AAAAAA
Results:
1-25
|
Results: 25
Authors:
CHIBAFALEK O
NISSIMRAFINIA M
ARGAMAN Z
GENEM A
MORAN I
KEREM E
KEREM B
Citation: O. Chibafalek et al., SCREENING OF CFTR MUTATIONS IN AN ISOLATED POPULATION - IDENTIFICATION OF CARRIERS AND PATIENTS, European journal of human genetics, 6(2), 1998, pp. 181-184
Authors:
CHIBAFALEK O
KEREM E
SHOSHANI T
AVIRAM M
AUGARTEN A
BENTUR L
TAL A
TULLIS E
RAHAT A
KEREM B
Citation: O. Chibafalek et al., THE MOLECULAR-BASIS OF DISEASE VARIABILITY AMONG CYSTIC-FIBROSIS PATIENTS CARRYING THE 3849-]T MUTATION(10 KB C), Genomics (San Diego, Calif.), 53(3), 1998, pp. 276-283
Authors:
GROSSTSUR V
MANOR O
KEREM B
FRIEDLANDER Y
SHALEV RS
Citation: V. Grosstsur et al., DEVELOPMENTAL DYSCALCULIA IS A FAMILIAL LEARNING-DISABILITY, Annals of neurology, 44(3), 1998, pp. 29-29
Authors:
GUTTENBACH M
NASSAR N
FEICHTINGER W
STEINLEIN C
NANDA I
WANNER G
KEREM B
SCHMID M
Citation: M. Guttenbach et al., AN INTERSTITIAL NUCLEOLUS ORGANIZER REGION IN THE LONG ARM OF HUMAN-CHROMOSOME-7 - CYTOGENETIC CHARACTERIZATION AND FAMILIAL SEGREGATION, Cytogenetics and cell genetics, 80(1-4), 1998, pp. 104-112
Authors:
MISHMAR D
RAHAT A
SCHERER SW
NYAKATURA G
HINZMANN B
KOHWI Y
MANDELGUTFROIND Y
LEE JR
DRESCHER B
SAS DE
MARGALIT H
PLATZER M
WEISS A
TSUI LC
ROSENTHAL A
KEREM B
Citation: D. Mishmar et al., MOLECULAR CHARACTERIZATION OF A COMMON FRAGILE SITE (FRA7H) ON HUMAN-CHROMOSOME-7 BY THE CLONING OF A SIMIAN-VIRUS-40 INTEGRATION SITE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(14), 1998, pp. 8141-8146
Authors:
AN RH
WANG XL
KEREM B
BENHORIN J
MEDINA A
GOLDMIT M
KASS RS
Citation: Rh. An et al., NOVEL LQT-3 MUTATION AFFECTS NA-SUBUNIT AND BETA(1)-SUBUNIT( CHANNEL ACTIVITY THROUGH INTERACTIONS BETWEEN ALPHA), Circulation research, 83(2), 1998, pp. 141-146
Authors:
AN RH
WANG XL
KEREM B
BENHORIN J
MEDINA A
KASS RS
Citation: Rh. An et al., NOVEL LQT-3 MUTATION AFFECTS NA-SUBUNIT AND BETA(1)-SUBUNIT INTERACTIONS( CHANNEL ACTIVITY THROUGH ALPHA), Biophysical journal, 74(2), 1998, pp. 25-25
Authors:
KEREM E
RAVEHAREL N
AUGARTEN A
MADGAR I
NISSIMRAFINIA M
YAHAV Y
GOSHEN R
BENTUR L
RIVLIN J
AVIRAM M
GENEM A
CHIBAFALEK O
KRAEMER MR
SIMON A
BRANSKI D
KEREM B
Citation: E. Kerem et al., A CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR SPLICE VARIANT WITH PARTIAL PENETRANCE ASSOCIATED WITH VARIABLE CYSTIC-FIBROSIS PRESENTATIONS, American journal of respiratory and critical care medicine, 155(6), 1997, pp. 1914-1920
Authors:
ESTIVILL X
BANCELLS C
RAMOS C
PIAZZA A
CARBONARA A
MASTELLA G
BONIZZATO A
CASTALDI G
DALCAMO E
FERRARI M
GASPARINI P
GUANTI G
