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Results: 1-25 | 26-30
Results: 1-25/30
SOMATIC MUTATION IN INDIVIDUAL LIVER CYSTS SUPPORTS A 2-HIT MODEL OF CYSTOGENESIS IN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE
Authors: WATNICK TJ TORRES VE GANDOLPH MA QIAN F ONUCHIC LF KLINGER KW LANDES G GERMINO GG
Citation: Tj. Watnick et al., SOMATIC MUTATION IN INDIVIDUAL LIVER CYSTS SUPPORTS A 2-HIT MODEL OF CYSTOGENESIS IN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE, MOLECULAR CELL, 2(2), 1998, pp. 247-251
HIGH-THROUGHPUT PARALLEL ANALYSIS OF HUNDREDS OF PATIENT SAMPLES FOR MORE THAN 100 MUTATIONS IN MULTIPLE DISEASE GENES
Authors: SHUBER AP MICHALOWSKY LA NASS GS SKOLETSKY J HIRE LM KOTSOPOULOS SK PHIPPS MF BARBERIO DM KLINGER KW
Citation: Ap. Shuber et al., HIGH-THROUGHPUT PARALLEL ANALYSIS OF HUNDREDS OF PATIENT SAMPLES FOR MORE THAN 100 MUTATIONS IN MULTIPLE DISEASE GENES, Human molecular genetics, 6(3), 1997, pp. 337-347
THE NTN2L GENE ENCODING A NOVEL HUMAN NETRIN MAPS TO THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE REGION ON CHROMOSOME 16P13.3
Authors: VANRAAY TJ FOSKETT SM CONNORS TD KLINGER KW LANDES GM BURN TC
Citation: Tj. Vanraay et al., THE NTN2L GENE ENCODING A NOVEL HUMAN NETRIN MAPS TO THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE REGION ON CHROMOSOME 16P13.3, Genomics, 41(2), 1997, pp. 279-282
THE CLONING OF A HUMAN ABC GENE (ABC3) MAPPING TO CHROMOSOME 16P13.3
Authors: CONNORS TD VANRAAY TJ PETRY LR KLINGER KW LANDES GM BURN TC
Citation: Td. Connors et al., THE CLONING OF A HUMAN ABC GENE (ABC3) MAPPING TO CHROMOSOME 16P13.3, Genomics, 39(2), 1997, pp. 231-234
EVALUATION OF DNA-SEQUENCING AMBIGUITIES USING TETRAMETHYLAMMONIUM CHLORIDE HYBRIDIZATION CONDITIONS
Authors: CONNORS TD BURN TC VANRAAY T GERMINO GG KLINGER KW LANDES GM
Citation: Td. Connors et al., EVALUATION OF DNA-SEQUENCING AMBIGUITIES USING TETRAMETHYLAMMONIUM CHLORIDE HYBRIDIZATION CONDITIONS, BioTechniques, 22(6), 1997, pp. 1088-1090
POLYCYSTIN - IN-VITRO SYNTHESIS, IN-VIVO TISSUE EXPRESSION, AND SUBCELLULAR-LOCALIZATION IDENTIFIES A LARGE MEMBRANE-ASSOCIATED PROTEIN
Authors: IBRAGHIMOVBESKROVNAYA O DACKOWSKI WR FOGGENSTEINER L COLEMAN N THIRU S PETRY LR BURN TC CONNORS TD VANRAAY T BRADLEY J QIAN F ONUCHIC LF WATNICK TJ PIONTEK K HAKIM RM LANDES GM GERMINO GG SANDFORD R KLINGER KW
Citation: O. Ibraghimovbeskrovnaya et al., POLYCYSTIN - IN-VITRO SYNTHESIS, IN-VIVO TISSUE EXPRESSION, AND SUBCELLULAR-LOCALIZATION IDENTIFIES A LARGE MEMBRANE-ASSOCIATED PROTEIN, Proceedings of the National Academy of Sciences of the United Statesof America, 94(12), 1997, pp. 6397-6402
DETECTION OF MALE FETAL DNA IN POSTPARTUM WOMEN WITH AUTOIMMUNE-DISEASE
Authors: BIANCHI DW KLINGER KW DERISO M FARINA A FURST DE MALONEY S EVANS PC NELSON JL
Citation: Dw. Bianchi et al., DETECTION OF MALE FETAL DNA IN POSTPARTUM WOMEN WITH AUTOIMMUNE-DISEASE, American journal of human genetics, 61(4), 1997, pp. 88-88
PCR QUANTITATION OF FETAL CELLS IN MATERNAL BLOOD IN NORMAL AND ANEUPLOID PREGNANCIES
Authors: BIANCHI DW WILLIAMS JM SULLIVAN LM HANSON FW KLINGER KW SHUBER AP
