ライフサイエンスコーパス: father

1 mother with moderate pain, and an unaffected father).

2 ct with the mother, and in some mammals, the father.

3 rwent transplant, as well as in his affected father.

4 was identified in the index patient and her father.

5 without a cohabiting, actively drug-abusing father.

6 ived a preemptive kidney transplant from his father.

7 bryos that inherit an Xist deletion from the father.

8 nal age when not adjusted for the age of the father.

9 on was found to be mosaic in an asymptomatic father.

10 sons are more responsive to cues from their father.

11 st germline mutations are inherited from the father.

12 There was no such reduction in CD risk among fathers.

13 ations as safe compared to male patients and fathers.

14 robust associations were seen in mothers or fathers.

15 difference in response to genetic vs. foster fathers.

16 arents; these were different for mothers and fathers.

17 omes for infants and increase quitting among fathers.

18 rs), 192 patients' mothers and 157 patients' fathers.

19 ed with total or cardiovascular mortality in fathers.

20 s self-reported by 43% of mothers and 34% of fathers.

21 ers and -0.22 (-0.31 to -0.15; P < .001) for fathers.

22 gnificantly elevated in offspring of exposed fathers.

23 ippocampus of the offspring and the sperm of fathers.

24 l paternal origin with higher risk for older fathers.

25 ue for EPRS from their successful extra-pair fathers.

26 control participants, 1233 mothers, and 1614 fathers.

27 essation interventions targeted at expectant fathers.

28 y and working memory deficit not observed in fathers.

29 ore associations emerging in mothers than in fathers.

30 health in promoting quitting among expectant fathers.

31 about half of them were first-time expectant fathers.

32 changes in neurogenomic state as they become fathers.

33 olonged grief in cancer-bereaved mothers and fathers 1 to 5 years after their child died of cancer.

34 25%; OR = 2.1; 95% CI, 1.0 to 4.3; P = .05; fathers: 10% vs 20%; OR = 2.3; 95% CI, 1.0 to 5.3; P = .

35 8%; OR = 6.5; 95% CI, 3.3 to 12.6; P < .001; fathers: 10% vs 47%; OR = 7.8; 95% CI, 3.7 to 16.8; P <

36 tal paternal depression symptoms affected 82 fathers (2.3%) and were associated with perceived stress

37 =2.23-3.38), intermediate for not-lived-with fathers (2.45, 95% CI=2.14-2.79), and lowest for stepfat

38 ariable (IV) analysis with data from 996,898 fathers (282,407 deaths) and 1,013,083 mothers (153,043

39 patients (aged 12-23 years), 103 mothers and fathers, 31 siblings (aged 12-26 years), and 42 friends

40 230 immunosuppressed renal transplanted men fathered 350 children (155 on MPA/195 not on MPA).

41 and were higher in brothers (64.0; P = .04), fathers (42.9; P = .004), and males (50.7; P < .001) tha

42 o [OR] = 9.9; 95% CI, 4.3 to 23.3; P < .001; fathers: 5% vs 36%; OR = 11.0; 95% CI, 4.1 to 29.6; P <

43 14%; OR = 2.9; 95% CI, 1.0 to 8.2; P = .04; fathers: 6% vs 19%; OR = 3.4; 95% CI, 1.3 to 9.0; P = .0

44 g themselves; 10060 mothers (85.1%) and 2688 fathers (83.4%), selecting other infant caregivers; and

45 atal surveys, 10958 mothers (91.0%) and 2950 fathers (88.6%) reported learning a lot about understand

46 ng as normal; 11023 mothers (92.2%) and 2923 fathers (88.9%), calming their infant, 11396 mothers (94

47 more likely to have an international migrant father (9.7% versus 4.0%) or brother (49.1% versus 30.3%

48 their infant, 11396 mothers (94.6%) and 3035 fathers (91.9%), calming themselves; 10060 mothers (85.1

49 regivers; and 11435 mothers (94.8%) and 3201 fathers (95.8%), that the information would decrease the

50 interval [CI], 1.23-2.53) versus nonchewing fathers (adjusted hazard ratio, 3.28; 95% CI, 1.67-6.43)

51 ctors for asthma were tertiary education for fathers (adjusted OR (95% CI); 2.32 (1.71-3.16)) and mot

52 In that group, the hazard ratio for fathers aged >/=35 years compared with <25 years at birt

53 The previously reported father (aged 95 years) and son (aged 64 years), and the

54 The sibling's father also carried the p.Ala13Thr variant, in whom an u

55 in a female patient with mild anemia, whose father also carries the trait and is from the Turkish ci

56 Having an older father also conferred an increased risk, with an odds ra

57 Offspring from old fathers also had transcriptional dysregulation of develo

58 is not just a "mother's problem"; 23% of new fathers also leave STEM after their first child.

