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Results: 1-20 |
Results: 20
PHYSIOLOGY AND PATHOPHYSIOLOGY OF ANDROGEN ACTION
Authors: HIORT O HOLTERHUS PM NITSCHE EM
Citation: O. Hiort et al., PHYSIOLOGY AND PATHOPHYSIOLOGY OF ANDROGEN ACTION, Bailliere's clinical endocrinology and metabolism, 12(1), 1998, pp. 115-132
IMMUNOHISTOCHEMISTRY AND IN-SITU HYBRIDIZATION OF THE ANDROGEN RECEPTOR IN THE DEVELOPING HUMAN PROSTATE
Authors: AUMULLER G HOLTERHUS PM KONRAD L VONRAHDEN B HIORT O ESQUENET M VERHOEVEN G
Citation: G. Aumuller et al., IMMUNOHISTOCHEMISTRY AND IN-SITU HYBRIDIZATION OF THE ANDROGEN RECEPTOR IN THE DEVELOPING HUMAN PROSTATE, Anatomy and embryology, 197(3), 1998, pp. 199-208
FROM GENOTYPE TO PHENOTYPE - MOLECULAR-GE NETIC ANALYSIS IN INTERSEX DISORDERS
Authors: HIORT O
Citation: O. Hiort, FROM GENOTYPE TO PHENOTYPE - MOLECULAR-GE NETIC ANALYSIS IN INTERSEX DISORDERS, Monatsschrift fur Kinderheilkunde, 146(2), 1998, pp. 86-91
INHERITED AND DE-NOVO ANDROGEN RECEPTOR GENE-MUTATIONS - INVESTIGATION OF SINGLE-CASE FAMILIES
Authors: HIORT O SINNECKER GHG HOLTERHUS PM NITSCHE EM KRUSE K
Citation: O. Hiort et al., INHERITED AND DE-NOVO ANDROGEN RECEPTOR GENE-MUTATIONS - INVESTIGATION OF SINGLE-CASE FAMILIES, The Journal of pediatrics, 132(6), 1998, pp. 939-943
FUNCTIONAL ASSESSMENT AND CLINICAL CLASSIFICATION OF ANDROGEN SENSITIVITY IN PATIENTS WITH MUTATIONS OF THE ANDROGEN RECEPTOR GENE
Authors: SINNECKER GHG HIORT O NITSCHE EM HOLTERHUS PM KRUSE K
Citation: Ghg. Sinnecker et al., FUNCTIONAL ASSESSMENT AND CLINICAL CLASSIFICATION OF ANDROGEN SENSITIVITY IN PATIENTS WITH MUTATIONS OF THE ANDROGEN RECEPTOR GENE, European journal of pediatrics, 156(1), 1997, pp. 7-14
MOSAICISM DUE TO A SOMATIC MUTATION OF THE ANDROGEN RECEPTOR GENE DETERMINES PHENOTYPE IN ANDROGEN INSENSITIVITY SYNDROME
Authors: HOLTERHUS PM BRUGGENWIRTH HT HIORT O KLEINKAUFHOUCKEN A KRUSE K SINNECKER GHG BRINKMANN AO
Citation: Pm. Holterhus et al., MOSAICISM DUE TO A SOMATIC MUTATION OF THE ANDROGEN RECEPTOR GENE DETERMINES PHENOTYPE IN ANDROGEN INSENSITIVITY SYNDROME, The Journal of clinical endocrinology and metabolism, 82(11), 1997, pp. 3584-3589
MOLECULAR-GENETIC ANALYSIS AND HUMAN CHORIONIC-GONADOTROPIN STIMULATION TESTS IN THE DIAGNOSIS OF PREPUBERTAL PATIENTS WITH PARTIAL 5-ALPHA-REDUCTASE DEFICIENCY
Authors: HIORT O WILLENBRING H ALBERS N HECKER W ENGERT J DIBBELT L SINNECKER GHG
Citation: O. Hiort et al., MOLECULAR-GENETIC ANALYSIS AND HUMAN CHORIONIC-GONADOTROPIN STIMULATION TESTS IN THE DIAGNOSIS OF PREPUBERTAL PATIENTS WITH PARTIAL 5-ALPHA-REDUCTASE DEFICIENCY, European journal of pediatrics, 155(6), 1996, pp. 445-451
