N. Barth

Gly15Gly polymorphism within the human adipocyte-specific apM-1gene but not Tyr111His polymorphism is associated with higher levels of cholesterol and LDL-cholesterol in caucasian patients with type 2 diabetes

J. Schölmerich, G. Schmitz, A. Schäffler, 2001, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Mutation analysis of the human adipocyte‐specific apM‐1 gene

J. Schölmerich, G. Schmitz, W. Drobnik, 2000, European journal of clinical investigation.

Identification of regulatory elements in the human adipose most abundant gene transcript-1 (apM-1) promoter: role of SP1/SP3 and TNF-α as regulatory pathways

T. Langmann, J. Schölmerich, G. Schmitz, 2003, Diabetologia.

Frequency and significance of Pro12Ala and Pro115Gln polymorphism in gene for peroxisome proliferation-activated receptor-gamma regarding metabolic parameters in a Caucasian cohort.

J. Schölmerich, G. Schmitz, A. Schäffler, 2001, Endocrine.

Frequency and significance of pro12Ala and Pro115Gln polymorphism in gene for peroxisome proliferation-activated receptor-γ2 regarding metabolic parameters in a caucasian cohortregarding metabolic parameters in a caucasian cohort

J. Schölmerich, G. Schmitz, A. Schäffler, 2001, Endocrine.

Identification of a new missense mutation (Gly95Glu) in a highly conserved codon within the high-mobility group box of the sex-determining region Y gene: report on a 46,XY female with gonadal dysgenesis and yolk-sac tumor.

J. Schölmerich, R. Knüchel, A. Schäffler, 2000, The Journal of clinical endocrinology and metabolism.

Pro12Ala polymorphism in the peroxisome proliferator-activated receptor-gamma2 (PPARgamma2) is associated with higher levels of total cholesterol and LDL-cholesterol in male caucasian type 2 diabetes patients.

J. Schölmerich, G. Schmitz, A. Schäffler, 2002, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Identification of regulatory elements in the human adipose most abundant gene transcript-1 (apM-1) promoter: role of SP1/SP3 and TNF-α as regulatory pathways

T. Langmann, J. Schölmerich, G. Schmitz, 2004, Diabetologia.

Identification of a new missense mutation (Gly95Glu) in a highly conserved codon within the high-mobility group box of the sex-determining region Y gene: report on a 46,XY female with gonadal dysgenesis and yolk-sac tumor.

J. Schölmerich, A. Schäffler, K. Palitzsch, 2000, The Journal of clinical endocrinology and metabolism.