نتایج جستجو برای: 4 man

تعداد نتایج: 1400498  

Journal: :Nature Reports Stem Cells 2007

Journal: :Stato, Chiese e Pluralismo Confessionale 2023

Constantine I The Great. Emperor, the man, leader
 ABSTRACT: History is not teacher of life, but perhaps reverse could be true if one looks at emblematic events and proceedings this interesting study conference, held University Bari from 17 to 18 November 2022, in which mysteries past are probed through eyes present. author reviews salient features figure Great as Man Commander reach perpl...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Ida Signe Bohse Larsen Yoshiki Narimatsu Hiren Jitendra Joshi Lina Siukstaite Oliver J Harrison Julia Brasch Kerry M Goodman Lars Hansen Lawrence Shapiro Barry Honig Sergey Y Vakhrushev Henrik Clausen Adnan Halim

The cadherin (cdh) superfamily of adhesion molecules carry O-linked mannose (O-Man) glycans at highly conserved sites localized to specific β-strands of their extracellular cdh (EC) domains. These O-Man glycans do not appear to be elongated like O-Man glycans found on α-dystroglycan (α-DG), and we recently demonstrated that initiation of cdh/protocadherin (pcdh) O-Man glycosylation is not depen...

Man

Journal: :Commonwealth 2022

This article examines the nature of will and its connection to representation in Hobbes's political philosophy. The argument is that notion willing not an empty formalism but hinges upon a dynamic fluid account human which informs sovereign subjects concerning dangers representing being represented. position taken stresses use metaphor stage his representation. In conclusion, advanced flawed by...

Journal: :acta medica iranica 0
v. tabibi h. khorsandi

two cases of advanced jaw destruction du e to act inomyces is mreported ; o ne with d iabetic d iathesis and a history o f too th ex tractio n the other had a t rauma o f the mandible wi th the fra cture; good results were obtained with penicillin thera py.

2011
Rita Lugovska

Phenylketonuria (PKU; OMIM 261600) is one of the most common inborn errors of metabolism in Caucasians, with a frequency of 1 : 10 000 newborns in Europe. It is an autosomal recessive trait caused by a deficiency of hepatic phenylalanine hydroxylase (PAH; 1 phenylalanine 4-monooxygenase, EC 1.14.16.1), the main clinical signs of which are impaired cognitive development and function (Eisensmith ...

Journal: :Bioinformatics 2005
Andrew C. R. Martin

MOTIVATION UniProtKB/SwissProt is the main resource for detailed annotations of protein sequences. This database provides a jumping-off point to many other resources through the links it provides. Among others, these include other primary databases, secondary databases, the Gene Ontology and OMIM. While a large number of links are provided to Protein Data Bank (PDB) files, obtaining a regularly...

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