LEONI GB
PIGNATTI PF
RONCHETTO P
SEIA M
TORRICELLI F
GOOSSENS M
CHEVALIERPORST F
BOZON D
SIMONBOUY B
FELDMANN D
ELION J
KAPLAN JC
FEREC C
CLAUSTRES M
CLAVEL C
PUCHELLE E
LUNARDI J
MATHIEU M
SCHEFFER H
HALLEY DJJ
VANDENOUWELAND AMW
TIJMENSEN ASLN
CASALS T
GIMENEZ FJ
RAMOS L
BENEYTO M
BENITEZ J
PALACIO A
TUMMLER B
BAUER I
MEITINGER T
CLAASS A
LINDNER M
SCHRODER E
STUHRMANN M
CASSIMAN J
CUPPENS H
COCHAUX P
PONCIN J
MESSIAN L
BARANOV VS
IVASCHENKO TE
BAKAY M
BAL J
WITT M
KANAVAKIS M
TZETIS M
ANTONIADI T
LAVINHA J
PACHECO P
DUARTE A
LOUREIRO P
KALAYDJIEVA L
ANGELICHEVA D
JORDANOVA A
SAVOV A
EIKLID K
HOLMBERG L
SCHAEDEL C
OZGUC M
GOCMEN A
ERDERN H
LIECHTIGALLATI S
NEMETI M
FEKETE G
KLAASSEN T
SCHWARZ M
SCHWARTZ M
MACEK M
MACEK M
KREBSOVA A
VAVROVA V
KEREM B
AVELIOVICH D
FERAK V
KADASI L
KAYSEROVA H
GLAVAC D
RAVNIKGLAVAC M
EFREMOV GD
CANKIKLEIN N
KERE J
Citation: X. Estivill et al., GEOGRAPHIC-DISTRIBUTION AND REGIONAL ORIGIN OF 272 CYSTIC-FIBROSIS INEUROPEAN POPULATIONS, Human mutation, 10(2), 1997, pp. 135-154
Authors:
KEREM E
NISSIMRAFINIA M
ARGAMAN Z
AUGARTEN A
BENTUR L
KLAR A
YAHAV Y
SZEINBERG A
HIBA O
BRANSKI D
COREY M
KEREM B
Citation: E. Kerem et al., A MISSENSE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR MUTATION WITH VARIABLE PHENOTYPE, Pediatrics, 100(3), 1997, pp. 51-56
Authors:
KEREM B
MISHMAR D
RAHAT A
SCHERER SW
LEE J
HINZMANN B
NYKATURA G
WEISS A
MANDELGUTFROIND Y
TSUR LC
ROSENTHAL A
Citation: B. Kerem et al., UNSTABLE REGIONS IN THE HUMAN GENOME - IDENTIFICATION AND CHARACTERIZATION OF THE COMMON FRAGILE SITE FRA7H IN HUMAN-CHROMOSOME-7, American journal of human genetics, 61(4), 1997, pp. 735-735
Authors:
BENHORIN J
GOLDMIT M
MACCLUER JW
BLANGERO J
WANG Q
MEDINA A
TOWBIN JA
KEREM B
Citation: J. Benhorin et al., A NEW MUTATION IN SCN5A ASSOCIATED WITH THE LONG QT SYNDROME, American journal of human genetics, 61(4), 1997, pp. 1909-1909
Authors:
RAVEHAREL N
KEREM E
NISSIMRAFINIA M
MADJAR I
GOSHEN R
AUGARTEN A
RAHAT A
HURWITZ A
DARVASI A
KEREM B
Citation: N. Raveharel et al., THE MOLECULAR-BASIS OF PARTIAL PENETRANCE OF SPLICING MUTATIONS IN CYSTIC-FIBROSIS, American journal of human genetics, 60(1), 1997, pp. 87-94
Authors:
KEREM E
KEREM B
Citation: E. Kerem et B. Kerem, GENOTYPE-PHENOTYPE CORRELATIONS IN CYSTIC-FIBROSIS, Pediatric pulmonology, 22(6), 1996, pp. 387-395
Authors:
KEREM B
KEREM E
Citation: B. Kerem et E. Kerem, THE MOLECULAR-BASIS FOR DISEASE VARIABILITY IN CYSTIC-FIBROSIS, European journal of human genetics, 4(2), 1996, pp. 65-73
Authors:
AVIDOR B
ZAKUT H
KEREM B
