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Results: << | 101-125 | 126-150 | 151-158
Results: 101-125/158
DISTRIBUTION OF EXTRACELLULAR MATRICES, MATRIX RECEPTORS, AND TRANSFORMING GROWTH-FACTOR-BETA-1 IN HUMAN AND EXPERIMENTAL LUNG GRANULOMATOUS INFLAMMATION
Authors: ROMAN J JEON YJ GAL A PEREZ RL
Citation: J. Roman et al., DISTRIBUTION OF EXTRACELLULAR MATRICES, MATRIX RECEPTORS, AND TRANSFORMING GROWTH-FACTOR-BETA-1 IN HUMAN AND EXPERIMENTAL LUNG GRANULOMATOUS INFLAMMATION, The American journal of the medical sciences, 309(3), 1995, pp. 124-133
MYOTUBULAR MYOPATHY IN A GIRL WITH A DELETION AT XQ27-Q28 AND UNBALANCED X-INACTIVATION ASSIGNS THE MTM1 GENE TO A 600-KB REGION
Authors: DAHL N HU LJ CHERY M FARDEAU M GILGENKRANTZ S NIVELONCHEVALLIER A SIDANERNOISETTE I MUGNERET F GOUYON JB GAL A KIOSCHIS P DURSO M MANDEL JL
Citation: N. Dahl et al., MYOTUBULAR MYOPATHY IN A GIRL WITH A DELETION AT XQ27-Q28 AND UNBALANCED X-INACTIVATION ASSIGNS THE MTM1 GENE TO A 600-KB REGION, American journal of human genetics, 56(5), 1995, pp. 1108-1115
BENGURION AND THE AMERICAN ALIGNMENT FOR A JEWISH STATE
Authors: GAL A
Citation: A. Gal, BENGURION AND THE AMERICAN ALIGNMENT FOR A JEWISH STATE, American Jewish archives, 47(1), 1995, pp. 172-175
CONSORTIUM FINE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE (CMTX1) - ADDITIONAL SUPPORT THAT CONNEXIN32 IS THE DEFECT IN CMTX1
Authors: PERICAKVANCE MA BARKER DF BERGOFFEN JA CHANCE P COCHRANE S DAHL N EXLER MC FAIN PR FAIRWEATHER ND FISCHBECK K GAL A HAITES N IONASESCU R IONASESCU VV KENNERSON ML MONACO AP MOSTACCUIOLO M NICHOLSON GA SILLEN A HAINES JL
Citation: Ma. Pericakvance et al., CONSORTIUM FINE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE (CMTX1) - ADDITIONAL SUPPORT THAT CONNEXIN32 IS THE DEFECT IN CMTX1, Human heredity, 45(3), 1995, pp. 121-128
THR4LYS RHODOPSIN MUTATION IS ASSOCIATED WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA OF THE CONE-ROD TYPE IN A SMALL DUTCH FAMILY
Authors: VANDENBORN LI VANSCHOONEVELD MJ DEJONG LAMS RIEMSLAG FCC DEJONG PTVM GAL A BLEEKERWAGEMAKERS EM
Citation: Li. Vandenborn et al., THR4LYS RHODOPSIN MUTATION IS ASSOCIATED WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA OF THE CONE-ROD TYPE IN A SMALL DUTCH FAMILY, Ophthalmic genetics, 15(2), 1994, pp. 51-60
MISSENSE RHODOPSIN MUTATION IN A FAMILY WITH RECESSIVE RP
Authors: KUMARAMANICKAVEL G MAW M DENTON MJ JOHN S SRIKUMARI CRS ORTH U OEHLMANN R GAL A
Citation: G. Kumaramanickavel et al., MISSENSE RHODOPSIN MUTATION IN A FAMILY WITH RECESSIVE RP, Nature genetics, 8(1), 1994, pp. 10-11
HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS (VOL 7,PG 64, 1994)
Authors: GAL A ORTH U BAEHR W SCHWINGER E ROSENBERG T
Citation: A. Gal et al., HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS (VOL 7,PG 64, 1994), Nature genetics, 7(4), 1994, pp. 551-551
HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS
Authors: GAL A ORTH U BAEHR W SCHWINGER E ROSENBERG T
Citation: A. Gal et al., HETEROZYGOUS MISSENSE MUTATION IN THE ROD CGMP PHOSPHODIESTERASE BETA-SUBUNIT GENE IN AUTOSOMAL-DOMINANT STATIONARY NIGHT BLINDNESS, Nature genetics, 7(1), 1994, pp. 64-68
