Table 3_Schimmelpenning-Feuerstein-Mims syndrome: a systematic review of clinical cases to identify genotype-phenotype associations.docx

Table 3_Schimmelpenning-Feuerstein-Mims syndrome: a systematic review of clinical cases to identify genotype-phenotype associations.docx

Background/objectives<p>Schimmelpenning-Feuerstein-Mims syndrome (SFMS) is a rare genodermatosis from the group of epidermal nevus syndromes with a wide range of clinical manifestations, including linear nevus sebaceous, ophthalmological disorders, cardiovascular abnormalities, nervous system...

وصف كامل

محفوظ في:

التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Ekaterina Zelenova (8658819) (author)
مؤلفون آخرون:	Tatiana Belysheva (22801718) (author), Elena Sharapova (22801721) (author), Vera Semenova (22801724) (author), Timur Valiev (22801727) (author), Tatiana Nasedkina (22801730) (author)
منشور في:	2025
الموضوعات:	Foetal Development and Medicine Schimmelpenning-Feuerstein-Mims syndrome KRAS HRAS NRAS mutation phenotype mosaicism dermal nevus
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!

مواد مشابهة

Table 2_Schimmelpenning-Feuerstein-Mims syndrome: a systematic review of clinical cases to identify genotype-phenotype associations.xlsx
حسب: Ekaterina Zelenova (8658819)
منشور في: (2025)

Table 1_Schimmelpenning-Feuerstein-Mims syndrome: a systematic review of clinical cases to identify genotype-phenotype associations.xlsx
حسب: Ekaterina Zelenova (8658819)
منشور في: (2025)

Data Sheet 1_Schimmelpenning-Feuerstein-Mims syndrome: a systematic review of clinical cases to identify genotype-phenotype associations.pdf
حسب: Ekaterina Zelenova (8658819)
منشور في: (2025)

Genomic analysis of adult case of ocular surface giant congenital melanocytic nevus and associated clinicopathological findings
حسب: Lindsay A McGrath (9281336)
منشور في: (2020)

Mitogen-Activated Protein Kinase Pathway: Genetic Analysis of 95 Adrenocortical Tumors
حسب: Marco Redaelli (713119)
منشور في: (2015)

Dissociation constants (K<sub>d</sub>) in μM for the interaction between RAS proteins and effectors.
حسب: Hossein Nakhaeizadeh (3390107)
منشور في: (2016)

Register of dissociation constants (K<sub>d</sub>) determined for the RAS-effector interactions.
حسب: Hossein Nakhaeizadeh (3390107)
منشور في: (2016)

RAS-effector interaction hotspots.
حسب: Hossein Nakhaeizadeh (3390107)
منشور في: (2016)

Superposition of all available RAS–effector complex structures.
حسب: Hossein Nakhaeizadeh (3390107)
منشور في: (2016)

Equilibrium dissociation constants for RAS-effector interaction determined Fluorescence polarization.
حسب: Hossein Nakhaeizadeh (3390107)
منشور في: (2016)

Domain organization of RAS effectors and different proteins used in this study.
حسب: Hossein Nakhaeizadeh (3390107)
منشور في: (2016)

The RAS-Effector Interface: Isoform-Specific Differences in the Effector Binding Regions
حسب: Hossein Nakhaeizadeh (3390107)
منشور في: (2016)

Supplementary Material for: Coexpression of SOX10/CD271 (p75<sup>NTR</sup>) and β-Galactosidase in Large to Giant Congenital Melanocytic Nevi of Pediatric Patients
حسب: Barysch M.J. (4145728)
منشور في: (2014)

<i>In vivo</i> confocal laser scan of a dermal nevus after intradermal ICG injection.
حسب: Constanze Jonak (134722)
منشور في: (2011)

DataSheet_1_Worldwide Prevalence and Clinical Characteristics of RAS Mutations in Head and Neck Cancer: A Systematic Review and Meta-Analysis.pdf
حسب: Ofra Novoplansky (3615527)
منشور في: (2022)

