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Results: 1-13 |
Results: 13
MUTATIONS IN PROP1 CAUSE FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY
Authors: WU W COGAN JD PFAFFLE RW DASEN JS FRISCH H OCONNELL SM FLYNN SE BROWN MR MULLIS PE PARKS JS PHILLIPS JA ROSENFELD MG
Citation: W. Wu et al., MUTATIONS IN PROP1 CAUSE FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY, Nature genetics, 18(2), 1998, pp. 147-149
CLINICAL AND MOLECULAR CHARACTERIZATION OF BRAZILIAN PATIENTS WITH GROWTH-HORMONE GENE DELETIONS
Authors: ARNHOLD IJP OSORIO MGF OLIVEIRA SB ESTEFAN V KAMIJO T KRISHNAMANI MRS COGAN JD PHILLIPS JA MENDONCA BB
Citation: Ijp. Arnhold et al., CLINICAL AND MOLECULAR CHARACTERIZATION OF BRAZILIAN PATIENTS WITH GROWTH-HORMONE GENE DELETIONS, Brazilian journal of medical and biological research, 31(4), 1998, pp. 491-497
THE PROP1 2-BASE PAIR DELETION IS A COMMON-CAUSE OF COMBINED PITUITARY-HORMONE DEFICIENCY
Authors: COGAN JD WU W PHILLIPS JA ARNHOLD IJP AGAPITO A FOFANOVA OV OSORIO MGF BIRCAN I MORENO A MENDONCA BB
Citation: Jd. Cogan et al., THE PROP1 2-BASE PAIR DELETION IS A COMMON-CAUSE OF COMBINED PITUITARY-HORMONE DEFICIENCY, The Journal of clinical endocrinology and metabolism, 83(9), 1998, pp. 3346-3349
A NOVEL MECHANISM OF ABERRANT PRE-MESSENGER-RNA SPLICING IN HUMANS
Authors: COGAN JD PRINCE MA LEKHAKULA S BUNDEY S FUTRAKUL A MCCARTHY EMS PHILLIPS JA
Citation: Jd. Cogan et al., A NOVEL MECHANISM OF ABERRANT PRE-MESSENGER-RNA SPLICING IN HUMANS, Human molecular genetics, 6(6), 1997, pp. 909-912
DETECTION OF GROWTH-HORMONE GENE DEFECTS BY DIDEOXY FINGERPRINTING (DDF)
Authors: MIYATA I COGAN JD PRINCE MA KAMIJO T OGAWA M PHILLIPS JA
Citation: I. Miyata et al., DETECTION OF GROWTH-HORMONE GENE DEFECTS BY DIDEOXY FINGERPRINTING (DDF), Endocrine journal, 44(1), 1997, pp. 149-154
ALLELIC VARIATIONS IN THE HUMAN GROWTH HORMONE-1 GENE PROMOTER OF GROWTH HORMONE-DEFICIENT PATIENTS AND NORMAL CONTROLS
Authors: WAGNER JK EBLE A COGAN JD PRINCE MA PHILLIPS JA MULLIS PE
Citation: Jk. Wagner et al., ALLELIC VARIATIONS IN THE HUMAN GROWTH HORMONE-1 GENE PROMOTER OF GROWTH HORMONE-DEFICIENT PATIENTS AND NORMAL CONTROLS, European journal of endocrinology, 137(5), 1997, pp. 474-481
GENETIC-MAPPING OF THE HUMAN PITUITARY-SPECIFIC TRANSCRIPTIONAL FACTOR GENE AND ITS ANALYSIS IN FAMILIAL PANHYPOPITUITARY DWARFISM
Authors: RASKIN S COGAN JD SUMMAR ML MORENO A KRISHNAMANI MRS PHILLIPS JA
