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Results: 1-25 | 26-36
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ABSENCE OF GERMLINE MUTATIONS IN THE PTEN GENE IN MEN WITH A POTENTIAL INHERITED PREDISPOSITION TO PROSTATE-CANCER
Authors: COONEY KA PETTY EM PEACOCKE M
Citation: Ka. Cooney et al., ABSENCE OF GERMLINE MUTATIONS IN THE PTEN GENE IN MEN WITH A POTENTIAL INHERITED PREDISPOSITION TO PROSTATE-CANCER, Journal of investigative medicine, 46(7), 1998, pp. 274-274
PTEN AND INHERITED HAMARTOMA-CANCER SYNDROMES
Authors: ENG C PEACOCKE M
Citation: C. Eng et M. Peacocke, PTEN AND INHERITED HAMARTOMA-CANCER SYNDROMES, Nature genetics, 19(3), 1998, pp. 223-223
MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE ANALYSES IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, 2 HAMARTOMA SYNDROMES WITH GERMLINE PTEN MUTATION
Authors: MARSH DJ COULON V LUNETTA KL ROCCASERRA P DAHIA PLM ZHENG ZM LIAW D CARON S DUBOUE B LIN AY RICHARDSON AL BONNETBLANC JM BRESSIEUX JM CABARROTMOREAU A CHOMPRET A DEMANGE L EELES RA YAHANDA AM FEARON ER FRICKER JP GORLIN RJ HODGSON SV HUSON S LACOMBE D LEPRAT F ODENT S TOULOUSE C OLOPADE OI SOBOL H TISHLER S WOODS CG ROBINSON BG WEBER HC PARSONS R PEACOCKE M LONGY M ENG C
Citation: Dj. Marsh et al., MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE ANALYSES IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, 2 HAMARTOMA SYNDROMES WITH GERMLINE PTEN MUTATION, Human molecular genetics, 7(3), 1998, pp. 507-515
SIMILARITIES OF CUTANEOUS AND BREAST PATHOLOGY IN COWDENS-SYNDROME
Authors: SCHRAGER CA SCHNEIDER D GRUENER AC TSOU HC PEACOCKE M
Citation: Ca. Schrager et al., SIMILARITIES OF CUTANEOUS AND BREAST PATHOLOGY IN COWDENS-SYNDROME, Experimental dermatology, 7(6), 1998, pp. 380-390
THE GENETIC-BASIS OF COWDENS-SYNDROME - 3 NOVEL MUTATIONS IN PTEN MMAC1/TEP1/
Authors: TSOU HC PING XL XIE XX GRUENER AC ZHANG H NINI R SWISSHELM K SYBERT V DIAMOND TM SUTPHEN R PEACOCKE M
Citation: Hc. Tsou et al., THE GENETIC-BASIS OF COWDENS-SYNDROME - 3 NOVEL MUTATIONS IN PTEN MMAC1/TEP1/, Human genetics, 102(4), 1998, pp. 467-473
PATTERNS OF X-CHROMOSOME INACTIVATION IN SPORADIC BASAL-CELL CARCINOMAS - EVIDENCE FOR CLONALITY
Authors: WALSH DS PEACOCKE M HARRINGTON A JAMES WD TSOU HC
Citation: Ds. Walsh et al., PATTERNS OF X-CHROMOSOME INACTIVATION IN SPORADIC BASAL-CELL CARCINOMAS - EVIDENCE FOR CLONALITY, Journal of the American Academy of Dermatology, 38(1), 1998, pp. 49-55
CLINICAL AND PATHOLOGICAL FEATURES OF BREAST DISEASE IN COWDENS-SYNDROME - AN UNDERRECOGNIZED SYNDROME WITH AN INCREASED RISK OF BREAST-CANCER
Authors: SCHRAGER CA SCHNEIDER D GRUENER AC TSOU HC PEACOCKE M
Citation: Ca. Schrager et al., CLINICAL AND PATHOLOGICAL FEATURES OF BREAST DISEASE IN COWDENS-SYNDROME - AN UNDERRECOGNIZED SYNDROME WITH AN INCREASED RISK OF BREAST-CANCER, Human pathology, 29(1), 1998, pp. 47-53
ALOPECIA UNIVERSALIS ASSOCIATED WITH A MUTATION IN THE HUMAN HAIRLESSGENE
Authors: AHMAD W HAQUE WFU BRANCOLINI V TSOU HC HAQUE SU LAM H AITA VM OWEN J DEBLAQUIERE M FRANK J CSERHALMIFRIEDMAN PB LEASK A MCGRATH JA PEACOCKE M AHMAD M OTT J CHRISTIANO AM
