TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism

2007 ◽  
Vol 30 (1) ◽  
pp. 13-19 ◽  
Author(s):  
L. Santarpia ◽  
M. Valenzise ◽  
G. Di Pasquale ◽  
T. Arrigo ◽  
G. San Martino ◽  
...  
Keyword(s):  
Congenital Hypothyroidism ◽  
Gene Polymorphisms ◽  
Foxe1 Gene

scholarly journals Network-Based Analysis Reveals Association of FOXE1 Gene Polymorphisms in Thyroid Cancer Patients; A Case-Control Study in Southeast of Iran

2020 ◽  
Vol 21 (9) ◽  
pp. 2771-2776
Author(s):  
Ahmad Mehrazin ◽  
Hossein Safarpour ◽  
Seyedeh Tahmineh Davoudi ◽  
Negin Parsamanesh ◽  
Farhad Saeedi ◽  
...  
Keyword(s):  
Thyroid Cancer ◽  
Cancer Patients ◽  
Gene Polymorphisms ◽  
Case Control Study ◽  
Case Control ◽  
Control Study ◽  
Foxe1 Gene

Mannan-binding lectin gene polymorphisms in ulcerative colitis and Crohn's disease

2001 ◽  
Vol 120 (5) ◽  
pp. A459-A459
Author(s):  
A RECTOR ◽  
P LEMEY ◽  
W LAFFUT ◽  
E KEYAERTS ◽  
F STRUYF ◽  
...  
Keyword(s):  
Ulcerative Colitis ◽  
Crohn’S Disease ◽  
Crohn's Disease ◽  
Gene Polymorphisms ◽  
Lectin Gene ◽  
Mannan Binding Lectin ◽  
Binding Lectin

Influence of pepsinogen gene polymorphisms on serum pepsinogen

1997 ◽  
Vol 61 (2) ◽  
pp. 93-97 ◽  
Author(s):  
Z. YAMAGATA ◽  
Y. ZHANG ◽  
S. SHINOZAKI ◽  
T. MIYAMURA ◽  
S. IIJIMA ◽  
...  
Keyword(s):  
Gene Polymorphisms ◽  
Serum Pepsinogen
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