Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP430980.RARh5Q9tg7317h8TMbV_HgpC7SXpKzKilVCCqsw9BJiiE130_assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430980.RARh5Q9tg7317h8TMbV_HgpC7SXpKzKilVCCqsw9BJiiE130_provenance.
• NP843749.RAT54FSJdDN6hOsKumch4dBMXglls32lK82YedT4g4J2o130_assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843749.RAT54FSJdDN6hOsKumch4dBMXglls32lK82YedT4g4J2o130_provenance.
• NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843766.RAXyguL3YVoX45PRES1nHiZqBOAC9H0RNk9P3QJUjY_Tc130_provenance.
• assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP745202.RAvoaWUtfCgWwhbjrZJPko-13IW48ZKEcTP7EC8Wh-ZW8130_assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745202.RAvoaWUtfCgWwhbjrZJPko-13IW48ZKEcTP7EC8Wh-ZW8130_provenance.
• NP745201.RA7YZSV4DKYrrKstSTt4K3z6ZIPnW2QU65COxQGjDWy7M130_assertion description "[Recent studies have shown that homozygous mutations in the HAX1 gene are associated with autosomal recessive forms of severe congenital neutropenia (also known as Kostmann disease), and results from studies in mice and men are beginning to unravel a prominent role for HAX-1 in apoptosis signaling not only in the hematopoietic compartment, but also in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745201.RA7YZSV4DKYrrKstSTt4K3z6ZIPnW2QU65COxQGjDWy7M130_provenance.