59 BD in the population-based Norwegian Mother, Father and Child Cohort Study (MoBa).

60 eferred MHC genotypes (i.e. MHC-heterozygous father and DAB*d-free mother).

61 Three affected family members, a father and his 2 daughters, were examined.

62 s important mentors in my life, including my father and Joe Gall, who is my "Doktor Vater." In turn,

63 s, we show that the H2A.B status of both the father and mother, but not of the zygote, affects embryo

64 maternal age is explained by the age of the father and that de novo mutations that occur more freque

65 In both the father and the aunt, histology of the surgical specimen

66 re inherited from the affected, asymptomatic father and the rare NKX2-5 variant (minor allele frequen

67 esolimbic reward brain regions of the F1-HFD father and the resultant HFD-tsRNA offspring.

68 es research on the effects of absence of the father and the transmission of paternal influences acros

69 male somatic phenotypes as observed in an XY father and XY daughter, respectively.

70 lia (RHINESSA) multigeneration study of 2044 fathers and 2549 mothers (age, 37-66 years) investigated

71 ies, what mechanisms allow nonmothers (i.e., fathers and alloparents) to demonstrate parental care?

72 n association between depressive symptoms in fathers and depressive symptoms in their adolescent offs

73 domly assigned (1:1) to invite or not invite fathers and male caregivers to participate.

74 more frequently between siblings and between fathers and offspring than between mothers and their off

75 longer parental life span (P 6.2 x 10-6 for fathers and P 2.0 x 10-3 for mothers), consistent with e

76 The risk of ADs was very similar in mothers, fathers and siblings of OCD probands, whereas it tended

77 of learning to sequence similarities between fathers and sons by experimentally tutoring juvenile Ben

78 males and affects the sperm transcriptome in fathers and sons.

79 mpaired long-term memory in both the exposed fathers and their offspring.

80 ularly lipid-derived metabolites, in exposed fathers and their offspring.

81 war orphans and collect information on their fathers and then paired each orphan with a nonorphan fro

82 l depression symptoms affected 153 (4.3%) of fathers and were associated with perceived stress in pre

83 ically significant associations between both fathers' and mothers' childhood overweight status and of

84 platforms for parent generation (mother and father) and F1 generation (male and female progeny).

85 ifestyles (e.g., divorced mother vs. married father), and 204 faculty compared same-gender candidates

86 n-Brown-Rahman syndrome (TBRS), their mosaic father, and 15 TBRS patients with distinct pathogenic de

87 to have experienced the death of a mother, a father, and a sibling from childhood through midlife.

88 o reared them, a "not-lived-with" biological father, and a stepfather.

89 s, E846D from the mother and R1063H from the father, and exhibited erythrocytosis and megakaryocytic

90 ne of which was corrected for the age of the father, and found that the fit was superior for the mode

91 are de novo, one is inherited from a mosaic father, and four offspring from two families have a pate

92 The study enrolled 95,278 mothers, 75,248 fathers, and 114,516 children.

93 erior temporal sulcus (STS) comparable to SC-Fathers, and functional connectivity between amygdala an

94 for mothers, intermediate for not-lived-with fathers, and lowest for stepfathers.

95 isms that subserve parental care in mothers, fathers, and others (i.e., alloparents).

96 ys and tested to what extent vertical (i.e., father- and/or mother-offspring relationships) or horizo

97 on abnormalities arising in the sperm of old fathers are a plausible mechanism to explain some of the

98 The offspring of younger mothers and older fathers are at risk for different mental health disorder

99 hin villages, particularly when children and fathers are coresident.