Citation: W. Ahmad et al., ALOPECIA UNIVERSALIS ASSOCIATED WITH A MUTATION IN THE HUMAN HAIRLESSGENE, Science, 279(5351), 1998, pp. 720-724
GERMLINE MUTATIONS OF THE PTEN GENE IN COWDEN-DISEASE, AN INHERITED BREAST AND THYROID-CANCER SYNDROME
Authors: LIAW D MARSH DJ LI J DAHIA PLM WANG SI ZHENG ZM BOSE S CALL KM TSOU HC PEACOCKE M ENG C PARSONS R
Citation: D. Liaw et al., GERMLINE MUTATIONS OF THE PTEN GENE IN COWDEN-DISEASE, AN INHERITED BREAST AND THYROID-CANCER SYNDROME, Nature genetics, 16(1), 1997, pp. 64-67
BETA-APO-14'-CAROTENOIC ACID TRANSACTIVATES THE RESPONSE ELEMENT OF THE RETINOIC ACID RECEPTOR BETA-2 GENE VIA ITS CONVERSION INTO RETINOICACID
Authors: WANG XD KRINSKY NI LIU C PEACOCKE M RUSSELL RM
Citation: Xd. Wang et al., BETA-APO-14'-CAROTENOIC ACID TRANSACTIVATES THE RESPONSE ELEMENT OF THE RETINOIC ACID RECEPTOR BETA-2 GENE VIA ITS CONVERSION INTO RETINOICACID, The FASEB journal, 11(3), 1997, pp. 1049-1049
MOLECULAR-BASIS OF VARIEGATE PORPHYRIA - A DE-NOVO INSERTION MUTATIONIN THE PROTOPORPHYRINOGEN OXIDASE GENE
Authors: LAM HM DRAGAN L TSOU HC MERK H PEACOCKE M GOERZ G SASSA S POHFITZPATRICK M BICKERS DR CHRISTIANO AM
Citation: Hm. Lam et al., MOLECULAR-BASIS OF VARIEGATE PORPHYRIA - A DE-NOVO INSERTION MUTATIONIN THE PROTOPORPHYRINOGEN OXIDASE GENE, Human genetics, 99(1), 1997, pp. 126-129
ERYTHROPOIETIC PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE
Authors: WANG XH PIOMELLI S PEACOCKE M CHRISTIANO AM POHFITZPATRICK MB
Citation: Xh. Wang et al., ERYTHROPOIETIC PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE, Journal of investigative dermatology, 109(5), 1997, pp. 688-691
THE MOLECULAR-BASIS OF COWDENS-SYNDROME
Authors: TSOU HC PING X XIE X YAO Y SCHRAGER C GRUENER A CHRISTIANO AM LIAW D PARSONS R ENG C PEACOCKE M
Citation: Hc. Tsou et al., THE MOLECULAR-BASIS OF COWDENS-SYNDROME, Journal of investigative dermatology, 109(1), 1997, pp. 5-5
ERYTHROPOIETIC-PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE
Authors: WANG XH PIOMELLI S PEACOCKE M CHRISTIANO AM POHFITZPATRICK MB
Citation: Xh. Wang et al., ERYTHROPOIETIC-PROTOPORPHYRIA - 4 NOVEL FRAMESHIFT MUTATIONS IN THE FERROCHELATASE GENE, Journal of investigative dermatology, 108(4), 1997, pp. 657-657
EXPRESSION OF RETINOID-X-RECEPTORS IN HUMAN DERMAL FIBROBLASTS
Authors: TSOU HC XIE XX YAO YJ PING XL PEACOCKE M
Citation: Hc. Tsou et al., EXPRESSION OF RETINOID-X-RECEPTORS IN HUMAN DERMAL FIBROBLASTS, Experimental cell research, 236(2), 1997, pp. 493-500
THE ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDEN-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES
Authors: TSOU HC TENG DHF PING XL BRANCOLINI V DAVIS T HU R XIE XX GRUENER AC SCHRAGER CA CHRISTIANO AM ENG C STECK P OTT J TAVTIGIAN SV PEACOCKE M
Citation: Hc. Tsou et al., THE ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDEN-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES, American journal of human genetics, 61(5), 1997, pp. 1036-1043
GERMLINE MUTATIONS OF THE PTEN GENE IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME
