low pCO2 conditions during gametogenesis.
88  a critical role in transposon silencing and gametogenesis.
89 tative cells and the different cell types of gametogenesis.
90 es in transposon silencing and regulation of gametogenesis.
91 ressing how many cell divisions occur before gametogenesis.
92 NMD and display defects in embryogenesis and gametogenesis.
93 n to optimize gamete quality through somatic gametogenesis.
94 e COII(G177S) might specifically impair male gametogenesis.
95 and cell wall synthesis during budding yeast gametogenesis.
96 tiating the switch from vegetative growth to gametogenesis.
97 velopmental control of these factors in male gametogenesis.
98  and functions including steroidogenesis and gametogenesis.
99 ay in epigenetic regulation during mammalian gametogenesis.
100 reening for environmental agents that affect gametogenesis.
101 anscriptionally active TEs for RdDM prior to gametogenesis.
102 tween homologous chromosomes as required for gametogenesis.
103 ecific translational control is required for gametogenesis.
104 regates to function as central regulators of gametogenesis.
105 cells adopt equal size cell divisions during gametogenesis.
106 als that FBL17 function is not restricted to gametogenesis.
107                                  During male gametogenesis, a developmentally regulated and cell type
108 rolled by blue and red light at the steps of gametogenesis along with its restoration and germination
109 of GnRH neurons at puberty onset, leading to gametogenesis and an increase in gonadal steroid hormone
110 transcription during specific stages of male gametogenesis and anther development.
111 gest that DGK2 and DGK4 are essential during gametogenesis and are required for ER-localized phosphol
112 psis thaliana) DGK2 and DGK4 are crucial for gametogenesis and biosynthesis of phosphatidylglycerol a
113 egions that are differentially marked during gametogenesis and can act over hundreds of kilobases to
114      The AS-IC imprint is established during gametogenesis and confers repression upon PWS-IC on the
115 volve evolutionary tradeoffs that compromise gametogenesis and contribute to infertility.
116  removes a large number of genes involved in gametogenesis and early embryogenesis.
117 ights into which genes are required for both gametogenesis and embryo development and might therefore
118 ed known and novel small RNA classes through gametogenesis and embryo development in the parasitic ne
119 ndicate that OGT activity is required during gametogenesis and embryogenesis with lethality occurring
120 orms required for centrosome function during gametogenesis and embryogenesis.
121  epigenome plays critical roles in mammalian gametogenesis and embryogenesis.
122 on is extensively remodeled during mammalian gametogenesis and embryogenesis.
123 ghter cells should play fundamental roles in gametogenesis and embryogenesis.
124                                          Via gametogenesis and fertilisation this lineage generates a
125 genome against transposon-induced defects in gametogenesis and fertility.
126 w that ROS play a crucial role during female gametogenesis and fertilization.
127 genetic programming events take place during gametogenesis and fetal development and are thought to h
128 S+ genomes is specifically suppressed during gametogenesis and germination of zygospores, a phenomeno
129 e diverse processes including melanogenesis, gametogenesis and hematopoeisis.
130 at the Wtf4 proteins can function outside of gametogenesis and in a distantly related species, Saccha
131 nctions in hematopoiesis, melanogenesis, and gametogenesis and in interstitial cells of Cajal.
132 een alga Chlamydomonas reinhardtii undergoes gametogenesis and mating upon nitrogen starvation.
133  key roles of the BRCA2 protein in mammalian gametogenesis and meiotic success.
134 atures in larval development, embryogenesis, gametogenesis and mRNA degradation.
135 ys, in part mimicking those occurring during gametogenesis and normal human development, as evidenced
136 rt studies on MID expression patterns during gametogenesis and on a second gene unique to the MT(-) l
137 rns at imprinted loci are established during gametogenesis and post fertilization and their alteratio
138         Although both sets of clones undergo gametogenesis and produce morphologically normal gametes
139 Argonaute proteins are expressed during male gametogenesis and promote male fertility.
140 lar mechanisms underlying sex determination, gametogenesis and reproductive physiology for most paras
141  mutants displayed unusual phenotypes during gametogenesis and resembled mutants in mitochondrial tra
142 protein (WDR55) required for male and female gametogenesis and seed development.
143 ckouts were discovered, with defects in both gametogenesis and seed development.
144 over, this work focused on genes involved in gametogenesis and sexual development.
145 complex plays an important role in mammalian gametogenesis and skeletal development.
146 ty at the chromatin interface and may impact gametogenesis and some developmental aspects of fragile
147 d gametocytogenesis in erythrocytes, nor for gametogenesis and sporogony in the mosquito vector.
