Mukowiscydoza rozpoznana u 36-letniego chorego.
Majka L, Witt M, Młynarczyk W, Nowicka A, Rutkiewicz E;
Pneumonol Alergol Pol, 2004; 72: 211-213.
Publications
Publikacje pracowników w ePub
The sequence variant of NOD2/CARD 15 in a Polish family on the background of Polish patients with Crohn's disease.
Dobrowolska-Zachwieja A, Kaczmarek M, Hoppe-Gołębiewska J, Słomski R;
Gastroenterolo Pol, 2004, 11 (4): 325-331.
The influence of the NOD2/CARD15 gene mutation variant on the incidence of extrainstestinal symptoms in patients with Crohn's disease in a Polish population.
Dobrowolska-Zachwieja A, Kaczmarek M, Hoppe-Gołębiewska J, Kalak R, Słomski R, Linke K;
Now Lek, 2004, 73 (5): 337-348.
The normotensive carriers of the MTHFR 677T allele, displaying the increased risk of development of the abdominal aortic aneurysm (AAA), occur at the highest frequency among the smoking patients.
Strauss E, Waliszewski K, Pawlak AL;
Prz Lek. 2004; 61 (10): 1086-1089.
Controversial aspect of using GFP as a marker for the production of transgenic cattle.
Duszewska AM, Lipiński D, Piliszek A, Słomski R, Pławski A, Wojdan J, Gawron W, Juzwa W, Zeyland J, Wenta-Muchalska E, Reklewski Z;
Pol J Vet Sci, 2004, 7 (4): 24124-9.
Assessment of transgene inheritance and transgene mapping in rabbits producing the human growth hormone in milk.
Kalak R, Lipiński D, Wielgus K, Jarmuż M, Jura J, Szalata M, Michalak M, Pławski A, Kaczmarek M, Nuc K, Korcz A, Gronek P, Smorąg Z, Pienkowski M, Słomski R;
Ann Anim Sc, 2004, 4; 241-252.
Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
Ballif BC, Wakui K, Gajęcka M, Shaffer LG;
Hum Genet, 2004, 114 (2): 196-206.
Rola bakterii Streptococcus mutans w patogenezie próchnicy.
Zandecka-Dziubak J, Tomaszewska M, Lipiński D, Mrozikiewicz PM;
Herba Polonica, 2004, 50 (2): 95-110.
Overexpression of gtfB gene fragments from Streptococcus mutans encoding Glu and Cat domains in Escherichia coli.
Lipiński D, Zandecka-Dziubak J, Juzwa W, Zeyland J, Mrozikiewicz PM, Słomski R;
Herba Polonica, 2004, 50 (2): 78-83.
Zmiany polimorficzne w genie CFTR a wrodzony obustronny brak nasieniowodów (CBAVD).
Kaczmarek M, Rutkiewicz E, Jędrzejczak P, Pawelczyk L, Witt M;
Pol Prz Nauk Zdr, 2004, 4: 78-83.