MUTATIONS IN THE HUMAN PERIPHERIN RDS GENE ASSOCIATED WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA/
Authors: GRUNING G MILLAN JM MEINS M BENEYTO M CABALLERO M APFELSTEDTSYLLA E BOSCH R ZRENNER E PRIETO F GAL A
Citation: G. Gruning et al., MUTATIONS IN THE HUMAN PERIPHERIN RDS GENE ASSOCIATED WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA/, Human mutation, 3(3), 1994, pp. 321-323
X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY - VALINE-38-METHIONINE SUBSTITUTION OF CONNEXIN-32
Authors: ORTH U FAIRWEATHER N EXLER MC SCHWINGER E GAL A
Citation: U. Orth et al., X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY - VALINE-38-METHIONINE SUBSTITUTION OF CONNEXIN-32, Human molecular genetics, 3(9), 1994, pp. 1699-1700
DETECTION OF POINT MUTATIONS IN THE ANDROGEN RECEPTOR GENE USING NONISOTOPIC SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS
Authors: HIORT O WODTKE A STRUVE D ZOLLNER A SINNECKER GHG ALBERS N BEYE M BEYER P BIRR C BLUNCK W BRACK C BRAMSWIG J DORR HG GAL A HECKER W HEIDEMANN P HEINRICH U HEISE HR HESSE V HINKEL M HOEPFFNER W HOLDER M KEIM L KLASEN M KORSCH E KRUGER G LANDENDORFER W MIX M MORLOT M MUHLENBERG R OTTEN A PARTSCH CJ PELZ L VONPETRYKOWSKI W RABL W REICH H SCHENK B SCHNABEL D SIPPELL W
Citation: O. Hiort et al., DETECTION OF POINT MUTATIONS IN THE ANDROGEN RECEPTOR GENE USING NONISOTOPIC SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS, Human molecular genetics, 3(7), 1994, pp. 1163-1166
3 NOVEL RHODOPSIN MUTATIONS (C110F, L131P, A164V) IN PATIENTS WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA
Authors: FUCHS S KRANICH H DENTON MJ ZRENNER E BHATTACHARYA SS HUMPHRIES P GAL A
Citation: S. Fuchs et al., 3 NOVEL RHODOPSIN MUTATIONS (C110F, L131P, A164V) IN PATIENTS WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA, Human molecular genetics, 3(7), 1994, pp. 1203-1203
MUCOPOLYSACCHARIDOSIS TYPE-I - IDENTIFICATION OF 8 NOVEL MUTATIONS AND DETERMINATION OF THE FREQUENCY OF THE 2 COMMON ALPHA-1-IDURONIDASE MUTATIONS (W402X AND Q70X) AMONG EUROPEAN PATIENTS
Authors: BUNGE S KLEIJER WJ STEGLICH C BECK M ZUTHER C MORRIS CP SCHWINGER E HOPWOOD JJ SCOTT HS GAL A
Citation: S. Bunge et al., MUCOPOLYSACCHARIDOSIS TYPE-I - IDENTIFICATION OF 8 NOVEL MUTATIONS AND DETERMINATION OF THE FREQUENCY OF THE 2 COMMON ALPHA-1-IDURONIDASE MUTATIONS (W402X AND Q70X) AMONG EUROPEAN PATIENTS, Human molecular genetics, 3(6), 1994, pp. 861-866
A MISSENSE POINT MUTATION (LEU13ARG) OF THE NORRIE DISEASE GENE IN A LARGE CUBAN KINDRED WITH NORRIE DISEASE
Authors: FUCHS S XU SY CABALLERO M SALCEDO M LAO A WEDEMANN H GAL A
Citation: S. Fuchs et al., A MISSENSE POINT MUTATION (LEU13ARG) OF THE NORRIE DISEASE GENE IN A LARGE CUBAN KINDRED WITH NORRIE DISEASE, Human molecular genetics, 3(4), 1994, pp. 655-656
GENE FOR AUTOSOMAL-DOMINANT CONGENITAL STATIONARY NIGHT BLINDNESS MAPS TO THE SAME REGION AS THE GENE FOR THE BETA-SUBUNIT OF THE ROD PHOTORECEPTOR CGMP PHOSPHODIESTERASE (PDEB) IN CHROMOSOME 4P16.3
Authors: GAL A XU SY PICZENIK Y EIBERG H DUVIGNEAU C SCHWINGER E ROSENBERG T