Citation: Dw. Bianchi et al., PCR QUANTITATION OF FETAL CELLS IN MATERNAL BLOOD IN NORMAL AND ANEUPLOID PREGNANCIES, American journal of human genetics, 61(4), 1997, pp. 822-829
THE REGION SURROUNDING THE PKD1 GENE - A 700-KB P1 CONTIG FROM A YAC-DEFICIENT INTERVAL
Authors: DACKOWSKI WR CONNORS TD BOWE AE STANTON V HOUSMAN D DOGGETT NA LANDES GM KLINGER KW
Citation: Wr. Dackowski et al., THE REGION SURROUNDING THE PKD1 GENE - A 700-KB P1 CONTIG FROM A YAC-DEFICIENT INTERVAL, PCR methods and applications, 6(6), 1996, pp. 515-524
GENERATION OF A TRANSCRIPTIONAL MAP FOR A 700-KB REGION SURROUNDING THE POLYCYSTIC KIDNEY-DISEASE TYPE-1 (PKD1) AND TUBEROUS SCLEROSIS TYPE-2 (TSC2) DISEASE GENES ON HUMAN-CHROMOSOME 16P13.3
Authors: BURN TC CONNORS TD VANRAAY TJ DACKOWSKI WR MILLHOLLAND JM KLINGER KW LANDES GM
Citation: Tc. Burn et al., GENERATION OF A TRANSCRIPTIONAL MAP FOR A 700-KB REGION SURROUNDING THE POLYCYSTIC KIDNEY-DISEASE TYPE-1 (PKD1) AND TUBEROUS SCLEROSIS TYPE-2 (TSC2) DISEASE GENES ON HUMAN-CHROMOSOME 16P13.3, PCR methods and applications, 6(6), 1996, pp. 525-537
A NOVEL RIBOSOMAL-PROTEIN L3-LIKE GENE (RPL3L) MAPS TO THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE GENE REGION
Authors: VANRAAY TJ CONNORS TD KLINGER KW LANDES GM BURN TC
Citation: Tj. Vanraay et al., A NOVEL RIBOSOMAL-PROTEIN L3-LIKE GENE (RPL3L) MAPS TO THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE GENE REGION, Genomics, 37(2), 1996, pp. 172-176
UTILIZATION OF EXON TRAPPING TO IDENTIFY TRANSCRIBED SEQUENCES IN THEREGION OF THE POLYCYSTIC KIDNEY-DISEASE (PKD1) GENE
Authors: BURN TC CONNORS TD DACKOWSKI WR MILLHOLLAND JM KLINGER KW LANDES GM
Citation: Tc. Burn et al., UTILIZATION OF EXON TRAPPING TO IDENTIFY TRANSCRIBED SEQUENCES IN THEREGION OF THE POLYCYSTIC KIDNEY-DISEASE (PKD1) GENE, Cytogenetics and cell genetics, 72(4), 1996, pp. 3-3
DEVELOPMENT OF A MODEL SYSTEM TO COMPARE CELL-SEPARATION METHODS FOR THE ISOLATION OF FETAL CELLS FROM MATERNAL BLOOD
Authors: BIANCHI DW KLINGER KW VADNAIS TJ DEMARIA MA SHUBER AP SKOLETSKY J MIDURA P DIRISO M PELLETIER C GENOVA M ERIKSON MS WILLIAMS JM
Citation: Dw. Bianchi et al., DEVELOPMENT OF A MODEL SYSTEM TO COMPARE CELL-SEPARATION METHODS FOR THE ISOLATION OF FETAL CELLS FROM MATERNAL BLOOD, Prenatal diagnosis, 16(4), 1996, pp. 289-298
FETAL CELL QUANTITATION IN MATERNAL BLOOD-SAMPLES FROM NORMAL AND ANEUPLOID PREGNANCIES
Authors: BIANCHI DW WILLIAMS JM PELLETIER C KLINGER KW SHUBER AP
Citation: Dw. Bianchi et al., FETAL CELL QUANTITATION IN MATERNAL BLOOD-SAMPLES FROM NORMAL AND ANEUPLOID PREGNANCIES, Pediatric research, 39(4), 1996, pp. 838-838
ALTERNATIVE SPLICING OF EXON-3 OF THE HUMAN GROWTH-HORMONE RECEPTOR IS THE RESULT OF AN UNUSUAL GENETIC-POLYMORPHISM
Authors: STALLINGSMANN ML LUDWICZAK RL KLINGER KW ROTTMAN F
Citation: Ml. Stallingsmann et al., ALTERNATIVE SPLICING OF EXON-3 OF THE HUMAN GROWTH-HORMONE RECEPTOR IS THE RESULT OF AN UNUSUAL GENETIC-POLYMORPHISM, Proceedings of the National Academy of Sciences of the United Statesof America, 93(22), 1996, pp. 12394-12399
PRENATAL DETECTION OF CHROMOSOME ANEUPLOIDIES IN UNCULTURED CHORIONICVILLUS SAMPLES BY FISH
