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Results: 1-25 | 26-35
Results: 1-25/35
SCREENING FOR TUMOR-SUPPRESSOR P16(CDKN2A) GERMLINE MUTATIONS IN ISRAELI MELANOMA FAMILIES
Authors: YAKOBSON EA ZLOTOGORSKI A SHAFIR R COHEN M ICEKSON M LANDAU M BRENNER S USHER S PERETZ H
Citation: Ea. Yakobson et al., SCREENING FOR TUMOR-SUPPRESSOR P16(CDKN2A) GERMLINE MUTATIONS IN ISRAELI MELANOMA FAMILIES, CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 36(8), 1998, pp. 645-648
PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17
Authors: FRENCH DL COLLER BS USHER S BERKOWITZ R ENG C SELIGSOHN U PERETZ H
Citation: Dl. French et al., PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17, British Journal of Haematology, 102(2), 1998, pp. 582-587
A SINGLE GENETIC-ORIGIN FOR THE COMMON PROTHROMBOTIC G20210A POLYMORPHISM IN THE PROTHROMBIN GENE
Authors: ZIVELIN A ROSENBERG N FAIER S KORNBROT N PERETZ H MANNHALTER C HORELLOU MH SELIGSOHN U
Citation: A. Zivelin et al., A SINGLE GENETIC-ORIGIN FOR THE COMMON PROTHROMBOTIC G20210A POLYMORPHISM IN THE PROTHROMBIN GENE, Blood, 92(4), 1998, pp. 1119-1124
A NOVEL MUTATION IN THE XDH GENE ACCOUNTS FOR XANTHINURIA AFFECTING AN ISRAELI PATIENT
Authors: LEYARTOVSKY D LAGZIEL A ICHIDA K SPERLING O LIBERMAN U YARON M PERETZ H
Citation: D. Leyartovsky et al., A NOVEL MUTATION IN THE XDH GENE ACCOUNTS FOR XANTHINURIA AFFECTING AN ISRAELI PATIENT, Arthritis and rheumatism, 41(9), 1998, pp. 717-717
CYS-618 ARG MUTATION IN THE RET PROTOONCOGENE ASSOCIATED WITH FAMILIAL MEDULLARY-THYROID CARCINOMA AND MATERNALLY TRANSMITTED HIRSCHSPRUNGS-DISEASE SUGGESTING A ROLE FOR IMPRINTING
Authors: PERETZ H LUBOSHITSKY R BARON E BITON A GERSHONI R USHER S GRYNBERG E YAKOBSON E GRAFF E LAPIDOT M
Citation: H. Peretz et al., CYS-618 ARG MUTATION IN THE RET PROTOONCOGENE ASSOCIATED WITH FAMILIAL MEDULLARY-THYROID CARCINOMA AND MATERNALLY TRANSMITTED HIRSCHSPRUNGS-DISEASE SUGGESTING A ROLE FOR IMPRINTING, Human mutation, 10(2), 1997, pp. 155-159
HIGHLY ELEVATED LACTATE-DEHYDROGENASE LEVEL IN A HEALTHY INDIVIDUAL -A CASE OF MACRO-LDH
Authors: PERRY C PERETZ H BENTAL O ELDOR A
Citation: C. Perry et al., HIGHLY ELEVATED LACTATE-DEHYDROGENASE LEVEL IN A HEALTHY INDIVIDUAL -A CASE OF MACRO-LDH, American journal of hematology, 55(1), 1997, pp. 39-40
RAPID DETECTION OF APOLIPOPROTEIN E2, E3 AND E4 POLYMORPHISMS BY A NEW PCR-BASED METHOD
Authors: ZIVELIN A ROSENBERG N PERETZ H AMIT Y KOMBROT N SELIGSOHN U
Citation: A. Zivelin et al., RAPID DETECTION OF APOLIPOPROTEIN E2, E3 AND E4 POLYMORPHISMS BY A NEW PCR-BASED METHOD, Thrombosis and haemostasis, 1997, pp. 1326-1326
2 NOVEL MUTATIONS CAUSING FACTOR-VII DEFICIENCY
Authors: TAMARY H FROMOVITCHAMIT Y SHALMON L ZIVELIN A PERETZ H LANIR N BRENNER B ZAIZOV R SELIGSOHN U
Citation: H. Tamary et al., 2 NOVEL MUTATIONS CAUSING FACTOR-VII DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 1686-1686
PHEOCHROMOCYTOMA DUE TO UNILATERAL ADRENAL-MEDULLARY HYPERPLASIA
Authors: QUPTY G ISHAY A PERETZ H DHARAN M KAUFMAN N LUBOSHITZKY R