THE CLINICAL AND MOLECULAR-SPECTRUM OF ANDROGEN INSENSITIVITY SYNDROMES
Authors: HIORT O SINNECKER GHG HOLTERHUS PM NITSCHE EM KRUSE K
Citation: O. Hiort et al., THE CLINICAL AND MOLECULAR-SPECTRUM OF ANDROGEN INSENSITIVITY SYNDROMES, American journal of medical genetics, 63(1), 1996, pp. 218-222
PHENOTYPIC CLASSIFICATION OF MALE PSEUDOHERMAPHRODITISM DUE TO STEROID 5-ALPHA-REDUCTASE-2 DEFICIENCY
Authors: SINNECKER GHG HIORT O DIBBELT L ALBERS N DORR HG HAUSS H HEINRICH U HEMMINGHAUS M HOEPFFNER W HOLDER M SCHNABEL D KRUSE K
Citation: Ghg. Sinnecker et al., PHENOTYPIC CLASSIFICATION OF MALE PSEUDOHERMAPHRODITISM DUE TO STEROID 5-ALPHA-REDUCTASE-2 DEFICIENCY, American journal of medical genetics, 63(1), 1996, pp. 223-230
RET PROTOONCOGENE POINT MUTATIONS IN SPORADIC NEUROENDOCRINE TUMORS
Authors: KOMMINOTH P MULETTAFEURER S SAREMASLANI P SEELENTAG WKF KUNZ EK HIORT O MATIASGUIU X ROTH J HEITZ PU
Citation: P. Komminoth et al., RET PROTOONCOGENE POINT MUTATIONS IN SPORADIC NEUROENDOCRINE TUMORS, Laboratory investigation, 74(1), 1996, pp. 270-270
THE ROLE OF ANDROGEN RECEPTOR GENE-MUTATIONS IN MALE BREAST-CARCINOMA
Authors: HIORT O NABER SP LEHNERS A MULETTAFEURER S SINNECKER GHG ZOLLNER A KOMMINOTH P
Citation: O. Hiort et al., THE ROLE OF ANDROGEN RECEPTOR GENE-MUTATIONS IN MALE BREAST-CARCINOMA, The Journal of clinical endocrinology and metabolism, 81(9), 1996, pp. 3404-3407
NONISOTOPIC SINGLE-STRAND CONFORMATION ANALYSIS OF THE 5-ALPHA-REDUCTASE TYPE-2 GENE FOR THE DIAGNOSIS OF 5-ALPHA-REDUCTASE DEFICIENCY
Authors: HIORT O SINNECKER GHG WILLENBRING H LEHNERS A ZOLLNER A STRUVE D
Citation: O. Hiort et al., NONISOTOPIC SINGLE-STRAND CONFORMATION ANALYSIS OF THE 5-ALPHA-REDUCTASE TYPE-2 GENE FOR THE DIAGNOSIS OF 5-ALPHA-REDUCTASE DEFICIENCY, The Journal of clinical endocrinology and metabolism, 81(9), 1996, pp. 3415-3418
CLINICAL, BIOCHEMICAL, AND GENETIC FINDINGS IN A LARGE PEDIGREE OF MALE AND FEMALE-PATIENTS WITH 5-ALPHA-REDUCTASE-2 DEFICIENCY
Authors: HOCHBERG Z CHAYEN R REISS N FALIK Z MAKLER A MUNICHOR M FARKAS A GOLDFARB H OHANA N HIORT O
Citation: Z. Hochberg et al., CLINICAL, BIOCHEMICAL, AND GENETIC FINDINGS IN A LARGE PEDIGREE OF MALE AND FEMALE-PATIENTS WITH 5-ALPHA-REDUCTASE-2 DEFICIENCY, The Journal of clinical endocrinology and metabolism, 81(8), 1996, pp. 2821-2827
MOLECULAR DIAGNOSIS OF MULTIPLE ENDOCRINE NEOPLASIA (MEN) IN PARAFFIN-EMBEDDED SPECIMENS
