(Q42240030)

English

Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia

scientific article published on January 1966

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scholarly article

1 reference

Europe PubMed Central

19 October 2017

Cytogenetische und cytologische Befunde bei enzymopenischen Panmyelopathien und Pancytopenien (German)

reason for deprecated rank

marking inconsistent with the registered/official identifier/name

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia (English)

reason for deprecated rank

marking inconsistent with the registered/official identifier/name

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5984971

19 July 2023

deficiency anemia

1 reference

based on heuristic

inferred from title

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

author name string

T. M. Schroeder

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5984971

19 July 2023

language of work or name

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5984971

19 July 2023

publication date

1 January 1966

1 reference

Europe PubMed Central

19 October 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00395947.pdf

Portable Document Format

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

http://link.springer.com/article/10.1007/BF00395947/fulltext.html

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

http://link.springer.com/content/pdf/10.1007/BF00395947

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

1 reference

Europe PubMed Central

19 October 2017

2

1 reference

Europe PubMed Central

19 October 2017

287-316

1 reference

Europe PubMed Central

19 October 2017

3

1 reference

Europe PubMed Central

19 October 2017

[STUDIES ON HEMOLYSIS IN FANCONI'S ANEMIA. INCREASE OF ATP-ASE AS A POSSIBLE CAUSE FOR DECEASED ATP VALUES.]

1 reference

https://api.crossref.org/works/10.1007%2FBF00395947

21 January 2018

[Cytogenetic research in pernicious anemia after treatment.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Cytophotometric determination of protein-bound thiols in mitosis & interphase of HeLa cells]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synchronous divisions in Tetrahymena pyriformis as studied in an inorganic medium; the effect of 2,4-dinitrophenol

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[THE SIGNIFICANCE OF FOLIC ACID AND VITAMIN B 12 FOR CELLULAR METABOLISM]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[METABOLIC INVESTIGATION OF HUMAN WHITE BLOOD CELLS. 3. ON THE CAUSES OF ENZYME LOSS FROM THE CELLS]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glutathione reductase deficiency with hematological and neurologic disorders. (Autosomal dominant hereditary formation of a pathological enzyme)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosal fragility in familial panmyelopathy (Fanconi type)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of spontaneous recurrent chromosome breakage in an untreated human tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal Mitotic Activity and Karyotype of Leucocytes from Pernicious Anæmia Patients cultured in Vitamin B12-deficient Medium

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[On different molecular mechanisms in the movement of cells.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interpretation of chromosome counts made on bone-marrow cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on sulfhydryl groups during cell division of sea urchin egg. I. Glutatione

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibition of Formation of Adenosine Triphosphate in Thiobacillus thioparus by 2 : 4-Dinitrophenol

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[On hexokinase in human blood cells]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome Abnormalities in Constitutional Aplastic Anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The significance of adenosinetriphosphate in cell division and nuclear division in anaphase]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[STUDIES OF METABOLIC PROCESSES IN WHITE BLOOD CELLS. II. ON THE PROBLEM OF ENZYME INDUCTION IN METABOLIC CHANGES: ENZYME PATTERNS IN DIABETES MELLITUS, UNDER VARIOUS NUTRITIONAL CONDITIONS AND UNDER THE INFLUENCE OF HORMONAL FACTORS]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The control of cell division; a review. I. General mechanisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHROMOSOMAL ABERRATIONS IN PERNICIOUS ANEMIA. STUDY OF THREE CASES BEFORE AND AFTER THERAPY

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-ray-induced chromosome damage in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical defects in the blood cells in familial panmyelopathy (Fanconi type)

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[STUDIES OF METABOLIC PROCESSES IN HUMAN WHITE BLOOD CELLS. I. ENZYME PATTERNS OF WHITE BLOOD CELLS IN NORMAL SUBJECTS]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Cytogenetic research in blood diseases: observations on the chromosomes in untreated pernicious anemia. I. Numerical changes.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship of pancytopenia to megaloblastic anemias; report of seven cases clinically confused with blood dyscrasias and subacute bacterial endocarditis

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple forms of hexokinase in the rat: tissue distribution, age dependency, and properties

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of leukemia in families of patients with hypoplasia of the marrow

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital telangiectatic erythema resembling lupus erythematosus in dwarfs; probably a syndrome entity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[On the effects of trenimon and endoxan on meiosis in male mice. I. Method of preparation and analysis of meiotic divisions].

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ACTION OF SULFHYDRYL COMPOUNDS ON HUMAN LEUKOCYTE MITOSIS IN VITRO

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Cytogenetic research in blood diseases: observations on the chromosomes in untreated pernicious anemia. II. Morphological changes.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome preparations of leukocytes cultured from human peripheral blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi anemia in an adult

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous chromosome aberrations in familial panmyelopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Chromosomal aberrations and their clinical significance.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[THE ENZYMOPENIC ERYTHROPATHIES.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the preservation of blood. V. The influence of the hydrogen ion concentration on certain changes in blood during storage

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN

1 reference

https://pubmed.ncbi.nlm.nih.gov/5984971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bollettino della Societa italiana di biologia sperimentale

1

38

111

author name string

G. Astaldi

publication date

1962

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

Bollettino della Societa italiana di biologia sperimentale

2

38

114

author name string

G. Astaldi

publication date

1962

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

[Biochemistry and pathogenesis of enzyme-deficiency hemolytic anemias]

31

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

Cancer Research

50

17

727

author name string

M. M. Swann

publication date

1957

1 reference

10.1007/BF00395947

https://api.crossref.org/works/10.1007/BF00395947

19 July 2023

Identifiers

10.1007/BF00395947

1 reference

Europe PubMed Central

19 October 2017

1 reference

Europe PubMed Central

19 October 2017

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