Citation: G. Qupty et al., PHEOCHROMOCYTOMA DUE TO UNILATERAL ADRENAL-MEDULLARY HYPERPLASIA, Clinical endocrinology, 47(5), 1997, pp. 613-617
IMPROVED METHOD FOR GENOTYPING APOLIPOPROTEIN-E POLYMORPHISMS BY A PCR-BASED ASSAY SIMULTANEOUSLY UTILIZING 2 DISTINCT RESTRICTION ENZYMES
Authors: ZIVELIN A ROSENBERG N PERETZ H AMIT Y KORNBROT N SELIGSOHN U
Citation: A. Zivelin et al., IMPROVED METHOD FOR GENOTYPING APOLIPOPROTEIN-E POLYMORPHISMS BY A PCR-BASED ASSAY SIMULTANEOUSLY UTILIZING 2 DISTINCT RESTRICTION ENZYMES, Clinical chemistry, 43(9), 1997, pp. 1657-1659
THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN JEWS STEM FROMDISTINCT FOUNDERS - ONE OF ANCIENT MIDDLE-EASTERN ORIGIN AND ANOTHER OF MORE RECENT EUROPEAN ORIGIN
Authors: PERETZ H MULAI A USHER S ZIVELIN A SEGAL A WEISMAN Z MITTELMAN M LUPO H LANIR N BRENNER B SHPILBERG O SELIGSOHN U
Citation: H. Peretz et al., THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN JEWS STEM FROMDISTINCT FOUNDERS - ONE OF ANCIENT MIDDLE-EASTERN ORIGIN AND ANOTHER OF MORE RECENT EUROPEAN ORIGIN, Blood, 90(7), 1997, pp. 2654-2659
GLANZMANN THROMBASTHENIA CAUSED BY AN 11.2-KB DELETION IN THE GLYCOPROTEIN IIIA (BETA(3)) IS A 2ND MUTATION IN IRAQI JEWS THAT STEMMED FROMA DISTINCT FOUNDER
Authors: ROSENBERG N YATUV R ORION Y ZIVELIN A DARDIK R PERETZ H SELIGSOHN U
Citation: N. Rosenberg et al., GLANZMANN THROMBASTHENIA CAUSED BY AN 11.2-KB DELETION IN THE GLYCOPROTEIN IIIA (BETA(3)) IS A 2ND MUTATION IN IRAQI JEWS THAT STEMMED FROMA DISTINCT FOUNDER, Blood, 89(10), 1997, pp. 3654-3662
GENETIC-EVIDENCE FOR A COMMON ORIGIN AMONG ROMAN JEWS AND ASHKENAZI JEWS
Authors: ODDOUX C GUILLENNAVARRO E CLAYTON CM NELSON H PERETZ H SELIGSOHN U LUZZATTO L NARDI M KARPATKIN M DITIVOLI C DICAVE E AXELROD F OSTRER H
Citation: C. Oddoux et al., GENETIC-EVIDENCE FOR A COMMON ORIGIN AMONG ROMAN JEWS AND ASHKENAZI JEWS, American journal of human genetics, 61(4), 1997, pp. 1200-1200
CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES
Authors: DARDIK R PERETZ H USHER S SELIGSOHN U MARTINOWITZ U
Citation: R. Dardik et al., CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES, Haemophilia, 2(1), 1996, pp. 11-17
A 14-BP DELETION (CODON-554 DEL AAGGTAACAGAGTG) AT EXON-14 INTRON N JUNCTION OF THE COAGULATION-FACTOR-XI GENE DISRUPTS SPLICING AND CAUSESSEVERE FACTOR-XI DEFICIENCY
Authors: PERETZ H ZIVELIN A USHER S SELIGSOHN U
Citation: H. Peretz et al., A 14-BP DELETION (CODON-554 DEL AAGGTAACAGAGTG) AT EXON-14 INTRON N JUNCTION OF THE COAGULATION-FACTOR-XI GENE DISRUPTS SPLICING AND CAUSESSEVERE FACTOR-XI DEFICIENCY, Human mutation, 8(1), 1996, pp. 77-78
PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17
Authors: FRENCH DL COLLER BS SELIGSOHN U PERETZ H
Citation: Dl. French et al., PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17, Blood, 88(10), 1996, pp. 110-110
THE 11BP DELETION IN GLYCOPROTEIN IIIA WHICH CAUSES GLANZMANN THROMBASTHENIA IN IRAQI-JEWS PROBABLY STEMS FROM A COMMON FOUNDER
