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Results: 1-21 |
Results: 21
BACULOVIRUS EXPRESSION CONFIRMS THAT DELETION OF CYSTEINE-369 IN LYSYL HYDROXYLASE (LH) RESULTS IN LOSS OF LH ACTIVITY IN 2 PATIENTS WITH EHLERS-DANLOS TYPE-VI
Authors: ALLEN JD WALKER LC THAI SF MURAD S PINNELL SR YEOWELL HN
Citation: Jd. Allen et al., BACULOVIRUS EXPRESSION CONFIRMS THAT DELETION OF CYSTEINE-369 IN LYSYL HYDROXYLASE (LH) RESULTS IN LOSS OF LH ACTIVITY IN 2 PATIENTS WITH EHLERS-DANLOS TYPE-VI, Journal of investigative dermatology, 110(4), 1998, pp. 502-502
CHARACTERIZATION OF THE REGULATORY AND MINOXIDIL-RESPONSIVE ELEMENTS IN THE 5'-FLANKING REGION OF THE LYSYL HYDROXYLASE GENE
Authors: THAI SF PINNELL SR YEOWELL HN
Citation: Sf. Thai et al., CHARACTERIZATION OF THE REGULATORY AND MINOXIDIL-RESPONSIVE ELEMENTS IN THE 5'-FLANKING REGION OF THE LYSYL HYDROXYLASE GENE, Journal of investigative dermatology, 110(4), 1998, pp. 605-605
MUTATIONS IN THE LYSYL HYDROXYLASE (LH) GENE ARE RESPONSIBLE FOR LH DEFICIENCY IN 8 PATIENTS WITH EHLERS-DANLOS TYPE-VI
Authors: WALKER LC FARMER BT YEOWELL HN
Citation: Lc. Walker et al., MUTATIONS IN THE LYSYL HYDROXYLASE (LH) GENE ARE RESPONSIBLE FOR LH DEFICIENCY IN 8 PATIENTS WITH EHLERS-DANLOS TYPE-VI, Journal of investigative dermatology, 110(4), 1998, pp. 613-613
PRENATAL ASSESSMENT OF CLINICAL PHENOTYPE BY MUTATIONAL SCREENING IN A FAMILY WITH EHLERS-DANLOS-SYNDROME TYPE-VI
Authors: YEOWELL HN WALKER LC
Citation: Hn. Yeowell et Lc. Walker, PRENATAL ASSESSMENT OF CLINICAL PHENOTYPE BY MUTATIONAL SCREENING IN A FAMILY WITH EHLERS-DANLOS-SYNDROME TYPE-VI, Journal of investigative dermatology, 110(4), 1998, pp. 613-613
ALTERED POSTTRANSLATIONAL MODIFICATIONS OF COLLAGEN IN KELOID
Authors: UZAWA K MARSHALL MK KATZ EP TANZAWA H YEOWELL HN YAMAUCHI M
Citation: K. Uzawa et al., ALTERED POSTTRANSLATIONAL MODIFICATIONS OF COLLAGEN IN KELOID, Biochemical and biophysical research communications (Print), 249(3), 1998, pp. 652-655
EHLERS-DANLOS-SYNDROME TYPE-VI RESULTS FROM A NONSENSE MUTATION AND ASPLICE SITE-MEDIATED EXON-SKIPPING MUTATION IN THE LYSYL HYDROXYLASE GENE
Authors: YEOWELL HN WALKER LC
Citation: Hn. Yeowell et Lc. Walker, EHLERS-DANLOS-SYNDROME TYPE-VI RESULTS FROM A NONSENSE MUTATION AND ASPLICE SITE-MEDIATED EXON-SKIPPING MUTATION IN THE LYSYL HYDROXYLASE GENE, Proceedings of the Association of American Physicians, 109(4), 1997, pp. 383-396
COMPOUND HETEROZYGOSITY FOR A NONSENSE MUTATION AND AN EXON DELETION IN THE LYSYL HYDROXYLASE GENE IS ASSOCIATED WITH DECREASED MESSENGER-RNA ACCUMULATION IN A PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI
Authors: YEOWELL HN WALKER LC
Citation: Hn. Yeowell et Lc. Walker, COMPOUND HETEROZYGOSITY FOR A NONSENSE MUTATION AND AN EXON DELETION IN THE LYSYL HYDROXYLASE GENE IS ASSOCIATED WITH DECREASED MESSENGER-RNA ACCUMULATION IN A PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI, Journal of investigative dermatology, 108(4), 1997, pp. 643-643
