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Results: 1-25 | 26-30
Results: 1-25/30
ASSIGNMENT OF THE HUMAN SEROTONIN-4 RECEPTOR GENE (HTR4) TO THE LONG ARM OF CHROMOSOME-5 (5Q31-Q33)
Authors: CICHON S KESPER K PROPPING P NOTHEN MM
Citation: S. Cichon et al., ASSIGNMENT OF THE HUMAN SEROTONIN-4 RECEPTOR GENE (HTR4) TO THE LONG ARM OF CHROMOSOME-5 (5Q31-Q33), Molecular membrane biology, 15(2), 1998, pp. 75-78
CLONING, GENOMIC ORGANIZATION, ALTERNATIVE TRANSCRIPTS AND MUTATIONALANALYSIS OF THE GENE RESPONSIBLE FOR AUTOSOMAL RECESSIVE UNIVERSAL CONGENITAL ALOPECIA (VOL 7, PG 1671, 1998)
Authors: CICHON S ANKER M VOGT IR ROHLEDER H PUTZSTUCK M HILLMER A FAROOQ SA ALDHAFRI KS AHMAD M HAQUE S RIETSCHEL M PROPPING P KRUSE R NOTHEN MM
Citation: S. Cichon et al., CLONING, GENOMIC ORGANIZATION, ALTERNATIVE TRANSCRIPTS AND MUTATIONALANALYSIS OF THE GENE RESPONSIBLE FOR AUTOSOMAL RECESSIVE UNIVERSAL CONGENITAL ALOPECIA (VOL 7, PG 1671, 1998), Human molecular genetics (Print), 7(12), 1998, pp. 1987-1988
CLONING, GENOMIC ORGANIZATION, ALTERNATIVE TRANSCRIPTS AND MUTATIONALANALYSIS OF THE GENE RESPONSIBLE FOR AUTOSOMAL RECESSIVE UNIVERSAL CONGENITAL ALOPECIA
Authors: CICHON S ANKER M VOGT IR ROHLEDER H PUTZSTUCK M HILLMER A FAROOQ SA ALDHAFRI KS AHMAD M HAQUE S RIETSCHEL M PROPPING P KRUSE R NOTHEN MM
Citation: S. Cichon et al., CLONING, GENOMIC ORGANIZATION, ALTERNATIVE TRANSCRIPTS AND MUTATIONALANALYSIS OF THE GENE RESPONSIBLE FOR AUTOSOMAL RECESSIVE UNIVERSAL CONGENITAL ALOPECIA, Human molecular genetics (Print), 7(11), 1998, pp. 1671-1679
POLYMORPHIC IMPRINTING OF THE SEROTONIN-2A (5-HT2A) RECEPTOR GENE IN HUMAN ADULT BRAIN
Authors: BUNZEL R BLUMCKE I CICHON S NORMANN S SCHRAMM J PROPPING P NOTHEN MM
Citation: R. Bunzel et al., POLYMORPHIC IMPRINTING OF THE SEROTONIN-2A (5-HT2A) RECEPTOR GENE IN HUMAN ADULT BRAIN, Molecular brain research, 59(1), 1998, pp. 90-92
A LINKAGE STUDY OF SPELLING DISORDER ON CHROMOSOME-1, CHROMOSOME-6, AND CHROMOSOME-15
Authors: SCHULTEKORNE G NOTHEN MM CICHON S GRIMM T MULLERMYHSOK B PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., A LINKAGE STUDY OF SPELLING DISORDER ON CHROMOSOME-1, CHROMOSOME-6, AND CHROMOSOME-15, American journal of medical genetics, 81(6), 1998, pp. 459-459
POLYMORPHIC IMPRINTING OF THE SEROTONIN-2A (5-HT2A) RECEPTOR GENE IN HUMAN ADULT BRAIN
Authors: BUNZEL R BLUMCKE I PROPPING P CICHON S NOTHEN MM
Citation: R. Bunzel et al., POLYMORPHIC IMPRINTING OF THE SEROTONIN-2A (5-HT2A) RECEPTOR GENE IN HUMAN ADULT BRAIN, American journal of medical genetics, 81(6), 1998, pp. 480-480
ASSIGNMENT OF THE HUMAN SEROTONIN-4 RECEPTOR GENE (HTR4) TO THE LONG ARM OF CHROMOSOME-5 (5Q31-Q33)
Authors: KESPER K CICHON S PROPPING P NOTHEN MM
