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Results: 1-25 | 26-50 | 51-53
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GY PROVIDES A MOUSE MODEL FOR SPERMINE SYNTHASE DEFICIENCY
Authors: LORENZ B FRANCIS F GEMPEL K BOEDDRICH A JOSTEN M SCHMAHL W SCHMIDT J LEHRACH H MEITINGER T STROM TM
Citation: B. Lorenz et al., GY PROVIDES A MOUSE MODEL FOR SPERMINE SYNTHASE DEFICIENCY, European journal of human genetics, 6, 1998, pp. 802-802
MAPPING OF 6 ISODICENTRIC XQ13 BREAKPOINTS ASSOCIATED WITH PRELEUKEMIA, CHARACTERIZATION OF THE REGION AND SEARCH FOR POTENTIAL EXPRESSED SEQUENCES
Authors: MCDONELL N BUCKLE V VINET MC RIDER S MONACO AP ROSS F KAHN A FRANCIS F KEARNEY L CHELLY J
Citation: N. Mcdonell et al., MAPPING OF 6 ISODICENTRIC XQ13 BREAKPOINTS ASSOCIATED WITH PRELEUKEMIA, CHARACTERIZATION OF THE REGION AND SEARCH FOR POTENTIAL EXPRESSED SEQUENCES, European journal of human genetics, 6, 1998, pp. 4172-4172
DOUBLECORTIN IS THE MAJOR GENE CAUSING X-LINKED SUBCORTICAL LAMINAR HETEROTOPIA (SCLH)
Authors: DESPORTES V FRANCIS F PINARD JM DESGUERRE I MOUTARD ML SNOECK I MEINERS LC CAPRON F CUSMAI R RICCI S MOTTE J ECHENNE B PONSOT G DULAC O CHELLY J BELDJORD C
Citation: V. Desportes et al., DOUBLECORTIN IS THE MAJOR GENE CAUSING X-LINKED SUBCORTICAL LAMINAR HETEROTOPIA (SCLH), Human molecular genetics (Print), 7(7), 1998, pp. 1063-1070
SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE
Authors: LORENZ B FRANCIS F GEMPEL K BODDRICH A JOSTEN M SCHMAHL W SCHMIDT J LEHRACH H MEITINGER T STROM TM
Citation: B. Lorenz et al., SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE, Human molecular genetics, 7(3), 1998, pp. 541-547
LAST NEWS - DOUBLECORTIN, A NEW GENE EXPR ESSED IN FETAL BRAIN, IS INVOLVED IN X-LINKED SUBCORTICAL LAMINAR HETEROTOPIA AND LISSENCEPHALY
Authors: DESPORTES V PINARD JM FRANCIS F CHELLY J
Citation: V. Desportes et al., LAST NEWS - DOUBLECORTIN, A NEW GENE EXPR ESSED IN FETAL BRAIN, IS INVOLVED IN X-LINKED SUBCORTICAL LAMINAR HETEROTOPIA AND LISSENCEPHALY, MS. Medecine sciences, 14(2), 1998, pp. 241-243
THE GENOMIC ORGANIZATION OF NKG2C, NKG2E, NKG2F AND NKG2D RECEPTOR GENES IN THE HUMAN NATURAL-KILLER GENE-COMPLEX
Authors: GLIENKE J SOBANOV Y BROSTJAN C STEFFENS C NGUYEN C LEHRACH H HOFER E FRANCIS F
Citation: J. Glienke et al., THE GENOMIC ORGANIZATION OF NKG2C, NKG2E, NKG2F AND NKG2D RECEPTOR GENES IN THE HUMAN NATURAL-KILLER GENE-COMPLEX, Immunogenetics (New York), 48(3), 1998, pp. 163-173
STRUCTURE OF THE HUMAN CD94 C-TYPE LECTIN GENE
Authors: RODRIGUEZ A CARRETERO M GLIENKE J BELLON T RAMIREZ A LEHRACH H FRANCIS F LOPEZBOTET M
