Template:2020 New References: Difference between revisions
From Embryology
mNo edit summary |
mNo edit summary |
||
(One intermediate revision by the same user not shown) | |||
Line 4: | Line 4: | ||
| [[User:Z8600021|Mark Hill]] ([[User talk:Z8600021|talk]]) 15:48, 8 January 2020 (AEDT) Added this new page to capture updated references added throughout the site in the "Some Recent Findings". Entries are listed alphabetically by topic page. Note that not all new references may be added to this current list. (More? [[New]]) | | [[User:Z8600021|Mark Hill]] ([[User talk:Z8600021|talk]]) 15:48, 8 January 2020 (AEDT) Added this new page to capture updated references added throughout the site in the "Some Recent Findings". Entries are listed alphabetically by topic page. Note that not all new references may be added to this current list. (More? [[New]]) | ||
|- | |- | ||
| {cerebellum}} | {{second trimester}} | | {{birth weight}} | {{birth}} | ||
* '''New Australian Birthweight Centiles'''{{#pmid:32608051|PMID32608051}} "All singleton births in Australia of 23-42 completed weeks' gestation and with spontaneous onset of labour, 2004-2013. Births initiated by obstetric intervention were excluded to minimise the influence of decisions to deliver small for gestational age babies before term. Current birthweight centile charts probably underestimate the incidence of intra-uterine growth restriction because obstetric interventions for delivering pre-term small for gestational age babies depress the curves at earlier gestational ages. Our curves circumvent this problem by excluding intervention-initiated births; they also incorporate more recent population data. These updated centile curves could facilitate more accurate diagnosis of small for gestational age babies in Australia." | |||
|- | |||
| {{blood}} | {{stem cell}} | |||
* '''CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation'''[https://www.pnas.org/content/117/38/23626 PNAS] "Hematopoietic stem and progenitor cell (HSPC) formation and lineage differentiation involve gene expression programs orchestrated by transcription factors and epigenetic regulators. Genetic disruption of the chromatin remodeler chromodomain-helicase-DNA-binding protein 7 (CHD7) expanded phenotypic HSPCs, erythroid, and myeloid lineages in {{zebrafish}} and {{mouse}} embryos. CHD7 acts to suppress hematopoietic differentiation. Binding motifs for RUNX and other hematopoietic transcription factors are enriched at sites occupied by CHD7, and decreased RUNX1 occupancy correlated with loss of CHD7 localization. CHD7 physically interacts with RUNX1 and suppresses RUNX1-induced expansion of HSPCs during development through modulation of RUNX1 activity. Consequently, the RUNX1:CHD7 axis provides proper timing and function of HSPCs as they emerge during hematopoietic development or mature in adults, representing a distinct and evolutionarily conserved control mechanism to ensure accurate hematopoietic lineage differentiation." [https://www.omim.org/entry/608892 OMIM - CHD7] | [https://www.omim.org/entry/151385 OMIM - RUNX1] | |||
|- | |||
| {{cerebellum}} | {{second trimester}} | |||
* '''Morphometric development of the human fetal {{cerebellum}} during the early {{second trimester}}'''{{#pmid:31751665|PMID31751665}} "The protracted nature of development makes the cerebellum vulnerable to a broad spectrum of pathologic conditions, especially during the early fetal period. This study aims to characterize normal cerebellar growth in human fetuses during the early second trimester. We manually segmented the fetal cerebellum using 7.0-T high-resolution MR images obtained in 35 specimens with gestational ages ranging from 15 to 22 weeks. Volume measurements and shape analysis were performed to quantitatively evaluate global and regional cerebellar growth. The absolute volume of the fetal cerebellum showed a quadratic growth with increasing gestational age, while the pattern of relative volume changes revealed that the cerebellum grew at a greater pace than the cerebrum after 17 gestational weeks. Shape analysis was used to examine the distinctive development of subregions of the cerebellum. The extreme lateral portions of both cerebellar hemispheres showed the lowest rate of growth. The anterior lobe grew faster than most of the posterior lobe. These findings expand our understanding of the early growth pattern of the human cerebellum and could be further used to assess the developmental conditions of the fetal brain." | * '''Morphometric development of the human fetal {{cerebellum}} during the early {{second trimester}}'''{{#pmid:31751665|PMID31751665}} "The protracted nature of development makes the cerebellum vulnerable to a broad spectrum of pathologic conditions, especially during the early fetal period. This study aims to characterize normal cerebellar growth in human fetuses during the early second trimester. We manually segmented the fetal cerebellum using 7.0-T high-resolution MR images obtained in 35 specimens with gestational ages ranging from 15 to 22 weeks. Volume measurements and shape analysis were performed to quantitatively evaluate global and regional cerebellar growth. The absolute volume of the fetal cerebellum showed a quadratic growth with increasing gestational age, while the pattern of relative volume changes revealed that the cerebellum grew at a greater pace than the cerebrum after 17 gestational weeks. Shape analysis was used to examine the distinctive development of subregions of the cerebellum. The extreme lateral portions of both cerebellar hemispheres showed the lowest rate of growth. The anterior lobe grew faster than most of the posterior lobe. These findings expand our understanding of the early growth pattern of the human cerebellum and could be further used to assess the developmental conditions of the fetal brain." | ||
|- | |- |
Latest revision as of 11:45, 28 September 2020
2020 New References (Expand to see list) |
---|
Mark Hill (talk) 15:48, 8 January 2020 (AEDT) Added this new page to capture updated references added throughout the site in the "Some Recent Findings". Entries are listed alphabetically by topic page. Note that not all new references may be added to this current list. (More? New) |
birth weight | birth
|
blood | Template:Stem cell
|
cerebellum | second trimester
|
cortex
|
Fetal Alcohol Syndrome
|
fly | molecular
|
gestational diabetes | tooth
|
Hippo
|
limb | Hox
|
inner ear
|
malaria
|
mammary gland
|
menstrual cycle | hippocampus,
|
renal
|
somitogenesis | mesoderm
|
zebrafish
|
References |
|