AAAAAA

   
Results: 1-25 | 26-50 | 51-69
Results: 1-25/69
IMMUNOMODULATION OF CYTOKINE PRODUCTION IN MYCOSIS-FUNGOIDES BY AS-101
Authors: SHOHAT M HODAK E SREDNI B SREDNI D DAVID M SHOHAT B
Citation: M. Shohat et al., IMMUNOMODULATION OF CYTOKINE PRODUCTION IN MYCOSIS-FUNGOIDES BY AS-101, European cytokine network, 9(3), 1998, pp. 315-315
CYTOKINE PROFILE IN ATOPIC-DERMATITIS AND THE IMMUNOMODULATORY EFFECTOF AS-101
Authors: SHOHAT M BENAMITAI D SHOHAT B SREDNI D SREDNI B DAVID M
Citation: M. Shohat et al., CYTOKINE PROFILE IN ATOPIC-DERMATITIS AND THE IMMUNOMODULATORY EFFECTOF AS-101, European cytokine network, 9(3), 1998, pp. 321-321
PREVALENCE OF GLUCOCEREBROSIDASE MUTATIONS IN THE ISRAELI ASHKENAZI JEWISH POPULATION
Authors: HOROWITZ M PASMANIKCHOR M BOROCHOWITZ Z FALIKZACCAI T HELDMANN K CARMI R PARVARI R BEITOR H GOLDMAN B PELEG L LEVYLAHAD E RENBAUM P LEGUM S SHOMRAT R YEGER H BENBENISTI D NAVON R DROR V SHOHAT M MAGAL N NAVOT N EYAL N
Citation: M. Horowitz et al., PREVALENCE OF GLUCOCEREBROSIDASE MUTATIONS IN THE ISRAELI ASHKENAZI JEWISH POPULATION, Human mutation, 12(4), 1998, pp. 240-244
ASSESSMENT OF PYRIN GENE-MUTATIONS IN TURKS WITH FAMILIAL MEDITERRANEAN FEVER (FMF)
Authors: CHEN XG FISCHELGHODSIAN N CERCEK A HAMON M OGUR G LOTAN R DANON Y SHOHAT M
Citation: Xg. Chen et al., ASSESSMENT OF PYRIN GENE-MUTATIONS IN TURKS WITH FAMILIAL MEDITERRANEAN FEVER (FMF), Human mutation, 11(6), 1998, pp. 456-460
REPLICATION TIMING OF THE VARIOUS FMR1 ALLELES DETECTED BY FISH - INFERENCES REGARDING THEIR TRANSCRIPTIONAL STATUS
Authors: YESHAYA J SHALGI R SHOHAT M AVIVI L
Citation: J. Yeshaya et al., REPLICATION TIMING OF THE VARIOUS FMR1 ALLELES DETECTED BY FISH - INFERENCES REGARDING THEIR TRANSCRIPTIONAL STATUS, Human genetics, 102(1), 1998, pp. 6-14
A DIFFERENT TRIPLE-TEST NOMOGRAM SHOULD BE DESIGNED FOR IN-VITRO FERTILIZATION PREGNANCIES
Authors: BARHAVA I YITZHAK M ORVIETO R CZITRON B BENRAFAEL Z SHOHAT M
Citation: I. Barhava et al., A DIFFERENT TRIPLE-TEST NOMOGRAM SHOULD BE DESIGNED FOR IN-VITRO FERTILIZATION PREGNANCIES, Human reproduction (Oxford. Print), 13, 1998, pp. 7-7
ABNORMAL LIVER TEST-RESULTS IN MYOTONIC-DYSTROPHY
Authors: ACHIRON A BARAK Y MAGAL N SHOHAT M COHEN M BARAR R GADOTH N
Citation: A. Achiron et al., ABNORMAL LIVER TEST-RESULTS IN MYOTONIC-DYSTROPHY, Journal of clinical gastroenterology, 26(4), 1998, pp. 292-295
CORRELATION OF LINKAGE DATA WITH PHENOTYPE IN 8 FAMILIES WITH STICKLER-SYNDROME
Authors: WILKIN DJ MORTIER GR JOHNSON CL JONES MC DEPAEPE A SHOHAT M WILDIN RS FALK RE COHN DH
Citation: Dj. Wilkin et al., CORRELATION OF LINKAGE DATA WITH PHENOTYPE IN 8 FAMILIES WITH STICKLER-SYNDROME, American journal of medical genetics, 80(2), 1998, pp. 121-127
EVIDENCE FOR COMPLEX NUCLEAR INHERITANCE IN A PEDIGREE WITH NONSYNDROMIC DEAFNESS DUE TO A HOMOPLASMIC MITOCHONDRIAL MUTATION
Authors: BYKHOVSKAYA Y SHOHAT M EHRENMAN K JOHNSON D HAMON M CANTOR RM AOUIZERAT B BU XD ROTTER JI JABER L FISCHELGHODSIAN N