100 The finding suggests that expectant and new fathers are not at greater risk of poor mental health.

101 de novo mutations in the offspring of older fathers are not only more numerous but also occur more f

102 These findings support the involvement of fathers as well as mothers in early interventions to red

103 hed light on sex differences through work on fathers as well as mothers, are affected by psychopathol

104 ults showed that the abstinence rates of the fathers at 6 months (adjusted OR: 3.60, 95% CI: 1.41-9.2

105 Z chromosome blocks was produced by daughter-father backcrosses, and inferred from marker loci positi

106 ed GDM/GH risk indicator in both mothers and fathers because of shared spousal behaviors and environm

107 adult lifespan of orphans who had lost their father before birth was 2.4 y (95% CI: 0.7, 3.9 y) and w

108 st the transmission of effects from the same father (before or after training) and from different fat

109 Taken together, our results demonstrate that fathering behavior in A. ocellaris occurs spontaneously,

110 ximately 30% of the fish displayed extensive fathering behavior within 90 min.

111 d overall cancer mortality (HR per SD higher fathers' BMI: 1.20 [1.16-1.24] and mothers' BMI: 1.29 [1

112 [95% confidence interval (CI)] per SD higher fathers' BMI: 1.29 [1.26-1.31] and mothers' BMI: 1.39 [1

113 The patient's father, brother and one aunt were identified as carriers

114 f genes from her mother and one set from her father but where males receive genes only from their mot

115 nating a diploid "mother" with a tetraploid "father") but repressed in the reciprocal cross.

116 ) a selective advantage in the testes of the father, but have a deleterious effect in offspring.

117 -additive: offspring with a predator-exposed father, but not two predator-exposed parents, had lower

118 e risk of adverse birth outcomes in children fathered by male kidney transplanted patients.

119 ence of congenital malformations in children fathered by male recipients, including patients on mycop

120 f knowledge regarding outcome of pregnancies fathered by men exposed to MPA.

121 We compared outcomes in pregnancies fathered by renal transplant men per whether they had be

122 Broods were fathered by up to 3 different males.

123 hat heritable mutations transmitted from the father can arise from either paternal or maternal misrep

124 through which epigenetic information from a father can shape offspring gene expression and developme

125 We studied whether fathers can transfer epigenetic information to their dau

126 porate long- and short-read data from mother-father-child trios, and therefore require relatively hig

127 nformation on the first 150 families (mother-father-child(ren)) enrolled.

128 xplain why younger men have a higher risk of fathering children with Down syndrome.

129 onse to the odour of their genetic mother or father compared to the odour of a non-relative of the sa

130 ter the onset of spermatogenesis, even young fathers contribute three times more mutations than young

131 arity of methylomes within patrilines (i.e., father-daughter subfamilies) than between patrilines in

132 and two family history (mother DSM-5 AUD and father DSM-5 AUD) features using supervised, Linear Supp

133 ase-parent trios, case-mother duos, and case-father duos.

134 these men had been identified as "expectant fathers" during the previous wave.

135 d Spectroscopy (fNIRS) was used on 24 mother-father dyads (N = 48) to measure prefrontal cortical (PF

136 was hypermethylated in the saccharin-exposed fathers, especially at dopamine receptor promoter region

137 PC-Fathers exhibited high amygdala activation similar to PC

138 Fathers exposed to high concentrations of dioxin-like PC

139 to test the hypothesis that if the mother or father (F1) had been exposed to their own mother's (F0)

140 s, families with a not-lived-with biological father, families with a stepfather, and adoptees and the

141 er this time, 349 men were identified as new fathers (first child aged <1 year), and 224 of these men

142 Research on the psychological adjustment of fathers following VPT birth is limited.

143 after receiving haploidentical HSCT from his father for the treatment of metastatic rhabdomyosarcoma.

144 ciations with diabetes were also observed in fathers (for either, HR = 1.2, 95% CI: 1.1, 1.3; for bot

145 Eleven mothers and 8 fathers from 13 families participated.

146 A sub-cohort (n = 50,736 mothers, n = 44,794 fathers) from survey data was analysed for risk factors.

147 ed-part-time employment (both part-time) and father full-time/mother part-time (1.5-earner).

148 Both the patient and her father had a His-58(E7) --> Leu mutation in alpha1.

149 , 42.8%-80.2%) for children whose mother and father had a history of sleepwalking.

