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Results: 76-100/105
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE HUMAN CD59 LOCUS
Authors: NOTHEN MM DEWALD G
Citation: Mm. Nothen et G. Dewald, DINUCLEOTIDE REPEAT POLYMORPHISM AT THE HUMAN CD59 LOCUS, Clinical genetics, 47(3), 1995, pp. 165-166
NO ASSOCIATION BETWEEN LENGTH OF THE (CAG)(N) REPEAT OF THE HUNTINGTONS-DISEASE GENE AND TOURETTES-SYNDROME
Authors: HEBEBRAND J NOTHEN MM KLUG B WETTKESCHAFER R CAMPS A LISCH S HEMMER S VONGONTARD A POUSTKA F LEHMKUHL G SCHMIDT M PROPPING P REMSCHMIDT H
Citation: J. Hebebrand et al., NO ASSOCIATION BETWEEN LENGTH OF THE (CAG)(N) REPEAT OF THE HUNTINGTONS-DISEASE GENE AND TOURETTES-SYNDROME, Biological psychiatry, 37(3), 1995, pp. 209-211
HUMAN ADENOSINE A(1) RECEPTOR GENE - SYSTEMATIC SCREENING FOR DNA-SEQUENCE VARIATION AND LINKAGE MAPPING ON CHROMOSOME 1Q31-32.1 USING A SILENT POLYMORPHISM IN THE CODING REGION
Authors: DECKERT J NOTHEN MM BRYANT SP REN HZ WOLF HK STILES GL SPURR NK PROPPING P
Citation: J. Deckert et al., HUMAN ADENOSINE A(1) RECEPTOR GENE - SYSTEMATIC SCREENING FOR DNA-SEQUENCE VARIATION AND LINKAGE MAPPING ON CHROMOSOME 1Q31-32.1 USING A SILENT POLYMORPHISM IN THE CODING REGION, Biochemical and biophysical research communications, 214(2), 1995, pp. 614-621
ASSOCIATION ANALYSIS OF THE MONOAMINE-OXIDASE-A GENE IN BIPOLAR AFFECTIVE-DISORDER BY USING FAMILY-BASED INTERNAL CONTROLS
Authors: NOTHEN MM EGGERMANN K ALBUS M BORRMANN M RIETSCHEL M KORNER J MAIER W MINGES J LICHTERMANN D FRANZEK E WEIGELT B KNAPP M PROPPING P
Citation: Mm. Nothen et al., ASSOCIATION ANALYSIS OF THE MONOAMINE-OXIDASE-A GENE IN BIPOLAR AFFECTIVE-DISORDER BY USING FAMILY-BASED INTERNAL CONTROLS, American journal of human genetics, 57(4), 1995, pp. 975-977
HUMAN DOPAMINE D4 RECEPTOR GENE - FREQUENT OCCURRENCE OF A NULL ALLELE AND OBSERVATION OF HOMOZYGOSITY
Authors: NOTHEN MM CICHON S HEMMER S HEBEBRAND J REMSCHMIDT H LEHMKUHL G POUSTKA F SCHMIDT M CATALANO M FIMMERS R KORNER J RIETSCHEL M PROPPING P
Citation: Mm. Nothen et al., HUMAN DOPAMINE D4 RECEPTOR GENE - FREQUENT OCCURRENCE OF A NULL ALLELE AND OBSERVATION OF HOMOZYGOSITY, Human molecular genetics, 3(12), 1994, pp. 2207-2212
DETECTION OF 4 POLYMORPHIC SITES IN THE HUMAN DOPAMINE D1 RECEPTOR GENE (DRD1)
Authors: CICHON S NOTHEN MM ERDMANN J PROPPING P
Citation: S. Cichon et al., DETECTION OF 4 POLYMORPHIC SITES IN THE HUMAN DOPAMINE D1 RECEPTOR GENE (DRD1), Human molecular genetics, 3(1), 1994, pp. 209-209
A COMMON AMINO-ACID POLYMORPHISM IN COMPLEMENT COMPONENT C1R
Authors: NOTHEN MM DEWALD G
Citation: Mm. Nothen et G. Dewald, A COMMON AMINO-ACID POLYMORPHISM IN COMPLEMENT COMPONENT C1R, Human molecular genetics, 3(1), 1994, pp. 217-217
DELINEATION OF MARKER CHROMOSOMES BY REVERSE CHROMOSOME PAINTING USING ONLY A SMALL NUMBER OF DOP-PCR AMPLIFIED MICRODISSECTED CHROMOSOMES
Authors: VIERSBACH R SCHWANITZ G NOTHEN MM