148 G3 is a crucial cohesin subunit in mammalian gametogenesis and supporting our proposal that STAG3 is
149 ic modifications that are established during gametogenesis and that are maintained throughout somatic
150 g-specific activities that are essential for gametogenesis and that regulation of subcellular Dalpha1
151 nto fundamental processes of male and female gametogenesis and the earliest phases of embryonic life
152 ernal conditions impact the offspring during gametogenesis and through fetal/early-postnatal life, th
153  other metazoans and have important roles in gametogenesis and transposon control.
154 d changes in osmoregulation, locomotion, and gametogenesis, and (b) compare the resultant profiles wi
155  (H4S1ph) is evolutionarily conserved during gametogenesis, and contributes to post-meiotic nuclear c
156 pment, including proliferation, meiosis, and gametogenesis, and ensures a robust response to RNA inte
157 f dicentric chromatids is synthesized during gametogenesis, and kinetochore protein dephosphorylation
158 s, plays an essential role in hematopoiesis, gametogenesis, and melanogenesis during both embryonic a
159 y essential roles in stem cell self-renewal, gametogenesis, and RNA interference in diverse organisms
160   Flagellar CrPKD2 increased fourfold during gametogenesis, and several CrPKD2 RNA interference strai
161 gue (Mvh), a gene that is essential for male gametogenesis, and show that Dazl stimulates translation
162 cal cellular processes including phototaxis, gametogenesis, and the biogenesis of the photosynthetic
163 blished in male and female germ cells during gametogenesis, and the de novo DNA methyltransferase DNM
164      De novo mutations (DNMs) originating in gametogenesis are an important source of genetic variati
165 e incidence of this defect and its impact on gametogenesis are not clear.
166 ession at specific stages during meiosis and gametogenesis, as compared to vegetative growth and star
167  vitro model system for studies of mammalian gametogenesis, as well as for the development of new str
168 on, whereas imprinting is established during gametogenesis at primary regions (H19 ICR).
169          The Dnmt3L gene is expressed during gametogenesis at stages where genomic imprints are estab
170 evels in February and July-August but during gametogenesis (August to January) and spawning (March to
171 ylation in this region is established during gametogenesis, being present in oocytes and absent in sp
172       Both isoforms are essential for normal gametogenesis but have opposite effects on male/female g
173 1 is not necessary for microsporogenesis and gametogenesis but is essential for pollen germination.
174    The two mutations do not affect embryonic gametogenesis but the KitY719F mutation blocks spermatog
175                  Therefore, H2Bubi represses gametogenesis by opposing the recruitment of RSC at the
176 ion and terminal differentiation during male gametogenesis by regulating chromatin conformation in pr
177  firm evidence that meiosis, the hallmark of gametogenesis, can be faithfully replicated outside of t
178                 Exposure at severe OA during gametogenesis caused disruption in oyster reproduction.
179 lyadenylation-regulated translation, such as gametogenesis, cell cycle progression, and synaptic plas
180 kinesis, transcription regulation, mammalian gametogenesis, centrosome duplication, and suppression o
181 mental transition that enables the resultant gametogenesis-competent cells to respond to feminizing o
182 t the Tmem48 mutation is responsible for the gametogenesis defects and skeletal malformations in the
183                             We show that the gametogenesis defects can be corrected by ASF1A and ASF1
184 doubly null mice were partially rescued from gametogenesis defects observed in Atm null mice.
185 ing in derepression of multiple TE families, gametogenesis defects, and sterility.
186  in mammals, is established and reset during gametogenesis; defects in this process in the parent can
187 shment of patterns of DNA methylation during gametogenesis depends in part on DNMT3L, an enzymaticall
188         Integrated probabilistic modeling of gametogenesis developed in response to our observations
189 or a variety of biological processes such as gametogenesis, developmental transitions, and sex determ
190 ge-component muations affect male and female gametogenesis differentially.
191 -interacting RNAs (piRNAs) are essential for gametogenesis, embryogenesis, and stem cell maintenance
192  is presumed to play a physiological role in gametogenesis, embryogenesis, or both.
193 ription factor essential for later stages of gametogenesis extends the replicative life span of aged
194 that the natural depletion of H1 during male gametogenesis facilitates DEMETER-directed DNA demethyla
195 atm; and 6.7, pCO2 18480 microatm) on oyster gametogenesis, fertilization, and early larval developme
196  Meiotic recombination is a critical step in gametogenesis for many organisms, enabling the creation
197 it 3, was disrupted in Arabidopsis thaliana, gametogenesis frequently failed due to defects in cell d
198             When first reported 4 years ago, gametogenesis from embryonic stem (ES) cells promised an
199 control of the developmental program of male gametogenesis, function to direct cell type- and stage-s
200 pecies of all four extant arthropod classes, gametogenesis functions without nurse cells.
