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Results: 1-17 |
Results: 17
MOLECULAR MAPPING OF ALZHEIMER-TYPE DEMENTIA IN DOWNS-SYNDROME
Authors: PRASHER VP FARRER MJ KESSLING AM FISHER EMC WEST RJ BARBER PC BUTLER AC
Citation: Vp. Prasher et al., MOLECULAR MAPPING OF ALZHEIMER-TYPE DEMENTIA IN DOWNS-SYNDROME, Annals of neurology, 43(3), 1998, pp. 380-383
MTHFR ASSOCIATION WITH ARTERIOSCLEROTIC VASCULAR-DISEASE
Authors: FLETCHER O KESSLING AM
Citation: O. Fletcher et Am. Kessling, MTHFR ASSOCIATION WITH ARTERIOSCLEROTIC VASCULAR-DISEASE, Human genetics, 103(1), 1998, pp. 11-21
GENETIC INITIATION, PROGRESSION AND PROGNOSTIC MARKERS IN TRANSITIONAL-CELL CARCINOMA OF THE BLADDER - A SUMMARY OF THE STRUCTURAL AND TRANSCRIPTIONAL CHANGES, AND THE ROLE OF DEVELOPMENTAL GENES
Authors: ADSHEAD JM KESSLING AM OGDEN CW
Citation: Jm. Adshead et al., GENETIC INITIATION, PROGRESSION AND PROGNOSTIC MARKERS IN TRANSITIONAL-CELL CARCINOMA OF THE BLADDER - A SUMMARY OF THE STRUCTURAL AND TRANSCRIPTIONAL CHANGES, AND THE ROLE OF DEVELOPMENTAL GENES, British Journal of Urology, 82(4), 1998, pp. 503-512
ALLELIC VARIABILITY IN D21S11, BUT NOT IN APP OR APOE, IS ASSOCIATED WITH COGNITIVE DECLINE IN DOWN-SYNDROME
Authors: FARRER MJ CRAYTON L DAVIES GE OLIVER C POWELL J HOLLAND AJ KESSLING AM
Citation: Mj. Farrer et al., ALLELIC VARIABILITY IN D21S11, BUT NOT IN APP OR APOE, IS ASSOCIATED WITH COGNITIVE DECLINE IN DOWN-SYNDROME, NeuroReport, 8(7), 1997, pp. 1645-1649
HUMAN COL6A1 - GENOMIC CHARACTERIZATION OF THE GLOBULAR DOMAINS, STRUCTURAL AND EVOLUTIONARY COMPARISON WITH COL6A2
Authors: TRIKKA D DAVIS T LAPENTA V BRAHE C KESSLING AM
Citation: D. Trikka et al., HUMAN COL6A1 - GENOMIC CHARACTERIZATION OF THE GLOBULAR DOMAINS, STRUCTURAL AND EVOLUTIONARY COMPARISON WITH COL6A2, Mammalian genome, 8(5), 1997, pp. 342-345
PHYSICAL MAPPING AND CHARACTERIZATION OF A CHROMOSOME-21 PERICENTROMERIC COSMID
Authors: MARATOU K HOWARD CM FARRER MJ MANCAMA DT KESSLING AM DAVIES GE
Citation: K. Maratou et al., PHYSICAL MAPPING AND CHARACTERIZATION OF A CHROMOSOME-21 PERICENTROMERIC COSMID, Cytogenetics and cell genetics, 77, 1997, pp. 30-30
INFLUENCE OF GENETIC-VARIABILITY IN THE NONDELETION LDL-RECEPTOR ALLELE ON PHENOTYPIC VARIATION IN FRENCH-CANADIAN FAMILIAL HYPERCHOLESTEROLEMIA HETEROZYGOTES SHARING A NULL LDL-RECEPTOR GENE DEFECT
Authors: BETARD C KESSLING AM ROY M DAVIGNON J
Citation: C. Betard et al., INFLUENCE OF GENETIC-VARIABILITY IN THE NONDELETION LDL-RECEPTOR ALLELE ON PHENOTYPIC VARIATION IN FRENCH-CANADIAN FAMILIAL HYPERCHOLESTEROLEMIA HETEROZYGOTES SHARING A NULL LDL-RECEPTOR GENE DEFECT, Atherosclerosis, 119(1), 1996, pp. 43-55
CONSERVED GENE-SEQUENCES FOR SPECIES IDENTIFICATION - PCR ANALYSIS OFTHE 3'-UTR OF THE SON GENE DISTINGUISHES HUMAN AND OTHER MAMMALIAN DNAS
Authors: SOTERIOU B FISHER RA KHAN IM KESSLING AM ARCHARD LC BULUWELA L
Citation: B. Soteriou et al., CONSERVED GENE-SEQUENCES FOR SPECIES IDENTIFICATION - PCR ANALYSIS OFTHE 3'-UTR OF THE SON GENE DISTINGUISHES HUMAN AND OTHER MAMMALIAN DNAS, Forensic science international, 73(3), 1995, pp. 171-181
CROSSING-OVER IN NONDISJOINED CHROMOSOMES-21
