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Everything about WASF1
Wiskott–Aldrich syndrome protein family member 1, also known as WASP-family verprolin homologous protein 1 (WAVE1), is a protein that in humans is encoded by the WASF1 gene. Wikipedia →
🧭 Start here: a 6-step reading path
- Read the overview: WASF1A 5-minute orientation
- Skim a recent paper: An asymptomatic WASF1 truncation reveals pathogenic mechanism and therapeutic strategy for neurodevelopmental disordersInfluential work since 2022
- Pick up a classic book: Cosmographia et geographia de AffricaThe most-reprinted book on the subject
- Read the landmark paper: De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with SeizuresCited 43 times
- Go sideways: WASF2A closely related topic
- Go sideways: Actin nucleation-promoting factor WASLA closely related topic
📖 Definitions
No dictionary entry for this exact phrase.
🗂️ The subject at a glance
🏆 Landmark papers (most cited)
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures
Expansion of the Genotypic and Phenotypic Spectrum of WASF1-Related Neurodevelopmental Disorder
Trio exome sequencing identified a novel de novo WASF1 missense variant leading to recurrent site substitution in a Chinese patient with developmental delay, microcephaly, and early-onset seizures: A mutational hotspot p.Trp161 and literature review
Recurrent de novo pathogenic variant of WASF1 in a Japanese patient with neurodevelopmental disorder with absent language and variable seizures
The recurrent WASF1 nonsense variant identified in two unaffected Chinese families with neurodevelopmental disorder: case report and review of the literatures
B-89: Neuropsychological Profile of WASF1 (Wiskott-Aldrich Syndrome Protein Family Member 1)
Study the function of GTPase related genes wasf1 and ect2 in zebrafish vascular development
The first description of a rare monogenic disease with polymicrogyria caused by a pathogenic variant in the gene WASF1 in monozygotic twins
🆕 Influential since 2022
📚 Books worth reading
Cosmographia et geographia de AffricaLeo Africanus, Robert Brown · 1556- 📕Dīwān Ḥāfiẓ IbrāhīmMuḥammad Ḥāfiẓ Ibrāhīm · 1948
- 📕Qalʻat al-ḤiṣnMuṣṭafá Ṭalās · 1989
- 📕Mawsūʻat riḥlāt al-ʻArab wa-al-Muslimīn ilá FilasṭīnTaysīr Khalaf · 2010
- 📕Qalʻat al-ḤiṣnMuṣṭafá Ṭalās · 1989
- 📕al-ShawqīyātAḥmad Shawqī · 1948
- 📕الشوقياتAḥmad Shawqī · 1935
- 📕al-ʻAqīdah awwalanṢāliḥ ibn Ṭāhā ʻAbd al-Wāḥid · 2005
Ranked by number of editions on Open Library, a rough measure of how lasting a book is.
🔗 Related topics
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- ACTR2 Actin-related protein 2 is a protein that in humans is encoded by the ACTR2 gene. The specific function of ACTR2 has not yet been determined. However,…
- Wiskott–Aldrich syndrome protein The Wiskott–Aldrich syndrome protein (WASp), or Actin nucleation-promoting factor WAS is a 502–amino acid protein expressed in cells of the hematopoietic…
- ACTR3 Actin-related protein 3 is a protein that in humans is encoded by the ACTR3 gene. The specific function of this gene has not yet been determined; however…
- Profilin 1 Profilin-1 is a protein that in humans is encoded by the PFN1 gene. The PFN1 protein, also known as profilin-1, is a small, monomeric protein composed…
- NCKIPSD NCK-interacting protein with SH3 domain is a protein that in humans is encoded by the NCKIPSD gene. The protein encoded by this gene is localized exclusively…