Storage of skin biopsies at -70 degrees C for future fibroblast culture.-Reference-Cited by-同舟云学术

Storage of skin biopsies at -70 degrees C for future fibroblast culture.

Published:1984-10-01 Issue:10 Volume:37 Page:1191-1193
ISSN:0021-9746
Container-title:Journal of Clinical Pathology
language:en
Short-container-title:Journal of Clinical Pathology

Author:

Fowler K J

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference19 articles.

1. Localization of prolactin in chromophobe pituitary adenomas: study of necropsy material by immunoperoxidase technique;Kovacs, K.; Corenblum, B.; Sirek, A.M.T.; Penz, G.; Ezrin, C.;J Clin Pathol,1976

2. The variability of blood group antigens in gastric carcinoma as demonstrated by the immunoperoxidase technique;Slocombe, G.W.; Berry, C.L.; Swettenham, K.V.;Virchows Arch (Pathol Anat),1980

3. Nachweis von Eisenoxyd in gewissen Pigmenten;M, Perls Von;Virchows Arch (Pathol Anat)

4. Method for enzymatic intensification of immunocytochemical reaction without use of labelled antibodies;Sternberger, L.A.; Cucullis, J.J.;J Histochem Cytochem,1969

5. Renin in renal cell carcinoma-an immunocytochemical study using antibody to pure human renin;Lindop, G.B.M.; Fleming, S.;J Clin Pathol,1984

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Integrated multi-omics for rapid rare disease diagnosis on a national scale;Nature Medicine;2023-06-08

2. Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma;International Journal of Molecular Sciences;2023-02-10

3. Expanding the Allelic Heterogeneity of ANO10 -Associated Autosomal Recessive Cerebellar Ataxia;Neurology Genetics;2023-02

4. Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function;International Journal of Molecular Sciences;2022-01-17

5. Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humans;Human Molecular Genetics;2021-09-07