Citation: Y. Bykhovskaya et al., EVIDENCE FOR COMPLEX NUCLEAR INHERITANCE IN A PEDIGREE WITH NONSYNDROMIC DEAFNESS DUE TO A HOMOPLASMIC MITOCHONDRIAL MUTATION, American journal of medical genetics, 77(5), 1998, pp. 421-426
SYNDROME OF ALOPECIA TOTALIS AND 17B-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY
Authors: KAUSCHANSKY A SHOHAT M FRYDMAN M ROSLER A GREENBAUM E SIROTA L
Citation: A. Kauschansky et al., SYNDROME OF ALOPECIA TOTALIS AND 17B-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY, American journal of medical genetics, 76(1), 1998, pp. 28-31
GENETIC INFLUENCE ON THE PREVALENCE OF TORUS PALATINUS
Authors: GORSKY M BUKAI A SHOHAT M
Citation: M. Gorsky et al., GENETIC INFLUENCE ON THE PREVALENCE OF TORUS PALATINUS, American journal of medical genetics, 75(2), 1998, pp. 138-140
MULTIPLE DE-NOVO MPZ (P-0) POINT MUTATIONS IN A SPORADIC DEJERINE-SOTTAS CASE
Authors: WARNER LE SHOHAT M SHORER Z LUPSKI JR
Citation: Le. Warner et al., MULTIPLE DE-NOVO MPZ (P-0) POINT MUTATIONS IN A SPORADIC DEJERINE-SOTTAS CASE, Human mutation, 10(1), 1997, pp. 21-24
CONNEXIN26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON-SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS
Authors: ZELANTE L GASPARINI P ESTIVILL X MELCHIONDA S DAGRUMA L GOVEA N MILA M DELLAMONICA M LUTFI J SHOHAT M MANSFIELD E DELGROSSO K RAPPAPORT E SURREY S FORTINA P
Citation: L. Zelante et al., CONNEXIN26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON-SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS, Human molecular genetics, 6(9), 1997, pp. 1605-1609
A HIGH-RESOLUTION GENETIC-MAP OF THE FAMILIAL MEDITERRANEAN FEVER CANDIDATE REGION ALLOWS IDENTIFICATION OF HAPLOTYPE-SHARING AMONG ETHNIC-GROUPS
Authors: BALOW JE SHELTON DA ORSBORN A MANGELSDORF M AKSENTIJEVICH I BLAKE T SOOD R GARDNER D LIU R PRAS E LEVY EN CENTOLA M DENG ZM ZAKS N WOOD G CHEN XG RICHARDS N SHOHAT M LIVNEH A PRAS M DOGGETT NA COLLINS FS LIU PP ROTTER JI FISCHELGHODSIAN N GUMUCIO D RICHARDS RI KASTNER DL
Citation: Je. Balow et al., A HIGH-RESOLUTION GENETIC-MAP OF THE FAMILIAL MEDITERRANEAN FEVER CANDIDATE REGION ALLOWS IDENTIFICATION OF HAPLOTYPE-SHARING AMONG ETHNIC-GROUPS, Genomics, 44(3), 1997, pp. 280-291
CONSTRUCTION OF A 1-MB RESTRICTION-MAPPED COSMID CONTIG CONTAINING THE CANDIDATE REGION FOR THE FAMILIAL MEDITERRANEAN FEVER LOCUS (MEFV) ON CHROMOSOME 16P13.3
Authors: SOOD R BLAKE T AKSENTIJEVICH I WOOD G CHEN X GARDNER D SHELTON DA MANGELSDORF M ORSBORN A PRAS E BALOW JE CENTOLA M DENG ZM ZAKS N CHEN XG RICHARDS N FISCHELGHODSIAN N ROTTER JI PRAS M SHOHAT M DEAVEN LL GUMUCIO DL CALLEN DF RICHARDS RI COLLINS FS LIU PP KASTNER DL DOGGETT NA
Citation: R. Sood et al., CONSTRUCTION OF A 1-MB RESTRICTION-MAPPED COSMID CONTIG CONTAINING THE CANDIDATE REGION FOR THE FAMILIAL MEDITERRANEAN FEVER LOCUS (MEFV) ON CHROMOSOME 16P13.3, Genomics, 42(1), 1997, pp. 83-95
CONGENITAL DEFICIENCY OF AFP AND DOWN-SYNDROME SCREENING
Authors: SHER C SHOHAT M
Citation: C. Sher et M. Shohat, CONGENITAL DEFICIENCY OF AFP AND DOWN-SYNDROME SCREENING, Prenatal diagnosis, 17(9), 1997, pp. 884-885
FURTHER DELINEATION OF CEREBRO-OSTEO-NEPHROSIS SYNDROME
