Mohammad Shahrooei

发表

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Jacques Fellay, Agatha Schlüter, Aurora Pujol, 2020, Science.

Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population

J. Casanova, L. Abel, R. Sherkat, 2023, Journal of Clinical Immunology.

Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

Mark S. Anderson, P. Gregersen, R. Nussbaum, 2021, Science Immunology.

Mark S. Anderson, J. Casanova, J. Fellay, 2021, The Journal of experimental medicine.

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

R. Nussbaum, J. Casanova, M. Gut, 2021, Science immunology.

Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin

J. Casanova, C. Wouters, L. Notarangelo, 2022, Science.

Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria

A. Teleman, D. Rinchai, Y. Seeleuthner, 2023, Cell.

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, W. Wasserman, 2023, The Journal of experimental medicine.

Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria

J. Casanova, S. Tangye, F. Sallusto, 2023, Science Immunology.

Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications

N. Brunetti‐Pierri, J. Hentschel, F. Alkuraya, 2022, American journal of human genetics.

Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy and periventricular calcifications

Abou, N. Brunetti‐Pierri, J. Hentschel, 2022, medRxiv.

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

J. Derisi, F. Rieux-Laucat, J. Fellay, 2023, Nature.

Impaired respiratory burst contributes to infections in PKCδ-deficient patients

J. Casanova, L. Abel, G. Uzel, 2021, The Journal of experimental medicine.

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

J. Casanova, J. Uitto, L. Abel, 2022, The Journal of experimental medicine.

Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).

J. L. Shephard, M. Vihinen, H. Kanegane, 2021, Blood cells, molecules & diseases.

X-linked hyper-IgM syndrome associated with pulmonary manifestations: A very rare case of functional mutation in CD40L gene in Iran.

M. Shahrooei, M. Nabavi, M. Torabizadeh, 2019, Current research in translational medicine.

Conocarpus trees have low allergenicity potential in patients suffering from asthma and allergic rhinitis living in southwestern Iran

M. Chehrazi, A. Fayezi, Mohammad Shahrooei, 2023, Allergo Journal International.

The immunopathological landscape of human pre-TCRα deficiency: from rare to common variants

Chaim A. Schramm, J. Kelsen, C. Deswarte, 2024, Science.

Purification and evaluation of glycerol teichoic acid from biofilm forming Staphylococcus epidermidis as a putative vaccine candidate

S. Siadat, M. Shahrooei, B. Mirzaei, 2015 .

Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency

Laura E. Covill, P. Gregersen, J. Casanova, 2022, The Journal of experimental medicine.

Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy

Mark M. Davis, J. Casanova, L. Notarangelo, 2021, Cell.

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

J. Casanova, S. Seligman, C. Rice, 2019, The Journal of experimental medicine.

Whole Exome Sequencing Revealed a Novel GJB1 Pathogenic Variant and a Rare BSCL2 Mutation in Two Iranian Large Pedigrees with Multiple Affected Cases of Charcot-Marie-Tooth

Hassan Rokni-Zadeh, A. Biglari, M. Maghbooli, 2019, International journal of molecular and cellular medicine.

A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

Jacques Fellay, Aurora Pujol, Claire Redin, 2020, Cell.

NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation

M. Konantz, C. Lengerke, Zhichao Miao, 2020, The Journal of experimental medicine.

Synthesis of conjugated PIA-rSesC and immunological evaluation against biofilm-forming Staphylococcus epidermidis.

M. Shafiee Ardestani, S. Siadat, J. van Eldere, 2019, Journal of medical microbiology.

Ses proteins as possible targets for vaccine development against Staphylococcus epidermidis infections.

E. Vanstreels, J. van Eldere, M. Shahrooei, 2018, The Journal of infection.

Immunoprophylaxis and immunotherapy of Staphylococcus epidermidis infections: challenges and prospects

J. Eldere, M. Shahrooei, L. Van Mellaert, 2012, Expert review of vaccines.

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Andrew J. Oler, Eglantine Ferrand Devouge, P. Gregersen, 2023, Genome Medicine.

Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis

M. Shabani, N. Parvaneh, H. Alimadadi, 2019, Pediatric blood & cancer.

Correction: Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency

J. Casanova, T. Ozcelik, L. Abel, 2022, The Journal of experimental medicine.

Leishmaniasis and autoimmunity in patient with LPS-responsive beige-like anchor protein (LRBA) deficiency.

A. Aghamohammadi, G. Azizi, R. Yazdani, 2020, Endocrine, metabolic & immune disorders drug targets.

Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector Engagement

S. Ehl, V. Ziaee, S. Ammann, 2020, Frontiers in Immunology.

Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature

A. Aghamohammadi, X. Bossuyt, G. Azizi, 2017, Immunological investigations.

Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency.

K. Dobbs, B. Boisson, J. Toguchida, 2024, Nature immunology.

Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect

H. Pircher, S. Ammann, S. Tholen, 2024, The Journal of experimental medicine.

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

S. Tangye, C. Deswarte, K. Claeys, 2024, Cell.

Human inherited CCR2 deficiency underlies progressive polycystic lung disease

D. Rinchai, S. Bahram, Y. Seeleuthner, 2023, Cell.

Inhibition of Staphylococcus epidermidis Biofilm Formation by Rabbit Polyclonal Antibodies against the SesC Protein

P. Hermans, B. Stijlemans, J. van Eldere, 2009, Infection and Immunity.

Atypical Omenn Syndrome Due to RAG2 Gene Mutation, a Case Report.

N. Rezaei, S. Shokri, M. Shahrooei, 2019, Iranian journal of immunology : IJI.

Bacillus Calmette–Guérin (BCG)‐associated hemophagocytic lymphohistiocytosis in the setting of IFN‐γR1 deficiency: A diagnostic dilemma

N. Parvaneh, L. Parvaneh, M. Shahrooei, 2020, EJHaem.

Isolation and characterization of a resistance Bacillus subtilis for soil stabilization and dust alleviation purposes

Maryam Zakavi, Mohammad Shahrooei, Hossein Askari, 2024, Scientific reports.