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Results of search for 'au:"Parrish, J E"'
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Authors
Berkowitz, S
Boyd, Y
Brown, H
Butler, L D
Chatterjee, A
Chen, E
Ciccodicola, A
Cox, G F
Fenner, M H
Field, J B
Fouts, R
Fouts, R L
Frydman, M
Haan, E A
Hamers, G J
Nelson, D L
Parrish, J E
Phadke, K
Wagner, M J
Wells, D E
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Topics
Aminoisobutyric Acids
Animals
Base Sequence
Cell Line
Chromosome Mapping
Chromosomes, Artificial, Yeast
Chromosomes, Human, Pair 8
Cloning, Molecular
Cricetinae
DNA, Complementary
Female
Humans
Hybrid Cells
Insulin
Male
Mice
Molecular Sequence Data
Mutation
X Chromosome
genetics
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English
Your search returned 18 results.
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1.
EFFECT OF NA ON SUGAR AND AMINO ACID TRANSPORT IN STRIATED MUSCLE.
[electronic resource]
by
PARRISH, J E
KIPNIS, D M
Producer:
19961201
In:
The Journal of clinical investigation
vol. 43
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2.
Role of Na+ and K+ on sugar (2-deoxyglucose) and amino acid (alpha-aminoisobutyric acid) transport in striated muscle.
[electronic resource]
by
Kipnis, D M
Parrish, J E
Producer:
19660108
In:
Federation proceedings
vol. 24
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3.
Regional assignment of 19 X-linked ESTs.
[electronic resource]
by
Parrish, J E
Nelson, D L
Producer:
19940217
In:
Human molecular genetics
vol. 2
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4.
Methods for finding genes. A major rate-limiting step in positional cloning.
[electronic resource]
by
Parrish, J E
Nelson, D L
Producer:
19931210
In:
Genetic analysis, techniques and applications
vol. 10
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5.
Collagen-induced and adjuvant-induced arthritis in rats. Post-immunization treatment with collagen to suppress or abrogate the arthritic response.
[electronic resource]
by
Phadke, K
Fouts, R
Parrish, J E
Producer:
19840820
In:
Arthritis and rheumatism
vol. 27
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6.
Factitious hypoglycemia. Why not diagnose before laparotomy?
[electronic resource]
by
Berkowitz, S
Parrish, J E
Field, J B
Producer:
19720125
In:
The American journal of medicine
vol. 51
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7.
Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophy.
[electronic resource]
by
Wulff, K
Parrish, J E
Herrmann, F H
Wehnert, M
Producer:
19970822
In:
Human mutation
vol. 9
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8.
Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions.
[electronic resource]
by
Chatterjee, A
Tanaka, T
Parrish, J E
Herman, G E
Producer:
19960423
In:
Mammalian genome : official journal of the International Mammalian Genome Society
vol. 6
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9.
Magnesium deficiency and carbohydrate metabolism.
[electronic resource]
by
Kahil, M E
Parrish, J E
Simons, E L
Brown, H
Producer:
19670130
In:
Diabetes
vol. 15
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10.
Alignment of physical and genetic maps of human 8q23-qter using somatic cell hybrid mapping panel.
[electronic resource]
by
Parrish, J E
Wang, Y
Wagner, M J
Wells, D E
Producer:
19940721
In:
Somatic cell and molecular genetics
vol. 20
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11.
Evaluation of the effects of various anti-arthritic drugs on type II collagen-induced mouse arthritis model.
[electronic resource]
by
Phadke, K
Fouts, R L
Parrish, J E
Butler, L D
Producer:
19851213
In:
Immunopharmacology
vol. 10
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12.
Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome.
[electronic resource]
by
Parrish, J E
Wagner, M J
Hecht, J T
Scott, C I
Wells, D E
Producer:
19920214
In:
Genomics
vol. 11
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13.
A muscle-specific DNase I-like gene in human Xq28.
[electronic resource]
by
Parrish, J E
Ciccodicola, A
Wehhert, M
Cox, G F
Chen, E
Nelson, D L
Producer:
19960214
In:
Human molecular genetics
vol. 4
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14.
Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti type 2.
[electronic resource]
by
Parrish, J E
Scheuerle, A E
Lewis, R A
Levy, M L
Nelson, D L
Producer:
19970311
In:
Human molecular genetics
vol. 5
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15.
The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney.
[electronic resource]
by
Wilson, A C
Parrish, J E
Massa, H F
Nelson, D L
Trask, B J
Herr, W
Producer:
19950721
In:
Genomics
vol. 25
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16.
MSG1 (melanocyte-specific gene 1): mapping to chromosome Xq13.1, genomic organization, and promoter analysis.
[electronic resource]
by
Fenner, M H
Parrish, J E
Boyd, Y
Reed, V
MacDonald, M
Nelson, D L
Isselbacher, K J
Shioda, T
Producer:
19981005
In:
Genomics
vol. 51
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17.
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
[electronic resource]
by
Parrish, J E
Oostra, B A
Verkerk, A J
Richards, C S
Reynolds, J
Spikes, A S
Shaffer, L G
Nelson, D L
Producer:
19950404
In:
Nature genetics
vol. 8
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18.
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome.
[electronic resource]
by
Lüdecke, H J
Wagner, M J
Nardmann, J
La Pillo, B
Parrish, J E
Willems, P J
Haan, E A
Frydman, M
Hamers, G J
Wells, D E
Producer:
19950516
In:
Human molecular genetics
vol. 4
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