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Literature DB >> 3717163

The heterozygote advantage in phenylketonuria.

L I Woolf.

Abstract

Entities: Disease

Mesh：

Year: 1986 PMID： 3717163 PMCID： PMC1684820

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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13 in total

1. The high frequency of phenylketonuria in Ireland and Western Scotland.

Authors: L I Woolf
Journal: J Inherit Metab Dis Date: 1978 Impact factor: 4.982

2. PHENYLKETONURIA IN YEMENITE JEWS.

Authors: B E COHEN; A SZEINBERG; H BOICHIS; E BODONYI
Journal: Pediatrics Date: 1963-12 Impact factor: 7.124

3. Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.

Authors:
Journal: Humangenetik Date: 1975-12-23

4. Teratogenic and toxic effects of ochratoxin A in rats.

Authors: M H Brown; G M Szczech; B P Purmalis
Journal: Toxicol Appl Pharmacol Date: 1976-08 Impact factor: 4.219

5. Balkan (endemic) nephropathy and foodborn ochratoxin A: preliminary results of a survey of foodstuffs.

Authors: P Krogh; B Hald; R Plestina; S Ceović
Journal: Acta Pathol Microbiol Scand B Date: 1977-06

6. [Clinical results of differential diagnosis of the so-called facial pain].

Authors: H G Bull; H G Luhr; W Schmidt-Hoberg
Journal: Zahnarztl Prax Date: 1974-04-19

7. Phenylketonuria. Mass screening of newborns in Ireland.

Authors: S F Cahalane
Journal: Arch Dis Child Date: 1968-04 Impact factor: 3.791

8. On estimating the actual rate of foetal loss in families with an autosomal recessive disorder and Woolf's data on PKU.

Authors: L P ten Kate
Journal: Ann Hum Genet Date: 1978-05 Impact factor: 1.670

9. Genetics of phenylketonuria. Heterozygosity for phenylketonuria.

Authors: L I Woolf; W I Cranston; B L Goodwin
Journal: Nature Date: 1967-03-04 Impact factor: 49.962

10. Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage.

Authors: L I Woolf; M S McBean; F M Woolf; S F Cahalane
Journal: Ann Hum Genet Date: 1975-05 Impact factor: 1.670

11 in total

Review 1. The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.

Authors: D S Konecki; U Lichter-Konecki
Journal: Hum Genet Date: 1991-08 Impact factor: 4.132

2. Phenotyping heterozygous carriers of juvenile neuronal ceroid lipofuscinosis with CLN3 mutations.

Authors: Richard Bergholz; Alfried Kohlschütter; Angela Schulz; Waltraud Hubert; Klaus Rüther
Journal: Graefes Arch Clin Exp Ophthalmol Date: 2014-10-22 Impact factor: 3.117

Review 3. Genetic etiology and clinical challenges of phenylketonuria.

Authors: Nasser A Elhawary; Imad A AlJahdali; Iman S Abumansour; Ezzeldin N Elhawary; Nagwa Gaboon; Mohammed Dandini; Abdulelah Madkhali; Wafaa Alosaimi; Abdulmajeed Alzahrani; Fawzia Aljohani; Ehab M Melibary; Osama A Kensara
Journal: Hum Genomics Date: 2022-07-19 Impact factor: 6.481

Review 4. Gene-environment interactions in development and disease.

Authors: C Lovely; Mindy Rampersad; Yohaan Fernandes; Johann Eberhart
Journal: Wiley Interdiscip Rev Dev Biol Date: 2016-09-14 Impact factor: 5.814

Review 5. Mycotoxins.

Authors: J W Bennett; M Klich
Journal: Clin Microbiol Rev Date: 2003-07 Impact factor: 26.132

6. Association of Polymorphisms in Connective Tissue Growth Factor and Epidermal Growth Factor Receptor Genes With Human Longevity.

Authors: Timothy A Donlon; Brian J Morris; Qimei He; Randi Chen; Kamal H Masaki; Richard C Allsopp; D Craig Willcox; Gregory J Tranah; Neeta Parimi; Daniel S Evans; Friederike Flachsbart; Almut Nebel; Duk-Hwan Kim; Joobae Park; Bradley J Willcox
Journal: J Gerontol A Biol Sci Med Sci Date: 2017-08-01 Impact factor: 6.053