Citation: A. Rodriguez et al., STRUCTURE OF THE HUMAN CD94 C-TYPE LECTIN GENE, Immunogenetics, 47(4), 1998, pp. 305-309
A PHEX GENE MUTATION IS RESPONSIBLE FOR ADULT-ONSET VITAMIN-D-RESISTANT HYPOPHOSPHATEMIC OSTEOMALACIA - EVIDENCE THAT THE DISORDER IS NOT ADISTINCT ENTITY FROM X-LINKED HYPOPHOSPHATEMIC RICKETS
Authors: ECONS MJ FRIEDMAN NE ROWE PSN SPEER MC FRANCIS F STROM TM OUDET C SMITH JA NINOMIYA JT LEE BE BERGEN H
Citation: Mj. Econs et al., A PHEX GENE MUTATION IS RESPONSIBLE FOR ADULT-ONSET VITAMIN-D-RESISTANT HYPOPHOSPHATEMIC OSTEOMALACIA - EVIDENCE THAT THE DISORDER IS NOT ADISTINCT ENTITY FROM X-LINKED HYPOPHOSPHATEMIC RICKETS, The Journal of clinical endocrinology and metabolism, 83(10), 1998, pp. 3459-3462
AN AUTOIMMUNE-DISEASE, APECED, CAUSED BY MUTATIONS IN A NOVEL GENE FEATURING 2 PHD-TYPE ZINC-FINGER DOMAINS
Authors: AALTONEN J BJORSES P PERHEENTUPA J HORELLIKUITUNEN N PALOTIE A PELTONEN L LEE YS FRANCIS F HENNIG S THIEL C LEHRACH H YASPO ML
Citation: J. Aaltonen et al., AN AUTOIMMUNE-DISEASE, APECED, CAUSED BY MUTATIONS IN A NOVEL GENE FEATURING 2 PHD-TYPE ZINC-FINGER DOMAINS, Nature genetics, 17(4), 1997, pp. 399-403
GENOMIC ORGANIZATION OF THE HUMAN PEX GENE MUTATED IN X-LINKED DOMINANT HYPOPHOSPHATEMIC RICKETS
Authors: FRANCIS F STROM TM HENNIG S BODDRICH A LORENZ B BRANDAU O MOHNIKE KL CAGNOLI M STEFFENS C KLAGES S BORZYM K POHL T OUDET C ECONS MJ ROWE PSN REINHARDT R MEITINGER T LEHRACH H
Citation: F. Francis et al., GENOMIC ORGANIZATION OF THE HUMAN PEX GENE MUTATED IN X-LINKED DOMINANT HYPOPHOSPHATEMIC RICKETS, PCR methods and applications, 7(6), 1997, pp. 573-585
AUTISM AND MULTIPLE EXOSTOSES ASSOCIATED WITH AN X-8 TRANSLOCATION OCCURRING WITHIN THE GRPR GENE AND 3' TO THE SDC2 GENE
Authors: ISHIKAWABRUSH Y POWELL JF BOLTON P MILLER AP FRANCIS F WILLARD HF LEHRACH H MONACO AP
Citation: Y. Ishikawabrush et al., AUTISM AND MULTIPLE EXOSTOSES ASSOCIATED WITH AN X-8 TRANSLOCATION OCCURRING WITHIN THE GRPR GENE AND 3' TO THE SDC2 GENE, Human molecular genetics, 6(8), 1997, pp. 1241-1250
DISTRIBUTION OF MUTATIONS IN THE PEX GENE IN FAMILIES WITH X-LINKED HYPOPHOSPHATEMIC RICKETS (HYP)
Authors: ROWE PSN OUDET CL FRANCIS F SINDING C PANNETIER S ECONS MJ STROM TM MEITINGER T GARABEDIAN M DAVID A MACHER MA QUESTIAUX E POPOWSKA E PRONICKA E READ AP MOKRZYCKI A GLORIEUX FH DREZNER MK HANAUER A LEHRACH H GOULDING JN ORIORDAN JLH
Citation: Psn. Rowe et al., DISTRIBUTION OF MUTATIONS IN THE PEX GENE IN FAMILIES WITH X-LINKED HYPOPHOSPHATEMIC RICKETS (HYP), Human molecular genetics, 6(4), 1997, pp. 539-549
