Angiotensin II stimulates proliferation of normal early erythroid progenitors.

Por Mrug, M, Stopka, T, Julian, B A, Prchal, J F, Prchal, J T
Publicado em 1997

Oral "hairy" leukoplakia: a clue to HIV-I exposure.

Por Dylewski, J, Prchal, J
Publicado em 1987

Rapid determination of clonality by detection of two closely-linked X chromosome exonic polymorphisms using allele-specific PCR.

Por Liu, Y, Phelan, J, Go, R C, Prchal, J F, Prchal, J T
Publicado em 1997

RFLP of the X chromosome-linked glucose-6-phosphate dehydrogenase locus in blacks.

Por Yoshida, A, Takizawa, T, Prchal, J T
Publicado em 1988

Defective spectrin dimer-dimer association with hereditary elliptocytosis.

Por Liu, S C, Palek, J, Prchal, J T
Publicado em 1982

Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia.

Por Kralovics, R, Sokol, L, Prchal, J T
Publicado em 1998

Persistent generalized lymphadenopathy in homosexual men: clinical, pathological and immunologic characteristics.

Por Gilmore, N. J., Prchal, J. F., Jothy, S.
Publicado em 1983

Hemoglobin Long Island is caused by a single mutation (adenine to cytosine) resulting in a failure to cleave amino-terminal methionine.

Por Prchal, J T, Cashman, D P, Kan, Y W
Publicado em 1986

A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.

Por Lawler, J, Liu, S C, Palek, J, Prchal, J
Publicado em 1984

Decreased population of Leu-7+ natural killer cells in lymph nodes of homosexual men with AIDS-related persistent lymphadenopathy.

Por Jothy, S, Gilmore, N, El'Gabalawy, H, Prchal, J
Publicado em 1985

Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.

Por Hittner, H M, Carroll, A J, Prchal, J T
Publicado em 1982

Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.

Por Liu, S C, Palek, J, Prchal, J, Castleberry, R P
Publicado em 1981

The origin of glucose-6-phosphate-dehydrogenase (G6PD) polymorphisms in African-Americans.

Por Kay, A C, Kuhl, W, Prchal, J, Beutler, E
Publicado em 1992

Pure red cell aplasia with an inhibitor to erythropoiesis.

Por Seidenfeld, A M, Owen, J, Prchal, J F, Glynn, M F
Publicado em 1979

Polycythemia vera. The in vitro response of normal and abnormal stem cell lines to erythropoietin.

Por Prchal, J F, Adamson, J W, Murphy, S, Steinmann, L, Fialkow, P J
Publicado em 1978

Presence of J chain in human lymphoid cells.

Por Mestecky, J, Preud'homme, J L, Crago, S S, Mihaesco, E, Prchal, J T, Okos, A J
Publicado em 1980

Hb Long Island: a hemoglobin variant with a methionyl extension at the NH2 terminus and a prolyl substitution for the normal histidyl residue 2 of the beta chain.

Por Barwick, R C, Jones, R T, Head, C G, Shih, M F, Prchal, J T, Shih, D T
Publicado em 1985

Clonal hematopoiesis and acquired thalassemia in common variable immunodeficiency.

Por Belickova, M., Schroeder, H. W., Guan, Y. L., Brierre, J., Berney, S., Cooper, M. D., Prchal, J. T.
Publicado em 1994

Isolation and characterization of cDNA clones for human erythrocyte beta-spectrin.

Por Prchal, J T, Morley, B J, Yoon, S H, Coetzer, T L, Palek, J, Conboy, J G, Kan, Y W
Publicado em 1987

Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.

Por Coetzer, T L, Sahr, K, Prchal, J, Blacklock, H, Peterson, L, Koler, R, Doyle, J, Manaster, J, Palek, J
Publicado em 1991