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Urate‐induced immune programming: Consequences for gouty arthritis and hyperuricemia
Georgiana Cabău,
T. Crișan,
V. Klück,
R. Popp,
L. Joosten
|
7 |
2019 |
7 🐬
|
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Convergent evolution in European and Rroma populations reveals pressure exerted by plague on Toll-like receptors
18 auth.
H. Laayouni,
M. Oosting,
P. Luisi,
M. Ioana,
S. Alonso,
I. Ricaño-Ponce,
G. Trynka,
A. Zhernakova,
T. Plantinga,
Shih-Chin Cheng,
...
J. V. D. van der Meer,
R. Popp,
A. Sood,
B. K. Thelma,
C. Wijmenga,
L. Joosten,
J. Bertranpetit,
M. Netea
|
6 |
2014 |
6 🐜
|
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Genetic determination of irritable bowel syndrome.
C. Hoţoleanu,
R. Popp,
A. Trifa,
L. Nedelcu,
D. Dumitrascu
|
5 |
2008 |
5 🐬
|
🐢
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MECOM, HBS1L‐MYB, THRB‐RARB, JAK2, and TERT polymorphisms defining the genetic predisposition to myeloproliferative neoplasms: A study on 939 patients
31 auth.
A. Trifa,
C. Bănescu,
A. Bojan,
Cristian M Voina,
S. Popa,
Simona Vișan,
A. Ciubean,
F. Tripon,
D. Dima,
V. Popov,
Ș. Vesa,
M. Andreescu,
Tünde Török-Vistai,
R. Mihaila,
Nicoleta P. Berbec,
...
I. Macarie,
A. Colita,
M. Iordache,
A. Cătană,
M. Farcas,
C. Tomuleasa,
K. Vasile,
C. Truica,
Adriana Todincă,
Lavinia Pop-Muntean,
R. Manolache,
H. Bumbea,
A. Vlădăreanu,
M. Găman,
C. Ciufu,
R. Popp
|
5 |
2018 |
5 🐢
|
🐢
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TERT rs2736100 A>C SNP and JAK2 46/1 haplotype significantly contribute to the occurrence of JAK2 V617F and CALR mutated myeloproliferative neoplasms – a multicentric study on 529 patients
25 auth.
A. Trifa,
C. Bănescu,
Mihaela Tevet,
A. Bojan,
D. Dima,
L. Urian,
Tünde Török-Vistai,
V. Popov,
M. Zdrenghea,
L. Petrov,
A. Vasilache,
Meilin Murat,
D. Georgescu,
M. Popescu,
O. Pătrinoiu,
...
M. Balea,
R. Costache,
E. Coleș,
C. Saguna,
Nicoleta P. Berbec,
A. Vlădăreanu,
R. Mihaila,
H. Bumbea,
A. Cucuianu,
R. Popp
|
5 |
2016 |
5 🐢
|
🐢
|
The G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms
8 auth.
A. Trifa,
A. Cucuianu,
L. Petrov,
L. Urian,
M. Militaru,
D. Dima,
...
I. Pop,
R. Popp
|
5 |
2010 |
5 🐢
|
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Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania.
9 auth.
C. Lazar,
R. Popp,
A. Trifa,
C. Mocanu,
G. Mihuț,
C. Al-Khzouz,
...
E. Tomescu,
I. Figan,
P. grigorescu-sido
|
4 |
2010 |
4 🐜
|
🐬
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The Role of Oxidative Stress and Vascular Insufficiency in Primary Open Angle Glaucoma
A. Ster,
R. Popp,
F. Petrişor,
C. Stan,
V. Pop
|
4 |
2014 |
4 🐬
|