Citation: A. Gal et al., GENE FOR AUTOSOMAL-DOMINANT CONGENITAL STATIONARY NIGHT BLINDNESS MAPS TO THE SAME REGION AS THE GENE FOR THE BETA-SUBUNIT OF THE ROD PHOTORECEPTOR CGMP PHOSPHODIESTERASE (PDEB) IN CHROMOSOME 4P16.3, Human molecular genetics, 3(2), 1994, pp. 323-325
3 SEQUENCE POLYMORPHISMS IN THE PDC GENE
Authors: MANSERGH FC JORDAN SA FARRAR GJ KUMARSINGH R GAL A BHATTACHARYA S HUMPHRIES P
Citation: Fc. Mansergh et al., 3 SEQUENCE POLYMORPHISMS IN THE PDC GENE, Human molecular genetics, 3(11), 1994, pp. 2077-2077
MISSENSE MUTATIONS ARE FREQUENT IN THE GENE FOR X-CHROMOSOMAL ADRENOLEUKODYSTROPHY (ALD)
Authors: FUCHS S SARDE CO WEDEMANN H SCHWINGER E MANDEL JL GAL A
Citation: S. Fuchs et al., MISSENSE MUTATIONS ARE FREQUENT IN THE GENE FOR X-CHROMOSOMAL ADRENOLEUKODYSTROPHY (ALD), Human molecular genetics, 3(10), 1994, pp. 1903-1905
ASSIGNMENT OF A GENE FOR AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA (RP12) TO CHROMOSOME 1Q31-Q32.1 IN AN INBRED AND GENETICALLY HETEROGENEOUS DISEASE POPULATION
Authors: VANSOEST S VANDENBORN LI GAL A FARRAR GJ BLEEKERWAGEMAKERS LM WESTERVELD A HUMPHRIES P SANDKUIJL LA BERGEN AAB
Citation: S. Vansoest et al., ASSIGNMENT OF A GENE FOR AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA (RP12) TO CHROMOSOME 1Q31-Q32.1 IN AN INBRED AND GENETICALLY HETEROGENEOUS DISEASE POPULATION, Genomics, 22(3), 1994, pp. 499-504
MAPPING OF THE AUTOSOMAL-DOMINANT EXUDATIVE VITREORETINOPATHY LOCUS (EVR1) BY MULTIPOINT LINKAGE ANALYSIS IN 4 FAMILIES
Authors: MULLER B ORTH U VANNOUHUYS CE DUVIGNEAU C FUHRMANN C SCHWINGER E LAQUA H GAL A
Citation: B. Muller et al., MAPPING OF THE AUTOSOMAL-DOMINANT EXUDATIVE VITREORETINOPATHY LOCUS (EVR1) BY MULTIPOINT LINKAGE ANALYSIS IN 4 FAMILIES, Genomics, 20(2), 1994, pp. 317-319
SCALAR AND VECTOR-MESON PRODUCTION IN (K-, K+) REACTIONS ON NUCLEI
Authors: GOBBI C DOVER CB GAL A
Citation: C. Gobbi et al., SCALAR AND VECTOR-MESON PRODUCTION IN (K-, K+) REACTIONS ON NUCLEI, Physical review. C. Nuclear physics, 50(3), 1994, pp. 1594-1605
DENSITY-DEPENDENCE IN SIGMA(-)-ATOMS AND IMPLICATIONS FOR SIGMA-HYPERNUCLEI
Authors: BATTY CJ FRIEDMAN E GAL A
Citation: Cj. Batty et al., DENSITY-DEPENDENCE IN SIGMA(-)-ATOMS AND IMPLICATIONS FOR SIGMA-HYPERNUCLEI, Progress of theoretical physics. Supplement, (117), 1994, pp. 227-240
WIDTHS OF XI-HYPERNUCLEAR STATES
Authors: MILLENER DJ DOVER CB GAL A
Citation: Dj. Millener et al., WIDTHS OF XI-HYPERNUCLEAR STATES, Progress of theoretical physics. Supplement, (117), 1994, pp. 307-324
APPLICATION OF MASS FORMULAS FOR MULTIPLY STRANGE NUCLEI
Authors: BALBERG S GAL A SCHAFFNER J
Citation: S. Balberg et al., APPLICATION OF MASS FORMULAS FOR MULTIPLY STRANGE NUCLEI, Progress of theoretical physics. Supplement, (117), 1994, pp. 325-337
DENSITY-DEPENDENT K- NUCLEAR OPTICAL POTENTIALS FROM KAONIC ATOMS
Authors: FRIEDMAN E GAL A BATTY CJ
Citation: E. Friedman et al., DENSITY-DEPENDENT K- NUCLEAR OPTICAL POTENTIALS FROM KAONIC ATOMS, Nuclear physics. A, 579(3-4), 1994, pp. 518-538
ON THE PRODUCTION AND DECAY OF STRANGENESS S=-2 HYPERNUCLEI
Authors: DOVER CB GAL A MILLENER DJ
Citation: Cb. Dover et al., ON THE PRODUCTION AND DECAY OF STRANGENESS S=-2 HYPERNUCLEI, Nuclear physics. A, 572(1), 1994, pp. 85-111
Risultati: << | 101-125 | 126-150 | 151-158