Results 221 to 230 of about 128,250 (259)

HMGB1 Assists in Overcoming Cisplatin Resistance in Chemoresistant Human Ovarian Cancer Cells

Molecular Carcinogenesis, EarlyView.
ABSTRACT Cisplatin is one of the most effective chemotherapeutic agents used in the treatment of ovarian cancer. However, the frequent development of cisplatin resistance remains a significant limitation, leading to therapeutic failure and poor patient outcomes.
Van Huynh, Guliang Wang, Anirban Mukherjee, Karen M. Vasquez   +3 more
wiley   +1 more source

Dental Implants as a Treatment Option for Prosthetic Rehabilitation of Children with Ectodermal Dysplasia: A Systematic Review. [PDF]

Int J Clin Pediatr Dent
Barve KD, Padawe DS, Takate VS.
europepmc   +1 more source

New Technologies Empower Hemophilic Arthropathy Treatment: Focusing on Regenerative Medicine, Molecular Targeting, and Gene Therapy

Medicine Bulletin, EarlyView.
ABSTRACT Hemophilic arthropathy (HA), a major complication of hemophilia, is a chronic osteoarthropathy driven by repeated joint bleeding. Although traditional therapies such as coagulation factor replacement, physical rehabilitation, and surgery can manage symptoms, they cannot fundamentally repair established joint damage or break the pathological ...
Lin Sun, Yingnan Wang, Leyuan Zhao, Liqiang Lu, Fushan Hou, Chuan Yin, Kun Zhang, Yongqiang Hao, Jingke Fu   +8 more
wiley   +1 more source

Challenges in diagnosing diaphragmatic eventration in a neonate with Fryns syndrome and cleft palate. [PDF]

Radiol Case Rep
Imdadoglu T, Unal I, Yasar E, Alomari O, Guzel B, Boyaci E, Altuncu E.   +6 more
europepmc   +1 more source

Expanding the Genetic and Phenotypic Spectrum of DYT‐VPS16: The Importance of Splice‐Site Variants

Movement Disorders, EarlyView.
Abstract Background DYT‐VPS16, an early‐onset isolated dystonia caused by variants in the VPS16 gene, has been reported in fewer than 70 patients. Methods We explored the clinical and genotypic spectrum of DYT‐VPS16 by investigating early‐onset dystonia patients with VPS16 variants discovered in our large Biodatabank and through gene‐matching ...
Ana Westenberger, Edgard Verdura, Mandy Radefeldt, Leslie E. Sanderson, Kornelia Tripolszki, Anna Marcé‐Grau, Ana Cazurro‐Gutiérrez, Anita Nikoncuk, Rebecca Herzog, Ruslan Al‐Ali, Mariana Ferreira, Ligia S. Almeida, Tainá Regina Damaceno Silveira, Suliman Khan, Raphael Doyle Maia, Péter Klivényi, András Salamon, Volkan Baltaci, Asli Subasioglu, Jeanette Prada‐Arismendy, Goran Čuturilo, Sebastian Loens, Vera Tadic, Isabelle Maystadt, Deniz Karadurmus, Barbara Leube, Jonathan De Winter, Alice Monticelli, Liesbeth De Waele, Jonathan Baets, Mateja Vinkšel, Aleš Maver, Lorena Tschopp, Gabriela Ziegler, Ana Sanguinetti, Katja Lohmann, Tahsin Stefan Barakat, Peter Bauer, Belén Perez‐Dueñas, Aida M. Bertoli‐Avella   +39 more
wiley   +1 more source

Developmental system drift in the patterning of the arthropod tarsus

Klementz BC, Neu SM, Laumer EM, Setton EV, Hinne IA, Barnett AA, Hämmerle M, Brenneis G, Gulia-Nuss M, Sharma PP.   +9 more
europepmc   +1 more source

Multiple Onychopapillomas and BAP1 Tumor Predisposition Syndrome.

JAMA Dermatol
Lebensohn A, Ghafoor A, Bloomquist L, Royer MC, Castelo-Soccio L, Karacki K, Hathaway O, Maglo T, Wagner C, Agra MG, Blakely AM, Schrump DS, Hassan R, Cowen EW.   +13 more
europepmc   +1 more source

A missense mutation in the highly conserved TNF-like domain of Ectodysplasin A is the candidate causative variant for X-linked hypohidrotic ectodermal dysplasia in Limousin cattle: Clinical, histological, and molecular analyses. [PDF]

PLoS One
Krull F, Bleyer M, Schäfer J, Brenig B.
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

The Early Prostehtic Management Of Hypohidrotic And Anhidrotic Ectodermal Dysplasia: About Two Clinical Cases

Journal of Dental Reports, 2022
Ectodermal dysplasia is a hereditary disorder. Patients with ectodermal dysplasia have ectodermally-derived organs disorders which can affect teeth, nails, hair and sweat glands.
Nihel Charfi
semanticscholar   +1 more source

Malformations of the index nails

Clinical and Experimental Dermatology, 2009
We report a 52-year-old woman with micronychia of the index fingers. Radiographic examination revealed a Y-shaped bifurcation of the distal phalanx of both index fingers. She was diagnosed with congenital onychodysplasia of the index fingers (COIF) or Iso-Kikuchi syndrome.
T P, Hussein, H R C, Brandt, T V B, Gabbi, M M S, Nico   +3 more
openaire   +2 more sources