DI GIULIO, MASSIMO
 Distribuzione geografica
Continente #
AS - Asia 1.364
NA - Nord America 853
SA - Sud America 288
EU - Europa 176
AF - Africa 30
OC - Oceania 2
Totale 2.713
Nazione #
US - Stati Uniti d'America 833
SG - Singapore 680
CN - Cina 268
BR - Brasile 231
HK - Hong Kong 160
VN - Vietnam 92
FR - Francia 82
KR - Corea 62
NL - Olanda 30
IT - Italia 21
AR - Argentina 19
JP - Giappone 15
ID - Indonesia 14
IN - India 13
EC - Ecuador 11
ZA - Sudafrica 11
BD - Bangladesh 10
CA - Canada 9
DE - Germania 9
GB - Regno Unito 9
CL - Cile 8
IL - Israele 8
TR - Turchia 7
MX - Messico 6
CO - Colombia 5
FI - Finlandia 5
PY - Paraguay 5
KE - Kenya 4
PK - Pakistan 4
PL - Polonia 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
PE - Perù 3
RU - Federazione Russa 3
SA - Arabia Saudita 3
UA - Ucraina 3
UY - Uruguay 3
DZ - Algeria 2
ET - Etiopia 2
IQ - Iraq 2
JO - Giordania 2
LB - Libano 2
LK - Sri Lanka 2
MA - Marocco 2
PS - Palestinian Territory 2
SN - Senegal 2
TN - Tunisia 2
VE - Venezuela 2
AM - Armenia 1
AT - Austria 1
AU - Australia 1
AZ - Azerbaigian 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BW - Botswana 1
CH - Svizzera 1
CY - Cipro 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
EG - Egitto 1
ES - Italia 1
HN - Honduras 1
HR - Croazia 1
IE - Irlanda 1
JM - Giamaica 1
KG - Kirghizistan 1
KZ - Kazakistan 1
ML - Mali 1
MN - Mongolia 1
MU - Mauritius 1
MY - Malesia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PH - Filippine 1
PR - Porto Rico 1
PT - Portogallo 1
QA - Qatar 1
SE - Svezia 1
SK - Slovacchia (Repubblica Slovacca) 1
SR - Suriname 1
Totale 2.713
Città #
Santa Clara 543
Singapore 402
Hong Kong 158
Hefei 128
Lauterbourg 77
Seoul 59
San Jose 53
Ashburn 47
Ho Chi Minh City 39
Beijing 26
Los Angeles 26
São Paulo 19
Buffalo 18
Hanoi 16
Minamishinagawa 8
New York 8
Rio de Janeiro 7
Dallas 6
Dhaka 5
Helsinki 5
Johannesburg 5
Thái Bình 5
Bengaluru 4
Brasília 4
Curitiba 4
Frankfurt am Main 4
Goiânia 4
Guayaquil 4
Jakarta 4
Nairobi 4
Santiago 4
Tokyo 4
Asunción 3
Belo Horizonte 3
Cape Town 3
Da Nang 3
Guangzhou 3
Hyderabad 3
Hải Dương 3
Ourinhos 3
Phoenix 3
Pittsburgh 3
Porto Alegre 3
Salvador 3
Shanghai 3
Surabaya 3
Tashkent 3
Vitória da Conquista 3
Addis Ababa 2
Amman 2
Anápolis 2
Aparecida de Goiânia 2
Bauru 2
Bắc Ninh 2
Cambridge 2
Campinas 2
Campos dos Goytacazes 2
Chapecó 2
City of Industry 2
Conselheiro Lafaiete 2
Dakar 2
Detroit 2
Duque de Caxias 2
Elk Grove Village 2
Erbil 2
Formosa 2
Fort Wayne 2
Gravataí 2
Guarulhos 2
Hicksville 2
Istanbul 2
Itu 2
Ituiutaba 2
Jacareí 2
Jeddah 2
Jundiaí 2
Lima 2
Maricá 2
Mexico City 2
Mogi das Cruzes 2
Montevideo 2
Nanjing 2
New Orleans 2
Newark 2
Orem 2
Osaka 2
Pará de Minas 2
Philadelphia 2
Piracicaba 2
Quito 2
Quảng Ngãi 2
Sebokeng 2
Shenzhen 2
Shijiazhuang 2
Sorocaba 2
São Gonçalo 2
São José 2
Talcahuano 2
Warsaw 2
Abu Dhabi 1
Totale 1.851
Nome #
The universal ancestor and the ancestors of Archaea and Bacteria were anaerobes whereas the ancestor of the Eukarya domain was an aerobe. 66
The extension reached by the minimization of the polarity distances during the evolution of the genetic code 65
An extension of the coevolution theory of the origin of the genetic code 62
Formal Proof that the Split Genes of tRNAs of Nanoarchaeum equitans Are an Ancestral Character. 60
The origin of protein synthesis: on some molecular fossils identified through comparison of protein sequences 47
The evolution of the genetic code took place in an anaerobic environment. 47
Some aspects of the organization and evolution of the genetic code 45
RNA editing and modifications of RNAs might have favoured the evolution of the triplet genetic code from an ennuplet code 39
An Autotrophic Origin for the Coded Amino Acids is Concordant with the Coevolution Theory of the Genetic Code. 38
On the origin of protein synthesis: a speculative model based on hairpin RNA structures 37
