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Alba Luengo Zhaoqi Li Dan Y. Gui Lucas B. Sullivan Maria Zagorulya Brian T. Do Raphael Ferreira Adi Naamati Ahmed Ali Caroline A. Lewis Craig J. Thomas Stefani Spranger Nicholas J. Matheson Matthew G. Vander Heiden 《Molecular cell》2021,81(4):691-707.e6
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Heidi Weberru? Raphael Pirzer Robert Dalla Pozza Heinrich Netz Renate Oberhoffer 《PloS one》2016,11(3)
Carotid intima-media thickness (cIMT) is a surrogate marker of early atherosclerotic changes in children. cIMT-studies are hard to compare, due to variations in ultrasound protocols, especially regarding the common carotid artery (CCA) segment measured in relation to the bulb. This study’s purpose was therefore to compare two distinct CCA segments in children, to see if cIMT values differ substantially according to the site of measurement. cIMT was assessed after power calculation in 30 children (15 girls) aged 8–17, using B-Mode ultrasound (5–13 MHz) at two CCA locations. The first measurement was performed over a distance of 1 cm immediately after the bulb (A), the second 1cm proximal the bulb (B) over the same distance of 1cm length. Means of end-diastolic far wall cIMT were compared between measurement A and B. cIMT in 30 participants was 0.51±0.06 mm for measurement A and 0.51±0.05 mm for measurement B. Results did not differ significantly (p = .947) over a distance of 2 cm after the bulb. According to our results, studies measuring CCA IMT within the first 2 cm, either close to the bulb or further proximal, can be compared. This will improve interpretation of data and application of reference values. 相似文献
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Keven D. Juaire Karine Lapouge Matthias M.M. Becker Irina Kotova Michelle Michelhans Raphael Carapito Klemens Wild Seiamak Bahram Irmgard Sinning 《Structure (London, England : 1993)》2021,29(1):15-28.e7
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Raphael Chijioke Njoku 《Dialectical Anthropology》2007,31(1-3):45-64
It is difficult to completely understand the life history of an intellectual excluding an understanding of his family upbringing
and formative years. Family upbringing and childhood environment, often the less known part of a life history, play crucial
roles in shaping the ideas and values individuals espouse in their adult life. Notwithstanding, this paper is not concerned
with Don C. Ohadike’s childhood. It rather focuses on the professional career of our able historian – that is the part of
his life as revealed by his most outstanding published writings. Ohadike’s published works contain a wellspring of idioms
that tell much about his values, quality of mind, and his mission as an African historian. Ohadike was a humanist, an African
patriot, and a nationalist crusader. His entire philosophy centered on safeguarding his African identity in an emergent world
of cultural imperialism.
The funds for this research were provided by a NEH-funded fellowship at the Schomburg Center, New York in the Spring of 2007.
I owe a lot of gratitude to Professor John McLeod and Dean Blaine Hudson for granting me the extra incentives to pursue my
research in New York. While all errors and misinterpretations are mine, I wish to thank the editors and anonymous reviewers
for Journal of Dialectical Anthropology for their perspective comments and suggestions on earlier drafts of this paper. 相似文献
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Peter Hechtman Bernard Boulay Marc De Braekeleer Eve Andermann Serge Melançon Jean Larochelle Claude Prevost Feige Kaplan 《Human genetics》1992,90(4):402-406
Mutations at the hexosaminidase A (HEXA) gene which cause Tay-Sachs disease (TSD) have elevated frequency in the Ashkenazi Jewish and French-Canadian populations. We report a novel TSD allele in the French-Canadian population associated with the infantile form of the disease. The mutation, a GA transition at the +1 position of intron 7, abolishes the donor splice site. Cultured human fibroblasts from a compound heterozygote for this transition (and for a deletion mutation) produce no detectable HEXA mRNA. The intron 7+1 mutation occurs in the base adjacent to the site of the adult-onset TSD mutation (G805A). In both mutations a restriction site for the endonuclease EcoRII is abolished. Unambiguous diagnosis, therefore, requires allele-specific oligonucleotide hybridization to distinguish between these two mutant alleles. The intron 7+1 mutation has been detected in three unrelated families. Obligate heterozygotes for the intron 7+1 mutation were born in the Saguenay-Lac-St-Jean region of Quebec. The most recent ancestors common to obligate carriers of this mutation were from the Charlevoix region of the province of Quebec. This mutation thus has a different geographic centre of diffusion and is probably less common than the exon 1 deletion TSD mutation in French Canadians. Neither mutation has been detected in France, the ancestral homeland of French Canada. 相似文献