DataSheet_2_Worldwide Prevalence and Clinical Characteristics of RAS Mutations in Head and Neck Cancer: A Systematic Review and Meta-Analysis.pdf
حسب: Ofra Novoplansky (3615527)
منشور في: (2022)

Distribution of genotypes from crossing <i>Hras</i><sup><i>+/-</i></sup><i>;Nras</i><sup><i>+/-</i></sup> mice.
حسب: Jamie D. Weyandt (811803)
منشور في: (2016)

Protein standard absolute quantification for measurement of cellular Ras abundance.
حسب: Craig J. Mageean (824869)
منشور في: (2015)

Isotopically-labelled Ras standards and proteotypic peptides used in this study.
حسب: Craig J. Mageean (824869)
منشور في: (2015)

Selected reaction monitoring of proteotypic Ras peptides in SW48 isogenic cell lines.
حسب: Craig J. Mageean (824869)
منشور في: (2015)

Cellular Ras abundance in isogenic colorectal cell lines.
حسب: Craig J. Mageean (824869)
منشور في: (2015)

Absolute Quantification of Endogenous Ras Isoform Abundance
حسب: Craig J. Mageean (824869)
منشور في: (2015)

Patient characteristics grouped by mutation status.
حسب: Jeremy A. Goss (8207379)
منشور في: (2019)

Intracranial arteriovenous malformation (AVM) specimens and genetic results.
حسب: Jeremy A. Goss (8207379)
منشور في: (2019)

Histopathology and immunohistochemical findings of VP and SCC induced by vemurafenib.
حسب: Eric Frouin (652646)
منشور في: (2014)

Immunohistological and molecular analyses.
حسب: Eric Frouin (652646)
منشور في: (2014)

Table S1 - Cutaneous Epithelial Tumors Induced by Vemurafenib Involve the MAPK and Pi3KCA Pathways but Not HPV nor HPyV Viral Infection
حسب: Eric Frouin (652646)
منشور في: (2014)

Loss of wild-type <i>Hras</i> alone or in combination with loss of wild-type <i>Nras</i> promotes lymphoid infiltration in the lungs of urethane-treated mice.
حسب: Jamie D. Weyandt (811803)
منشور في: (2016)

Immunohistochemical staining in urethane-induced lung lesions.
حسب: Jamie D. Weyandt (811803)
منشور في: (2016)

Effects of concomitant loss of wild-type <i>Hras</i> and <i>Nras</i> on urethane-induced tumorigenesis.
حسب: Jamie D. Weyandt (811803)
منشور في: (2016)

Loss of wild-type <i>Hras</i>, but not <i>Nras</i>, promotes formation of urethane induced lung tumors.
حسب: Jamie D. Weyandt (811803)
منشور في: (2016)

Immunohistochemical staining in urethane-induced lung lesions.
حسب: Jamie D. Weyandt (811803)
منشور في: (2016)

Image 1_Case Report: Prenatal ultrasound presentation of congenital melanocytic nevus syndrome.jpeg
حسب: ZhiH Shi (20471459)
منشور في: (2024)

Table1_Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation.DOCX
حسب: Roberta Zuntini (11187786)
منشور في: (2023)

Table2_Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation.docx
حسب: Roberta Zuntini (11187786)
منشور في: (2023)

Image1_Case Report: Sequential postzygotic HRAS mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving HRAS in oncogenic transformation.JPEG
حسب: Roberta Zuntini (11187786)
منشور في: (2023)

Early boost following MIM and PP training.
حسب: Ursula Debarnot (341042)
منشور في: (2013)

Mutational status and detailed mutation classes found.
حسب: Muhammad Awidi (5931629)
منشور في: (2019)

Characteristics of the 190 patients.
حسب: Muhammad Awidi (5931629)
منشور في: (2019)

S1 Dataset -
حسب: Muhammad Awidi (5931629)
منشور في: (2019)