Authors: ENG C MARSH D LIAW D DAHIA P LI J ZHENG Z TSOU H PEACOCKE M GORLIN R PARSONS R
Citation: C. Eng et al., GERMLINE MUTATIONS OF THE PTEN GENE IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 69-69
ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDENS-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES
Authors: TSOU HC TENG D PING XL BRONCOLINI V DAVIS T HU R XIE XX GRUENER AC SCHRAGER AC CHRISTIANO AC ENG C STECK P OTT J TAVITIGIAN S PEACOCKE M
Citation: Hc. Tsou et al., ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDENS-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES, American journal of human genetics, 61(4), 1997, pp. 468-468
ANTIOXIDANT VITAMINS, CANCER, AND CARDIOVASCULAR-DISEASE
Authors: KRINSKY NI PEACOCKE M RUSSELL RM
Citation: Ni. Krinsky et al., ANTIOXIDANT VITAMINS, CANCER, AND CARDIOVASCULAR-DISEASE, The New England journal of medicine, 335(14), 1996, pp. 1066-1067
MOLECULAR-BASIS OF VARIEGATE PORPHYRIA - FRAMESHIFT MUTATIONS IN THE PROTOPORPHYRINOGEN OXIDASE GENE
Authors: LAM HM DRAGAN L TSOU HC MERK H PEACOCKE M GOERZ G SASSA S POHFITZPATRICK M BICKERS DR CHRISTIANO AM
Citation: Hm. Lam et al., MOLECULAR-BASIS OF VARIEGATE PORPHYRIA - FRAMESHIFT MUTATIONS IN THE PROTOPORPHYRINOGEN OXIDASE GENE, Journal of investigative dermatology, 107(1), 1996, pp. 144-144
CLONALITY OF BASAL-CELL CARCINOMA - MOLECULAR ANALYSIS OF AN INTERESTING CASE
Authors: WALSH DS TSOU HC HARRINGTON A JAMES WD PEACOCKE M
Citation: Ds. Walsh et al., CLONALITY OF BASAL-CELL CARCINOMA - MOLECULAR ANALYSIS OF AN INTERESTING CASE, Journal of investigative dermatology, 106(3), 1996, pp. 579-582
AGE-ASSOCIATED CHANGES IN BASAL C-FOS TRANSCRIPTION FACTOR-BINDING ACTIVITY IN RAT HEARTS
Authors: TSOU H AZHAR G LU XG KOVACS S PEACOCKE M WEI JY
Citation: H. Tsou et al., AGE-ASSOCIATED CHANGES IN BASAL C-FOS TRANSCRIPTION FACTOR-BINDING ACTIVITY IN RAT HEARTS, Experimental cell research, 229(2), 1996, pp. 432-437
RAR-BETA-2-MEDIATED GROWTH-INHIBITION IN HELA-CELLS
Authors: SI SP LEE XH TSOU HC BUCHSBAUM R TIBADUIZA E PEACOCKE M
Citation: Sp. Si et al., RAR-BETA-2-MEDIATED GROWTH-INHIBITION IN HELA-CELLS, Experimental cell research, 223(1), 1996, pp. 102-111
A DIAGNOSTIC ASSAY FOR THE WISKOTT-ALDRICH SYNDROME AND ITS VARIANT FORMS
Authors: SIMINOVITCH KA GREER WL NOVOGRODSKY A AXELSSON B SOMANI AK PEACOCKE M
Citation: Ka. Siminovitch et al., A DIAGNOSTIC ASSAY FOR THE WISKOTT-ALDRICH SYNDROME AND ITS VARIANT FORMS, Journal of investigative medicine, 43(2), 1995, pp. 159-169
IDENTIFICATION OF WASP MUTATIONS IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND ISOLATED THROMBOCYTOPENIA REVEALS ALLELIC HETEROGENEITY AT THE WAS LOCUS
Authors: KOLLURI R SHEHABELDIN A PEACOCKE M LAMHONWAH AM TEICHERTKULISZEWSKA K WEISMAN SM SIMINOVITCH KA
Citation: R. Kolluri et al., IDENTIFICATION OF WASP MUTATIONS IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND ISOLATED THROMBOCYTOPENIA REVEALS ALLELIC HETEROGENEITY AT THE WAS LOCUS, Human molecular genetics, 4(7), 1995, pp. 1119-1126
Risultati: 1-25 | 26-36