Citation: B. Avidor et al., SIMPLE, RAPID NONRADIOACTIVE METHOD TO DETECT MAJOR CYSTIC-FIBROSIS MUTATIONS IN ASHKENAZI-JEWS, Clinical chemistry, 42(1), 1996, pp. 103-105
Authors:
DARVASI A
KEREM B
Citation: A. Darvasi et B. Kerem, DELETION AND INSERTION MUTATIONS IN SHORT TANDEM REPEATS IN THE CODING REGIONS OF HUMAN GENES, European journal of human genetics, 3(1), 1995, pp. 14-20
Authors:
KEREM E
KALMAN YM
YAHAV Y
SHOSHANI T
ABELIOVICH D
SZEINBERG A
RIVLIN J
BLAU H
TAL A
BENTUR L
SPRINGER C
AUGARTEN A
GODFREY S
LERER I
BRANSKI D
FRIEDMAN M
KEREM B
Citation: E. Kerem et al., HIGHLY VARIABLE INCIDENCE OF CYSTIC-FIBROSIS AND DIFFERENT MUTATION DISTRIBUTION AMONG DIFFERENT JEWISH ETHNIC-GROUPS IN ISRAEL, Human genetics, 96(2), 1995, pp. 193-197
Authors:
RESHEF D
RAHAT A
KEREM B
Citation: D. Reshef et al., IDENTIFICATION AND CHARACTERIZATION OF UNSTABLE REGIONS IN HUMAN-CHROMOSOMES - CHROMOSOME-7 AS A MODEL, Cytogenetics and cell genetics, 71(1), 1995, pp. 22-23
Authors:
KEREM B
RAVEHAREL N
NISSIMRAFINIA M
GOSHEN R
MADGAR I
AUGARTEN A
KEREM E
Citation: B. Kerem et al., VARIABLE LEVELS OF ABERRANTLY SPLICED CFTR MESSENGER-RNA TRANSCRIBED FROM THE 5T ALLELE - THE CAUSE FOR VARIABLE DISEASE SEVERITY AMONG INDIVIDUALS AND BETWEEN ORGANS OF THE NAME INDIVIDUAL, American journal of human genetics, 57(4), 1995, pp. 1412-1412
Authors:
RAVEHAREL N
MADGAR I
GOSHEN R
NISSIMRAFINIA M
ZIADNI A
RAHAT A
CHIBA O
KALMAN YM
BRAUTBAR C
LEVINSON D
AUGARTEN A
KEREM E
KEREM B
Citation: N. Raveharel et al., CFTR HAPLOTYPE ANALYSIS REVEALS GENETIC-HETEROGENEITY IN THE ETIOLOGYOF CONGENITAL BILATERAL APLASIA OF THE VAS-DEFERENS, American journal of human genetics, 56(6), 1995, pp. 1359-1366
Authors:
SHOSHANI T
AUGARTEN A
YAHAV J
GAZIT E
KEREM B
Citation: T. Shoshani et al., 2 NOVEL MUTATIONS IN THE CFTR GENE - W1089X IN EXON 17B AND 4010DELTATT IN EXON-21, Human molecular genetics, 3(4), 1994, pp. 657-658
Authors:
EHRLICH G
GINZBERG D
LOEWENSTEIN Y
GLICK D
KEREM B
BENARI S
ZAKUT H
SOREQ H
Citation: G. Ehrlich et al., POPULATION DIVERSITY AND DISTINCT HAPLOTYPE FREQUENCIES ASSOCIATED WITH ACHE AND BCHE GENES OF ISRAELI JEWS FROM TRANS-CAUCASIAN GEORGIA AND FROM EUROPE, Genomics, 22(2), 1994, pp. 288-295
Authors:
KALMAN YM
KEREM B
Citation: Ym. Kalman et B. Kerem, INFERENCE OF CF CARRIER FREQUENCIES FROM CF PATIENTS DATA, IS IT JUSTIFIED, American journal of human genetics, 53(3), 1993, pp. 1492-1492
Authors:
DARVASI A
KEREM B
Citation: A. Darvasi et B. Kerem, SLIPPAGE DURING REPLICATION AS A MECHANISM CAUSING DELETION AND INSERTION MUTATIONS IN THE CF GENE, American journal of human genetics, 53(3), 1993, pp. 1614-1614
Risultati:
1-25
|