Citation: R. Viersbach et al., DELINEATION OF MARKER CHROMOSOMES BY REVERSE CHROMOSOME PAINTING USING ONLY A SMALL NUMBER OF DOP-PCR AMPLIFIED MICRODISSECTED CHROMOSOMES, Human genetics, 93(6), 1994, pp. 663-667
ASSOCIATION ANALYSIS OF THE DOPAMINE D-2 RECEPTOR GENE IN TOURETTES-SYNDROME USING THE HAPLOTYPE RELATIVE RISK METHOD
Authors: NOTHEN MM HEBEBRAND J KNAPP M HEBEBRAND K CAMPS A VONGONTARD A WETTKESCHAFER R LISCH S CICHON S POUSTKA F SCHMIDT M LEHMKUHL G REMSCHMIDT H PROPPING P
Citation: Mm. Nothen et al., ASSOCIATION ANALYSIS OF THE DOPAMINE D-2 RECEPTOR GENE IN TOURETTES-SYNDROME USING THE HAPLOTYPE RELATIVE RISK METHOD, American journal of medical genetics, 54(3), 1994, pp. 249-252
NO EVIDENCE OF ASSOCIATION BETWEEN DOPAMINE D4 RECEPTOR VARIANTS AND BIPOLAR AFFECTIVE-DISORDER
Authors: LIM LCC NOTHEN MM KORNER J RIETSCHEL M CASTLE D HUNT N PROPPING P MURRAY R GILL M
Citation: Lcc. Lim et al., NO EVIDENCE OF ASSOCIATION BETWEEN DOPAMINE D4 RECEPTOR VARIANTS AND BIPOLAR AFFECTIVE-DISORDER, American journal of medical genetics, 54(3), 1994, pp. 259-263
DOPAMINE D2 RECEPTOR MOLECULAR VARIANT AND SCHIZOPHRENIA
Authors: NOTHEN MM WILDENAUER D CICHON S ALBUS M MAIER W MINGES J LICHTERMANN D BONDY B RIETSCHEL M KORNER J FIMMERS P PROPPING P
Citation: Mm. Nothen et al., DOPAMINE D2 RECEPTOR MOLECULAR VARIANT AND SCHIZOPHRENIA, Lancet, 343(8908), 1994, pp. 1301-1302
ASSOCIATION TESTS IN PSYCHIATRIC-DISORDER S - CONCEPTS AND FINDINGS
Authors: PROPPING P NOTHEN MM KORNER J RIETSCHEL M MAIER W
Citation: P. Propping et al., ASSOCIATION TESTS IN PSYCHIATRIC-DISORDER S - CONCEPTS AND FINDINGS, Nervenarzt, 65(11), 1994, pp. 725-740
HAILEY-HAILEY DISEASE AND BIPOLAR AFFECTI VE-DISORDER IN 3 MEMBERS OFTHE SAME FAMILY
Authors: WILK M RIETSCHEL M KORNER J MOLLER HJ NOTHEN MM BAUER R KREYSEL HW
Citation: M. Wilk et al., HAILEY-HAILEY DISEASE AND BIPOLAR AFFECTI VE-DISORDER IN 3 MEMBERS OFTHE SAME FAMILY, Hautarzt, 45(5), 1994, pp. 313-317
HUMAN-COMPLEMENT COMPONENT C8 - MOLECULAR-BASIS OF THE BETA-CHAIN POLYMORPHISM
Authors: DEWALD G HEMMER S NOTHEN MM
Citation: G. Dewald et al., HUMAN-COMPLEMENT COMPONENT C8 - MOLECULAR-BASIS OF THE BETA-CHAIN POLYMORPHISM, FEBS letters, 340(3), 1994, pp. 211-215
SINGLE-STRAND CONFORMATION ANALYSIS (SSCA) OF THE DOPAMINE D1 RECEPTOR GENE (DRD1) REVEALS NO SIGNIFICANT MUTATION IN PATIENTS WITH SCHIZOPHRENIA AND MANIC-DEPRESSION
Authors: CICHON S NOTHEN MM RIETSCHEL M KORNER J PROPPING P
Citation: S. Cichon et al., SINGLE-STRAND CONFORMATION ANALYSIS (SSCA) OF THE DOPAMINE D1 RECEPTOR GENE (DRD1) REVEALS NO SIGNIFICANT MUTATION IN PATIENTS WITH SCHIZOPHRENIA AND MANIC-DEPRESSION, Biological psychiatry, 36(12), 1994, pp. 850-853
IDENTIFICATION OF GENETIC-VARIATION IN THE HUMAN SEROTONIN 1D-BETA RECEPTOR GENE
Authors: NOTHEN MM ERDMANN J SHIMRONABARBANELL D PROPPING P
Citation: Mm. Nothen et al., IDENTIFICATION OF GENETIC-VARIATION IN THE HUMAN SEROTONIN 1D-BETA RECEPTOR GENE, Biochemical and biophysical research communications, 205(2), 1994, pp. 1194-1200
A COMMON SER THR POLYMORPHISM IN THE PERFORIN HOMOLOGOUS REGION OF HUMAN-COMPLEMENT COMPONENT C7/
