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Literature DB >> 14206613

A SUGGESTED CONTROL GENE MECHANISM FOR THE EXCESSIVE PRODUCTION OF TYPES I AND 3 PORPHYRINS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA.

C J WATSON, W RUNGE, L TADDEINI, I BOSSENMAIER, R CARDINAL.

Abstract

Keywords: AMINOHYDROLASES; BONE MARROW CELLS; BONE MARROW EXAMINATION; CATTLE DISEASES; ERYTHROCYTES; ISOMERASES; MUTATION; PORPHYRIA; UROBILINOGEN

Mesh：

Substances：

Year: 1964 PMID： 14206613 PMCID： PMC300302 DOI： 10.1073/pnas.52.2.478

Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN： 0027-8424 Impact factor: 11.205

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31 in total

1. delta-aminolaevulate dehydratase from Rhodopseudomonas spheroides.

Authors: B F BURNHAM; W S PIERCE; K R WILLIAMS; M H BOYER; C K KIRBY
Journal: Biochem J Date: 1963-06 Impact factor: 3.857

2. ERYTHROPOIETIC PROTOPORPHYRIA. A NEW TYPE OF INBORN ERROR OF METABOLISM.

Authors: B HAEGER-ARONSEN
Journal: Am J Med Date: 1963-10 Impact factor: 4.965

3. Erythropoietic (congenital) porphyria: A rare abnormality of the normoblasts.

Authors: R SCHMID; S SCHWARTZ; R D SUNDBERG
Journal: Blood Date: 1955-05 Impact factor: 22.113

4. A qualitative and quantitative study of the separation of uroporphyrin octamethyl esters I and III by dioxan chromatography.

Authors: P A CORNFORD; A BENSON
Journal: J Chromatogr Date: 1963-02

5. Genetic regulatory mechanisms in the synthesis of proteins.

Authors: F JACOB; J MONOD
Journal: J Mol Biol Date: 1961-06 Impact factor: 5.469

6. A metabolic myopathy due to absence of muscle phosphorylase.

Authors: C M PEARSON; D G RIMER; W F MOMMAERTS
Journal: Am J Med Date: 1961-04 Impact factor: 4.965

7. Erythropoietic protoporphyria. A new porphyria syndrome with solar urticaria due to protoporphyrinaemia.

Authors: I A MAGNUS; A JARRETT; T A PRANKERD; C RIMINGTON
Journal: Lancet Date: 1961-08-26 Impact factor: 79.321

8. Porphyrin content of bone marrow and liver in the various forms of porphyria.

Authors: R SCHMID; S SCHWARTZ; C J WATSON
Journal: AMA Arch Intern Med Date: 1954-02

9. The manifestations of the different forms of porphyria in relation to chemical findings.

Authors: C J WATSON; P T LOWRY; R SCHMID; V E HAWKINSON; S SCHWARTZ
Journal: Trans Assoc Am Physicians Date: 1951

10. Photosensitive or congenital porphyria with hemolytic anemia. II. Isotopic studies of porphyrin and hemoglobin metabolism.

Authors: M GRINSTEIN; R A ALDRICH; V HAWKINSON; P LOWRY; C J WATSON
Journal: Blood Date: 1951-08 Impact factor: 22.113

14 in total

1. ACUTE INTERMITTENT PORPHYRIA: THE FIRST "OVERPRODUCTION DISEASE" LOCALIZED TO A SPECIFIC ENZYME.

Authors: D P TSCHUDY; M G PERLROTH; H S MARVER; A COLLINS; G HUNTER; M RECHCIGL
Journal: Proc Natl Acad Sci U S A Date: 1965-04 Impact factor: 11.205

Review 2. The porphyrias: a review.

Authors: G H Elder; C H Gray; D C Nicholson
Journal: J Clin Pathol Date: 1972-12 Impact factor: 3.411

A SUGGESTED CONTROL GENE MECHANISM FOR THE EXCESSIVE PRODUCTION OF TYPES I AND 3 PORPHYRINS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA.

1. delta-aminolaevulate dehydratase from Rhodopseudomonas spheroides.

2. ERYTHROPOIETIC PROTOPORPHYRIA. A NEW TYPE OF INBORN ERROR OF METABOLISM.

3. Erythropoietic (congenital) porphyria: A rare abnormality of the normoblasts.

4. A qualitative and quantitative study of the separation of uroporphyrin octamethyl esters I and III by dioxan chromatography.

5. Genetic regulatory mechanisms in the synthesis of proteins.

6. A metabolic myopathy due to absence of muscle phosphorylase.

7. Erythropoietic protoporphyria. A new porphyria syndrome with solar urticaria due to protoporphyrinaemia.

8. Porphyrin content of bone marrow and liver in the various forms of porphyria.

9. The manifestations of the different forms of porphyria in relation to chemical findings.

10. Photosensitive or congenital porphyria with hemolytic anemia. II. Isotopic studies of porphyrin and hemoglobin metabolism.

1. ACUTE INTERMITTENT PORPHYRIA: THE FIRST "OVERPRODUCTION DISEASE" LOCALIZED TO A SPECIFIC ENZYME.

Review 2. The porphyrias: a review.

3. [Enzyme determination in erythrocytes of patients with porphyria cutanea tarda].

Review 4. [Genetic aspects of metabolic disorders].

5. Uroporphyrinogen 3 cosynthetase in asymptomatic carriers of congenital erythpoietic porphyria.

6. Hepatic porphyrias.

7. Erythropoietic porphyria of the fox squirrel Sciurus niger.

8. Repression by hematin of porphyrin biosynthesis in erythrocyte precursors in congenital erythropoietic porphyria.

Review 9. Enzymatic defects of hereditary porphyrias: an explanation of dominance at the molecular level.

10. Presynaptic neuromuscular inhibition by porphobilinogen and porphobilin.