150 ts consistently show that participants whose father had a manual (as compared to nonmanual) occupatio

151 ed inflammatory burden in participants whose father had a manual occupation, through increased plasma

152 His father had childhood type 1 diabetes in poor glycemic co

153 Affected eyes appeared ovoid on MRI and the father had thin optic nerves.

154 Daughters of overweight fathers had higher rates of carcinogen-induced mammary t

155 g of HFD mothers and F1 daughters of HFD-fed fathers had increased weight gain compared to controls.

156 The offspring of older fathers had reduced exploratory and startle behaviors an

157 in whom the index parent (315 mothers and 22 fathers) had experienced at least 2 episodes of MDD (rec

158 f a Japanese mother and a Norwegian engineer father, he was educated in Japan and later graduated fro

159 A segments (mega-NUMTs) transmitted from the father in all 7 families.

160 The proband and her affected father in Family 2 were homozygous for a single nucleoti

161 Fathers in multiplex families have marginally greater si

162 Including fathers in the intervention had no measurable effect on

163 presumptive "inbreeding avoidance delay," or father-induced reproductive suppression).

164 ther has Sickle cell anaemia (Hb SS) and his father is a carrier of heterozygous alpha-thalassemia st

165 Surprisingly, the patient's father is not anemic, but he is a smoker with high level

166 X6) between a diploid mother and a hexaploid father, leading to the seed abortion.

167 nts cause severe GD in F1 daughters when Har fathers mate with mothers lacking P-element-piRNAs (i.e.

168 [SD] age at birth, 32.7 [5.3] years) and 101 fathers (mean [SD] age at birth, 34.7 [6.4] years) of 14

169 [SD] age at birth, 32.9 [4.8] years) and 110 fathers (mean [SD] age at birth, 35.9 [5.3] years) of 15

170 Women preferred divorced mothers to married fathers; men preferred mothers who took leaves to mother

171 ddressing the differing needs of mothers and fathers more effectively.

172 Identifying fathers most at risk of depressive symptoms and when bes

173 fspring, we are collecting biospecimens from father-mother-offspring constellations to study de novo

174 Compared with cohabiting fathers, mothers had a greater reduction in risk for dru

175 ved to age 50 (n = 661,031) to offspring and fathers (n = 691,124).

176 King Philip II was the father of Alexander the Great.

177 over a century ago by Elie Metchnikoff, the "father of innate immunity," who is credited with discove

178 tenary of the death of Elie Metchnikoff, the father of innate immunity.

179 iversary of the death of Harvey Cushing, the father of modern neurosurgery.

180 To quote Carolus Linnaeus ( 1 , p. 19), the father of taxonomy, "The first step in wisdom is to know

181 19), the father of taxonomy, "The first step in wisdom is to know

182 three of the cases, and the mildly affected father of the fourth affected individual was confirmed a

183 Paraphrasing the Swiss physician and father of toxicology Paracelsus (1493-1541) on chemical

184 ng the rate of epilepsy among mothers versus fathers of affected individuals; and (3) lineage analysi

185 incidence of recent T. gondii infections in fathers of congenitally infected children indicates that

186 nd South America led us to determine whether fathers of congenitally infected infants in the National

187 hereas it tended to be higher in mothers and fathers of TD/CTD probands (compared with siblings).

188 Mothers and fathers of VPT infants had elevated rates of depression

189 tly dispersed to the group in which they had fathered offspring more likely than expected.

190 irs, there were 241 mother-offspring and 297 father-offspring pairs with a mean (SD) offspring age of

191 to 26,057 mother-offspring pairs (and 19,792 father-offspring pairs) from the Nord-Trondelag Health (

192 n BP (N = 32,227 mother-offspring and 27,535 father-offspring pairs).

193 circumference, using data from 68,244 mother-father-offspring trios from the Norwegian Mother and Chi

194 e IPD meta-analysis (N = 5327 to 5377 mother-father-offspring trios) showed that increasing maternal

195 found a statistically significant effect of fathers' onset of being overweight in puberty on offspri

196 hs of age, as compared with offspring with a father or sibling with T1D.