PEX GENE DELETIONS IN GY AND HYP MICE PROVIDE MOUSE MODELS FOR X-LINKED HYPOPHOSPHATEMIA
Authors: STROM TM FRANCIS F LORENZ B BODDRICH A ECONS MJ LEHRACH H MEITINGER T
Citation: Tm. Strom et al., PEX GENE DELETIONS IN GY AND HYP MICE PROVIDE MOUSE MODELS FOR X-LINKED HYPOPHOSPHATEMIA, Human molecular genetics, 6(2), 1997, pp. 165-171
CHARACTERIZATION OF THE C3 YAC CONTIG FROM PROXIMAL MOUSE-CHROMOSOME-17 AND ANALYSIS OF ALLELIC EXPRESSION OF GENES FLANKING THE IMPRINTED IGF2R GENE
Authors: SCHWEIFER N VALK PJM DELWEL R COX R FRANCIS F MEIEREWERT S LEHRACH H BARLOW DP
Citation: N. Schweifer et al., CHARACTERIZATION OF THE C3 YAC CONTIG FROM PROXIMAL MOUSE-CHROMOSOME-17 AND ANALYSIS OF ALLELIC EXPRESSION OF GENES FLANKING THE IMPRINTED IGF2R GENE, Genomics, 43(3), 1997, pp. 285-297
A PEX GENE MUTATION IS RESPONSIBLE FOR ADULT-ONSET VITAMIN-D-RESISTANT HYPOPHOSPHATEMIC OSTEOMALACIA - EVIDENCE THAT THE DISORDER IS NOT A DISTINCT ENTITY FROM X-LINKED HYPOPHOSPHATEMIC RICKETS (HYP)
Authors: ECONS MJ FRIEDMAN NE ROWE PSN SPEER MC FRANCIS F STROM TM OUDET C LEE B BERGEN H
Citation: Mj. Econs et al., A PEX GENE MUTATION IS RESPONSIBLE FOR ADULT-ONSET VITAMIN-D-RESISTANT HYPOPHOSPHATEMIC OSTEOMALACIA - EVIDENCE THAT THE DISORDER IS NOT A DISTINCT ENTITY FROM X-LINKED HYPOPHOSPHATEMIC RICKETS (HYP), Journal of bone and mineral research, 12, 1997, pp. 316-316
POSITIONAL CLONING OF THE PEX GENE - NEW INSIGHTS INTO THE PATHOPHYSIOLOGY OF X-LINKED HYPOPHOSPHATEMIC RICKETS
Authors: ECONS MJ FRANCIS F
Citation: Mj. Econs et F. Francis, POSITIONAL CLONING OF THE PEX GENE - NEW INSIGHTS INTO THE PATHOPHYSIOLOGY OF X-LINKED HYPOPHOSPHATEMIC RICKETS, American journal of physiology. Renal, fluid and electrolyte physiology, 42(4), 1997, pp. 489-498
ATRIAL FUNCTION ASSESSMENT FOR HEART-TRANSPLANT ANASTOMOSIS - CARDIACMR-IMAGING WITH SEMIAUTOMATIC CARDIAC ANALYSIS AND FLOW MEASUREMENT
Authors: LIU Y NARASIMHAN A BLECHINGER J FRANCIS F WANN LS
Citation: Y. Liu et al., ATRIAL FUNCTION ASSESSMENT FOR HEART-TRANSPLANT ANASTOMOSIS - CARDIACMR-IMAGING WITH SEMIAUTOMATIC CARDIAC ANALYSIS AND FLOW MEASUREMENT, Radiology, 205, 1997, pp. 1012-1012
THE BALANCHINE-TRUST + ANSWERING SOME QUESTIONS ON THE PRINCIPLES UPON WHICH THE TRUST WORKS
Authors: FRANCIS F
Citation: F. Francis, THE BALANCHINE-TRUST + ANSWERING SOME QUESTIONS ON THE PRINCIPLES UPON WHICH THE TRUST WORKS, DANCING TIMES, 87(1042), 1997, pp. 885-885
SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE
Authors: LORENZ B FRANCIS F GEMPEL K BODDRICH A JOSTEN M SCHMAHL W GERBITZ KD LEHRACH H MEITINGER T STROM TM