Citation: K. Kesper et al., ASSIGNMENT OF THE HUMAN SEROTONIN-4 RECEPTOR GENE (HTR4) TO THE LONG ARM OF CHROMOSOME-5 (5Q31-Q33), American journal of medical genetics, 81(6), 1998, pp. 503-503
SURGICAL-TREATMENT OF GOITER IN ELDERLY PATIENTS
Authors: CICHON S BARCZYNSKI M KONTUREK A GUCWA J BARCZYNSKI ML SLOWIACZEK M ANIELSKI R
Citation: S. Cichon et al., SURGICAL-TREATMENT OF GOITER IN ELDERLY PATIENTS, British Journal of Surgery, 85, 1998, pp. 133-133
SURGICAL-TREATMENT OF SECONDARY HYPERPARATHYROIDISM IN PATIENTS WITH KIDNEY SUBSTITUTION THERAPY
Authors: BARCZYNSKI ML BARCZYNSKI M CICHON S KOPEC J RES F SLOWIACZEK M SULOWICZ W
Citation: Ml. Barczynski et al., SURGICAL-TREATMENT OF SECONDARY HYPERPARATHYROIDISM IN PATIENTS WITH KIDNEY SUBSTITUTION THERAPY, British Journal of Surgery, 85, 1998, pp. 133-133
EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15
Authors: SCHULTEKORNE G GRIMM T NOTHEN MM MULLERMYHSOK B CICHON S VOGT IR PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15, American journal of human genetics, 63(1), 1998, pp. 279-282
A GENE FOR UNIVERSAL CONGENITAL ALOPECIA MAPS TO CHROMOSOME 8P21-22
Authors: NOTHEN MM CICHON S VOGT IR HEMMER S KRUSE R KNAPP M HOLLER T ULHAQUE MF HAQUE S PROPPING P AHMAD M RIETSCHEL M
Citation: Mm. Nothen et al., A GENE FOR UNIVERSAL CONGENITAL ALOPECIA MAPS TO CHROMOSOME 8P21-22, American journal of human genetics, 62(2), 1998, pp. 386-390
DESCRIPTION OF THE GENETIC-ANALYSIS WORKSHOP-10 BIPOLAR DISORDER LINKAGE DATA SETS
Authors: GOLDIN LR GERSHON ES BERRETTINI WH STINE OC DEPAULO R MCMAHON F MEYERS D NOTHEN M PROPPING P CICHON S FIMMERS R BAUR M ALBUS M FRANZEK E KREINER R MAIER W RIETSCHEL M BARON M KNOWLES J GILLIAM C ENDICOTT J GURLING H CURTIS D SMYTH C KELSOE J
Citation: Lr. Goldin et al., DESCRIPTION OF THE GENETIC-ANALYSIS WORKSHOP-10 BIPOLAR DISORDER LINKAGE DATA SETS, Genetic epidemiology, 14(6), 1997, pp. 563-568
SYSTEMIC SEARCH FOR SUSCEPTIBILITY GENES IN BIPOLAR AFFECTIVE-DISORDER - EVIDENCE FOR DISEASE LOCI AT 18P AND 4P
Authors: NOTHEN MM CICHON S FRANZEK E ALBUS M BORRMANN M RIETSCHEL M LICHTERMANN D WEIGELT B LERER B MAIER W FIMMERS R PROPPING P
Citation: Mm. Nothen et al., SYSTEMIC SEARCH FOR SUSCEPTIBILITY GENES IN BIPOLAR AFFECTIVE-DISORDER - EVIDENCE FOR DISEASE LOCI AT 18P AND 4P, American journal of medical genetics, 74(6), 1997, pp. 674-675
INVESTIGATION OF A BIPOLAR AFFECTIVE-DISORDER LOCUS ON THE SHORT ARM OF CHROMOSOME-18
Authors: ROHLEDER H CICHON S PROPPING P NOTHEN MM
Citation: H. Rohleder et al., INVESTIGATION OF A BIPOLAR AFFECTIVE-DISORDER LOCUS ON THE SHORT ARM OF CHROMOSOME-18, American journal of medical genetics, 74(6), 1997, pp. 675-675
SYSTEMATIC SEARCH FOR SUSCEPTIBILITY GENES IN BIPOLAR AFFECTIVE-DISORDER EVIDENCE FOR DISEASE LOCI AT 18P AND 4P