197 We exposed mothers, fathers or both parents to visual cues of predation risk

198 If married or in established relationships, fathers or male caregivers aged 18 years or older were a

199 und for F2 offspring of analgesic-exposed F1 fathers or mothers, we interpret this as potentially ind

200 ve analyses did not explore the influence of fathers, other children in the home, or length of NICU s

201 r, a growing body of research indicates that fathers play a significant role through presently unknow

202 The current findings from BaYaka fathers point to testosterone as a psychobiological corr

203 s among offspring of affected mothers versus fathers (prevalence ratio = 1.0, 95% confidence interval

204 We used mother-father-proband (trio) information from multiple technica

205 Predator-exposed fathers produced sons that were more risk-prone, whereas

206 ent fathers to compare sedentary- and runner-father progenies.

207 that male sticklebacks-a small fish in which fathers provide care-experience dramatic changes in neur

208 tterns and micro-RNA content in the sperm of fathers, providing a potential mechanism for the transge

209 their mothers (r = 0.14) compared with their fathers (r = 0.03).

210 ce (29 of 81; 36%) of T. gondii infection in fathers, relative to the average seropositivity rate of

211 LEAR RNA POLYMERASE D1 (NRPD1) in tetraploid fathers represses seed abortion in paternal excess cross

212 to the average age of a new mother and a new father, respectively, Fishers equal-investment conclusio

213 In fathers, rigid personality was related to increased repe

214 's testosterone was linked to locally-valued fathering roles, we found that fathers who were seen as

215 terval) 2.66 (1.42-4.99) compared to rural]; father's [2.62 (1.79-3.83)] and mother's history of alle

216 history of allergies, mother's age at birth, father's age at birth and highest parental education.

217 Father's age, low gestational age, obstetric characteris

218 ior for the model without adjustment for the father's age.

219 al age effect of three mutations per year of father's age.

220 2.92)) and (2.79 (1.79-4.35)), respectively; father's and mother's history of asthma; children's own

221 Social Class) was ascertained in childhood (father's class at 10/11 y) and adulthood (42/43 years),

222 y good-your mother's baking-or very bad-your father's cooking.

223 Adult lifespan was not reduced when the father's death occurred after the infant's birth.

224 ealth is well characterized, the role that a father's diet has on his offspring's health remains poor

225 c disorders in offspring can result from the father's diet, but the mechanism remains unclear.

226 Lower father's education tended to increase the odds of type 2

227 sharing) increases the average fitness of a father's gametes.

228 e of conception can epigenetically reprogram father's germ-line and modulate their daughters' birth w

229 A father's lifetime experiences can be transmitted to his

230 Patient's and father's lymphocytes showed reduced pSTAT4, nuclear tran

231 equently modelled by the interaction between father's occupation and the highest household occupation

232 d for sex, education, age, country of birth, father's occupation, ever-consumed alcohol, and asset in

233 Patient's and father's peripheral blood mononuclear cells and macropha

234 EBOV RNA in the mother's breast milk and the father's seminal fluid.

235 hen compared the methylation profile of each father's somatic tissue and semen with the methylation p

236 present in an offspring and evident only in father's sperm, and identified single-nucleotide, struct

237 ed the sequence statistics of their tutor's (father's) songs at multiple levels of organization (e.g.

238 TD/CTD and their first- (siblings, mothers, fathers), second- (half siblings) and third-degree (cous

239 However, they were able to father sex-converted progeny when presented with cold-an

240 over, heterozygous embryos sired by pi6(-/-) fathers show reduced viability in utero.

241 ce of AF in a first-degree relative: mother, father, sibling, or children.

242 of cigarettes during pregnancy, or when only fathers smoke.

243 o differentiate between the Y chromosomes of father-son pairs, and imputed Y-STR genotypes.