Authors: HOWARD CM DAVIES GE FARRER MJ BENNETT LB WYSE RKH ASHCROFT K KESSLING AM
Citation: Cm. Howard et al., CROSSING-OVER IN NONDISJOINED CHROMOSOMES-21, Cytogenetics and cell genetics, 70(3-4), 1995, pp. 166-166
A MICRODISSECTED CHROMOSOME 21P MINI-LIBRARY
Authors: BENNETT LB CLAUSSEN U FARRER MJ KESSLING AM
Citation: Lb. Bennett et al., A MICRODISSECTED CHROMOSOME 21P MINI-LIBRARY, Cytogenetics and cell genetics, 70(3-4), 1995, pp. 168-168
GENETIC-VARIATION IN THE COL6A1 REGION IS ASSOCIATED WITH CONGENITAL HEART-DEFECTS IN TRISOMY-21 (DOWNS-SYNDROME)
Authors: DAVIES GE HOWARD CM FARRER MJ COLEMAN MM BENNETT LB CULLEN LM WYSE RKH BURN J WILLIAMSON R KESSLING AM
Citation: Ge. Davies et al., GENETIC-VARIATION IN THE COL6A1 REGION IS ASSOCIATED WITH CONGENITAL HEART-DEFECTS IN TRISOMY-21 (DOWNS-SYNDROME), Annals of Human Genetics, 59, 1995, pp. 253-269
CLADISTIC-ANALYSIS OF THE APOLIPOPROTEIN AI-CIII-AIV GENE-CLUSTER USING A HEALTHY FRENCH-CANADIAN SAMPLE .1. HAPLOID ANALYSIS
Authors: HAVILAND MB KESSLING AM DAVIGNON J SING CF
Citation: Mb. Haviland et al., CLADISTIC-ANALYSIS OF THE APOLIPOPROTEIN AI-CIII-AIV GENE-CLUSTER USING A HEALTHY FRENCH-CANADIAN SAMPLE .1. HAPLOID ANALYSIS, Annals of Human Genetics, 59, 1995, pp. 211-231
UNUSUAL GENOTYPES IN THE COL6A1 GENE IN PARENTS OF CHILDREN WITH TRISOMY-21 AND MAJOR CONGENITAL HEART-DEFECTS
Authors: DAVIES GE HOWARD CM FARRER MJ COLEMAN MM CULLEN LM WILLIAMSON R WYSE RKH KESSLING AM
Citation: Ge. Davies et al., UNUSUAL GENOTYPES IN THE COL6A1 GENE IN PARENTS OF CHILDREN WITH TRISOMY-21 AND MAJOR CONGENITAL HEART-DEFECTS, Human genetics, 93(4), 1994, pp. 443-446
THE SON GENE ENCODES A CONSERVED DNA-BINDING PROTEIN MAPPING TO HUMAN-CHROMOSOME-21
Authors: KHAN IM FISHER RA JOHNSON KJ BAILEY MES SICILIANO MJ KESSLING AM FARRER M KAMALATI T BULUWELA L CARRITT B
Citation: Im. Khan et al., THE SON GENE ENCODES A CONSERVED DNA-BINDING PROTEIN MAPPING TO HUMAN-CHROMOSOME-21, Annals of Human Genetics, 58, 1994, pp. 25-34
GENETIC-VARIATION IN THE COLLAGEN-VI (ALPHA-1) GENE CONTRIBUTES TO PATHOGENESIS OF ATRIOVENTRICULAR SEPTAL-DEFECT IN TRISOMY-21 (DOWN-SYNDROME)
Authors: DAVIES GE HOWARD CM FARRER MJ CULLEN LM COLEMAN MM WILLIAMSON R BURN J KESSLING AM
Citation: Ge. Davies et al., GENETIC-VARIATION IN THE COLLAGEN-VI (ALPHA-1) GENE CONTRIBUTES TO PATHOGENESIS OF ATRIOVENTRICULAR SEPTAL-DEFECT IN TRISOMY-21 (DOWN-SYNDROME), Circulation, 88(4), 1993, pp. 290-290
MEIOTIC CROSSING-OVER IN NONDISJOINED CHROMOSOMES OF CHILDREN WITH TRISOMY-21
Authors: HOWARD CM DAVIES GE FARRER MJ COLEMAN MM WYSE RKH BURN J WILLIAMSON R KESSLING AM
Citation: Cm. Howard et al., MEIOTIC CROSSING-OVER IN NONDISJOINED CHROMOSOMES OF CHILDREN WITH TRISOMY-21, American journal of human genetics, 53(3), 1993, pp. 562-562
MEIOTIC CROSSING-OVER IN NONDISJOINED CHROMOSOMES OF CHILDREN WITH TRISOMY-21 AND A CONGENITAL HEART DEFECT
Authors: HOWARD CM DAVIES GE FARRER MJ CULLEN LM COLEMAN MM WILLIAMSON R WYSE RKH PALMER R KESSLING AM
Citation: Cm. Howard et al., MEIOTIC CROSSING-OVER IN NONDISJOINED CHROMOSOMES OF CHILDREN WITH TRISOMY-21 AND A CONGENITAL HEART DEFECT, American journal of human genetics, 53(2), 1993, pp. 462-471
Risultati: 1-17 |