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All mouse models of pulmonary hypertension with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | persistent fetal circulation syndrome | Foxf1em1Vvk/Foxf1+ | involves: C57BL/6 * DBA/2 | J:296328 | View | |||
| | persistent fetal circulation syndrome | Nos3tm1Unc/Nos3tm1Unc | B6.129P2-Nos3tm1Unc/J | J:98913 | View | |||
| persistent fetal circulation syndrome |
Ptentm1Hwu/Ptentm1Hwu Twist2tm1.1(cre)Dor/Twist2+ |
B6.129-Twist2tm1.1(cre)Dor Ptentm1Hwu | J:192736 | View | ||||
| pulmonary hypertension | Cavin1tm1Pfp/Cavin1tm1Pfp | B6.129S6-Cavin1tm1Pfp/J | J:217258 | View | ||||
| pulmonary venoocclusive disease | Aplnrtm1.1Path/Aplnrtm1.1Path | Not Specified | J:227456 | View | ||||
| pulmonary venoocclusive disease |
Aplnrtm1Path/Aplnrtm1Path Tg(Kdr-cre)#Brei/0 |
involves: C57BL/6 | J:227456 | View | ||||