Authors: BRYNDORF T CHRISTENSEN B VAD M PARNER J CARELLI MP WARD BE KLINGER KW BANG J PHILIP J
Citation: T. Bryndorf et al., PRENATAL DETECTION OF CHROMOSOME ANEUPLOIDIES IN UNCULTURED CHORIONICVILLUS SAMPLES BY FISH, American journal of human genetics, 59(4), 1996, pp. 918-926
A SIMPLIFIED PROCEDURE FOR DEVELOPING MULTIPLEX PCRS
Authors: SHUBER AP GRONDIN VJ KLINGER KW
Citation: Ap. Shuber et al., A SIMPLIFIED PROCEDURE FOR DEVELOPING MULTIPLEX PCRS, PCR methods and applications, 5(5), 1995, pp. 488-493
ANALYSIS OF THE GENOMIC SEQUENCE FOR THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (PKD1) GENE PREDICTS THE PRESENCE OF A LEUCINE-RICH REPEAT
Authors: BURN TC CONNORS TD DACKOWSKI WR PETRY LR VANRAAY TJ MILLHOLLAND JM VENET M MILLER G HAKIM RM LANDES GM KLINGER KW FENG Q ONUCHIC LF WATNICK T GERMINO GG DOGGETT NA
Citation: Tc. Burn et al., ANALYSIS OF THE GENOMIC SEQUENCE FOR THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (PKD1) GENE PREDICTS THE PRESENCE OF A LEUCINE-RICH REPEAT, Human molecular genetics, 4(4), 1995, pp. 575-582
INCREASED EXON-TRAPPING EFFICIENCY THROUGH MODIFICATIONS TO THE PSPL3SPLICING VECTOR
Authors: BURN TC CONNORS TD KLINGER KW LANDES GM
Citation: Tc. Burn et al., INCREASED EXON-TRAPPING EFFICIENCY THROUGH MODIFICATIONS TO THE PSPL3SPLICING VECTOR, Gene, 161(2), 1995, pp. 183-187
CHROMOSOME 16P13.3 - ENRICHMENT OF KIDNEY CDNAS
Authors: LANDES G PETRY LR DACKOWSKI WR HAKIM R DOGGETT NA KLINGER KW
Citation: G. Landes et al., CHROMOSOME 16P13.3 - ENRICHMENT OF KIDNEY CDNAS, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 183-183
RAPID PRENATAL-DIAGNOSIS OF 14 CASES OF TRIPLOIDY USING FISH WITH MULTIPLE PROBES
Authors: GERSEN SL CARELLI MP KLINGER KW WARD BE
Citation: Sl. Gersen et al., RAPID PRENATAL-DIAGNOSIS OF 14 CASES OF TRIPLOIDY USING FISH WITH MULTIPLE PROBES, Prenatal diagnosis, 15(1), 1995, pp. 1-5
MULTIPLE ALLELE-SPECIFIC DIAGNOSTIC ASSAY (MASDA) - A HIGH-THROUGHPUT, LOW-COST PROCEDURE FOR DNA DIAGNOSTICS
Authors: SHUBER AP MICHALOWSKY L NASS S SKOLETSKY J KOTSOPOULOS S BARBERIO D HIRE L KLINGER KW
Citation: Ap. Shuber et al., MULTIPLE ALLELE-SPECIFIC DIAGNOSTIC ASSAY (MASDA) - A HIGH-THROUGHPUT, LOW-COST PROCEDURE FOR DNA DIAGNOSTICS, American journal of human genetics, 57(4), 1995, pp. 1316-1316
FLUORESCENT IN-SITU HYBRIDIZATION AND 2ND-TRIMESTER SONOGRAPHIC ANOMALIES - USES AND LIMITATIONS
Authors: ISADA NB HUME RF REICHLER A JOHNSON MP KLINGER KW EVANS MI WARD BE
Citation: Nb. Isada et al., FLUORESCENT IN-SITU HYBRIDIZATION AND 2ND-TRIMESTER SONOGRAPHIC ANOMALIES - USES AND LIMITATIONS, Fetal diagnosis and therapy, 9(6), 1994, pp. 367-370
WHATS IN A SPOT
Authors: HOUSEAL TW KLINGER KW
Citation: Tw. Houseal et Kw. Klinger, WHATS IN A SPOT, Human molecular genetics, 3(8), 1994, pp. 1215-1216
INTEGRATING THE GENETIC AND PHYSICAL MAP OF CHROMOSOME 1P
Authors: HOUSEAL TW LEVERONE B DRACOPOLI N KLINGER KW LANDES GM
Citation: Tw. Houseal et al., INTEGRATING THE GENETIC AND PHYSICAL MAP OF CHROMOSOME 1P, Cytogenetics and cell genetics, 67(3), 1994, pp. 168-169
Risultati: 1-25 | 26-30