A COMMON DUPLICATION IN THE LYSYL HYDROXYLASE GENE OF PATIENTS WITH EHLERS-DANLOS-SYNDROME TYPE-VI RESULTS IN PREFERENTIAL STIMULATION OF LYSYL HYDROXYLASE-ACTIVITY AND MESSENGER-RNA BY HYDRALAZINE
Authors: YEOWELL HN WALKER LC MURAD S PINNELL SR
Citation: Hn. Yeowell et al., A COMMON DUPLICATION IN THE LYSYL HYDROXYLASE GENE OF PATIENTS WITH EHLERS-DANLOS-SYNDROME TYPE-VI RESULTS IN PREFERENTIAL STIMULATION OF LYSYL HYDROXYLASE-ACTIVITY AND MESSENGER-RNA BY HYDRALAZINE, Archives of biochemistry and biophysics, 347(1), 1997, pp. 126-131
COMPOUND HETEROZYGOSITY FOR A NONSENSE MUTATION AND AN EXON DELETION IN THE LYSYL HYDROXYLASE GENE OF A PATIENT WITH EHLERS-DANLOS SYNDROMETYPE-VI
Authors: YEOWELL HN WALKER LC YEOWELL MN PINNELL SR
Citation: Hn. Yeowell et al., COMPOUND HETEROZYGOSITY FOR A NONSENSE MUTATION AND AN EXON DELETION IN THE LYSYL HYDROXYLASE GENE OF A PATIENT WITH EHLERS-DANLOS SYNDROMETYPE-VI, Matrix biology, 15(3), 1996, pp. 185-185
LYSYL HYDROXYLASE-ACTIVITY AND MESSENGER-RNA ARE SIGNIFICANTLY UP-REGULATED BY ADMINISTRATION OF HYDRALAZINE AND ASCORBATE TO FIBROBLASTS FROM EHLERS-DANLOS SYNDROME TYPE-VI PATIENTS WITH A COMMON DUPLICATION IN THE LYSYL HYDROXYLASE GENE
Authors: YEOWELL HN WALKER LC MURAD S PINNELL SR
Citation: Hn. Yeowell et al., LYSYL HYDROXYLASE-ACTIVITY AND MESSENGER-RNA ARE SIGNIFICANTLY UP-REGULATED BY ADMINISTRATION OF HYDRALAZINE AND ASCORBATE TO FIBROBLASTS FROM EHLERS-DANLOS SYNDROME TYPE-VI PATIENTS WITH A COMMON DUPLICATION IN THE LYSYL HYDROXYLASE GENE, Journal of investigative dermatology, 106(4), 1996, pp. 102-102
NORMAL AND SHORTENED TRANSCRIPTS FROM THE LYSYL HYDROXYLASE GENE MAY EXPLAIN LYSYL HYDROXYLASE DEFICIENCY IN FIBROBLASTS FROM A PATIENT WITH EHLERS-DANLOS SYNDROME TYPE-VI
Authors: WALKER LC MURAD S PINNELL SR YEOWELL HN
Citation: Lc. Walker et al., NORMAL AND SHORTENED TRANSCRIPTS FROM THE LYSYL HYDROXYLASE GENE MAY EXPLAIN LYSYL HYDROXYLASE DEFICIENCY IN FIBROBLASTS FROM A PATIENT WITH EHLERS-DANLOS SYNDROME TYPE-VI, Journal of investigative dermatology, 106(4), 1996, pp. 607-607
THE EXPRESSION OF A FUNCTIONAL, SECRETED HUMAN LYSYL HYDROXYLASE IN ABACULOVIRUS SYSTEM
Authors: KROL BJ MURAD S WALKER LC MARSHALL MK CLARK WL PINNELL SR YEOWELL HN
Citation: Bj. Krol et al., THE EXPRESSION OF A FUNCTIONAL, SECRETED HUMAN LYSYL HYDROXYLASE IN ABACULOVIRUS SYSTEM, Journal of investigative dermatology, 106(1), 1996, pp. 11-16
A DUPLICATION IN THE LYSYL HYDROXYLASE GENE MAY BE A COMMON MUTATION IN A SUBSET OF PATIENTS WITH EHLERS-DANLOS SYNDROME TYPE-VI
Authors: YEOWELL HN WALKER LC MARSHALL MK PINNELL SR
Citation: Hn. Yeowell et al., A DUPLICATION IN THE LYSYL HYDROXYLASE GENE MAY BE A COMMON MUTATION IN A SUBSET OF PATIENTS WITH EHLERS-DANLOS SYNDROME TYPE-VI, Journal of cellular biochemistry, 1995, pp. 374-374
THE MESSENGER-RNA AND ACTIVITY OF LYSYL HYDROXYLASE ARE STIMULATED BYADMINISTRATION OF ASCORBATE AND HYDRALAZINE TO HUMAN SKIN FIBROBLASTSFROM A PATIENT WITH EHLERS-DANLOS SYNDROME TYPE-VI
Authors: YEOWELL HN MARSHALL LC MURAD MK PINNELL SR