244 Among obligate carriers with affected fathers, sons, or both, 53 of 55 (96%) had abnormal base

245 and higher embryo mortality, possibly due to fathers spending less time within nests and less frequen

246 Our observations revealed that fathers subjected to wheel-running for 12 wk produced of

247 nsmission for these syndromes in mothers and fathers, supporting the representativeness of results fr

248 Mothers, not fathers, take the lead in the endocrinological and behav

249 ned cooperation to human life history, human fathers' testosterone may be linked to these two behavio

250 When transmitted by a homozygous father (Tg/Tg), the Tg fails to show imprinted expressio

251 When transmitted from a hemizygous father (+/Tg), the Xist Tg demonstrates paternal-specifi

252 ltural changes have increased the numbers of fathers that are involved in direct caregiving in Wester

253 smoking cessation intervention for expectant fathers that focused on explaining the ramifications of

254 My father, the oldest of six children, was the first in his

255 ers and -0.39 (-0.56 to -0.21; P < .001) for fathers; the mean (95% CI) change in anxiety score per w

256 revealed more affected mothers than affected fathers; this effect was similar for affected and unaffe

257 length (LTL) is well established, with older fathers thought to pass on longer telomeres to their off

258 s as potential mediators of the effects from father to offspring.

259 characterization of viruses isolated from a father to son transmission event.

260 perfectly during inferred transmission from father to son, and during nearly two decades of episodes

261 before or after training) and from different fathers to compare sedentary- and runner-father progenie

262 New mothers are more likely than new fathers to leave STEM, to switch to part-time work, and

263 contrast, evolution generally leads diploid fathers to mask mutations in their gametes to the maximu

264 ain gene expression: exposing mothers versus fathers to predation risk activated different transcript

265 This father-to-child effect is reproduced in several mouse mo

266 nt markers identified to date explain 37% of father-to-son familial risk, 8% of which can be attribut

267 10-3 (95% CI 1.94 x 10-3 to 2.48 x 10-3) per father-to-son Y-transmission, higher than many short tan

268 9,702) and approximately 2.4% lower risk for fathers (total ndeaths = 97,630).

269 As in humans, older macaque fathers transmit more mutations to their offspring, incr

270 om a approximately 70-repeat allele from the father (unaffected by ALS or FTLD at age 89 years) expan

271 Exome sequencing revealed that the father was heterozygous for a de novo 5 bp deletion in M

272 more likely to inform the daughter that her father was sick enough to die (68% vs 43%; 95% CI, 5-44%

273 As down-regulated in daughters of overweight fathers, was activated in their mammary tissues and tumo

274 dependently detecting mega-NUMTs in 0.13% of fathers, we see autosomal transmission of the haplotype.

275 The parents and siblings of the father were healthy.

276 F1 daughters of HFD fathers were also heavier (p=0.01).

277 Expectant fathers were at risk of depression symptoms if they felt

278 cally significantly associated variables for fathers were having said farewell to the deceased child

279 ality of individuals born in 1914-1916 whose fathers were killed during World War 1.

280 were more resistant to infection when their fathers were reared on medicinal milkweed, while materna

281 t an appointment on behalf of his fictitious father who had severe itch for several months, asked whe

282 s transmitted from the clinically unaffected father who was a mosaic carrier of the variant.

283 ialysis, the patient received a KTx from her father who was already the HSCT donor.

284 ionwide survey, including 133 mothers and 92 fathers who had lost a child to cancer 1 to 5 years earl

285 Smoking expectant fathers who registered with their pregnant partners were

286 BaYaka fathers who were better providers also tended to have lo

287 ocally-valued fathering roles, we found that fathers who were seen as better community sharers had lo

288 In the proband's father, who had 0.0 logMAR visual acuity, significant co

289 spring with large expansions, but not in the father, who has the approximately 70-repeat allele.

290 lains the phenotypic differences between the father, who is a smoker, and his daughter.

291 y163Ser) variant in MYLPF arose de novo in a father, who transmitted it to his son.

292 polymorphic ventricular tachycardia and his father with left ventricular noncompaction and catechola

293 splantation for diastolic heart failure, her father with left ventricular noncompaction, and 2 fourth

294 g protective against the following: having a father with T2D, being overweight, having higher blood p

295 diagnosed with GDM and GTD as well as in her father with type 2 DM but was absent in control patients

296 d mortality has been observed in mothers and fathers with male offspring but little is known regardin

297 xpected incidence of recent infections among fathers with serum samples collected by the 1-year visit

298 and only slightly more than was observed for fathers with siblings with ASD (relative risk, 2.08; 95%

299 olic disease in mothers and with diabetes in fathers, with stronger associations when both GDM and GH

300 anhattan (my mother was a Vogue model and my father worked in retail), and I traveled to college at t