A. Eblé

C. Flück, A. Pandey, P. Mullis, 2011, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

New N-terminal located mutation (Q4ter) within the POU1F1-gene (PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype.

S. Gallati, P. Mullis, R. Pfäffle, 2003, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn2+ for Normal Growth and Development

Primus E. Mullis, C. Flück, P. Mullis, 2013, International journal of endocrinology.

Prevalence of Human GH-1 Gene Alterations in Patients with Isolated Growth Hormone Deficiency

P. Hindmarsh, P. Mullis, A. Eblé, 1998, Pediatric Research.

Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line.

M. Dattani, C. Flück, P. Mullis, 2000, The Journal of endocrinology.

Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiency.

M. Dattani, P. Hindmarsh, C. Flück, 2008, The Journal of clinical endocrinology and metabolism.

Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosis.

I. Robinson, H. Simon, S. Yousefi, 2007, Endocrinology.

Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls.

J. Cogan, P. Mullis, J. Phillips, 1997, European journal of endocrinology.

Isolated growth hormone (GH) deficiency type IA associated with a 45-kilobase gene deletion within the human GH gene cluster.

N. Akar, P. Mullis, A. Akıncı, 1992, The Journal of clinical endocrinology and metabolism.

Prevalence of Human Growth Hormone-1 Gene Deletions among Patients with Isolated Growth Hormone Deficiency from Different Populations

P. Mullis, A. Akıncı, C. Brook, 1992, Pediatric Research.

"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.

Wei Wu, P. Hindmarsh, C. Flück, 1999, The Journal of clinical endocrinology and metabolism.

Rescue of Isolated GH Deficiency Type II (IGHD II) via Pharmacologic Modulation of GH-1 Splicing.

C. Flück, P. Mullis, Maria Consolata Miletta, 2016, Endocrinology.

Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C).

C. Flück, P. Mullis, U. Marti, 1998, The Journal of clinical endocrinology and metabolism.

Growth hormone (GH)-releasing hormone increases the expression of the dominant-negative GH isoform in cases of isolated GH deficiency due to GH splice-site mutations.

I. Robinson, C. Flück, P. Mullis, 2010, Endocrinology.

Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and stature.

M. Thevis, C. Flück, P. Mullis, 2007, The Journal of clinical endocrinology and metabolism.

Monoclonal antibodies reveal the alteration of the rhodocetin structure upon alpha2beta1 integrin binding

J. Stetefeld, T. Bracht, L. Sorokin, 2020 .

Regulation of growth-hormone-receptor gene expression by growth hormone and pegvisomant in human mesangial cells.

C. Strasburger, U. Meinhardt, P. Mullis, 2003, Kidney international.

Isolated GH deficiency type II: knockdown of the harmful Delta3GH recovers wt-GH secretion in rat tumor pituitary cells.

I. Robinson, M. Bidlingmaier, C. Flück, 2010, Endocrinology.

Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and action.

M. Dattani, C. Flück, A. Pandey, 2010, The Journal of clinical endocrinology and metabolism.

Alteration of ZnT5-Mediated Zinc Import into the Early Secretory Pathway Affects the Secretion of Growth Hormone from Rat Pituitary Cells

C. Flück, P. Mullis, Maria Consolata Miletta, 2014, Hormone Research in Paediatrics.

Influence of growth hormone receptor d3 and full-length isoforms on growth hormone response and final height in patients with severe growth hormone deficiency

M. Dattani, P. Hindmarsh, C. Flück, 2007 .

Isolated GH deficiency type II: knockdown of the harmful Delta3GH recovers wt-GH secretion in rat tumor pituitary cells.

I. Robinson, M. Bidlingmaier, C. Flück, 2010, Endocrinology.