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Results of search for 'au:"HUMPHRIES, P"', page 3 of 6
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Authors
Ayuso, C
Bhattacharya, S
Bradley, D G
Bush, R A
Campbell, M
DOBRINER, K
Daiger, S P
Farrar, G J
Gal, A
Humphries, M M
Humphries, P
Jordan, S A
Kenna, P
Kenna, P F
Kiang, A S
Kumar-Singh, R
Lawler, M
McCann, S R
McWilliam, P
Sharp, E M
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Topics
Adult
Animals
Base Sequence
Chromosome Mapping
Female
Genes, Dominant
Genetic Linkage
Genetic Markers
Humans
Male
Mice
Molecular Sequence Data
Mutation
Pedigree
Polymerase Chain Reaction
Polymorphism, Genetic
Retinitis Pigmentosa
Rhodopsin
genetics
methods
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English
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Your search returned 117 results.
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Results
41.
Human nidogen gene: identification of multiple RFLP and exclusion as candidate gene in a family with epidermolysis bullosa (EBS2) with evidence for linkage to chromosome 1.
[electronic resource]
by
Humphries, M
Nagayoshi, T
Sheils, D
Humphries, P
Uitto, J
Producer:
19901221
In:
The Journal of investigative dermatology
vol. 95
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42.
Long-term dosing studies using mutagenic carcinogens indicate a highly significant correlation between elevations in the level of rat glutathione S-transferase P messenger RNA and liver tumours of hepatocellular origin.
[electronic resource]
by
Russell, S E
Pearson, C
Kelly, M
McQuaid, S
Humphries, P
Producer:
19880324
In:
The Biochemical journal
vol. 249
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43.
Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosa.
[electronic resource]
by
Kumar-Singh, R
Kenna, P F
Farrar, G J
Humphries, P
Producer:
19930316
In:
Genomics
vol. 15
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44.
Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus.
[electronic resource]
by
Kumar-Singh, R
Jordan, S A
Farrar, G J
Humphries, P
Producer:
19911202
In:
Nucleic acids research
vol. 19
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45.
Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophy.
[electronic resource]
by
Mansergh, F
Meitinger, T
Rodolph, G
Humphries, P
Farrar, G J
Producer:
19980326
In:
Journal of medical genetics
vol. 35
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46.
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouse.
[electronic resource]
by
Campbell, M
Humphries, M
Kennan, A
Kenna, P
Humphries, P
Brankin, B
Producer:
20061106
In:
Experimental eye research
vol. 83
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47.
Molecular cloning of extensive sequences of the in vitro synthesized chicken ovalbumin structural gene.
[electronic resource]
by
Humphries, P
Cochet, M
Krust, A
Gerlinger, P
Kourilsky, P
Chambon, P
Producer:
19771130
In:
Nucleic acids research
vol. 4
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48.
Isolation of a polymorphic DNA segment unique to human chromosome 7 by molecular cloning of hybrid cell DNA.
[electronic resource]
by
Humphries, P
Barton, D
McKay, A M
Humphries, M M
Carritt, B
Producer:
19830729
In:
Molecular & general genetics : MGG
vol. 190
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49.
Evidence against a second autosomal dominant retinitis pigmentosa locus close to rhodopsin on chromosome 3q.
[electronic resource]
by
Inglehearn, C
Farrar, J
Denton, M
Gal, A
Humphries, P
Bhattacharya, S
Producer:
19930809
In:
American journal of human genetics
vol. 53
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50.
Early detection of leukaemic relapse after bone marrow transplantation using the polymerase chain reaction.
[electronic resource]
by
Browne, P V
Lawler, M
O'Riordan, J
Humphries, P
McCann, S R
Producer:
19910725
In:
Bone marrow transplantation
vol. 7
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51.
Studies in steroid metabolism. XIV. The isolation from human urine of delta9 17-ketosteroids.
[electronic resource]
by
LIEBERMAN, S
HARITON, L B
HUMPHRIES, P
RHOADS, C P
DOBRINER, K
Producer:
20030501
In:
The Journal of biological chemistry
vol. 196
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52.
Gene-based therapies for dominantly inherited retinopathies.
[electronic resource]
by
Farrar, G J
Millington-Ward, S
Chadderton, N
Humphries, P
Kenna, P F
Producer:
20120830
In:
Gene therapy
vol. 19
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53.
Persistent donor chimaerism is consistent with disease-free survival following BMT for chronic myeloid leukaemia.
[electronic resource]
by
Gardiner, N
Lawler, M
O'Riordan, J
DeArce, M
Humphries, P
McCann, S R
Producer:
19970923
In:
Bone marrow transplantation
vol. 20
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54.
Further evidence consistent with Yqh as an indicator of risk of gonadal blastoma in Y-bearing mosaic Turner syndrome.
[electronic resource]
by
De Arce, M A
Costigan, C
Gosden, J R
Lawler, M
Humphries, P
Producer:
19920824
In:
Clinical genetics
vol. 41
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55.
A sequence polymorphism in the human peripherin/RDS gene.
[electronic resource]
by
Farrar, G J
Kenna, P
Jordan, S A
Kumar-Singh, R
Humphries, P
Producer:
19920211
In:
Nucleic acids research
vol. 19
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56.
Recombinant plasmids containing Xenopus laevis globin structural genes derived from complementary DNA.
[electronic resource]
by
Humphries, P
Old, R
Coggins, L W
McShane, T
Watson, C
Paul, J
Producer:
19780612
In:
Nucleic acids research
vol. 5
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57.
Structural and transcriptional properties associated with a member of a new family of conserved short dispersed repeated elements in human DNA.
[electronic resource]
by
Humphries, P
MacCabe, A P
Spencer, R A
Humphries, M M
Pearson, C
Producer:
19860403
In:
Gene
vol. 39
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58.
MRI in the assessment of congenital vaginal anomalies.
[electronic resource]
by
Humphries, P D
Simpson, J C
Creighton, S M
Hall-Craggs, M A
Producer:
20080605
In:
Clinical radiology
vol. 63
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59.
Observations on the structure of two human 7SK pseudogenes and on homologous transcripts in vertebrate species.
[electronic resource]
by
Humphries, P
Russell, S E
McWilliam, P
McQuaid, S
Pearson, C
Humphries, M M
Producer:
19871105
In:
The Biochemical journal
vol. 245
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60.
Comparative ultrastructural analyses of mouse, rabbit, and human platelets and fibrin networks.
[electronic resource]
by
Pretorius, E
Humphries, P
Ekpo, O E
Smit, E
van der Merwe, C F
Producer:
20071126
In:
Microscopy research and technique
vol. 70
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