Authors: KOMMINOTH P MULETTAFEURER S SAREMASLANI P KUNZ EK MATIASGUIU X HIORT O SCHRODER S SEELENTAG WKF ROTH J HEITZ PU
Citation: P. Komminoth et al., MOLECULAR DIAGNOSIS OF MULTIPLE ENDOCRINE NEOPLASIA (MEN) IN PARAFFIN-EMBEDDED SPECIMENS, Endocrine pathology, 6(4), 1995, pp. 267-278
TRUE HERMAPHRODITISM WITH 46,XY KARYOTYPE AND A POINT MUTATION IN THESRY GENE
Authors: HIORT O KLAUBER GT
Citation: O. Hiort et Gt. Klauber, TRUE HERMAPHRODITISM WITH 46,XY KARYOTYPE AND A POINT MUTATION IN THESRY GENE, The Journal of pediatrics, 126(6), 1995, pp. 1022-1022
ANALYSIS OF RET PROTOONCOGENE POINT MUTATIONS DISTINGUISHES HERITABLEFROM NONHERITABLE MEDULLARY-THYROID CARCINOMAS
Authors: KOMMINOTH P KUNZ EK MATIASGUIU X HIORT O CHRISTENSEN G COLOMER A ROTH J HEITZ PU
Citation: P. Komminoth et al., ANALYSIS OF RET PROTOONCOGENE POINT MUTATIONS DISTINGUISHES HERITABLEFROM NONHERITABLE MEDULLARY-THYROID CARCINOMAS, Cancer, 76(3), 1995, pp. 479-489
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
MOLECULAR CHARACTERIZATION OF THE ANDROGEN RECEPTOR GENE IN BOYS WITHHYPOSPADIAS
Authors: HIORT O KLAUBER G CENDRON M SINNECKER GHG KEIM L SCHWINGER E WOLFE HJ YANDELL DW
Citation: O. Hiort et al., MOLECULAR CHARACTERIZATION OF THE ANDROGEN RECEPTOR GENE IN BOYS WITHHYPOSPADIAS, European journal of pediatrics, 153(5), 1994, pp. 317-321
DETECTION OF RET PROTOONCOGENE POINT MUTATIONS IN PARAFFIN-EMBEDDED PHEOCHROMOCYTOMA SPECIMENS BY NONRADIOACTIVE SINGLE-STRAND CONFORMATIONPOLYMORPHISM ANALYSIS AND DIRECT SEQUENCING
Authors: KOMMINOTH P KUNZ E HIORT O SCHRODER S MATIASGUIU X CHRISTIANSEN G ROTH J HEITZ PU
Citation: P. Komminoth et al., DETECTION OF RET PROTOONCOGENE POINT MUTATIONS IN PARAFFIN-EMBEDDED PHEOCHROMOCYTOMA SPECIMENS BY NONRADIOACTIVE SINGLE-STRAND CONFORMATIONPOLYMORPHISM ANALYSIS AND DIRECT SEQUENCING, The American journal of pathology, 145(4), 1994, pp. 922-929
SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS OF ANDROGEN RECEPTORGENE-MUTATIONS IN PATIENTS WITH ANDROGEN INSENSITIVITY SYNDROMES - APPLICATION FOR DIAGNOSIS, GENETIC-COUNSELING, AND THERAPY
Authors: HIORT O HUANG Q SINNECKER GHG SADEGHINEJAD A KRUSE K WOLFE HJ YANDELL DW
Citation: O. Hiort et al., SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS OF ANDROGEN RECEPTORGENE-MUTATIONS IN PATIENTS WITH ANDROGEN INSENSITIVITY SYNDROMES - APPLICATION FOR DIAGNOSIS, GENETIC-COUNSELING, AND THERAPY, The Journal of clinical endocrinology and metabolism, 77(1), 1993, pp. 262-266
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