A polyphyletic model for the origin of tRNAs has more support than a monophyletic model. 37
A model of the origin of the 5S ribosomal RNA molecule. 37
The Last Universal Common Ancestor (LUCA) and the Ancestors of Archaea and Bacteria were Progenotes 37
The origin of the genetic code: matter of metabolism or physicochemical determinism? 37
tRNA creation by hairpin duplication 36
The origin of the tRNA molecule: Independent data favor a specific model of its evolution. 36
A Model for the Origin of the First mRNAs 36
The Non-Biological Meaning of the Term "Prokaryote" and Its Implications 36
On Earth, there would be a number of fundamental kinds of primary cells - cellular domains - greater than or equal to four 35
The phylogeny of tRNA molecules and the origin of the genetic code 34
The Origin of the 5S Ribosomal RNA Molecule Could Have Been Caused by a Single Inverse Duplication: Strong Evidence from Its Sequences 34
A novel three-unit tRNA splicing endonuclease found in ultrasmall Archaea possesses broad substrate specificity. 34
Progenote 33
The robust statistical bases of the coevolution theory of genetic code origin 33
Biological evidence against the panspermia theory. 33
A comparison among the models proposed to explain the origin of the tRNA molecule: A synthesis. 33
Structuring of the genetic code took place at acidic pH 32
The 'recently' split transfer RNA genes may be close to merging the two halves of the tRNA rather than having just separated them 32
The level and landscape of optimization in the origin of the genetic code 32
., Was it an ancient gene codifyng for a hairpin RNA that, by means of direct duplication, gave rise to the primitive tRNA molecule? 32
The genetic code is not an optimal code in a model taking into account both the biosynthetic relationships between amino acids and their physicochemical properties 32
The coevolution theory of the origin of the genetic code 31
Why the Genetic Code Originated. Implications for the origin of protein synthesis 31
The lack of foundation in the mechanism on which are based the physico-chemical theories for the origin of the genetic code is counterposed to the credible and natural mechanism suggested by the coevolution theory 31
Genetic code origin: are the pathways of type Glu-trnagln->Gln-trnagln molecular fossils or not? 31
The ancestor of the Bacteria domain was a hyperthermophile . 30
The non-universality of the genetic code: The universal ancestor was a progenote 30
On the optimization of the physicochemical distances between amino acids in the evolution of the genetic code 30
The Presence in tRNA Molecule Sequences of the Double Hairpin, an Evolutionary Stage Through Which the Origin of this Molecule is Thought to have Passed 30
Transfer RNA genes in pieces are an ancestral character 30
Research on the origin of life. Introduction 29
Physicochemical optimization in the genetic code origin as the number of codified amino acids increases 29
The tree of life might be rooted in the branch leading to Nanoarchaeota 28
The origin of the genetic code in the ocean abysses: new comparisons confirm old observations 28
THE HISTORICAL FACTOR - THE BIOSYNTHETIC RELATIONSHIPS BETWEEN AMINO-ACIDS AND THEIR PHYSICOCHEMICAL PROPERTIES IN THE ORIGIN OF THE GENETIC-CODE 28
The non-monophyletic origin of the tRNA molecule and the origin of genes only after the evolutionary stage of the last universal common ancestor (LUCA) 28
On the origin of the genetic code 27
The ?-sheets of proteins, the biosynthetic relationships between amino acids, and the origin of the genetic code 27
The origin of the tRNA molecule: implications for the origin of protein synthesis 27
Origin of glutaminyl-tRNA synthetase: an example of palimpsest? 26
Split genes, ancestral genes 26
Nanoarchaeum equitans is a living fossil 26
