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Results: 1-25 | 26-50 | 51-63 |
Results: 51-63/63
DIFFERENTIAL PHYLOGENETIC FOOTPRINTING AS A MEANS TO IDENTIFY BASE CHANGES RESPONSIBLE FOR RECRUITMENT OF THE ANTHROPOID GAMMA-GENE TO A FETAL EXPRESSION PATTERN
Authors: GUMUCIO DL SHELTON DA BLANCHARDMCQUATE K GRAY T TARLE S HEILSTEDTWILLIAMSON H SLIGHTOM JL COLLINS F GOODMAN M
Citation: Dl. Gumucio et al., DIFFERENTIAL PHYLOGENETIC FOOTPRINTING AS A MEANS TO IDENTIFY BASE CHANGES RESPONSIBLE FOR RECRUITMENT OF THE ANTHROPOID GAMMA-GENE TO A FETAL EXPRESSION PATTERN, The Journal of biological chemistry, 269(21), 1994, pp. 15371-15380
DETECTION OF FUSION TRANSCRIPTS GENERATED BY THE INVERSION 16-CHROMOSOME IN ACUTE MYELOGENOUS LEUKEMIA
Authors: CLAXTON DF LIU P HSU HB MARLTON P HESTER J COLLINS F DEISSEROTH AB ROWLEY JD SICILIANO MJ
Citation: Df. Claxton et al., DETECTION OF FUSION TRANSCRIPTS GENERATED BY THE INVERSION 16-CHROMOSOME IN ACUTE MYELOGENOUS LEUKEMIA, Blood, 83(7), 1994, pp. 1750-1756
THE DISTINCTION BETWEEN MULTIPLE RETINAL-PIGMENT EPITHELIAL HAMARTOMATA (MRPEH) IN FAMILIAL ADENOMATOUS POLYPOSIS (FAP) AND CONGENITAL HYPERTROPHY OF THE RETINAL-PIGMENT EPITHELIUM (CHRPE)
Authors: HENNESSY MP COLLINS F CORONEO MT
Citation: Mp. Hennessy et al., THE DISTINCTION BETWEEN MULTIPLE RETINAL-PIGMENT EPITHELIAL HAMARTOMATA (MRPEH) IN FAMILIAL ADENOMATOUS POLYPOSIS (FAP) AND CONGENITAL HYPERTROPHY OF THE RETINAL-PIGMENT EPITHELIUM (CHRPE), Australian and New Zealand journal of ophthalmology, 21(4), 1993, pp. 275-276
PATHOLOGY OF OSSEOUS AND GENITOURINARY LESIONS OF PROTEUS SYNDROME
Authors: BALE PM WATSON G COLLINS F
Citation: Pm. Bale et al., PATHOLOGY OF OSSEOUS AND GENITOURINARY LESIONS OF PROTEUS SYNDROME, Pediatric pathology, 13(6), 1993, pp. 797-809
ORAL-FACIAL-DIGITAL SYNDROME AND RETINAL ABNORMALITIES WITH AUTOSOMALRECESSIVE INHERITANCE
Authors: JAMIESON R COLLINS F
Citation: R. Jamieson et F. Collins, ORAL-FACIAL-DIGITAL SYNDROME AND RETINAL ABNORMALITIES WITH AUTOSOMALRECESSIVE INHERITANCE, American journal of medical genetics, 47(2), 1993, pp. 304-305
MULTIPLE CONGENITAL-DEFECTS ASSOCIATED WITH MATERNAL USE OF TOPICAL TRETINOIN
Authors: LIPSON AH COLLINS F WEBSTER WS
Citation: Ah. Lipson et al., MULTIPLE CONGENITAL-DEFECTS ASSOCIATED WITH MATERNAL USE OF TOPICAL TRETINOIN, Lancet, 341(8856), 1993, pp. 1352-1353
A NEW 5-YEAR PLAN FOR THE UNITED-STATES HUMAN GENOME PROJECT
Authors: COLLINS F GALAS D
Citation: F. Collins et D. Galas, A NEW 5-YEAR PLAN FOR THE UNITED-STATES HUMAN GENOME PROJECT, Science, 262(5130), 1993, pp. 43-46
GDNF - A GLIAL-CELL LINE DERIVED NEUROTROPHIC FACTOR FOR MIDBRAIN DOPAMINERGIC-NEURONS
Authors: LIN LFH DOHERTY DH LILE JD BEKTESH S COLLINS F
Citation: Lfh. Lin et al., GDNF - A GLIAL-CELL LINE DERIVED NEUROTROPHIC FACTOR FOR MIDBRAIN DOPAMINERGIC-NEURONS, Science, 260(5111), 1993, pp. 1130-1132
GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR IS EXPRESSED IN THE DEVELOPING BUT NOT ADULT STRIATUM AND STIMULATES DEVELOPING DOPAMINE NEURONS IN-VIVO
Authors: STROMBERG I BJORKLUND L JOHANSSON M TOMAC A COLLINS F OLSON L HOFFER B HUMPEL C
Citation: I. Stromberg et al., GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR IS EXPRESSED IN THE DEVELOPING BUT NOT ADULT STRIATUM AND STIMULATES DEVELOPING DOPAMINE NEURONS IN-VIVO, Experimental neurology, 124(2), 1993, pp. 401-412
MOLECULAR DIAGNOSIS AND MONITORING IN AML WITH INVERSION 16 (INV16)
Authors: CLAXTON DF LIU P HSU HB MARLTON P ROWLEY J COLLINS F DEISSEROTH A SICILIANO M
Citation: Df. Claxton et al., MOLECULAR DIAGNOSIS AND MONITORING IN AML WITH INVERSION 16 (INV16), Blood, 82(10), 1993, pp. 10000190-10000190
ANALYSIS OF ALTERNATIVE SPLICING PATTERNS OF THE HUNTINGTON DISEASE GENE
Authors: VALDES J TAGLE D ELMER L COLLINS F
Citation: J. Valdes et al., ANALYSIS OF ALTERNATIVE SPLICING PATTERNS OF THE HUNTINGTON DISEASE GENE, American journal of human genetics, 53(3), 1993, pp. 737-737
HETERODUPLEX DETECTION AND RNA ANALYSIS OF NE1 MUTATIONS
Authors: COLMAN S ABERNATHY C HO V KAMATH R KOUSSEFF B WILLIAMS C DRISCOLL DJ ZORI R COLLINS F WALLACE MR
Citation: S. Colman et al., HETERODUPLEX DETECTION AND RNA ANALYSIS OF NE1 MUTATIONS, American journal of human genetics, 53(3), 1993, pp. 1145-1145
CYSTIC-FIBROSIS (CF) GENE-PRODUCT IS EXPRESSED IN RETINA AND RETINAL-PIGMENT EPITHELIUM
Authors: MILLER SS RABIN J STRONG T IANNUZZI M ADAMS A COLLINS F REENSTRA W MCCRAY P
Citation: Ss. Miller et al., CYSTIC-FIBROSIS (CF) GENE-PRODUCT IS EXPRESSED IN RETINA AND RETINAL-PIGMENT EPITHELIUM, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1009-1009
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