Z. Ren

发表

Ultraviolet light induces expression of p53 and p21 in human skin: effect of sunscreen and constitutive p21 expression in skin appendages.

F. Pontén, M. Nistér, B. Berne, 1995, The Journal of investigative dermatology.

Benign clonal keratinocyte patches with p53 mutations show no genetic link to synchronous squamous cell precancer or cancer in human skin.

F. Pontén, M. Uhlén, J. Lundeberg, 1997, The American journal of pathology.

Molecular pathology in basal cell cancer with p53 as a genetic marker

F. Pontén, M. Uhlén, J. Lundeberg, 1997, Oncogene.

The role of p53 codon 72 and human papilloma virus status of cutaneous squamous cell carcinoma in the Swedish population.

F. Pontén, A. Asplund, J. Lundeberg, 2004, Acta dermato-venereologica.

Early metastatic progression of bladder carcinoma: molecular profile of primary tumor and sentinel lymph node.

K. Wester, Z. Ren, P. Malmström, 2002, The Journal of urology.

VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy

J. Rilstone, C. Ackerley, I. Nishino, 2013, Acta Neuropathologica.

Constitutive and inducible expression of PDGF in the human basophilic cell line, KU 812.

G. Nilsson, L. Hellman, M. Nistér, 1993, Growth factors.

Two distinct p53 immunohistochemical patterns in human squamous‐cell skin cancer, precursors and normal epidermis

F. Pontén, M. Nistér, Z. Ren, 1996, International journal of cancer.

Expression of platelet-derived growth factor beta receptor in chondrogenesis of perichondrial transplants.

M. Nistér, Z. Ren, L. Ohlsén, 1995, Scandinavian journal of plastic and reconstructive surgery and hand surgery.

Epithelial-stromal interactions in basal cell cancer: the PDGF system.

F. Pontén, M. Nistér, Z. Ren, 1993, The Journal of investigative dermatology.

Human epidermal cancer and accompanying precursors have identical p53 mutations different from p53 mutations in adjacent areas of clonally expanded non-neoplastic keratinocytes.

F. Pontén, M. Uhlén, J. Lundeberg, 1996, Oncogene.

High expression of B4GALT1 is associated with poor prognosis in acute myeloid leukemia

Z. Ren, Mingyong Wang, Yiming Lei, 2022, Frontiers in Genetics.

TP53 mutations predict for poor survival in de novo diffuse large B-cell lymphoma of germinal center subtype.

R. Rosenquist, Z. Ren, R. Amini, 2009, Leukemia research.

Genetic alterations in tp53 in recurrent urothelial cancer: a longitudinal study.

C. Cordon-Cardo, V. Reuter, G. Dalbagni, 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.

Molecular genetic and epigenetic analysis of NCX2/SLC8A2 at 19q13.3 in human gliomas

J. Kere, M. Nistér, Z. Ren, 2010, Neuropathology and applied neurobiology.

Differential effects of TGF-beta1 on telomerase activity in thyroid carcinoma cell lines.

Z. Ren, N. Heldin, Y. Paulsson-Karlsson, 2005, Biochemical and biophysical research communications.

Recovering DNA and Optimizing PCR Conditions from Microdissected Formalin-Fixed and Paraffin-Embedded Materials

M. Nistér, Z. Ren, C. Sundström, 2001, Pathobiology.

Biobanking of fresh frozen tissue: RNA is stable in nonfixed surgical specimens

F. Pontén, Simin Tahmasebpoor, Z. Ren, 2006, Laboratory Investigation.

Genetic instability in the 9q22.3 region is a late event in the development of squamous cell carcinoma

F. Pontén, M. Uhlén, J. Odeberg, 1998, Oncogene.

Molecular Genetic Analysis of p53 Intratumoral Heterogeneity in Human Astrocytic Brain Tumors

T. Soussi, M. Nistér, Z. Ren, 2007, Journal of neuropathology and experimental neurology.

Planning for intracavitary anti-EGFR radionuclide therapy of gliomas. Literature review and data on EGFR expression.

K. Wester, H. Lundqvist, M. Nistér, 2006, Journal of neuro-oncology.

Pigmentosum Patient Gene Mutations in a Xeroderma p 53 a Multitude of Simultaneously Present Epidermal Neoplastic Lesions Contain Clones of Normal Keratinocytes and a Variety of Updated

J. Lundeberg, Z. Ren, A. Ahmadian, 2006 .

Clones of normal keratinocytes and a variety of simultaneously present epidermal neoplastic lesions contain a multitude of p53 gene mutations in a xeroderma pigmentosum patient.

F. Pontén, M. Uhlén, J. Lundeberg, 1998, Cancer research.

RETRACTED: VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification

J. Rilstone, C. Ackerley, I. Nishino, 2009, Cell.

VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification (Retracted article. See vol. 142, pg. 984, 2010)

J. Rilstone, C. Ackerley, I. Nishino, 2009 .

Lafora Progressive Myoclonus Epilepsy: Disease Course Homogeneity in a Genetic Isolate

C. Ackerley, Z. Ren, B. Minassian, 2008, Journal of child neurology.

Genetically distinct astrocytic and oligodendroglial components in oligoastrocytomas

M. Nistér, Z. Ren, H. Kalimo, 2007, Acta Neuropathologica.

Reconstruction of the two-dimensional distribution of p53 positive staining patches in sun-exposed morphologically normal skin.

F. Pontén, M. Nistér, Z. Ren, 1997, International journal of oncology.

Role of mutations in the p53 gene for the development of human squamous cell skin cancer : a correlative molecular and morphological study

Z. Ren, 1996 .

Retraction Notice to: VMA21 Deficiency Causes an Autophagic Myopathy by Compromising V-ATPase Activity and Lysosomal Acidification

J. Rilstone, C. Ackerley, I. Nishino, 2010, Cell.

The carcinogenic role of oncogenic HPV and p53 gene mutation in cervical adenocarcinomas

E. Wilander, Z. Ren, A. Hellström, 2006, Medical oncology.