The RNA world, the genetic code and the tRNA molecule 26
Genetic code origin and the strength of natural selection 26
The origin of the genetic code: theories and their relationships, a review 25
The universal ancestor and the ancestor of Bacteria were hyperthermophiles . 25
The origin of the genetic code cannot be studied using measurements based on the PAM matrix because this matrix reflects the code itself, making any such analyses tautologous 25
The evolution of aminoacyl-tRNA synthetases, the biosynthetic pathways of amino acids and the genetic code 25
A methanogen hosted the origin of the genetic code. 25
Reflections on the origin of the genetic code: a hypothesis 25
The evidence that the tree of life is not rooted within the Archaea is unreliable: a reply to Skophammer et al. 25
on the optimization of the physicochemical distances between amino acids in the evolution of the genetic code 25
The origin of the genetic code. 25
The universal ancestor was a thermophile or a hyperthermophile 24
On the origin of the transfer RNA molecule 24
Second codon positions of genes and the secondary structures of proteins. Relationships and implications for the origin of the genetic code 24
The early phases of genetic code origin: conjectures on the evolution of coded catalysis. 24
A comparison of proteins from Pyrococcus furiosus and Pyrococcus abyssi: barophily in the physicochemical properties of amino acids and in the genetic code 24
The non-monophyletic origin of the tRNA molecule 24
The historical factor: the biosynthetic relationships between amino acids, and the optimization of their physicochemical properties in the origin of the genetic code 23
Physicochemical optimization in the genetic code origin as the number of codified amino acids increases 23
The origin of the genetic code 23
The ocean abysses witnessed the origin of the genetic code 23
A blind empiricism against the coevolution theory of the origin of the genetic code 23
On the relationships between the genetic code coevolution hypothesis and the physicochemical hypothesis 22
The close relationship between the biosynthetic families of amino acids and the organisation of the genetic code 22
The split genes of Nanoarchaeum equitans are an ancestral character 22
On the RNA world: evidence in favour of an early ribonucleopeptide world 22
Molecular parasitism in the E.coli-Bdellovibrio bacteriovorus system: translocation of the matrix protein from the host to the parassite outer membrane 22
The origin of genes could be polyphyletic 22
Permuted tRNA genes of Cyanidioschyzon merolae, the origin of the tRNA molecule and the root of the Eukarya domain 21
The Universal Ancestor Lived in a Thermophilic or hyperthermophilic environment 21
The universal ancestor was a thermophile or a hyperthermophile: tests and further evidence . 21
The basal phylogenetic position of Nanoarchaeum equitans (Nanoarchaeota) 21
Absorbent Markov chains as a model for the study of the evolution of proteins 20
On the origin of the genetic code 20
The phylogeny of tRNAs seems to confirm the predictions of the coevolution theory of the origin of the genetic code 19
The robust statistical bases of the coevolution theory of genetic code origin 19
., The late stage of genetic code structuring took place at a high temperature 18
The first lines of divergence in the Bacteria domain were the hyperthermophilic organisms, the Thermotogales and the Aquificales, and not the mesophilic Planctomycetales 18
The coevolution theory of the origin of the genetic code 17
Totale 2.713
Categoria #
all - tutte 8.522
article - articoli 8.220
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 302
Totale 17.044


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/20251.267 0 4 86 47 544 2 1 32 3 28 276 244
2025/20261.446 65 146 129 251 305 36 262 101 63 55 33 0
Totale 2.713