Authors:
KORKKO J
KUIVANIEMI H
PAASSILTA P
ZHUANG JP
TROMP G
DEPAEPE A
PROCKOP DJ
ALAKOKKO L
Citation: J. Korkko et al., 2 NEW RECURRENT NUCLEOTIDE MUTATIONS IN THE COL1A1 GENE IN 4 PATIENTSWITH OSTEOGENESIS IMPERFECTA - ABOUT 1 5TH ARE RECURRENT/, Human mutation, 9(2), 1997, pp. 148-156
Authors:
LIU XC
PAN J
XU ZF
ZHUANG JP
LIU M
YU DM
SHI ZX
FU HZ
Citation: Xc. Liu et al., MACHINABLE REPM WITH EXCELLENT INTRINSIC COERCIVE FORCE PREPARED BY DS TECHNOLOGY, JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY, 13(6), 1997, pp. 475-478
Citation: Jp. Zhuang et al., THE CAMPYLOBACTER-JEJUNI PORIN TRIMERS PACK INTO DIFFERENT LATTICE TYPES WHEN RECONSTITUTED IN THE PRESENCE OF LIPID, European journal of biochemistry, 244(2), 1997, pp. 575-579
Authors:
ZHUANG JP
TROMP G
KUIVANIEMI H
CASTELLS S
BUGGE M
PROCKOP DJ
Citation: Jp. Zhuang et al., DIRECT SEQUENCING OF PCR PRODUCTS DERIVED FROM CDNAS FOR THE PRO-ALPHA-1 AND PRO-ALPHA-2 CHAINS OF TYPE-I PROCOLLAGEN AS A SCREENING METHODTO DETECT MUTATIONS IN PATIENTS WITH OSTEOGENESIS IMPERFECTA, Human mutation, 7(2), 1996, pp. 89-99
Authors:
ZHUANG JP
TROMP G
KUIVANIEMI H
CASTELLS S
PROCKOP DJ
Citation: Jp. Zhuang et al., SUBSTITUTION OF ARGININE FOR GLYCINE AT POSITION-154 OF THE ALPHA-1 CHAIN OF TYPE-I COLLAGEN IN A VARIANT OF OSTEOGENESIS IMPERFECTA - COMPARISON TO PREVIOUS CASES WITH THE SAME MUTATION, American journal of medical genetics, 61(2), 1996, pp. 111-116
Authors:
ZHUANG JP
TROMP G
KUIVANIEMI H
NAKAYASU K
PROCKOP DJ
Citation: Jp. Zhuang et al., DELETION OF 19 BASE-PAIRS IN INTRON-13 OF THE GENE FOR THE PRO-ALPHA-2(I) CHAIN OF TYPE-I PROCOLLAGEN (COL1A2) CAUSES EXON SKIPPING IN A PROBAND WITH TYPE-I OSTEOGENESIS IMPERFECTA, Human genetics, 91(3), 1993, pp. 210-216
Authors:
TROMP G
WU YL
PROCKOP DJ
MADHATHERI SL
KLEINERT C
EARLEY JJ
ZHUANG JP
NORRGARD O
DARLING RC
ABBOTT WM
COLE CW
JAAKKOLA P
RYYNANEN M
PEARCE WH
YAO JST
MAJAMAA K
SMULLENS SN
GATALICA Z
FERRELL RE
JIMENEZ SA
JACKSON CE
MICHELS VV
KAYE M
KUIVANIEMI H
Citation: G. Tromp et al., SEQUENCING OF CDNA FROM 50 UNRELATED PATIENTS REVEALS THAT MUTATIONS IN THE TRIPLE-HELICAL DOMAIN OF TYPE-III PROCOLLAGEN ARE AN INFREQUENTCAUSE OF AORTIC-ANEURYSMS, The Journal of clinical investigation, 91(6), 1993, pp. 2539-2545