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YERKES E
SCHULMAN M
FOGO A
KON V
HOGAN BML
PHILLIPS JA
BROCK JW
INAGAMI T
ICHIKAWA I
Citation: H. Nishimura et al., NULL MUTATION OF THE MURINE ANGIOTENSIN TYPE-2 RECEPTOR GENE PRODUCESA SPECTRUM OF PHENOTYPES RESEMBLING HUMAN CONGENITAL URINARY-TRACT ANOMALIES (CUTA), Journal of the American Society of Nephrology, 8, 1997, pp. 1680-1680
Authors:
YERKES E
NISHIMURA H
HOHENFELLNER K
HUNLEY TE
YOSHIDA H
KON V
PHILLIPS JA
BROCK JW
ICHIKAWA I
Citation: E. Yerkes et al., ASSOCIATION BETWEEN THE ANGIOTENSIN TYPE-2 RECEPTOR (AT2) GENOTYPE AND CONGENITAL URINARY-TRACT ANOMALIES (CUTA) IN 2 INDEPENDENT COHORTS, Journal of the American Society of Nephrology, 8, 1997, pp. 1837-1837
Citation: Ja. Phillips et Ir. Price, A CATALOG OF PHAEOPHYTA (BROWN-ALGAE) FROM QUEENSLAND, AUSTRALIA, Australian systematic botany, 10(5), 1997, pp. 683-721
Citation: Ja. Phillips, GENUS AND SPECIES CONCEPTS IN ZONARIA AND HOMOEOSTRICHUS (DICTYOTALES, PHAEOPHYCEAE), INCLUDING THE DESCRIPTION OF EXALLOSORUS GEN. NOV, European journal of phycology, 32(3), 1997, pp. 303-311
Citation: Ja. Phillips et Mn. Clayton, COMPARATIVE-STUDIES ON GAMETANGIAL DISTRIBUTION AND STRUCTURE IN SPECIES OF ZONARIA AND HOMOEOSTRICHUS (DICTYOTALES, PHAEOPHYCEAE) FROM AUSTRALIA, European journal of phycology, 32(1), 1997, pp. 25-34
Authors:
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REXER B
SIRRIPURAPU S
JOHN S
GOLDSTEIN R
PHILLIPS JA
HALEY LL
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SHOWS TB
SMITH CM
GERHARD DS
Citation: Jb. Williams et al., THE HUMAN HNP36 GENE IS LOCALIZED TO CHROMOSOME 11Q13 AND PRODUCES ALTERNATIVE TRANSCRIPTS THAT ARE NOT MUTATED IN MULTIPLE ENDOCRINE NEOPLASIA, TYPE-1 (MEN-I) SYNDROME, Genomics, 42(2), 1997, pp. 325-330
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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
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AMBLER J
MITCHELSON A
BAYLEY D
PHILLIPS JA
CRAIG SJ
MONIA BP
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WILLIAMS TM
DOBSON GP
MATHIEUCOSTELLO O
MORSBACH D
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PHILLIPS JA
Citation: Tm. Williams et al., SKELETAL-MUSCLE HISTOLOGY AND BIOCHEMISTRY OF AN ELITE SPRINTER, THE AFRICAN CHEETAH, Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology, 167(8), 1997, pp. 527-535
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DASOUKI M
JURECIC V
PHILLIPS JA
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BALDINI A
Citation: M. Dasouki et al., DIGEORGE-ANOMALY AND CHROMOSOME 10P DELETIONS - ONE OR 2 LOCI, American journal of medical genetics, 73(1), 1997, pp. 72-75
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PHILLIPS JA
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DENNEBERG T
CARLSON J
GEORGE AL
Citation: Jk. Endsley et al., GENOMIC ORGANIZATION OF A HUMAN CYSTINE TRANSPORTER GENE (SLC3A1) ANDIDENTIFICATION OF NOVEL MUTATIONS CAUSING CYSTINURIA, Kidney international, 51(6), 1997, pp. 1893-1899
Citation: Ac. Alberts et al., EFFECTS OF INCUBATION-TEMPERATURE AND WATER POTENTIAL ON GROWTH AND THERMOREGULATORY BEHAVIOR OF HATCHLING CUBAN ROCK IGUANAS (CYCLURA-NUBILA), Copeia, (4), 1997, pp. 766-776
Authors:
YERKES E
NISHIMURA H
HUNLEY TE
KON V
PHILLIPS JA
BROCK JW
ICHIKAWA I
Citation: E. Yerkes et al., ASSOCIATION BETWEEN THE ANGIOTENSIN TYPE-2 RECEPTOR (AT2) GENOTYPE AND CONGENITAL URINARY-TRACT ANOMALIES (CUTA) IN MICE AND MEN, Pediatrics, 100(3), 1997, pp. 568-568
Authors:
MCELLIGOTT DL
PHILLIPS JA
STILLMAN CA
KOCH RJ
MOSIER DE
HOBBS MV
Citation: Dl. Mcelligott et al., CD4(-CELLS FROM IRF-1-DEFICIENT MICE EXHIBIT ALTERED PATTERNS OF CYTOKINE EXPRESSION AND CELL SUBSET HOMEOSTASIS() T), The Journal of immunology, 159(9), 1997, pp. 4180-4186
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REPASKE DR
MEDLEJ R
GULTEKIN EK
KRISHNAMANI MRS
HALABY G
FINDLING JW
PHILLIPS JA
Citation: Dr. Repaske et al., HETEROGENEITY IN CLINICAL MANIFESTATION OF AUTOSOMAL-DOMINANT NEUROHYPOPHYSEAL DIABETES-INSIPIDUS CAUSED BY A MUTATION ENCODING ALA(-1)-]VAL IN THE SIGNAL PEPTIDE OF THE ARGININE-VASOPRESSIN NEUROPHYSIN-II COPEPTIN PRECURSOR, The Journal of clinical endocrinology and metabolism, 82(1), 1997, pp. 51-56
Authors:
RASKIN S
PHILLIPS JA
KRISHNAMANI MRS
VNENCAKJONES C
PARKER RA
ROZOV T
CARDIERI JM
MAROSTICA P
ABREU F
GIUGLIANI R
REIS F
ROSARIO NA
LUDWIG N
CULPI L
Citation: S. Raskin et al., CYSTIC-FIBROSIS IN THE BRAZILIAN POPULATION - DF508 MUTATION AND KM-19 XV-2C HAPLOTYPE DISTRIBUTION/, Human biology, 69(4), 1997, pp. 499-508
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LOYD JE
SLOVIS B
PHILLIPS JA
BUTLER MG
FOROUD TM
CONNEALLY PM
NEWMAN JH
Citation: Je. Loyd et al., THE PRESENCE OF GENETIC ANTICIPATION SUGGESTS THAT THE MOLECULAR-BASIS OF FAMILIAL PRIMARY PULMONARY-HYPERTENSION MAY BE TRINUCLEOTIDE REPEAT EXPANSION, Chest, 111(6), 1997, pp. 82-83