Authors: ROSENBERG N YATUV R PERETZ H SELIGSOHN U
Citation: N. Rosenberg et al., THE 11BP DELETION IN GLYCOPROTEIN IIIA WHICH CAUSES GLANZMANN THROMBASTHENIA IN IRAQI-JEWS PROBABLY STEMS FROM A COMMON FOUNDER, Thrombosis and haemostasis, 73(6), 1995, pp. 1189-1189
RECOMBINATION DISTANCE BETWEEN PLATELET GLYCOPROTEIN-IIB AND GLYCOPROTEIN-IIIA GENES
Authors: PERETZ H YAKOBSON E KOROSTISHEVSKY M USHER S SELIGSOHN U
Citation: H. Peretz et al., RECOMBINATION DISTANCE BETWEEN PLATELET GLYCOPROTEIN-IIB AND GLYCOPROTEIN-IIIA GENES, Thrombosis and haemostasis, 73(6), 1995, pp. 1195-1195
CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES
Authors: DARDIK R PERETZ H USHER S KORNBROT N SHAKI R SELIGSOHN U MARTINOWITZ U
Citation: R. Dardik et al., CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES, Thrombosis and haemostasis, 73(6), 1995, pp. 1220-1220
NEGOTIATING CLOTHING IDENTITIES ON THE SALES FLOOR
Authors: PERETZ H
Citation: H. Peretz, NEGOTIATING CLOTHING IDENTITIES ON THE SALES FLOOR, Symbolic interaction, 18(1), 1995, pp. 19-37
2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN ASHKENAZI-JEWS MAYPOINT TO A EUROPEAN ORIGIN - RESPONSE
Authors: SELIGSOHN U PERETZ H ZIVELIN A SHPILBERG O
Citation: U. Seligsohn et al., 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN ASHKENAZI-JEWS MAYPOINT TO A EUROPEAN ORIGIN - RESPONSE, Blood, 86(8), 1995, pp. 3268-3268
GLANZMANNS-THROMBASTHENIA ASSOCIATED WITH DELETION INSERTION AND ALTERNATIVE SPLICING IN THE GLYCOPROTEIN IIB GENE
Authors: PERETZ H ROSENBERG N USHER S GRAFF E NEWMAN PJ COLLER BS SELIGSOHN U
Citation: H. Peretz et al., GLANZMANNS-THROMBASTHENIA ASSOCIATED WITH DELETION INSERTION AND ALTERNATIVE SPLICING IN THE GLYCOPROTEIN IIB GENE, Blood, 85(2), 1995, pp. 414-420
ONE OF THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN ASHKENAZI JEWS (TYPE-II) IS ALSO PREVALENT IN IRAQI JEWS, WHO REPRESENT THE ANCIENT GENE POOL OF JEWS
Authors: SHPILBERG O PERETZ H ZIVELIN A YATUV R CHETRIT A KULKA T STERN C WEISS E SELIGSOHN U
Citation: O. Shpilberg et al., ONE OF THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN ASHKENAZI JEWS (TYPE-II) IS ALSO PREVALENT IN IRAQI JEWS, WHO REPRESENT THE ANCIENT GENE POOL OF JEWS, Blood, 85(2), 1995, pp. 429-432
DIFFERENTIAL PROLIFERATIVE CHARACTERISTICS OF ALVEOLAR FIBROBLASTS ININTERSTITIAL LUNG-DISEASES - REGULATIVE ROLE OF IL-1 AND PGE(2)
Authors: FIREMAN E BENEFRAIM S GREIF J PERETZ H KIVITY S TOPILSKY M RODRIG Y YELLIN A APTE RN
Citation: E. Fireman et al., DIFFERENTIAL PROLIFERATIVE CHARACTERISTICS OF ALVEOLAR FIBROBLASTS ININTERSTITIAL LUNG-DISEASES - REGULATIVE ROLE OF IL-1 AND PGE(2), Mediators of inflammation, 3(6), 1994, pp. 445-452
SCREENING FOR DOWN-SYNDROME IN THE 2ND TRIMESTER OF PREGNANCY
Authors: LEGUM C GLASSNER M PERETZ H YAFFO A YEDWAB G AMSTER R SAGAI Y
Citation: C. Legum et al., SCREENING FOR DOWN-SYNDROME IN THE 2ND TRIMESTER OF PREGNANCY, European journal of obstetrics, gynecology, and reproductive biology, 55(1), 1994, pp. 15-16
Risultati: 1-25 | 26-35