Authors: NOTHEN MM CICHON S FRANZEK E ALBUS M BORRMANN M RIETSCHEL M LICHTERMANN D WEIGELT B LERER B MAIER W FIMMERS R PROPPING P
Citation: Mm. Nothen et al., SYSTEMATIC SEARCH FOR SUSCEPTIBILITY GENES IN BIPOLAR AFFECTIVE-DISORDER EVIDENCE FOR DISEASE LOCI AT 18P AND 4P, American journal of human genetics, 61(4), 1997, pp. 1679-1679
CNTF AND PSYCHIATRIC-DISORDERS
Authors: NOTHEN MM CICHON S EGGERMANN K PROPPING P KNAPP M MAIER W RIETSCHEL M
Citation: Mm. Nothen et al., CNTF AND PSYCHIATRIC-DISORDERS, Nature genetics, 13(2), 1996, pp. 142-143
SYSTEMATIC SCREENING FOR MUTATIONS IN THE 5'-REGULATORY REGION OF THEHUMAN DOPAMINE D-1 RECEPTOR (DRD1) GENE IN PATIENTS WITH SCHIZOPHRENIA AND BIPOLAR AFFECTIVE-DISORDER
Authors: CICHON S NOTHEN MM STOBER G SCHROERS R ALBUS M MAIER W RIETSCHEL M KORNER J WEIGELT B FRANZEK E WILDENAUER D FIMMERS R PROPPING P
Citation: S. Cichon et al., SYSTEMATIC SCREENING FOR MUTATIONS IN THE 5'-REGULATORY REGION OF THEHUMAN DOPAMINE D-1 RECEPTOR (DRD1) GENE IN PATIENTS WITH SCHIZOPHRENIA AND BIPOLAR AFFECTIVE-DISORDER, American journal of medical genetics, 67(4), 1996, pp. 424-428
LACK OF IMPRINTING OF THE HUMAN DOPAMINE D4 RECEPTOR (DRD4) GENE
Authors: CICHON S NOTHEN MM WOLF HK PROPPING P
Citation: S. Cichon et al., LACK OF IMPRINTING OF THE HUMAN DOPAMINE D4 RECEPTOR (DRD4) GENE, American journal of medical genetics, 67(2), 1996, pp. 229-231
LINKAGE STUDIES OF BIPOLAR DISORDER TO CHROMOSOME-18 MARKERS
Authors: NOTHEN MM CICHON S CRADDOCK N ALBUS M MAIER W LICHTERMANN D WEIGELT B FRANZEK E RIETSCHEL R KORNER J FIMMERS R PROPPING P
Citation: Mm. Nothen et al., LINKAGE STUDIES OF BIPOLAR DISORDER TO CHROMOSOME-18 MARKERS, Biological psychiatry, 39(7), 1996, pp. 396-396
THE HUMAN-COMPLEMENT C8G GENE, A MEMBER OF THE LIPOCALIN GENE FAMILY - POLYMORPHISMS AND MAPPING TO CHROMOSOME 9Q34.3
Authors: DEWALD G CICHON S BRYANT SP HEMMER S NOTHEN MM SPURR NK
Citation: G. Dewald et al., THE HUMAN-COMPLEMENT C8G GENE, A MEMBER OF THE LIPOCALIN GENE FAMILY - POLYMORPHISMS AND MAPPING TO CHROMOSOME 9Q34.3, Annals of Human Genetics, 60, 1996, pp. 281-291
SYSTEMATIC SCREENING FOR MUTATIONS IN THE PROMOTER AND THE CODING REGION OF THE 5-HT1A GENE
Authors: ERDMANN J SHIMRONABARBANELL D CICHON S ALBUS M MAIER W LICHTERMANN D MINGES J REUNER U FRANZEK E ERTL MA HEBEBRAND J REMSCHMIDT H LEHMKUHL G POUSTKA F SCHMIDT M FIMMERS R KORNER J RIETSCHEL M PROPPING P NOTHEN MM
Citation: J. Erdmann et al., SYSTEMATIC SCREENING FOR MUTATIONS IN THE PROMOTER AND THE CODING REGION OF THE 5-HT1A GENE, American journal of medical genetics, 60(5), 1995, pp. 393-399
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
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
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
Risultati: 1-25 | 26-30