201 , spermatogenesis, testicular determination, gametogenesis, gonad differentiation, and possibly sex d
202                         The role of Brca2 in gametogenesis has been obscure because of embryonic leth
203 cue experiments suggest that male and female gametogenesis have distinct requirements for importin al
204 eniles) abundant spermatogonia committing to gametogenesis (high KIT(+)).
205 s an important role in meiosis induction and gametogenesis in adult medaka but contrary to common exp
206 rs during larval and metamorphic stages, and gametogenesis in adults.
207 light a crucial role for RanBPM in mammalian gametogenesis in both genders.
208 l number of genes whose elimination disrupts gametogenesis in both sexes after the major events of me
209 l of differentiating early germ cells during gametogenesis in both sexes.
210        We also show that pCRY is involved in gametogenesis in Chlamydomonas pCRY is down-regulated in
211 eveal a specific requirement of Hbs1 in male gametogenesis in Drosophila and indicate an essential ro
212 rtant for germline stem cell maintenance and gametogenesis in males, whereas ectopic expression in fe
213     Thus, the majority of genes required for gametogenesis in mammals remain unidentified.
214 ts of ATZ exposure on meiosis, a key step in gametogenesis in mammals.
215                                       Female gametogenesis in most flowering plants depends on the pr
216 ET domain proteins may function similarly in gametogenesis in other species.
217 quality can explain the stability of somatic gametogenesis in plants and basal metazoans, the evoluti
218 he fundamental mechanisms that regulate male gametogenesis in plants and demonstrate that their sensi
219 /26S proteasome system is important for male gametogenesis in plants and suggest that deubiquitinatio
220  different form of cytokinesis occurs during gametogenesis in Saccharomyces cerevisiae, in which four
221 vation that eIF4E levels are elevated during gametogenesis in several organisms suggests that eIF4E m
222 cates that the t(8;22) arises de novo during gametogenesis in some, but not all, individuals.
223     Finally, reduced fertility and irregular gametogenesis in the Arabidopsis SWR1 mutants indicate a
224 tyrosine kinase (RTK) genes expressed during gametogenesis in the cnidarian Hydra vulgaris, we isolat
225                  Based on this, we show that gametogenesis in the marine green alga, Monostroma angic
226 nd gametocytogenesis, but essential for male gametogenesis in the mosquito vector.
227 agphinins regulate cell proliferation during gametogenesis in the mouse.
228 ables nonrandom segregation is primed during gametogenesis in the parents.
229 Thus, our results show that investigation of gametogenesis in yeast provides novel insights into chro
230 f two lncRNAs governs mating-type control of gametogenesis in yeast.
231 thylation, during meiotic spore development (gametogenesis) in Saccharomyces.
232 strain Ho_CS develop an aging phenotype upon gametogenesis induction, initiated by the loss of inters
233                              Successful male gametogenesis involves orchestration of sequential gene
234                                              Gametogenesis is a complex process subject to strict con
235                                              Gametogenesis is a highly regulated process in all organ
236                                              Gametogenesis is a thermosensitive process in numerous m
237                                     However, gametogenesis is affected in several ways and tissue mas
238                                              Gametogenesis is dependent on intercellular communicatio
239                                              Gametogenesis is dependent on the expression of germline
240            The cell-fate decision leading to gametogenesis is essential for sexual reproduction.
241 ice appear to develop and function normally, gametogenesis is severely compromised.
242 n priming, which may be downregulated during gametogenesis, is indispensable for robust maintenance o
243 , expression of IME1, the central inducer of gametogenesis, is inhibited in cis by transcription of t
244 ) self-renew (Thy1(+) enriched) or commit to gametogenesis (Kit(+) enriched).
245 t not haploid MATa or MATalpha cells undergo gametogenesis, known as sporulation.
246 AF-like gene (At5g26290) exhibiting aberrant gametogenesis led us to investigate the developmental ro
247 ty of invertebrates in the initial stages of gametogenesis, male and female germ cells develop in ful
248 osaicism together with sexual differences in gametogenesis might explain a considerable fraction of u
249   Depletion of GCalpha impairs XA-stimulated gametogenesis, mimicking the defect of GEP1 disruption.
250 iterated) events in adult animals, including gametogenesis, movement, behavior, and learning.
