| P2093 | author name string | Alison P Galvani | |
| | Eric M Poolman | |
| P2860 | cites work | Evaluating plague and smallpox as historical selective pressures for the CCR5-Delta 32 HIV-resistance allele | Q22066229 |
| | Cystic Fibrosis Heterozygote Resistance to Cholera Toxin in the Cystic Fibrosis Mouse Model | Q22299398 |
| | Identification of the cystic fibrosis gene: chromosome walking and jumping | Q22299423 |
| | The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study | Q24530092 |
| | Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: an evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion | Q24538931 |
| | Genomewide pattern of synonymous nucleotide substitution in two complete genomes of Mycobacterium tuberculosis | Q24658353 |
| | Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA | Q28119124 |
| | Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening | Q28217255 |
| | Molecular cloning and expression of a novel glycolipid sulfotransferase in Mycobacterium tuberculosis | Q28486449 |
| | Identification of the cystic fibrosis gene: genetic analysis | Q29614402 |
| | The global burden of typhoid fever | Q29619215 |
| | Intense selection in an age-structured population | Q79855574 |
| | Effect of population structure on the amount of polymorphism and the fixation probability under overdominant selection | Q81473002 |
| | Susceptibility to typhoid fever is associated with a polymorphism in the cystic fibrosis transmembrane conductance regulator (CFTR). | Q33221005 |
| | Case-control study of enteropathogens associated with childhood diarrhea in Dhaka, Bangladesh | Q33963440 |
| | Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics | Q34019037 |
| | The origin of the major cystic fibrosis mutation (delta F508) in European populations. | Q34059578 |
| | Salmonella typhi uses CFTR to enter intestinal epithelial cells. | Q34066552 |
| | Mycobacterium tuberculosis complex DNA from an extinct bison dated 17,000 years before the present | Q34083039 |
| | Does deficiency of arylsulfatase B have a role in cystic fibrosis? | Q34204396 |
| | Cystic fibrosis in the Ohio Amish: gene frequency and founder effect | Q34265519 |
| | Genetic and geographical variability in cystic fibrosis: evolutionary considerations. | Q34399381 |
| | De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling | Q34443974 |
| | Prevention of phagosome-lysosome fusion in cultured macrophages by sulfatides of Mycobacterium tuberculosis | Q35012546 |
| | Mycobacterial isolations in young adults with cystic fibrosis | Q36136663 |
| | Prospective study of mycobacterial infections in patients with cystic fibrosis | Q36221006 |
| | Tuberculosis control in the era of HIV. | Q36274930 |
| | Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies. | Q37361324 |
| | Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation | Q37377671 |
| | Generalizing Fisher's "reproductive value": overlapping and nonoverlapping generations with competing genotypes | Q37593485 |
| | Activation of intestinal CFTR Cl- channel by heat-stable enterotoxin and guanylin via cAMP-dependent protein kinase. | Q37629420 |
| | Mutations of the cystic fibrosis gene in patients with chronic pancreatitis | Q38502091 |
| | Why is the cystic fibrosis gene so frequent? | Q38749495 |
| | TUBERCULOSIS IN ANCIENT EGYPT | Q39271207 |
| | Typhoid fever in children aged less than 5 years | Q39517030 |
| | Hypothesis: a selective advantage for cystic fibrosis heterozygotes | Q41431660 |
| | Gene frequency and fitness change in an age-structured population | Q41497675 |
| | Chloride secretion in response to guanylin in colonic epithelial from normal and transgenic cystic fibrosis mice | Q42701115 |
| | Genetic evidence for CFTR dysfunction in Japanese: background for chronic pancreatitis | Q43073732 |
| | Nontuberculous Mycobacteria in Adult Patients with Cystic Fibrosis | Q44146527 |
| | The history of tuberculosis as a global epidemic | Q47251146 |
| | Is Mycobacterium tuberculosis 15,000 years old? | Q48078215 |
| | Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival. | Q50955831 |
| | Cystic fibrosis in Asian Indians. | Q51034540 |
| | Life table studies of mortality | Q53027599 |
| | Do ΔF508 heterozygotes have a selective advantage? | Q56084192 |
| | Cystic fibrosis and chloride-secreting diarrhoea | Q59044623 |
| | Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis | Q72097755 |
| | Comments on the possible existence and nature of a heterozygote advantage in cystic fibrosis | Q72298951 |
| | Escherichia coli heat-stable enterotoxin-mediated colonic Cl- secretion is absent in cystic fibrosis | Q72718158 |
| | The estimated incidence of cystic fibrosis in Japan | Q73362781 |
| | Identification of cystic fibrosis mutations in the United Arab Emirates. Mutations in brief no. 133. Online | Q77335047 |
| | The arcana of tuberculosis with a brief epidemiologic history of the disease in the U.S.A. | Q78263212 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | biophysics | Q7100 |
| | cystic fibrosis | Q178194 |
| | bioengineering | Q580689 |
| | biomedical engineering | Q327092 |
| P304 | page(s) | 91-8 | |
| P577 | publication date | 2007-02-22 | |
| P1433 | published in | Journal of the Royal Society Interface | Q2492390 |
| P1476 | title | Evaluating candidate agents of selective pressure for cystic fibrosis | |
| P478 | volume | 4 | |