Authors: UDLER Y HALPERN GJ SHER C DAVIDOVITZ M SHOHAT M
Citation: Y. Udler et al., FURTHER DELINEATION OF CEREBRO-OSTEO-NEPHROSIS SYNDROME, American journal of medical genetics, 72(4), 1997, pp. 383-385
CORRELATION BETWEEN THE INCIDENCE OF MYOTONIC-DYSTROPHY IN DIFFERENT GROUPS IN ISRAEL AND THE NUMBER OF CTG TRINUCLEOTIDE REPEATS IN THE MYOTONIN GENE
Authors: MORCOHEN R MAGAL N GADOTH N SHOHAT T SHOHAT M
Citation: R. Morcohen et al., CORRELATION BETWEEN THE INCIDENCE OF MYOTONIC-DYSTROPHY IN DIFFERENT GROUPS IN ISRAEL AND THE NUMBER OF CTG TRINUCLEOTIDE REPEATS IN THE MYOTONIN GENE, American journal of medical genetics, 71(2), 1997, pp. 156-159
CONSANGUINITY AND COMMON ADULT DISEASES IN ISRAELI ARAB COMMUNITIES
Authors: JABER L SHOHAT T ROTTER JI SHOHAT M
Citation: L. Jaber et al., CONSANGUINITY AND COMMON ADULT DISEASES IN ISRAELI ARAB COMMUNITIES, American journal of medical genetics, 70(4), 1997, pp. 346-348
AGENESIS OF THE CORPUS-CALLOSUM IN A MOTHER AND SON
Authors: INBAR D HALPERN GJ WEITZ R SADEH M SHOHAT M
Citation: D. Inbar et al., AGENESIS OF THE CORPUS-CALLOSUM IN A MOTHER AND SON, American journal of medical genetics, 69(2), 1997, pp. 152-154
ANCIENT MISSENSE MUTATIONS IN A NEW MEMBER OF THE RORET GENE FAMILY ARE LIKELY TO CAUSE FAMILIAL MEDITERRANEAN FEVER
Authors: AKSENTIJEVICH I CENTOLA M DENG ZM SOOD R BALOW JE WOOD G ZAKS N MANSFIELD E CHEN X EISENBERG S VEDULA A SHAFRAN N RABEN N PRAS E PRAS M KASTNER DL BLAKE T BAXEVANIS AD ROBBINS C KRIZMAN D COLLINS FS LIU PP CHEN XG SHOHAT M HAMON M KAHAN T CERCEK A ROTTER JI FISCHELGHODSIAN N RICHARDS N SHELTON DA GUMUCIO D YOKOYAMA Y MANGELSDORF M ORSBORN A RICHARDS RI RICKE DO BUCKINGHAM JM MOYZIS RK DEAVEN LL DOGGETT NA
Citation: I. Aksentijevich et al., ANCIENT MISSENSE MUTATIONS IN A NEW MEMBER OF THE RORET GENE FAMILY ARE LIKELY TO CAUSE FAMILIAL MEDITERRANEAN FEVER, Cell, 90(4), 1997, pp. 797-807
EFFECTS OF CONSANGUINEOUS MARRIAGE ON REPRODUCTIVE OUTCOME IN AN ARABCOMMUNITY IN ISRAEL
Authors: JABER L MERLOB P GABRIEL R SHOHAT M
Citation: L. Jaber et al., EFFECTS OF CONSANGUINEOUS MARRIAGE ON REPRODUCTIVE OUTCOME IN AN ARABCOMMUNITY IN ISRAEL, Journal of Medical Genetics, 34(12), 1997, pp. 1000-1002
DENTAL MANIFESTATIONS OF BULIMIA-NERVOSA
Authors: MARKITZIU A SHOHAT M BEERI E BONE A ZALKIND M
Citation: A. Markitziu et al., DENTAL MANIFESTATIONS OF BULIMIA-NERVOSA, Journal of dental research, 76(5), 1997, pp. 1165-1165
SPEECH DISORDERS IN ISRAELI ARAB CHILDREN
Authors: JABER L NAHMANI A SHOHAT M
Citation: L. Jaber et al., SPEECH DISORDERS IN ISRAELI ARAB CHILDREN, Israel journal of medical sciences, 33(10), 1997, pp. 663-665
A GENE FOR ARTHROGRYPOSIS MULITPLEX CONGENITA NEUROPATHIC TYPE IS LINKED TO D5S394 ON CHROMOSOME 5QTER
Authors: SHOHAT M LOTAN R MAGAL N SHOHAT T FISCHELGHODSIAN N ROTTER JI JABER L
Citation: M. Shohat et al., A GENE FOR ARTHROGRYPOSIS MULITPLEX CONGENITA NEUROPATHIC TYPE IS LINKED TO D5S394 ON CHROMOSOME 5QTER, American journal of human genetics, 61(5), 1997, pp. 1139-1143
Risultati: 1-25 | 26-50 | 51-69