251  Reduction of the genetic information before gametogenesis occurs in meiosis, when cross-overs (COs)
252                                   In plants, gametogenesis occurs late in development, and somatic mu
253                                  Remarkably, gametogenesis occurs without significant changes in DNAm
254            Here, we examine the role in male gametogenesis of the Doublesex-related gene Dmrt6 (Dmrtb
255 (hermaphrodite, female, or male) and type of gametogenesis (oogenesis or spermatogenesis).
256 and the timing of insertion events in either gametogenesis or early embryonic development.
257 re of accurate chromosome segregation during gametogenesis or early embryonic divisions.
258 hytes, indicating that PpMET plays a role in gametogenesis or early sporophyte development.
259                                       During gametogenesis, PfCCps are released and localize surround
260  through meiotic development and migrate for gametogenesis-processes that require LINC complex functi
261 e identification of GEP1 being essential for gametogenesis provides a potential new target for interv
262 ng Mrp4(-/-) mice had significantly impaired gametogenesis, reduced testicular testosterone, and disr
263 rimordial germ cells is robust, but terminal gametogenesis remains inefficient and doubts about gamet
264 puts influence early meiotic progression and gametogenesis remains poorly understood in metazoans.
265 cing these environmental signals to initiate gametogenesis remains unknown.
266 asis of germline encapsulation in Drosophila gametogenesis, reporting that it is not driven solely by
267                    Germ cell development and gametogenesis require genome-wide transitions in epigene
268 lants is distinct from that in animals since gametogenesis requires production of haploid spores, whi
269 ic marks imposed on the X chromosomes during gametogenesis, responsible for normal imprinted X inacti
270 ur model suggests that sexual dimorphisms in gametogenesis result in a greater proportion of somatica
271 ethylation marks are erased and reset during gametogenesis, resulting in paternal or maternal imprint
272   During the extended prophase of Drosophila gametogenesis, spermatocytes undergo robust gene transcr
273                                We determined gametogenesis stage- and male-specific expression and lo
274 dk2) is not necessary for mouse viability or gametogenesis stages prior to meiotic prophase I, mice b
275  for its function in germline specification, gametogenesis, stem cell maintenance, transposon silenci
276 n, epigenetic information established during gametogenesis, such as gametic imprints, cannot be resto
277 ologs may perform conserved functions during gametogenesis, that in C. elegans certain aspects of ooc
278 es demonstrate that PfPATPL1 plays a role in gametogenesis, thereby identifying PLA2 phospholipases s
279  communicate directly with each other during gametogenesis through intercellular bridges, often calle
280 these ranged from defects in early stages of gametogenesis to later defects affecting pollen germinat
281 ents processes that normally function during gametogenesis to prepare the gamete genomes to support d
282 stigation of chromatin reorganization during gametogenesis, using the model eukaryote Saccharomyces c
283 e intra-species, intra-individual, and intra-gametogenesis variations in the meiotic program, A. rhod
284                          In contrast, female gametogenesis was not affected by the absence of major O
285            A causative role for AHA3 in male gametogenesis was proven by complementation with a norma
286 and how chromatin regulates AGSC biology and gametogenesis, we derived stage-specific high-resolution
287 h the known requirements of JAK signaling in gametogenesis, we find that mutants of upd3 show an age-
288  cause defects in germ cell proliferation or gametogenesis, we identified sets of genes with germline
289           Consistent with ASF1 importance in gametogenesis, we show that ASF1A and ASF1B are expresse
290 xpressed and play a crucial role during male gametogenesis, whereas endo-siRNAs are essential for ooc
291                              This process of gametogenesis, which is key to malaria transmission, inv
292 ivated a subset of control genes involved in gametogenesis while down-regulating protein biosynthesis
293 d germ cells survive to complete meiosis and gametogenesis with high efficiency.
294 dial germ cell development and the timing of gametogenesis with respect to stressor exposure.
295             Genomic imprinting begins during gametogenesis with the establishment of epigenetic marks
296 rease in the number of cell divisions before gametogenesis, with a concomitant increase in mutations
297 the sporophyte and gametophyte affect female gametogenesis, with different developmental outcomes det
298      Gametocytes differentiation to gametes (gametogenesis) within mosquitos is essential for malaria
299 ermline stem cell proliferation, meiosis and gametogenesis, yet how these key transitions are coordin
300 cluding stem cell proliferation, meiosis and gametogenesis, yet the nature of these fundamental signa

 
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