Literature DB >> 5098070

An inherited kidney disease of mice resembling human nephronophthisis.

M F Lyon, E V Hulse.   

Abstract

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Year:  1971        PMID： 5098070      PMCID： PMC1468974          DOI： 10.1136/jmg.8.1.41

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  21 in total

1.  Congenital nephrotic syndrome.

Authors:  N HALLMAN; L HJELT
Journal:  J Pediatr       Date:  1959-08       Impact factor: 4.406

2.  GLOMERULONEPHRITIS AND LATE ONSET DISEASE OF MICE FOLLOWING NEONATAL VIRUS INFECTION.

Authors:  J HOTCHIN; D N COLLINS
Journal:  Nature       Date:  1964-09-26       Impact factor: 49.962

3.  FAMILIAL JUVENILE NEPHRONOPHTHISIS. AN UNRECOGNIZED RENAL DISEASE IN THE UNITED STATES.

Authors:  J A MANGOS; J M OPITZ; C C LOBECK; D U COOKSON
Journal:  Pediatrics       Date:  1964-09       Impact factor: 7.124

4.  RAPID ESTIMATION OF UREA IN WHOLE BLOOD WITH URASTRAT.

Authors:  D N BARON; G HUGHES
Journal:  Br Med J       Date:  1965-01-23

5.  NATURALLY OCCURRING AND SULFONAMIDE-INDUCED LESIONS IN RATS DURING A 1-YEAR TOXICITY STUDY.

Authors:  J E GRAY
Journal:  Am J Vet Res       Date:  1963-09       Impact factor: 1.156

6.  Juvenile nephronophthisis. Part 2. A histologic and microangiographic study.

Authors:  B I IVEMARK; A LJUNGQVIST; A BARRY
Journal:  Acta Paediatr       Date:  1960-07       Impact factor: 2.299

7.  Juvenile nephronophthisis. Part 1. A genetically determined nephropathy with hypotonic polyuria and azotaemia.

Authors:  O BROBERGER; J WINBERG; R ZETTERSTROM
Journal:  Acta Paediatr       Date:  1960-07       Impact factor: 2.299

8.  A case of Fanconi's familial juvenile nephronophthisis.

Authors:  C HOOFT; H ROELS; J HERPOL
Journal:  Helv Paediatr Acta       Date:  1959-09

9.  [Knowledge and differential diagnosis of familial juvenile nephronophthisis].

Authors:  R GRUTTNER; W LENZ
Journal:  Arch Kinderheilkd       Date:  1957

10.  Effects of old age and over-nutrition on the kidney.

Authors:  G C KENNEDY
Journal:  Br Med Bull       Date:  1957-01       Impact factor: 4.291
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  32 in total

Review 1.  Mouse chromosome 10.

Authors:  B A Taylor; W N Frankel; R H Reeves
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders.

Authors:  Michio Hirano; Caterina Garone; Catarina M Quinzii
Journal:  Biochim Biophys Acta       Date:  2012-01-18

Review 3.  Mouse chromosome 10.

Authors:  B A Taylor; M J Justice; R Reeves
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

Review 4.  The enigmatic parietal epithelial cell is finally getting noticed: a review.

Authors:  Takamoto Ohse; Jeffrey W Pippin; Alice M Chang; Ronald D Krofft; Jeffrey H Miner; Michael R Vaughan; Stuart J Shankland
Journal:  Kidney Int       Date:  2009-10-21       Impact factor: 10.612

5.  176th ENMC International Workshop: diagnosis and treatment of coenzyme Q₁₀ deficiency.

Authors:  Shamima Rahman; Catherine F Clarke; Michio Hirano
Journal:  Neuromuscul Disord       Date:  2011-07-01       Impact factor: 4.296

6.  An overview of current mouse models recapitulating coenzyme q10 deficiency syndrome.

Authors:  Floriana Licitra; Hélène Puccio
Journal:  Mol Syndromol       Date:  2014-07

7.  Parkinson's disease-like neuromuscular defects occur in prenyl diphosphate synthase subunit 2 (Pdss2) mutant mice.

Authors:  Carly G K Ziegler; Min Peng; Marni J Falk; Erzsebet Polyak; Elpida Tsika; Harry Ischiropoulos; Dana Bakalar; Julie A Blendy; David L Gasser
Journal:  Mitochondrion       Date:  2011-10-01       Impact factor: 4.160

8.  A simple capillary tube method for the determination of the specific gravity of 25 and 50 micro l quantities of urine.

Authors:  R H Watts
Journal:  J Clin Pathol       Date:  1971-10       Impact factor: 3.411

Review 9.  Contrasuppression in autoimmunity.

Authors:  C J Kelly; E G Neilson
Journal:  Immunol Res       Date:  1988       Impact factor: 2.829

10.  Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice.

Authors:  Catarina M Quinzii; Caterina Garone; Valentina Emmanuele; Saba Tadesse; Sindu Krishna; Beatriz Dorado; Michio Hirano
Journal:  FASEB J       Date:  2012-11-12       Impact factor: 5.191
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