Citation: B. Lorenz et al., SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE, American journal of human genetics, 61(4), 1997, pp. 1982-1982
MUTATIONS IN THE PEX GENE - EVIDENCE FOR ALTERATIONS IN GENE-FUNCTION, AND IMPLICATIONS FOR X-LINKED RICKETS (HYP)
Authors: ROWE PSM GOULDING JN FRANCIS F OUDET C STROM T ECONS M MOKRYCZKI A READ AP ORIORDAN JLH
Citation: Psm. Rowe et al., MUTATIONS IN THE PEX GENE - EVIDENCE FOR ALTERATIONS IN GENE-FUNCTION, AND IMPLICATIONS FOR X-LINKED RICKETS (HYP), Journal of bone and mineral research, 11(11), 1996, pp. 12-12
THE GENE FOR X-LINKED HYPOPHOSPHATEMIC RICKETS MAPS TO A 200-300 KB REGION IN XP22.1, AND IS LOCATED ON A SINGLE YAC CONTAINING A PUTATIVE VITAMIN-D RESPONSE ELEMENT (VDRE)
Authors: ROWE PSN GOULDING JN FRANCIS F OUDET C ECONS MJ HANAUER A LEHRACH H READ AP MOUNTFORD RC SUMMERFIELD T WEISSENBACH J FRASER W DREZNER MK DAVIES KE ORIORDAN JLH
Citation: Psn. Rowe et al., THE GENE FOR X-LINKED HYPOPHOSPHATEMIC RICKETS MAPS TO A 200-300 KB REGION IN XP22.1, AND IS LOCATED ON A SINGLE YAC CONTAINING A PUTATIVE VITAMIN-D RESPONSE ELEMENT (VDRE), Human genetics, 97(3), 1996, pp. 345-352
UNIVERSAL MULTIFRACTAL SCALING OF SYNTHETIC-APERTURE RADAR IMAGES OF SEA-ICE
Authors: FALCO T FRANCIS F LOVEJOY S SCHERTZER D KERMAN B DRINKWATER M
Citation: T. Falco et al., UNIVERSAL MULTIFRACTAL SCALING OF SYNTHETIC-APERTURE RADAR IMAGES OF SEA-ICE, IEEE transactions on geoscience and remote sensing, 34(4), 1996, pp. 906-914
SINONASAL UNDIFFERENTIATED CARCINOMA - A 10-YEAR EXPERIENCE
Authors: RIGHI PD FRANCIS F ARON BS WEITZNER S WILSON KM GLUCKMAN J
Citation: Pd. Righi et al., SINONASAL UNDIFFERENTIATED CARCINOMA - A 10-YEAR EXPERIENCE, American journal of otolaryngology, 17(3), 1996, pp. 167-171
A GENE (PEX) WITH HOMOLOGIES TO ENDOPEPTIDASES IS MUTATED IN PATIENTSWITH X-LINKED HYPOPHOSPHATEMIC RICKETS
Authors: FRANCIS F HENNIG S KORN B REINHARDT R DEJONG P POUSTKA A LEHRACH H ROWE PSN GOULDING JN SUMMERFIELD T MOUNTFORD R READ AP POPOWSKA E PRONICKA E DAVIES KE ORIORDAN JLH ECONS MJ NESBITT T DREZNER MK OUDET C PANNETIER S HANAUER A STROM TM MEINDL A LORENZ B CAGNOLI M MOHNIKE KL MURKEN J MEITINGER T
Citation: F. Francis et al., A GENE (PEX) WITH HOMOLOGIES TO ENDOPEPTIDASES IS MUTATED IN PATIENTSWITH X-LINKED HYPOPHOSPHATEMIC RICKETS, Nature genetics, 11(2), 1995, pp. 130-136
MAPPING AROUND THE FUSED LOCUS ON MOUSE CHROMOSOME-17
Authors: SUTHERLAND HF PICK E FRANCIS F LEHRACH H FRISCHAUF AM
Citation: Hf. Sutherland et al., MAPPING AROUND THE FUSED LOCUS ON MOUSE CHROMOSOME-17, Mammalian genome, 6(7), 1995, pp. 449-453
Risultati: 1-25 | 26-50 | 51-53