G. Rodgers

发表

Hemin-induced acceleration of hemoglobin production in immature cultured erythroid cells: preferential enhancement of fetal hemoglobin.

A. Schechter, P. Kollia, C. Noguchi, 1995, Blood.

Color vision defects in sickle cell anemia.

R. Gunkel, M. Roy, C. Noguchi, 1987, Archives of ophthalmology.

Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E disease.

A. Schechter, S. Fucharoen, N. Poolsup, 1996, Blood.

Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease.

A. Schechter, J. Jais, C. Noguchi, 1994, Blood.

Enhanced fetal hemoglobin production by phenylacetate and 4- phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and beta-thalassemia

D. Samid, E. Fibach, G. Rodgers, 1993 .

Enhanced fetal hemoglobin production by phenylacetate and 4-phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and beta-thalassemia.

D. Samid, E. Fibach, G. Rodgers, 1993, Blood.

Olfactomedin 4 deletion induces colon adenocarcinoma in ApcMin/+ mice

G. Piszczek, Hongchuan Li, H. Li, 2016, Oncogene.

Expression of hGC‐1 is correlated with differentiation of gastric carcinoma

G. Rodgers, L. Cao, W. Liu, 2007, Histopathology.

OLFM4 (olfactomedin 4)

W. Liu, G. Rodgers, 2011 .

Recombinant erythropoietin improves the anemia associated with Gaucher's disease.

L. Lessin, G. Rodgers, 1989, Blood.