Citation: S. Raskin et al., GENETIC-MAPPING OF THE HUMAN PITUITARY-SPECIFIC TRANSCRIPTIONAL FACTOR GENE AND ITS ANALYSIS IN FAMILIAL PANHYPOPITUITARY DWARFISM, Human genetics, 98(6), 1996, pp. 703-705
PHENOTYPIC DETERMINANTS OF ADENOVIRUS E1A GENE AUTOREGULATION - VARIABLE REGION BETWEEN CONSERVED CODING DOMAIN-2 AND DOMAIN-3
Authors: HAMID R COGAN JD JONES SN TIBBETTS C
Citation: R. Hamid et al., PHENOTYPIC DETERMINANTS OF ADENOVIRUS E1A GENE AUTOREGULATION - VARIABLE REGION BETWEEN CONSERVED CODING DOMAIN-2 AND DOMAIN-3, Virology, 213(2), 1995, pp. 666-670
A RECURRING DOMINANT-NEGATIVE MUTATION CAUSES AUTOSOMAL-DOMINANT GROWTH-HORMONE DEFICIENCY - A CLINICAL RESEARCH-CENTER STUDY
Authors: COGAN JD RAMEL B LEHTO M PHILLIPS J PRINCE M BLIZZARD RM DERAVEL TJL BRAMMERT M GROOP L
Citation: Jd. Cogan et al., A RECURRING DOMINANT-NEGATIVE MUTATION CAUSES AUTOSOMAL-DOMINANT GROWTH-HORMONE DEFICIENCY - A CLINICAL RESEARCH-CENTER STUDY, The Journal of clinical endocrinology and metabolism, 80(12), 1995, pp. 3591-3595
FAMILIAL GROWTH-HORMONE DEFICIENCY - A MODEL OF DOMINANT AND RECESSIVE MUTATIONS AFFECTING A MONOMERIC PROTEIN
Authors: COGAN JD PHILLIPS JA SCHENKMAN SS MILNER RDG SAKATI N
Citation: Jd. Cogan et al., FAMILIAL GROWTH-HORMONE DEFICIENCY - A MODEL OF DOMINANT AND RECESSIVE MUTATIONS AFFECTING A MONOMERIC PROTEIN, The Journal of clinical endocrinology and metabolism, 79(5), 1994, pp. 1261-1265
GENETIC-BASIS OF ENDOCRINE DISEASE-6 - MOLECULAR-BASIS OF FAMILIAL HUMAN GROWTH-HORMONE DEFICIENCY
Authors: PHILLIPS JA COGAN JD
Citation: Ja. Phillips et Jd. Cogan, GENETIC-BASIS OF ENDOCRINE DISEASE-6 - MOLECULAR-BASIS OF FAMILIAL HUMAN GROWTH-HORMONE DEFICIENCY, The Journal of clinical endocrinology and metabolism, 78(1), 1994, pp. 11-16
HETEROGENEOUS GROWTH-HORMONE (GH) GENE-MUTATIONS IN FAMILIAL GH DEFICIENCY
Authors: COGAN JD PHILLIPS JA SAKATI N FRISCH H SCHOBER E MILNER RDG
Citation: Jd. Cogan et al., HETEROGENEOUS GROWTH-HORMONE (GH) GENE-MUTATIONS IN FAMILIAL GH DEFICIENCY, The Journal of clinical endocrinology and metabolism, 76(5), 1993, pp. 1224-1228
MOLECULAR-BASIS OF AUTOSOMAL RECESSIVE AND AUTOSOMAL-DOMINANT INHERITANCE OF FAMILIAL GH DEFICIENCY
Authors: PHILLIPS JA COGAN JD MILLENDAVIS S MILNER RDG SAKATI NA SCHENKMAN SS BUNDEY SE
Citation: Ja. Phillips et al., MOLECULAR-BASIS OF AUTOSOMAL RECESSIVE AND AUTOSOMAL-DOMINANT INHERITANCE OF FAMILIAL GH DEFICIENCY, American journal of human genetics, 53(3), 1993, pp. 6-6
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