Zabel B - Search Results

1

Distribution of cartilage proteoglycan (aggrecan) core protein and link protein gene expression during human skeletal development.

Mundlos S, Meyer R, Yamada Y, Zabel B. Mundlos S, et al. Among authors: zabel b. Matrix. 1991 Nov;11(5):339-46. doi: 10.1016/s0934-8832(11)80205-2. Matrix. 1991. PMID: 1725805

2

Developmental expression of human cartilage matrix protein.

Mundlos S, Zabel B. Mundlos S, et al. Among authors: zabel b. Dev Dyn. 1994 Mar;199(3):241-52. doi: 10.1002/aja.1001990308. Dev Dyn. 1994. PMID: 8018988 Free article.

3

Distribution of osteonectin mRNA and protein during human embryonic and fetal development.

Mundlos S, Schwahn B, Reichert T, Zabel B. Mundlos S, et al. Among authors: zabel b. J Histochem Cytochem. 1992 Feb;40(2):283-91. doi: 10.1177/40.2.1552170. J Histochem Cytochem. 1992. PMID: 1552170

4

Distribution of type I and type II collagen gene expression during the development of human long bones.

Mundlos S, Engel H, Michel-Behnke I, Zabel B. Mundlos S, et al. Among authors: zabel b. Bone. 1990;11(4):275-9. doi: 10.1016/8756-3282(90)90080-i. Bone. 1990. PMID: 2242293

5

Nuclear localization of the protein encoded by the Wilms' tumor gene WT1 in embryonic and adult tissues.

Mundlos S, Pelletier J, Darveau A, Bachmann M, Winterpacht A, Zabel B. Mundlos S, et al. Among authors: zabel b. Development. 1993 Dec;119(4):1329-41. doi: 10.1242/dev.119.4.1329. Development. 1993. PMID: 8306891

6

Regulation of chondrocyte differentiation by Cbfa1.

Kim IS, Otto F, Zabel B, Mundlos S. Kim IS, et al. Among authors: zabel b. Mech Dev. 1999 Feb;80(2):159-70. doi: 10.1016/s0925-4773(98)00210-x. Mech Dev. 1999. PMID: 10072783 Free article.

7

An unknown spondylo-meta-epiphyseal dysplasia in sibs with extreme short stature.

Menger H, Mundlos S, Becker K, Spranger J, Zabel B. Menger H, et al. Among authors: zabel b. Am J Med Genet. 1996 May 3;63(1):80-3. doi: 10.1002/(SICI)1096-8628(19960503)63:1<80::AID-AJMG16>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8723091

8

Detection of hepatitis B virus DNA in the liver of children with chronic hepatitis B by in situ hybridization and its relation to other viral markers.

Wirth S, Hueter A, Blaha I, Mundlos S, Keller KM, Zabel B. Wirth S, et al. Among authors: zabel b. J Pediatr Gastroenterol Nutr. 1992 Feb;14(2):128-34. doi: 10.1097/00005176-199202000-00002. J Pediatr Gastroenterol Nutr. 1992. PMID: 1593366

9

Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasia.

Spranger J, Menger H, Mundlos S, Winterpacht A, Zabel B. Spranger J, et al. Among authors: zabel b. Pediatr Radiol. 1994;24(6):431-5. doi: 10.1007/BF02011911. Pediatr Radiol. 1994. PMID: 7700721

10

Alternative splicing as the result of a type II procollagen gene (COL2A1) mutation in a patient with Kniest dysplasia.

Winterpacht A, Schwarze U, Mundlos S, Menger H, Spranger J, Zabel B. Winterpacht A, et al. Among authors: zabel b. Hum Mol Genet. 1994 Oct;3(10):1891-3. doi: 10.1093/hmg/3.10.1891. Hum Mol Genet. 1994. PMID: 7849719 No abstract available.

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