Matches in Nanopublications for { ?s ?p "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 12 of
12
with 100 items per page.
- assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655787.RArA4QV-dWTlNMsl6qefTzGMbFLJx3I1XUu7HNodkOJRI130_provenance.
- NP232750.RA-rMSQ2GJU0C8EpMdVSs6aRsnR31zRBwtPuHXS1vjxNI130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232750.RA-rMSQ2GJU0C8EpMdVSs6aRsnR31zRBwtPuHXS1vjxNI130_provenance.
- assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702469.RAg_wkXGNATNkGeqAGn3KlI5Xwkp6TaYHbj_5P1znYeMk130_provenance.
- NP343573.RAf6KaLCqKOG9DCK3b__OyTV4muFBBqutF4-VQAtO4lrI130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343573.RAf6KaLCqKOG9DCK3b__OyTV4muFBBqutF4-VQAtO4lrI130_provenance.
- NP222456.RA6HCdf9M7V18UizFF6XpOMI9qNbYhZTPX8c1bNjwa5zQ130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222456.RA6HCdf9M7V18UizFF6XpOMI9qNbYhZTPX8c1bNjwa5zQ130_provenance.
- NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- NP343569.RA1KMSMHOrY4FhHEXVyuHlOhBys3lm9z3t-9kvSz5A0-Q130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343569.RA1KMSMHOrY4FhHEXVyuHlOhBys3lm9z3t-9kvSz5A0-Q130_provenance.
- NP343571.RA8jaBas6rQEGVQU_TNroYjpz7cKi_A0YBkqg2-hp0E5o130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343571.RA8jaBas6rQEGVQU_TNroYjpz7cKi_A0YBkqg2-hp0E5o130_provenance.