Citation: Hn. Yeowell et al., THE MESSENGER-RNA AND ACTIVITY OF LYSYL HYDROXYLASE ARE STIMULATED BYADMINISTRATION OF ASCORBATE AND HYDRALAZINE TO HUMAN SKIN FIBROBLASTSFROM A PATIENT WITH EHLERS-DANLOS SYNDROME TYPE-VI, Journal of investigative dermatology, 104(4), 1995, pp. 670-670
EXPRESSION OF A SECRETED FUNCTIONAL HUMAN LYSYL HYDROXYLASE IN A BACULOVIRUS EXPRESSION SYSTEM
Authors: KROL BJ WALKER LC MURAD S MARSHALL MK PINELL SR YEOWELL HN
Citation: Bj. Krol et al., EXPRESSION OF A SECRETED FUNCTIONAL HUMAN LYSYL HYDROXYLASE IN A BACULOVIRUS EXPRESSION SYSTEM, Journal of investigative dermatology, 104(4), 1995, pp. 675-675
THE MESSENGER-RNA AND THE ACTIVITY OF LYSYL HYDROXYLASE ARE UP-REGULATED BY THE ADMINISTRATION OF ASCORBATE AND HYDRALAZINE TO HUMAN SKIN FIBROBLASTS FROM A PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI
Authors: YEOWELL HN WALKER LC MARSHALL MK MURAD S PINNELL SR
Citation: Hn. Yeowell et al., THE MESSENGER-RNA AND THE ACTIVITY OF LYSYL HYDROXYLASE ARE UP-REGULATED BY THE ADMINISTRATION OF ASCORBATE AND HYDRALAZINE TO HUMAN SKIN FIBROBLASTS FROM A PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI, Archives of biochemistry and biophysics, 321(2), 1995, pp. 510-516
INHERITANCE ANALYSIS CONFIRMS COMPOUND HETEROZYGOSITY MUTATIONS IN LYSYL HYDROXYLASE GENE FROM A PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI
Authors: YEOWELL HN HA V MARSHALL MK PINNELL SR
Citation: Hn. Yeowell et al., INHERITANCE ANALYSIS CONFIRMS COMPOUND HETEROZYGOSITY MUTATIONS IN LYSYL HYDROXYLASE GENE FROM A PATIENT WITH EHLERS-DANLOS-SYNDROME TYPE-VI, Journal of investigative dermatology, 102(4), 1994, pp. 575-575
SEQUENCE-ANALYSIS OF A CDNA FOR LYSYL HYDROXYLASE ISOLATED FROM HUMANSKIN FIBROBLASTS FROM A NORMAL DONOR - DIFFERENCES FROM HUMAN PLACENTAL LYSYL HYDROXYLASE CDNA
Authors: YEOWELL HN HA V CLARK WL MARSHALL MK PINNELL SR
Citation: Hn. Yeowell et al., SEQUENCE-ANALYSIS OF A CDNA FOR LYSYL HYDROXYLASE ISOLATED FROM HUMANSKIN FIBROBLASTS FROM A NORMAL DONOR - DIFFERENCES FROM HUMAN PLACENTAL LYSYL HYDROXYLASE CDNA, Journal of investigative dermatology, 102(3), 1994, pp. 382-384
A PATIENT WITH EHLERS-DANLOS SYNDROME TYPE-VI IS A COMPOUND HETEROZYGOTE FOR MUTATIONS IN THE LYSYL HYDROXYLASE GENE
Authors: HA VT MARSHALL MK ELSAS LJ PINNELL SR YEOWELL HN
Citation: Vt. Ha et al., A PATIENT WITH EHLERS-DANLOS SYNDROME TYPE-VI IS A COMPOUND HETEROZYGOTE FOR MUTATIONS IN THE LYSYL HYDROXYLASE GENE, The Journal of clinical investigation, 93(4), 1994, pp. 1716-1721
REGULATION OF LYSYL OXIDASE MESSENGER-RNA IN DERMAL FIBROBLASTS FROM NORMAL DONORS AND PATIENTS WITH INHERITED CONNECTIVE-TISSUE DISORDERS
Authors: YEOWELL HN MARSHALL MK WALKER LC HA V PINNELL SR
Citation: Hn. Yeowell et al., REGULATION OF LYSYL OXIDASE MESSENGER-RNA IN DERMAL FIBROBLASTS FROM NORMAL DONORS AND PATIENTS WITH INHERITED CONNECTIVE-TISSUE DISORDERS, Archives of biochemistry and biophysics, 308(1), 1994, pp. 299-305
THE EHLERS-DANLOS SYNDROMES
Authors: YEOWELL HN PINNELL SR
Citation: Hn. Yeowell et Sr. Pinnell, THE EHLERS-DANLOS SYNDROMES, Seminars in dermatology, 12(3), 1993, pp. 229-240
Risultati: 1-21 |