Authors: DEWALD G NOTHEN MM RUTHER K
Citation: G. Dewald et al., A COMMON SER THR POLYMORPHISM IN THE PERFORIN HOMOLOGOUS REGION OF HUMAN-COMPLEMENT COMPONENT C7/, Human heredity, 44(6), 1994, pp. 301-304
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D18S365 LOCUS
Authors: ABELS S ERDMANN J NOTHEN MM
Citation: S. Abels et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D18S365 LOCUS, Human molecular genetics, 2(10), 1993, pp. 1747-1747
RETROSPECTIVE STUDY OF THE PARENTAL ORIGIN OF THE EXTRA CHROMOSOME INTRISOMY-18 (EDWARDS-SYNDROME)
Authors: NOTHEN MM EGGERMANN T ERDMANN J EIBEN B HOFMANN D PROPPING P SCHWANITZ G
Citation: Mm. Nothen et al., RETROSPECTIVE STUDY OF THE PARENTAL ORIGIN OF THE EXTRA CHROMOSOME INTRISOMY-18 (EDWARDS-SYNDROME), Human genetics, 92(4), 1993, pp. 347-349
A SERINE TO GLYCINE SUBSTITUTION AT POSITION-9 IN THE EXTRACELLULAR N-TERMINAL PART OF THE DOPAMINE-D3 RECEPTOR PROTEIN - NO ROLE IN THE GENETIC PREDISPOSITION TO BIPOLAR AFFECTIVE-DISORDER
Authors: RIETSCHEL M NOTHEN MM LANNFELT L SOKOLOFF P SCHWARTZ JC LANCZIK M FRITZE J CICHON S FIMMERS R KORNER J MOLLER HJ PROPPING P
Citation: M. Rietschel et al., A SERINE TO GLYCINE SUBSTITUTION AT POSITION-9 IN THE EXTRACELLULAR N-TERMINAL PART OF THE DOPAMINE-D3 RECEPTOR PROTEIN - NO ROLE IN THE GENETIC PREDISPOSITION TO BIPOLAR AFFECTIVE-DISORDER, Psychiatry research, 46(3), 1993, pp. 253-259
STEINFELD SYNDROME - REPORT OF A 2ND FAMILY AND FURTHER DELINEATION OF A RARE AUTOSOMAL-DOMINANT DISORDER
Authors: NOTHEN MM KNOPFLE G FODISCH HJ ZERRES K
Citation: Mm. Nothen et al., STEINFELD SYNDROME - REPORT OF A 2ND FAMILY AND FURTHER DELINEATION OF A RARE AUTOSOMAL-DOMINANT DISORDER, American journal of medical genetics, 46(4), 1993, pp. 467-470
TOURETTES-SYNDROME AND HOMOZYGOSITY FOR THE DOPAMINE-D3 RECEPTOR GENE
Authors: HEBEBRAND J NOTHEN MM LEHMKUHL G POUSTKA F SCHMIDT M PROPPING P REMSCHMIDT H
Citation: J. Hebebrand et al., TOURETTES-SYNDROME AND HOMOZYGOSITY FOR THE DOPAMINE-D3 RECEPTOR GENE, Lancet, 341(8858), 1993, pp. 1483-1483
ASSOCIATION VERSUS LINKAGE STUDIES IN PSYCHOSIS GENETICS
Authors: NOTHEN MM PROPPING P FIMMERS R
Citation: Mm. Nothen et al., ASSOCIATION VERSUS LINKAGE STUDIES IN PSYCHOSIS GENETICS, Journal of Medical Genetics, 30(8), 1993, pp. 634-637
EXCESS OF HOMOZYGOSITY AT THE DOPAMINE-D3 RECEPTOR GENE IN SCHIZOPHRENIA NOT CONFIRMED
Authors: NOTHEN MM CICHON S PROPPING P FIMMERS R SCHWAB SG WILDENAUER DB
Citation: Mm. Nothen et al., EXCESS OF HOMOZYGOSITY AT THE DOPAMINE-D3 RECEPTOR GENE IN SCHIZOPHRENIA NOT CONFIRMED, Journal of Medical Genetics, 30(8), 1993, pp. 708-708
FAMILIAL COSEGREGATION OF AFFECTIVE-DISORDER AND HAILEY-HAILEY DISEASE
Authors: KORNER J RIETSCHEL M NOTHEN MM WILK CM BAUER R PROPPING P MOLLER HJ
Citation: J. Korner et al., FAMILIAL COSEGREGATION OF AFFECTIVE-DISORDER AND HAILEY-HAILEY DISEASE, British Journal of Psychiatry, 163, 1993, pp. 109-110
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