Authors:
POPAWAGNER A
SCHRODER E
SCHMOLL H
WALKER LC
KESSLER C
Citation: A. Popawagner et al., UP-REGULATION OF MAP1B AND MAP2 IN THE RAT-BRAIN FOLLOWING MIDDLE CEREBRAL-ARTERY OCCLUSION - EFFECT OF AGE, European journal of neuroscience, 10, 1998, pp. 11623-11623
Citation: Eh. Bradley et Lc. Walker, EDUCATION AND ADVANCE CARE PLANNING IN NURSING-HOMES - THE IMPACT OF OWNERSHIP TYPE, Nonprofit and voluntary sector quarterly, 27(3), 1998, pp. 339-357
Authors:
WARZOK RW
KESSLER C
APEL G
SCHWARZ A
EGENSPERGER R
SCHREIBER D
HERBST EW
WOLF E
WALTHER R
WALKER LC
Citation: Rw. Warzok et al., APOLIPOPROTEIN E4 PROMOTES INCIPIENT ALZHEIMER PATHOLOGY IN THE ELDERLY, Alzheimer disease and associated disorders, 12(1), 1998, pp. 33-39
Authors:
POPAWAGNER A
SCHRODER E
WALKER LC
KESSLER C
Citation: A. Popawagner et al., BETA-AMYLOID PRECURSOR PROTEIN AND BETA-AMYLOID PEPTIDE IMMUNOREACTIVITY IN THE RAT-BRAIN AFTER MIDDLE CEREBRAL-ARTERY OCCLUSION - EFFECT OF AGE, Stroke, 29(10), 1998, pp. 2196-2202
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
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
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
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
Authors:
WALKER LC
VENGLARIK CJ
AUBIN G
WEATHERLY MR
MCCARTY NA
LESNICK B
RUIZ F
CLANCY JP
SORSCHER EJ
Citation: Lc. Walker et al., RELATIONSHIP BETWEEN AIRWAY ION-TRANSPORT AND A MILD PULMONARY-DISEASE MUTATION IN CFTR, American journal of respiratory and critical care medicine, 155(5), 1997, pp. 1684-1689
Citation: Eh. Bradley et al., INSTITUTIONAL EFFORTS TO PROMOTE ADVANCE CARE PLANNING IN NURSING-HOMES - CHALLENGES AND OPPORTUNITIES, The Journal of law, medicine & ethics, 25(2-3), 1997, pp. 150-159
Citation: Hs. Yang et al., PYRIDOXAL BENZOYL HYDRAZONE - THE ACTIVE FORM OF BENZOIC-ACID HYDRAZIDE AS A FIBROSUPPRESSIVE AGENT IN CELL-CULTURE, Journal of investigative dermatology, 108(4), 1997, pp. 525-525
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
Authors:
SAWAMURA N
TAMAOKA A
SHOJI S
KOO EH
WALKER LC
MORI H
Citation: N. Sawamura et al., CHARACTERIZATION OF AMYLOID-BETA PROTEIN SPECIES IN CEREBRAL AMYLOID ANGIOPATHY OF A SQUIRREL-MONKEY BY IMMUNOCYTOCHEMISTRY AND ENZYME-LINKED-IMMUNOSORBENT-ASSAY, Brain research, 764(1-2), 1997, pp. 225-229
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
Authors:
WALKER LC
PARKER CA
LIPINSKI WJ
CALLAHAN MJ
CARROLL RT
GANDY SE
SMITH JD
JUCKER M
BISGAIER CL
Citation: Lc. Walker et al., CEREBRAL LIPID DEPOSITION IN AGED APOLIPOPROTEIN-E-DEFICIENT MICE, The American journal of pathology, 151(5), 1997, pp. 1371-1377
Authors:
GHILARDI JR
CATTON M
STIMSON ER
ROGERS S
WALKER LC
MAGGIO JE
MANTYH PW
Citation: Jr. Ghilardi et al., INTRAARTERIAL INFUSION OF [I-125] A-BETA-1-40 LABELS AMYLOID DEPOSITSIN THE AGED PRIMATE BRAIN IN-VIVO, NeuroReport, 7(15-17), 1996, pp. 2607-2611
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
Authors:
KUO H
INGRAM DK
WALKER LC
TIAN M
HENGEMIHLE JM
JUCKER M
Citation: H. Kuo et al., SIMILARITIES IN THE AGE-RELATED HIPPOCAMPAL DEPOSITION OF PERIODIC ACID-SCHIFF-POSITIVE GRANULES IN THE SENESCENCE-ACCELERATED MOUSE P8 ANDC57BL 6 MOUSE STRAINS/, Neuroscience, 74(3), 1996, pp. 733-740
Citation: Lh. Wei et al., CYSTATIN-C - ICELANDIC-LIKE MUTATION IN AN ANIMAL-MODEL OF CEREBROVASCULAR BETA-AMYLOIDOSIS, Stroke, 27(11), 1996, pp. 2080-2085
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